Inger Nennesmo

Publikationer
Populärvetenskap och samverkan

Artiklar

Article: NPJ PARKINSONS DISEASE. 2024;10(1):93
PARKIN is not required to sustain OXPHOS function in adult mammalian tissues
Filograna R; Gerlach J; Choi H-N; Rigoni G; Barbaro M; Oscarson M; Lee S; Tiklova K; Ringner M; Koolmeister C; Wibom R; Riggare S; Nennesmo I; Perlmann T; Wredenberg A; Wedell A; Motori E; Svenningsson P; Larsson N-G
Article: NEUROLOGY-GENETICS. 2023;9(6):e200100
Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3
Ben-Shabat I; Kvarnung M; Sperker W; Bruhn H; Wredenberg A; Wibom R; Nennesmo I; Engvall M; Paucar M
Article: EMBO MOLECULAR MEDICINE. 2023;15(10):e17240
Single-cell profiling of muscle-infiltrating T cells in idiopathic inflammatory myopathies
Argyriou A; Horuluoglu B; Galindo-Feria AS; Diaz-Boada JS; Sijbranda M; Notarnicola A; Dani L; van Vollenhoven A; Ramskold D; Nennesmo I; Dastmalchi M; Lundberg IE; Diaz-Gallo L-M; Chemin K
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: SYNAPSE. 2023;77(4):e22269
[¹¹C]PBB3 binding in Aβ(-) or Aβ(+) corticobasal syndrome
Cselenyi Z; Wallin J; Tjerkoski J; Bloth B; Svensson S; Nennesmo I; Sunnemark D; Jelic V; Farde L; Svenningsson P
Article: FRONTIERS IN NEUROLOGY. 2023;14:1170005
Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders
Ek M; Nilsson D; Engvall M; Malmgren H; Thonberg H; Pettersson M; Anderlid B-M; Hammarsjo A; Helgadottir HT; Arnardottir S; Naess K; Nennesmo I; Paucar M; Hjartarson HT; Press R; Solders G; Sejersen T; Lindstrand A; Kvarnung M
Article: NUTRIENTS. 2022;14(18):3733
Variability in Skeletal Muscle Protein Synthesis Rates in Critically Ill Patients
Tjader I; Klaude M; Hssain AA; Guillet C; Nennesmo I; Wernerman J; Rooyackers O
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: FRONTIERS IN IMMUNOLOGY. 2022;13:866701
Screening for Anti-HMGCR Antibodies in a Large Single Myositis Center Reveals Infrequent Exposure to Statins and Diversiform Presentation of the Disease
Szczesny P; Barsotti S; Nennesmo I; Danielsson O; Dastmalchi M
Article: JOURNAL OF BIOLOGICAL CHEMISTRY. 2021;297(6):101355
A missense mutation converts the Na⁺,K⁺-ATPase into an ion channel and causes therapy-resistant epilepsy
Ygberg S; Akkuratov EE; Howard RJ; Taylan F; Jans DC; Mahato DR; Katz A; Kinoshita PF; Portal B; Nennesmo I; Lindskog M; Karlish SJD; Andersson M; Lindstrand A; Brismar H; Aperia A
Article: MOLECULAR PSYCHIATRY. 2021;26(10):5833-5847
Astroglial tracer BU99008 detects multiple binding sites in Alzheimer's disease brain
Kumar A; Koistinen NA; Malarte M-L; Nennesmo I; Ingelsson M; Ghetti B; Lemoine L; Nordberg A
Article: MOLECULAR PSYCHIATRY. 2021;26(10):5609-5619
Amyloid, tau, and astrocyte pathology in autosomal-dominant Alzheimer's disease variants: AβPParc and PSEN1DE9
Lemoine L; Gillberg P-G; Bogdanovic N; Nennesmo I; Saint-Aubertlfis L; Viitanen M; Graff C; Ingelsson M; Nordberg A
Article: NEUROLOGY-GENETICS. 2021;7(2):e566
