Jose Laffita Mesa

Publications
Public outreach and news

Articles

Article: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 2025;26(18):9213
Repeat Variants, Biomarkers, and Molecular Signatures in Parkinson's Disease: ATXN2, ATXN3, CACNA1A, PRNP, TBP, C9ORF72, TOMM40, APOE, and POLG-A Swedish Perspective
Laffita-Mesa JM; Paucar M; Svenningsson P
Article: MOVEMENT DISORDERS. 2025;40(4):672-682
An X-Linked Ataxia Syndrome in a Family with Hearing Loss Associated with a Novel Variant in the BCAP31 Gene
Paucar M; Li T; Bergendal A; Savitcheva I; Pourhamidi K; Laffita-Mesa JM; Nordgren A; Engvall M; Uhlen P; Lagerstedt-Robinson K; Svenningsson P
Article: MOVEMENT DISORDERS. 2025;40(2):363-369
The ZFHX3 GGC Repeat Expansion Underlying Spinocerebellar Ataxia Type 4 has a Common Ancestral Founder
Chen Z; Alvarez Jerez P; Anderson C; Paucar M; Lee J; Nilsson D; Macpherson H; Scardamaglia A; Montgomery K; Hardy J; Singleton AB; Tucci A; Mathews KD; Fu Y-H; Engvall M; Laffita-Mesa J; Nennesmo I; Wedell A; Ptacek LJ; Blauwendraat C; Gustavsson EK; Svenningsson P; Ryten M; Houlden H
Article: SCIENTIFIC REPORTS. 2025;15(1):2912
A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer disease
Ehn E; Eisfeldt J; Laffita-Mesa JM; Thonberg H; Schoumans J; Portaankorva AM; Viitanen M; Lindstrand A; Nennesemo I; Graff C
Article: ALZHEIMERS RESEARCH & THERAPY. 2024;16(1):207
Gene-variant specific effects of plasma amyloid-β levels in Swedish autosomal dominant Alzheimer disease
Johansson C; Thordardottir S; Laffita-Mesa J; Pannee J; Rodriguez-Vieitez E; Zetterberg H; Blennow K; Graff C
Article: JOURNAL OF INTERNAL MEDICINE. 2024;296(3):234-248
Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs
Paucar M; Nilsson D; Engvall M; Laffita-Mesa J; Soderhall C; Skorpil M; Halldin C; Fazio P; Lagerstedt-Robinson K; Solders G; Angeria M; Varrone A; Risling M; Jiao H; Nennesmo I; Wedell A; Svenningsson P
Article: JOURNAL OF THE NEUROLOGICAL SCIENCES. 2023;451:120707
Genetic screening for Huntington disease phenocopies in Sweden: A tertiary center case series focused on short tandem repeat (STR) disorders
Paucar M; Laffita-Mesa J; Niemela V; Malmgren H; Nennesmo I; Lagerstedt-Robinson K; Nordenskjold M; Svenningsson P
Article: BRAIN. 2023;146(3):1132-1140
Plasma biomarker profiles in autosomal dominant Alzheimer's disease
Johansson C; Thordardottir S; Laffita-Mesa J; Rodriguez-Vieitez E; Zetterberg H; Blennow K; Graff C
Article: EUROPEAN JOURNAL OF NEUROLOGY. 2022;29(12):3580-3589
APOE ε4 influences cognitive decline positively in APP and negatively in PSEN1 mutation carriers with autosomal-dominant Alzheimer's disease
Almkvist O; Johansson C; Laffita-Mesa J; Thordardottir S; Graff C
Article: JOURNAL OF NEUROLOGY. 2022;269(6):3037-3049
TBK1 haploinsufficiency results in changes in the K63-ubiquitination profiles in brain and fibroblasts from affected and presymptomatic mutation carriers
Khoshnood B; Ullgren A; Laffita-Mesa J; Oijerstedt L; Patra K; Nennesmo I; Graff C
Article: ACTA NEUROPATHOLOGICA COMMUNICATIONS. 2021;9(1):132
Single-cell multimodal analysis in a case with reduced penetrance of Progranulin-Frontotemporal Dementia
Natarajan K; Eisfeldt J; Hammond M; Laffita-Mesa JM; Patra K; Khoshnood B; Oijerstedt L; Graff C
Article: ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY. 2021;8(3):579-591
Plasma metabolomics of presymptomatic PSEN1-H163Y mutation carriers: a pilot study
Natarajan K; Ullgren A; Khoshnood B; Johansson C; Laffita-Mesa JM; Pannee J; Zetterberg H; Blennow K; Graff C
Article: MOVEMENT DISORDERS. 2021;36(2):508-514
A Novel Duplication inATXN2as Modifier for Spinocerebellar Ataxia 3 (SCA3) andC9ORF72-ALS
Laffita-Mesa JM; Nennesmo I; Paucar M; Svenningsson P
Article: PARKINSONISM & RELATED DISORDERS. 2020;79:135-137
Involuntary movements, vocalizations and cognitive decline
Sveinsson O; Udd B; Svenningsson P; Gassner C; Engstrom C; Laffita-Mesa J; Solders G; Hertegard S; Savitcheva I; Jung HH; Tolnay M; Frey BM; Paucar M
Article: PARKINSONISM & RELATED DISORDERS. 2018;:S1353-8020(18)30399-7
WITHDRAWN: Novel Xp21.1 deletion associated with unusual features in a large McLeod syndrome kindred.
Sveinsson O; Udd B; Svenningsson P; Gassner C; Engström C; Laffita-Mesa JM; Solders G; Hertegård S; Savitcheva I; Jung HH; Tolnay M; Frey BM; Paucar M
Journal article: CLINICAL GENETICS. 2018;94(3-4):346-350
Factors associated with ATXN2 CAG/CAA repeat intergenerational instability in Spinocerebellar ataxia type 2
Almaguer-Mederos LE; Mesa JML; Gonzalez-Zaldivar Y; Almaguer-Gotay D; Cuello-Almarales D; Aguilera-Rodriguez R; Falcon NS; Gispert S; Auburger G; Velazquez-Perez L
Article: CEREBELLUM. 2018;17(4):465-476
Novel Features and Abnormal Pattern of Cerebral Glucose Metabolism in Spinocerebellar Ataxia 19
Paucar M; Bergendal A; Gustavsson P; Nordenskjold M; Laffita-Mesa J; Savitcheva I; Svenningsson P
Article: JOURNAL OF PARKINSONS DISEASE. 2017;7(4):619-628
Correlations Between Methionine Cycle Metabolism, COMT Genotype, and Polyneuropathy in L-Dopa Treated Parkinson's Disease: A Preliminary Cross-Sectional Study
Andreasson M; Brodin L; Laffita-Mesa JM; Svenningsson P
Article: ARCHIVES OF MEDICAL RESEARCH. 2017;48(3):297-302
Buccal Cell Micronucleus Frequency Is Significantly Elevated in Patients with Spinocerebellar Ataxia Type 2
Cuello-Almarales DA; Almaguer-Mederos LE; Vazquez-Mojena Y; Almaguer-Gotay D; Zayas-Feria P; Laffita-Mesa JM; Gonzalez-Zaldivar Y; Aguilera-Rodriguez R; Rodriguez-Estupinan A; Velazquez-Perez L
Article: JOURNAL OF THE NEUROLOGICAL SCIENCES. 2017;372:324-328
Association of glutathione S-transferase omega polymorphism and spinocerebellar ataxia type 2
Almaguer-Mederos LE; Almaguer-Gotay D; Aguilera-Rodriguez R; Gonzalez-Zaldivar Y; Cuello-Almarales D; Laffita-Mesa J; Vazquez-Mojena Y; Zayas-Feria P; Rodriguez-Labrada R; Velazquez-Perez L; MacLeod P
Article: JOURNAL OF COMMUNITY GENETICS. 2015;6(3):265-273
SCA2 predictive testing in Cuba: challenging concepts and protocol evolution
Cruz-Marino T; Vazquez-Mojena Y; Velazquez-Perez L; Gonzalez-Zaldivar Y; Aguilera-Rodriguez R; Velazquez-Santos M; Estupinan-Rodriguez A; Miguel Laffita-Mesa J; Almaguer-Mederos LE; Paneque M
Article: CEREBELLUM AND ATAXIAS. 2015;2:1
Epidemiological, clinical, and molecular characterization of Cuban families with spinocerebellar ataxia type 3/Machado-Joseph disease.
González-Zaldívar Y; Vázquez-Mojena Y; Laffita-Mesa JM; Almaguer-Mederos LE; Rodríguez-Labrada R; Sánchez-Cruz G; Aguilera-Rodríguez R; Cruz-Mariño T; Canales-Ochoa N; MacLeod P; Velázquez-Pérez L
Journal article: IEEE MAGNETICS LETTERS. 2015;6:1-4
Single Point Gradiometer for Planetary Applications
Luis Mesa J; Diaz Michelena M; Ciudad D; Schoenthal W; McHenry ME; Maicas M; Aroca C
Journal article: ACTA CRYSTALLOGRAPHICA SECTION E: STRUCTURE REPORTS ONLINE. 2014;70(Pt 11):309-311
Crystal structure of (NH₄)₂[Fe^II₅(HPO₃)₆], a new open-framework phosphite
Berrocal T; Mesa JL; Larrea E; Arrieta JM
Article: BRAIN AND COGNITION. 2014;91:28-34
Executive deficit in spinocerebellar ataxia type 2 is related to expanded CAG repeats: Evidence from antisaccadic eye movements
Rodriguez-Labrada R; Velazquez-Perez L; Aguilera-Rodriguez R; Seifried-Oberschmidt C; Pena-Acosta A; Canales-Ochoa N; Medrano-Montero J; Estupinan-Rodriguez A; Vazquez-Mojena Y; Gonzalez-Zaldivar Y; Laffita Mesa JM
Article: CEREBELLUM. 2014;13(5):568-579
Comprehensive Study of Early Features in Spinocerebellar Ataxia 2: Delineating the Prodromal Stage of the Disease
Velazquez-Perez L; Rodriguez-Labrada R; Cruz-Rivas EM; Fernandez-Ruiz J; Vaca-Palomares I; Lilia-Campins J; Cisneros B; Pena-Acosta A; Vazquez-Mojena Y; Diaz R; Magana-Aguirre JJ; Cruz-Marino T; Estupinan-Rodriguez A; Laffita-Mesa JM; Gonzalez-Pina R; Canales-Ochoa N; Gonzalez-Zaldivar Y
Article: JOURNAL OF THE NEUROLOGICAL SCIENCES. 2014;341(1-2):41-45
Role of glutathione S-transferases in the spinocerebellar ataxia type 2 clinical phenotype
Almaguer-Gotay D; Almaguer-Mederos LE; Aguilera-Rodriguez R; Estupinan-Rodriguez A; Gonzalez-Zaldivar Y; Cuello-Almarales D; Laffita-Mesa JM; Vazquez-Mojena Y
Article: LANCET NEUROLOGY. 2014;13(5):482-489
Progression of early features of spinocerebellar ataxia type 2 in individuals at risk: a longitudinal study
Velazquez-Perez L; Rodriguez-Labrada R; Canales-Ochoa N; Medrano Montero J; Sanchez-Cruz G; Aguilera-Rodriguez R; Almaguer-Mederos LE; Laffita-Mesa JM
Article: JOURNAL OF GENETIC COUNSELING. 2014;23(1):89-96
Large Normal and Intermediate Alleles in the Context of SCA2 Prenatal Diagnosis
Cruz-Marino T; Miguel Laffita-Mesa J; Gonzalez-Zaldivar Y; Velazquez-Santos M; Aguilera-Rodriguez R; Estupinan-Rodriguez A; Vazquez-Mojena Y; Macleod P; Paneque M; Velazquez-Perez L
Article: JOURNAL OF THE NEUROLOGICAL SCIENCES. 2013;335(1-2):101-104
Genetic features of Huntington disease in Cuban population: Implications for phenotype, epidemiology and predictive testing
Vazquez-Mojena Y; Laguna-Salvia L; Laffita-Mesa JM; Gonzalez-Zaldivar Y; Almaguer-Mederos LE; Rodriguez-Labrada R; Almaguer-Gotay D; Zayas-Feria P; Velazquez-Perez L
Article: JOURNAL OF COMMUNITY GENETICS. 2013;4(4):451-460
Couples at risk for spinocerebellar ataxia type 2: the Cuban prenatal diagnosis experience
Cruz-Marino T; Velazquez-Perez L; Gonzalez-Zaldivar Y; Aguilera-Rodriguez R; Velazquez-Santos M; Vazquez-Mojena Y; Estupinan-Rodriguez A; Reynaldo-Arminan R; Enrique Almaguer-Mederos L; Miguel Laffita-Mesa J; Tamayo-Chiang V; Paneque M
Article: PLOS ONE. 2013;8(8):e70560
De Novo Mutations in Ataxin-2 Gene and ALS Risk
Miguel Laffita-Mesa J; Rodriguez Pupo JM; Moreno Sera R; Vazquez Mojena Y; Kouri V; Laguna-Salvia L; Martinez-Godales M; Valdevila Figueira JA; Bauer PO; Rodriguez-Labrada R; Gonzalez Zaldivar Y; Paucar M; Svenningsson P; Velazquez Perez L
Article: CLINICAL GENETICS. 2013;83(6):518-524
The Cuban program for predictive testing of SCA2: 11 years and 768 individuals to learn from
Cruz-Marino T; Velazquez-Perez L; Gonzalez-Zaldivar Y; Aguilera-Rodriguez R; Velazquez-Santos M; Vazquez-Mojena Y; Estupinan-Rodriguez A; Laffita-Mesa JM; Reynaldo-Arminan R; Almaguer-Mederos LE; Paneque M
Journal article: ISRN DENTISTRY. 2013;2013(1):1-5
Cuban Adolescents Requesting Presymptomatic Testing for Spinocerebellar Ataxia Type 2
Cruz-Mariño T; Velázquez-Pérez L; González-Zaldivar Y; Aguilera-Rodríguez R; Velázquez-Santos M; Vázquez-Mojena Y; Estupiñán-Rodríguez A; Laffita-Mesa JM; Reynaldo-Armiñán R; Almaguer-Mederos LE; Paneque M
Article: HUMAN GENETICS. 2012;131(4):625-638
Epigenetics DNA methylation in the core ataxin-2 gene promoter: novel physiological and pathological implications
Miguel Laffita-Mesa J; Bauer PO; Kouri V; Pena Serrano L; Roskams J; Almaguer Gotay D; Montes Brown JC; Martinez Rodriguez PA; Gonzalez-Zaldivar Y; Almaguer Mederos L; Cuello-Almarales D; Aguiar Santiago J
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2012;20(1):41-49
Unexpanded and intermediate CAG polymorphisms at the SCA2 locus (ATXN2) in the Cuban population: evidence about the origin of expanded SCA2 alleles
Miguel Laffita-Mesa J; Velazquez-Perez LC; Santos Falcon N; Cruz-Marino T; Gonzalez Zaldivar Y; Vazquez Mojena Y; Almaguer-Gotay D; Almaguer Mederos LE; Rodriguez Labrada R
Article: NEUROCHEMICAL RESEARCH. 2011;36(10):1793-1800
Oral Zinc Sulphate Supplementation for Six Months in SCA2 Patients: A Randomized, Double-Blind, Placebo-Controlled Trial
Velazquez-Perez L; Rodriguez-Chanfrau J; Cesar Garcia-Rodriguez J; Sanchez-Cruz G; Aguilera-Rodriguez R; Rodriguez-Labrada R; Cesar Rodriguez-Diaz J; Canales-Ochoa N; Almaguer Gotay D; Almaguer Mederos LE; Laffita Mesa JM; Porto-Verdecia M; Gonzalez Triana C; Rodriguez Pupo N; Hidalgo Batista I; Lopez-Hernandez OD; Diaz Polanco I; Jayme Novas A
Article: JOURNAL OF THE NEUROLOGICAL SCIENCES. 2011;306(1-2):103-107
Saccadic latency is prolonged in Spinocerebellar Ataxia type 2 and correlates with the frontal-executive dysfunctions
Rodriguez-Labrada R; Velazquez-Perez L; Seigfried C; Canales-Ochoa N; Auburger G; Medrano-Montero J; Sanchez-Cruz G; Aguilera-Rodriguez R; Laffita-Mesa J; Vazquez-Mojena Y; Verdecia-Ramirez M; Motta M; Quevedo-Batista Y
Article: JOURNAL OF GENETIC COUNSELING. 2011;20(3):241-248
Ethical Dilemmas in Genetic Testing: Examples from the Cuban Program for Predictive Diagnosis of Hereditary Ataxias
Cruz Marino T; Reynaldo Arminan R; Jorge Cedeno H; Laffita Mesa JM; Gonzalez Zaldivar Y; Aguilera Rodriguez R; Velazquez Santos M; Almaguer Mederos LE; Herrera MP; Velazquez Perez L
Article: MOVEMENT DISORDERS. 2011;26(2):347-350
Subtle Rapid Eye Movement Sleep Abnormalities in Presymptomatic Spinocerebellar Ataxia Type 2 Gene Carriers
Rodriguez-Labrada R; Velazquez-Perez L; Canales Ochoa N; Galicia Polo L; Haro Valencia R; Sanchez Cruz G; Medrano Montero J; Laffita-Mesa JM; Almaguer Mederos LE; Gonzalez Zaldivar Y; Torres Parra C; Pena Acosta A; Cruz Marino T
Journal article: ENDOSCOPY. 2011;43:E206-E207
Malignant fibrous histiocytoma of the small bowel with colon metastasis
Villa Jimenez OM; Hernandez Garces HR; Ruenes Domech C; Hano Garcia OM; Quintero Cayola S; Guerra Mesa JL; Perez Triana F; Wood Rodriguez L
Article: NEURODEGENERATIVE DISEASES. 2011;8(6):447-454
Sleep Disorders in Spinocerebellar Ataxia Type 2 Patients
Velazquez-Perez L; Voss U; Rodriguez-Labrada R; Auburger G; Canales Ochoa N; Sanchez Cruz G; Galicia Polo L; Haro Valencia R; Aguilera Rodriguez R; Medrano Montero J; Laffita Mesa JM; Tuin I
Article: CLINICAL GENETICS. 2010;78(2):169-174
Estimation of the age at onset in spinocerebellar ataxia type 2 Cuban patients by survival analysis
Almaguer-Mederos LE; Falcon NS; Almira YR; Zaldivar YG; Almarales DC; Gongora EM; Herrera MP; Batallan KE; Arminan RR; Manresa MV; Cruz GS; Laffita-Mesa J; Cyuz TM; Chang V; Auburger G; Gispert S; Perez LV
Article: NEUROSCIENCE LETTERS. 2010;472(2):85-89
Uncommon features in Cuban families affected with Friedreich ataxia
Cruz-Marino T; Gonzalez-Zaldivar Y; Miguel Laffita-Mesa J; Almaguer-Mederos L; Aguilera-Rodriguez R; Almaguer-Gotay D; Rodriguez-Labrada R; Canales-Ochoa N; MacLeod P; Velazquez-Perez L
Journal article: SLEEP MEDICINE. 2009;10:S15
053 CLINICAL AND POLYSOMNOGRAPH EVALUATION OF SLEEP DISORDERS IN SCA2 PATIENTS: A PHENOTYPICAL AND MOLECULAR CORRELATION
Velazquez-Perez L; Rodriguez-Labrada R; Tuin I; Galicia-Polo L; Canales-Ochoa N; Sanchez-Cruz G; Haro-Valencia R; Laffita-Mesa J; Auburger G
Article: NEUROSCIENCE LETTERS. 2009;454(2):157-160
Molecular epidemiology of spinocerebellar ataxias in Cuba: Insights into SCA2 founder effect in Holguin
Velazquez Perez L; Sanchez Cruz G; Santos Falcon N; Almaguer Mederos LE; Escalona Batallan K; Rodriguez Labrada R; Paneque Herrera M; Laffita Mesa JM; Rodriguez Diaz JC; Aguilera Rodriguez R; Gonzalez Zaldivar Y; Coello Almarales D; Almaguer Gotay D; Jorge Cedeno H
Article: CLINICAL NEUROPHYSIOLOGY. 2009;120(3):632-635
Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2
Velazquez-Perez L; Seifried C; Abele M; Wirjatijasa F; Rodriguez-Labrada R; Santos-Falcon N; Sanchez-Cruz G; Almaguer-Mederos L; Tejeda R; Canales-Ochoa N; Fetter M; Ziemann U; Klockgether T; Medrano-Montero J; Rodriguez-Diaz J; Laffita-Mesa JM; Auburger G
Journal article: CLINICAL NEUROPHYSIOLOGY. 2008;119:S173
Age at onset in spinocerebellar ataxia type 2 Cuban patients is affected by junctophilin-3 CTG repeat polymorphism
Mederos LEA; Zaldívar YG; Almarales DC; Gotay DA; Mesa JL; Santiago JA; Aguilera R; Cruz GS; Auburger G; Gispert S; Pérez LV
Journal article: JOURNAL OF ENDOCRINOLOGY. 2008;198(2):367-374
Prolonged interleukin-6 administration enhances glucose tolerance and increases skeletal muscle PPARα and UCP2 expression in rats
Holmes AG; Mesa JL; Neill BA; Chung J; Carey AL; Steinberg GR; Kemp BE; Southgate RJ; Lancaster GI; Bruce CR; Watt MJ; Febbraio MA
Journal article: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 2008;105(5):1739-1744
HSP72 protects against obesity-induced insulin resistance
Chung J; Nguyen A-K; Henstridge DC; Holmes AG; Chan MHS; Mesa JL; Lancaster GI; Southgate RJ; Bruce CR; Duffy SJ; Horvath I; Mestril R; Watt MJ; Hooper PL; Kingwell BA; Vigh L; Hevener A; Febbraio MA
Article: JOURNAL OF THE NEUROLOGICAL SCIENCES. 2007;263(1-2):158-164
Electrophysiological features in patients and presymptomatic relatives with spinocerebellar ataxia type 2.
Velázquez Pérez L; Sánchez Cruz G; Canales Ochoa N; Rodríguez Labrada R; Rodríguez Díaz J; Almaguer Mederos L; Laffita Mesa J
Article: AMERICAN JOURNAL OF HUMAN BIOLOGY. 2007;19(6):801-808
Cardiovascular fitness in adolescents:: The influence of sexual maturation status-the AVENA and EYHS studies
Ortega FB; Ruiz JR; Mesa JL; Gutierrez A; Sjostrom M
Article: REVISTA ESPANOLA DE CARDIOLOGIA. 2007;60(6):581-588
Lipid and metabolic profiles in adolescents are affected more by physical fitness than physical activity (AVENA study)
Garcia-Artero E; Ortega FB; Ruiz JR; Mesa JL; Delgado M; Gonzalez-Gross M; Garcia-Fuentes M; Vicente-Rodriguez G; Gutierrez A; Castillo MJ
Article: OBESITY. 2007;15(6):1589-1599
Cardiorespiratory fitness and sedentary activities are associated with adiposity in adolescents
Ortega FB; Tresaco B; Ruiz JR; Moreno LA; Martin-Matillas M; Mesa JL; Warnberg J; Bueno M; Tercedor P; Gutierrez A; Castillo MJ
Journal article: DIABETES. 2007;56(3):884-889
Lamin A/C polymorphisms, type 2 diabetes, and the metabolic syndrome - Case-control and quantitative trait studies
Mesa JL; Loos RJF; Franks PW; Ong KK; Luan J; O'Rahilly S; Wareham NJ; Barroso I
Journal article: NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES. 2007;17(2):104-124
Gene-lifestyle interaction on risk of type 2 diabetes
Franks PW; Mesa J-L; Harding AH; Wareham NJ
Article: HORMONE AND METABOLIC RESEARCH. 2006;38(12):832-837
Serum lipids, body mass index and waist circumference during pubertal development in Spanish adolescents:: The AVENA study
Ruiz JR; Ortega FB; Tresaco B; Warnberg J; Mesa JL; Gonzalez-Gross M; Moreno LA; Marcos A; Gutierrez A; Castillo MJ
Journal article: ZEITSCHRIFT FUR GESUNDHEITSWISSENSCHAFTEN. 2006;14(3):178-180
The importance of cardiorespiratory fitness for healthy metabolic traits in children and adolescents: the AVENA Study
Mesa JL; Ortega FB; Ruiz JR; Castillo MJ; Hurtig-Wennlof A; Sjostrom M; Gutierrez A
Article: NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES. 2006;16(4):285-293
Aerobic physical fitness in relation to blood lipids and fasting glycaemia in adolescents:: Influence of weight status
Mesa JL; Ruiz JR; Ortega FB; Warnberg J; Gonzalez-Lamuno D; Moreno LA; Gutierrez A; Castillo MJ
Article: ANNALS OF NUTRITION AND METABOLISM. 2006;50(6):519-527
Anthropometric determinants of a clustering of lipid-related metabolic risk factors in overweight and non-overweight adolescents influence of cardiorespiratory fitness -: The AVENA study
Mesa JL; Ortega FB; Ruiz JR; Castillo MJ; Tresaco B; Carreno F; Moreno LA; Gutierrez A; Bueno M
Journal article: AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM. 2004;287(1):E120-E127
Reduced plasma FFA availability increases net triacylglycerol degradation, but not GPAT or HSL activity, in human skeletal muscle
Watt MJ; Holmes AG; Steinberg GR; Mesa JL; Kemp BE; Febbraio MA
Article: REVISTA ESPANOLA DE CARDIOLOGIA. 2004;57(6):499-506
Sports requiring stressful physical exertion cause abnormalities in plasma lipid profile
Ruiz JR; Mesa JLM; Mingorance I; Rodríguez-Cuartero A; Castillo MJ
Article: JOURNAL OF SPORTS MEDICINE AND PHYSICAL FITNESS. 2003;43(4):554-558
Acute exposure to moderate high altitude decreases growth hormone response to physical exercise in untrained subjects
Gutiérrez A; González-Gross M; Ruiz JR; Mesa JLM; Castillo MJ
Article: INTERNATIONAL JOURNAL OF SPORTS MEDICINE. 2003;24(7):518-522
Sauna-induced rapid weight loss decreases explosive power in women but not in men
Gutiérrez A; Mesa JLM; Ruiz JR; Chirosa LJ; Castillo MJ
Article: JOURNAL OF HAND SURGERY-AMERICAN VOLUME. 2002;27A(5):897-901
Hand size influences optimal grip span in women but not in men
Ruiz-Ruiz J; Mesa JLM; Gutiérrez A; Castillo MJ
Article: ARCHIVOS LATINOAMERICANOS DE NUTRICION. 2001;51(4):321-331
Nutrition and sport practice. Adaptation of the food guide pyramid to the characteristics of sport diet.
González-Gross M; Gutiérrez A; Mesa JL; Ruiz-Ruiz J; Castillo MJ
Journal article: REVISTA DE NEUROLOGIA. 1999;28(7):726-728
Multiple progressive occlusions of intracranial arteries
Jover M; García JM; Mesa JM; Gata JM; Izquierdo G
Journal article: ITE JOURNAL-INSTITUTE OF TRANSPORTATION ENGINEERS. 1997;67(7):9-10
Beyond CMS implementation - Providing a context for project prioritization and programming
McLeod D; Sanderson M; DeArazoza R; Mesa JL
Journal article: POLYHEDRON. 1991;10(23-24):2725-2728
FERROMAGNETIC EXCHANGE INTERACTIONS IN 2 NEW BINUCLEAR NICKEL(II) COMPLEXES - [NI(PYMEP)(X)2]2.NH2O (X = N3, NCS, N = 2,0, PYMEP = N-(6-METHYL-2-PYRIDYLMETHYLENE)-2-(2-PYRIDYL) ETHYLAMINE)
ROJO T; CORTES R; LARRAMENDI JIR; LEZAMA L; MESA JL
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All other publications

Corrigendum: SCIENTIFIC REPORTS. 2025;15(1):10121
A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer disease (vol 15, 2912, 2025)
Ehn E; Eisfeldt J; Laffita-Mesa JM; Thonberg H; Schoumans J; Portaankorva AM; Viitanen M; Lindstrand A; Nennesmo I; Graff C
Letter: MOVEMENT DISORDERS. 2024;39(6):1077
Comment to: "SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies"
Paucar M; Nilsson D; Engvall M; Laffita-Mesa J; Wedell A; Svenningsson P
Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2023;31:469
A complex chromosome 21 rearrangement causes APP triplication and autosomal dominant early onset Alzheimer disease
Ehn E; Eisfeldt J; Thonberg H; Laffita J; Schoumans J; Remes A; Viitanen M; Lindstrand A; Nennesemo I; Graff C
Editorial: NEURAL REGENERATION RESEARCH. 2022;17(11):2445-2447
Are ATXN2 variants modifying our understanding about neural pathogenesis, phenotypes, and diagnostic?
Laffita-Mesa JM; Paucar M; Svenningsson P
Review: CURRENT OPINION IN NEUROLOGY. 2021;34(4):578-588
Ataxin-2 gene: a powerful modulator of neurological disorders
Laffita-Mesa JM; Paucar M; Svenningsson P
Conference publication: MOVEMENT DISORDERS. 2019;34:S183
The potential modifier effect of C9orf72 DNA methylation in C9ORF72 carriers
Laffita-Mesa JM; Kreidy C; Paucar M; Svenningsson P
Conference publication: MOVEMENT DISORDERS. 2019;34:S106
Ataxin-2 gene in the Cuban population: Mutagenesis and epigenetic DNA methylation disease influencing phenotype
Laffita-Mesa J; Perez LV
Editorial: NEUROLOGY. 2018;91(15):710-712
Chorea, psychosis, acanthocytosis, and prolonged survival associated with ELAC2 mutations
Paucar M; Pajak A; Freyer C; Bergendal A; Dory M; Laffita-Mesa JM; Stranneheim H; Lagerstedt-Robinson K; Savitcheva I; Walker RH; Wedell A; Wredenberg A; Svenningsson P
Conference publication: MOVEMENT DISORDERS. 2018;33:S97-S98
Nucleotide Repeats as Genetic Risk Factors in a Swedish Parkinson's Disease Cohort
Laffita-Mesa J; Brodin L; Svenningsson P
Conference publication: MOVEMENT DISORDERS. 2018;33:S98
(Epi)-genetic Alterations in c9orf72 and ATXN2: Gene Partners in ALS/FTD, Spinocerebellar Ataxias and in Parkinson Disease
Laffita-Mesa J; Svenningsson P
Conference publication: MOVEMENT DISORDERS. 2018;33:S16
Ataxin-2 Gene in the Cuban Population: Mutagenesis and Epigenetic DNA Methylation Influencing Disease Phenotype
Laffita-Mesa J; Velazquez-Perez L
Conference publication: MOVEMENT DISORDERS. 2018;33:S14-S15
Nuclear Anomalies and Genetic Polymorphism Associated to Patients with Spinocerebellar Ataxia Type 2
Cuello-Almarales D; Almaguer-Mederos L; Vazquez-Mojena Y; Almaguer-Gotay D; Zayas-Feria P; Laffita-Mesa J; Gonzalez-Zaldivar Y; Aguilera-Rodriguez R; Rodriguez-Estupinan A; Velazquez-Perez L
Review: MOVEMENT DISORDERS. 2017;32(5):708-718
Prodromal Spinocerebellar Ataxia Type 2: Prospects for Early Interventions and Ethical Challenges
Velazquez-Perez L; Rodriguez-Labrada R; Miguel Laffita-Mesa J
Conference publication: EUROPEAN CHILD & ADOLESCENT PSYCHIATRY. 2015;24:S234-S235
Arachnoid cyst and child psychiatric disorders. A case report
Sanchez Lorenzo I; Mora Mesa J
Review: MEDICINA CLINICA. 2014;143(8):360-365
Epigenetic heredity (deoxyribonucleic acid methylation): Clinical context in neurodegenerative disorders and ATXN2 gene
Miguel Laffita-Mesa J; Bauer P
Letter: CLINICAL GENETICS. 2014;86(1):96-98
Large normal alleles and SCA2 prevalence: lessons from a nationwide study and analysis of the literature
Laffita-Mesa JM; Almaguer-Mederos LE; Kouri V; Bauer PO; Vazquez-Mojena Y; Cruz Marino T; Velazquez-Perez L
Conference publication: JOURNAL OF APPLIED PHYSICS. 2014;115(17):17a934
Synthesis and magnetic properties of single phase titanomagnetites
Schoenthal W; Liu X; Cox T; Mesa JL; Maicas M; Diaz-Michelena M; Laughlin DE; McHenry ME
Conference publication: MOVEMENT DISORDERS. 2014;29:S475
De novo mutations in ataxin-2 gene, ALS risk and meta-analysis
Laffita-Mesa JM; Rodriguez Pupo JM; Moreno Sera R; Vazquez Mojena Y; Kouri V; Laguna-Salvia L; Martinez-Godales M; Valdevila Figueira JA; Bauer PO; Rodriguez-Labrada R; Gonzalez Zaldivar Y; Paucar M; Svenningsson P; Velazquez Perez LC
Conference publication: MOVEMENT DISORDERS. 2013;28:S247
Cuban families with spinocerebellar ataxia type 7
Gonzalez-Zaldivar Y; Vazquez-Mojena Y; Aguilera-Rodriguez R; Velazquez-Perez LC; Zaldivar-Vaillan T; Castro-Lopez M; Landa-Muniz M; Rodriguez-Labrada R; Cruz-Marino T; Sanchez-Cruz G; Canales-Ochoa N; Cuello-Almarales DA; Almaguer-Mederos LE; Laffita-Mesa JM
Conference publication: MOVEMENT DISORDERS. 2013;28:S243-S245
Mutated ATXN2 gene expression and changes in cellularity of cerebellar Purkinje cells are associated with specific ultra structure disruptions
Cuello-Almarales DA; Aguiar-Santiago JA; Fernandez-Masso JR; Vazquez MM; Mendosa-Mari I; Velazquez-Perez LC; Almaguer-Mederos LE; Laffita-Mesa JM; Amaguer-Gotay D; Garcia JC
Conference publication: MOVEMENT DISORDERS. 2013;28:S242-S243
Antioxidant status of superoxide dismutase/catalase enzymatic system modifies the clinic progression in spinocerebellar ataxia type 2 Cuban patients
Almaguer-Gotay D; Aguilera-Rodriguez R; Rodriguez-Labrada R; Velazquez-Perez LC; Gonzalez-Triana C; Almaguer-Mederos LE; Estupinan-Dominguez A; Cuellos-Almarales DA; Laffita-Mesa JM; Gonzalez-Zaldivar Y; Vazquez-Mojena Y
Conference publication: MOVEMENT DISORDERS. 2013;28:S236
Preclinical features of spinocerebellar ataxia type 2: Insight into early pathological effects of CAG expansion
Velazquez-Perez L; Rodriguez-Labrada R; Canales-Ochoa N; Cruz Marino T; Laffita-Mesa JM; Fernandez-Ruiz J; Diaz R; Galicia-Polo L; Haro-Valencia R; Moreno-Masmela S; Medrano-Montero J; Cruz-Rivas E
Conference publication: MOVEMENT DISORDERS. 2013;28:S237
No co-segregation of periodic legs movements/restless legs syndrome and spinocerebellar ataxia type 2: Premilinary evidences
Vazquez-Mojena Y; Velazquez-Perez LC; Laffita-Mesa JM; Rodriguez-Labrada R; Canales-Ochoa N; Pena Acosta A; Gonzalez-Zaldiva Y
Letter: CLINICAL GENETICS. 2013;83(3):293-294
Estimation of survival in Spinocerebellar Ataxia type 2 Cuban patients
Almaguer-Mederos LE; Aguilera Rodriguez R; Gonzalez Zaldivar Y; Almaguer Gotay D; Cuello Almarales D; Laffita Mesa J; Vazquez Mojena Y; Zayas Feria P; Auburger G; Gispert S; Velasquez Perez L
Conference publication: MOVEMENT DISORDERS. 2012;27:S487
Epigenetics and ataxin-2 locus
Laffita-Mesa JM; Bauer P; Kouri V; Pena Serrano L; Roskams J; Almaguer-Gotay D; Aguiar Santiago J; Gonzalez-Zaldivar Y; Velazquez-Perez LC; Montes Brown J
Conference publication: MOVEMENT DISORDERS. 2012;27:S486-S487
The contribution of the self PolyQ load [somatic mosaicism] in the CNS to the onset, disease duration and progression rate of SCA2 and phenotypic delineation
Laffita-Mesa JM; Vazquez Mojena Y; Cuello Almarales DA; Velazquez-Perez LC
Conference publication: MOVEMENT DISORDERS. 2012;27:S460
CAG analysis, haplotypes, unstable repeats, recombination, pedigrees, gene dosage, genotype-phenotype relationship and genetics polymorphisms in the SCA2 (ATXN2) locus
Laffita-Mesa JM; Velazquez-Perez LC; Vazquez Mojena Y; Kouri V; Martinez A; Miranda A; Pena Serrano L; Cuello Almarales DA; Aguilera Rodriguez R; Berovides V
Conference publication: MOVEMENT DISORDERS. 2012;27:S447
Intergenerational instability and genetic flow of the CAG repeat at the ATXN2 gene in Cuban families with spinocerebellar ataxia type 2
Almaguer-Mederos LE; Gonzalez-Zaldivar Y; Almaguer-Gotay D; Laffita-Mesa JM; Mejias-Brito S; Cuello-Almarales D
Conference publication: MOVEMENT DISORDERS. 2012;27:S197
Frontal-executive dysfunctions precede cerebellar syndrome in spinocerebellar ataxia type 2
Velazquez-Perez L; Rodriguez-Labrada R; Aguilera-Rodriguez R; Estupinan-Rodriguez A; Cruz-Marino T; Canales-Ochoa N; Laffita-Mesa JM; Rodriguez Diaz JC
Conference publication: MOVEMENT DISORDERS. 2012;27:S180-S181
Are Cuban ATXN2 large normal alleles prone to expand? Implications for the prenatal testing program
Cruz-Marino T; Laffita-Mesa JM; Velazquez-Santos M; Aquilera-Rodriguez R; Estupinan-Rodriguez A; Gonzalez-Zaldivar Y; Vazquez-Mojena Y; Velazquez-Perez LC
Conference publication: MOVEMENT DISORDERS. 2012;27:S183
First families diagnosed with Machado Joseph disease/SCA3 in Cuban population
Gonzalez-Zaldivar Y; Almaguer-Mederos LE; Laffita-Mesa JM; Vazquez-Mojena Y; Sanchez-Cruz G; Cruz-Marino T; Cuello Almarales DA; Almaguer-Gotay D; Aguilera-Rodriguez R; Estupinan-Rodriguez A; Rodriguez-Labrada R; Canales-Ochoa N; Velazquez-Perez LC
Conference publication: MOVEMENT DISORDERS. 2012;27:S181
Buccal cell micronucleus frequency is significantly increased in Cuban patients with spinocerebellar ataxia type 2
Cuello-Almarales DA; Almaguer-Mederos LE; Vazquez-Mojena Y; Almaguer-Gotay D; Laffita-Mesa JM; Aguilera-Rodriguez R; Zayas-Feria P; Gonzalez-Zaldivar Y; Rodriguez-Estupinan A
Conference publication: MOVEMENT DISORDERS. 2012;27:S179
Somatic mosaicism in SCA2 linked with decreased antioxidant defense. Ataxin-2 polyQ load underlies the antioxidative impairment in SCA2
Almaguer-Gotay D; Laffita-Mesa JM; Gonzalez-Zaldivar Y; Almaguer-Mederos LE; Sanchez-Cruz G; Mejias-Brito S; Velazquez-Perez LC
Conference publication: MOVEMENT DISORDERS. 2012;27:S61
Molecular analysis of Huntington's disease in a Cuban population
Vazquez-Mojena Y; Laffita-Mesa JM; Laguna-Salvia L; Gonzalez-Zaldivar Y; Almaguer-Gotay D; Zayas-Feria P; Almaguer-Mederos LE; Rodriguez-Labrada R; Velazquez-Perez L
Conference publication: MOVEMENT DISORDERS. 2012;27:S3
Epidemiology and age at onset analysis of Parkinson's disease in the eastern region of Cuba (Holguin)
Laguna-Salvia L; Valdevila-Figueira JA; Laffita-Mesa JM
Book chapter: GENOMICS AND HEALTH IN THE DEVELOPING WORLD. 2012;p. 1244-1253
. Hereditary Ataxias in Cuba
Velázquez-Pérez L; Laffita-Mesa JM; Rodríguez-Labrada R
Review: CEREBELLUM. 2011;10(2):184-198
A Comprehensive Review of Spinocerebellar Ataxia Type 2 in Cuba
Velazquez-Perez L; Rodriguez-Labrada R; Cesar Garcia-Rodriguez J; Enrique Almaguer-Mederos L; Cruz-Marino T; Miguel Laffita-Mesa J
Conference publication: MOVEMENT DISORDERS. 2011;26:S340
Population study of (CAG/CAA)n allele variation in the TATA box-binding protein and ATXN2-TBP mutations in a familiy with typical Parkinson
Laffita-Mesa JM; Vazquez Mojena Y; Laguna Salvia L; Velazquez Perez LC; Verdecia Ramirez M; Valdevila Figueira JA; Cruz Marino T; Rodriguez Labrada R
Conference publication: MOVEMENT DISORDERS. 2011;26:S7
The contribution of the self PolyQ load [somatic mosaicism] in the CNS to the onset, disease duration and progression rate of SCA2
Laffita-Mesa JM; Vazquez Mojena Y; Coello Almarales DA; Velazquez Perez LC
Conference publication: MOVEMENT DISORDERS. 2011;26:S6-S7
Delineating the de novo methylation pattern of the ataxin-2 promoter
Laffita-Mesa JM; Almaguer Gotay D; Pena-Serrano L; Peter BO; Coello Almarales DA; Kouri V
Conference publication: MOVEMENT DISORDERS. 2011;26:S3
Friedreich ataxia gene in Cuban population
Cruz-Marino T; Gonzalez-Zaldivar Y; Laffita-Mesa JM; Almaguer-Mederos LE; Aguilera-Rodriguez R; Alaguer-Gotay D; Rodriguez-Labrada R; Rodriguez-Labrada R; Canales-Ochoa N; MacLeod P; Velazquez-Perez L
Conference publication: MOVEMENT DISORDERS. 2011;26:S1
Genetic, biochemical and genotoxicity investigations on Cuban families affected by spinocerebellar ataxia type 2
Almaguer-Mederos LE; Aguilera-Rodriguez R; Gonzalez Zaldivar Y; Almaguer-Gotay D; Cuello-Almarales D; Alvarez Sosa A; Laffita-Mesa J; Sanchez Cruz G; Montes-Brown J; Mejias Brito S; Avila Avila G; Vazquez-Mojena Y; Zayas-Feria P; Estupinan-Rodriguez A; Bahr-Valcarcel P; Aguiar-Santiago J; Auburger G
Letter: CLINICAL GENETICS. 2010;77(6):598-600
Low predisposition to instability of the Friedreich ataxia gene in Cuban population
Marino TC; Zaldivar YG; Mesa JML; Mederos LA; Rodriguez RA; Gotay DA; Labrada RR; Ochoa NC; MacLeod P; Perez LV
Conference publication: MOVEMENT DISORDERS. 2010;25(7):S200
An integrative characterization of SCA2 in Cuba: Epidemiological, genetic neurochemical and electrophysiological findings in 7 926 Cuban carriers
Velazquez-Perez L; Sanchez-Cruz G; Conzalez Y; Herrera-Paneque M; Rodriguez-Diaz J; Rodriguez-Labrada R; Laffita-Mesa JM; Almaguer-Mederos L; Aguilera R; Canales-Ochoa N; Garcia JC; Medranao J
Conference publication: MOVEMENT DISORDERS. 2010;25(7):S199
Loss of CAA interruption in large normal alleles ATX2 is a risk factor to SCA2 gene instability: A haplotype and sequence based study in large Cuban kindreds
Laffita-Mesa JM; Velazquez-Perez L; Auburger G; Susan O; Gilberto S; Santos N; Almaguer L; Nay C; Gonzalez Y; Santiago AJ
Conference publication: MOVEMENT DISORDERS. 2010;25(7):S193-S194
Large normal polyQ runs underlies the highest prevalence of SCA2 in Cuba
Laffita-Mesa JM; Velazquez LC; Gonzalez Y; Vazquez YA; Gotay D; Cruz-Marino T; Rodriguez Y; Almaguer LE; Santos N; Sanchez G; Cuello D; Rodriguez R; Pena A; Paneque M; Rodriguez R
Conference publication: PARKINSONISM & RELATED DISORDERS. 2009;15:S157
The Cuban pathological CAG mutation causing SCA2 was introduced between 1408CE and 1733CE in the Cuban population
Laffita-Mesa J; Velasquez-Perez L; Auburger G; Gispert S; Serrano L; Sanchez-Cruz G
Conference publication: PARKINSONISM & RELATED DISORDERS. 2009;15:S157
Loss of CAA interruption in large SCA2 alleles is a risk factor to ATX2 gene instability
Laffita-Mesa J; Velasquez-Perez L; Auburger G; Gispert S; Pena-Serrano L; Sanchez-Cruz G; Santos N; Santiago J
Conference publication: EUROPEAN JOURNAL OF NEUROLOGY. 2009;16:291
Loss of CAA interruption in large SCA2 alleles is a risk factor to ATX2 gene instability
Perez LV; Laffita-Mesa J
Conference publication: JOURNAL OF NEUROLOGY. 2009;256:S154
Are the somatic mosaicisms of the CAG repeat expansions in similar Machado-Joseph disease/SCA3 and SCA2 patients?
Laffita-Mesa JM; Gonzalez-Zaldivar Y; Pena-Serrano L; Almaguer-Mederos L; Velazquez-Perez L
Conference publication: JOURNAL OF NEUROLOGY. 2009;256:S154
The Cuban pathological CAG mutation causing SCA2 was introduced by Hispanics and probably originated between 1408 and 1733 in the Cuban population
Laffita-Mesa JM; Velaquez-Perez L; Auburger G; Gispert S; Pena-Serrano L; Sanchez-Cruz G; Rodriguez-Labrada R; Cuello D
Conference publication: JOURNAL OF NEUROLOGY. 2009;256:S139
Sleep pathology in SCA2 patients reveal early degeneration in pons, thalamus, and striatum
Velazquez-Perez L; Labrada RR; Canales-Ochoa N; Cruz GS; Polo LG; Laffita-Mesa JM; Aguilera RG; Mederos LA; Valencia HR; Rodriguez J
Conference publication: JOURNAL OF NEUROLOGY. 2009;256:S101
Addressing the predictivity of electrophysiological biomarkers in SCA2: 20-year long-term follow-up study
Velazquez-Perez L; Sanchez-Cruz G; Canales-Ochoa N; Rodrigues-Labrada R; Laffita-Mesa JM
Conference publication: JOURNAL OF NEUROLOGY. 2009;256:S67
An integrative characterisation of SCA2 in Cuba: epidemiological, genetic neurochemical and electrophysiological findings in 7926 Cuban carriers
Velazquez-Perez L; Sanchez-Cruz G; Galicia-Polo L; Auburger G; Garcia-Rodriguez J; Rodriguez-Labrada R; Laffita-Mesa JM; Almaguer-Mederos L; Rodriguez RA; Gonzalez C; Canales-Ochoa N
Conference publication: JOURNAL OF NEUROLOGY. 2009;256:S52
Loss of CAA interruption in large normal alleles atx2 is a risk factor to SCA2 gene instability: a haplotype and sequence-based study in large Cuban kindreds
Laffita-Mesa JM; Velazquez-Perez L; Auburger G; Gispert S; Pena-Serrano L; Sanchez-Cruz G; Santos-Falcon N; Santiago J; Rodriguez-Labrada R; Cuello D; Gonzalez Y
Conference publication: JOURNAL OF NEUROLOGY. 2009;256:S45-S46
Restless legs and SCA2 are co-morbid phenotypes in ataxin 2 mutation carriers: common genotypes or modifiers?
Velazquez-Perez L; Rodriguez Labrada R; Canales-Ochoa N; Sanchez Cruz G; Galicia Polo L; Laffita-Mesa JM; Garcia Aguilera R; Almaguer Mederos L; Reyes-Valencia H; Rodriguez J
Conference publication: JOURNAL OF NEUROLOGY. 2009;256:S15
Ocular maximal saccade velocity is reduced even in presymptomatic stages resulting from polyQ toxicity in SCA2
Labrada RR; Velazquez-Perez L; Seifried C; Sontos-Falcon N; Abele M; Ziemann U; Martinez-Gongora E; Sanchez-Cruz G; Rodriguez J; Canales-Ochoa N; Laffita-Mesa JM; Perez-Gonzalez R; Mederos LA; Viebahn B; Stuckrad-Barre S; Fetter M; Klockgether T; Auburger G
Conference publication: JOURNAL OF NEURAL TRANSMISSION. 2009;116(2):245
Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2
Seifried C; Velazquez-Perez L; Abele M; Wirjatijasa F; Rodriguez-Labrada R; Santos-Falcon N; Almaguer-Mederos L; Tejeda R; Canales-Ochoa N; Hilker R; Fetter M; Ziemann U; Klockgether T; Medrano-Montero J; Rodriguez-Diaz J; Laffita-Mesa J; Auburger G
Conference publication: MOVEMENT DISORDERS. 2009;24:S14
Loss of CAA interruption in large normal alleles ATX2 is a risk factor to SCA2 gene instability: A haplotype and sequence based study in large Cuban kindreds
Laffita-Mesa JM; Velazquez-Perez L; Auburger G; Gispert S; Sanchez G; Santiago J; Rodriguez R
Conference publication: MOVEMENT DISORDERS. 2009;24:S14
The Cuban pathological CAG mutation causing SCA2 was introduced by Hispanics and probably originated between 1408CE and 1733CE in the Cuban population
Laffita-Mesa JM; Velazquez-Perez L; Auburger G; Gispert S; Pena-Serrano L
Conference publication: MOVEMENT DISORDERS. 2009;24:S24
Spinocerebellar ataxia type 2: A clinical, molecular, neurochemical and electrophysiological study of the mutation in 106 Cuban families
Velazquez-Perez L; Sanchez-Cruz G; Galicia-Polo L; Auburger G; Garcia-Rodriguez J; Rodriguez-Labrada R; Almaguer-Mederos L; Coello-Almarales D; Laffita-Mesa J; Aguilera-Rodriguez R; Gonzalez C; Cannales-Ochoa N
Conference publication: JACC-JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY. 2004;43(5):289A-290A
Primary angioplasty versus facilitated intervention (tenecteplase plus stenting) in patients with ST elevated acute myocardial infarction: Final results of the GRACIA-2 trial
Fernandez-Aviles F; Alonso JJ; Castro-Beiras A; Goicolea J; Blanco J; Alonso J; Mesa JL; Diaz-Llera L; Vazquez N; Hernandez R; Perez A; Moreu J
Conference publication: PHYSICA B-CONDENSED MATTER. 2002;320(1-4):423-426
Theory and experiment of the ESR of Co²⁺ in Zn₂(OH)PO₄ and Mg₂(OH)AsO₄
Foglio ME; dos Santos MC; Barberis GE; Rojo JM; Mesa JL; Lezama L; Rojo T
Review: SPORTS MEDICINE. 2002;32(14):903-944
Oral creatine supplementation and skeletal muscle metabolism in physical exercise
Mesa JLM; Ruiz JR; González-Gross MM; Sainz AG; Garzón MJC
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