Novel Mutation m.10372A>G in MT-ND3 Causing Sensorimotor Axonal Polyneuropathy
Bruhn H; Samuelsson K; Schober FA; Engvall M; Lesko N; Wibom R; Nennesmo I; Calvo-Garrido J; Press R; Stranneheim H; Freyer C; Wedell A; Wredenberg A
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: JOURNAL OF PEDIATRICS. 2021;228:240-251.e2
Clinical Presentation, Genetic Etiology, and Coenzyme Q10 Levels in 55 Children with Combined Enzyme Deficiencies of the Mitochondrial Respiratory Chain
Naess K; Bruhn H; Stranneheim H; Freyer C; Wibom R; Mourier A; Engvall M; Nennesmo I; Lesko N; Wredenberg A; Wedell A; von Dobeln U
Article: JOURNAL OF WRIST SURGERY. 2020;9(06):481-486
Structural Changes in the Posterior Interosseous Nerve from Patients with Wrist Osteoarthritis and Asymptomatic Controls
Sward E; Nennesmo I; Wilcke M
Article: DIAGNOSTICS. 2020;10(11):E966-966
Neurogenic vs. Myogenic Origin of Acquired Muscle Paralysis in Intensive Care Unit (ICU) Patients: Evaluation of Different Diagnostic Methods
Marrero HDJG; Stalberg EV; Cooray G; Corpeno Kalamgi R; Hedstrom Y; Bellander B-M; Nennesmo I; Larsson L
Article: CLINICAL AND EXPERIMENTAL RHEUMATOLOGY. 2020;38(1):42-49
Features of repeated muscle biopsies and phenotypes of monocytes in paired blood samples and clinical long-term response to treatment in patients with idiopathic inflammatory myopathy: a pilot study
Tang Q; Gheorghe KR; Zhang X-M; Lindroos E; Alexanderson H; Wick C; Bruton M; Fernandes-Cerqueira C; Harris RA; Nennesmo I; Lundberg IE
Article: CLINICAL GENETICS. 2019;96(2):118-125
Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth
Frisk S; Taylan F; Blaszczyk I; Nennesmo I; Anneren G; Herm B; Stattin E-L; Zachariadis V; Lindstrand A; Tesi B; Laurell T; Nordgren A
Article: HUMAN MOLECULAR GENETICS. 2019;28(11):1919-1929
Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24
Hedberg-Oldfors C; Abramsson A; Osborn DPS; Danielsson O; Fazlinezhad A; Nilipour Y; Hubbert L; Nennesmo I; Visuttijai K; Bharj J; Petropoulou E; Shoreim A; Vona B; Ahangari N; Lopez MD; Doosti M; Banote RK; Maroofian R; Edling M; Taherpour M; Zetterberg H; Karimiani EG; Oldfors A; Jamshidi Y
Article: FRONTIERS IN GENETICS. 2018;9:317
Pathological Study of a FMR1 Premutation Carrier With Progressive Supranuclear Palsy
Paucar M; Nennesmo I; Svenningsson P
Article: NEUROMUSCULAR DISORDERS. 2017;27(7):627-630
Late-onset limb-girdle muscular dystrophy caused by GMPPB mutations
Balcin H; Palmio J; Penttila S; Nennesmo I; Lindfors M; Solders G; Udd B
Article: HUMAN MOLECULAR GENETICS. 2017;26(13):2515-2525
A multi-systemic mitochondrial disorder due to a dominant p.Y955H disease variant in DNA polymerase gamma
Siibak T; Clemente P; Bratic A; Bruhn H; Kauppila TES; Macao B; Schober FA; Lesko N; Wibom R; Naess K; Nennesmo I; Wedell A; Peter B; Freyer C; Falkenberg M; Wredenberg A
Article: ORPHANET JOURNAL OF RARE DISEASES. 2017;12(1):73
Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model
Tegelberg S; Tomasic N; Kallijarvi J; Purhonen J; Elmer E; Lindberg E; Nord DG; Soller M; Lesko N; Wedell A; Bruhn H; Freyer C; Stranneheim H; Wibom R; Nennesmo I; Wredenberg A; Eklund EA; Fellman V
Article: SCIENTIFIC REPORTS. 2017;7:45496
Cortical laminar tau deposits and activated astrocytes in Alzheimer's disease visualised by ³H-THK5117 and ³H-deprenyl autoradiography
Lemoine L; Saint-Aubert L; Nennesmo I; Gillberg P-G; Nordberg A
Article: ALZHEIMERS & DEMENTIA. 2017;13(4):419-430
Amyloid tracers binding sites in autosomal dominant and sporadic Alzheimer's disease
Ni R; Gillberg P-G; Bogdanovic N; Viitanen M; Myllykangas L; Nennesmo I; Langstrom B; Nordberg A
Article: JOURNAL OF HUMAN GENETICS. 2017;62(2):321-324
No common founder for C9orf72 expansion mutation in Sweden
Chiang H-H; Forsell C; Lindstrom A-K; Lilius L; Thonberg H; Nennesmo I; Graff C
Article: ALZHEIMERS RESEARCH & THERAPY. 2016;8(1):30
Targeted delivery of nerve growth factor to the cholinergic basal forebrain of Alzheimer's disease patients: application of a second-generation encapsulated cell biodelivery device
Eyjolfsdottir H; Eriksdotter M; Linderoth B; Lind G; Juliusson B; Kusk P; Almkvist O; Andreasen N; Blennow K; Ferreira D; Westman E; Nennesmo I; Karami A; Darreh-Shori T; Kadir A; Nordberg A; Sundstrom E; Wahlund L-O; Wall A; Wiberg M; Winblad B; Seiger A; Wahlberg L; Almqvist P
Article: ARTHRITIS RESEARCH & THERAPY. 2016;18(1):136
Effects on muscle tissue remodeling and lipid metabolism in muscle tissue from adult patients with polymyositis or dermatomyositis treated with immunosuppressive agents
Loell I; Raouf J; Chen Y-W; Shi R; Nennesmo I; Alexanderson H; Dastmalchi M; Nagaraju K; Korotkova M; Lundberg IE
Article: ALZHEIMER DISEASE & ASSOCIATED DISORDERS. 2016;30(2):178-182
Same Ages, Same Genes: Same Brains, Same Pathologies? Dementia Timings, Co-Occurring Brain Pathologies, ApoE Genotypes in Identical and Fraternal Age-matched Twins at Autopsy
Iacono D; Volkmann I; Nennesmo I; Pedersen NL; Fratiglioni L; Johansson B; Karlsson D; Winblad B; Gatz M
Article: JOURNAL OF CLINICAL INVESTIGATION. 2015;125(12):4612-4624
Development of autoantibodies against muscle-specific FHL1 in severe inflammatory myopathies
Albrecht I; Wick C; Hallgren A; Tjarnlund A; Nagaraju K; Andrade F; Thompson K; Coley W; Phadke A; Diaz-Gallo L-M; Bottai M; Nennesmo I; Chemin K; Herrath J; Johansson K; Wikberg A; Ytterberg AJ; Zubarev RA; Danielsson O; Krystufkova O; Vencovsky J; Landegren N; Wahren-Herlenius M; Padyukov L; Kampe O; Lundberg IE
Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2015;97(5):761-768
Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26
Kishita Y; Pajak A; Bolar NA; Marobbio CMT; Maffezzini C; Miniero DV; Monne M; Kohda M; Stranneheim H; Murayama K; Naess K; Lesko N; Bruhn H; Mourier A; Wibom R; Nennesmo I; Jespers A; Goyaert P; Ohtake A; Van Laer L; Loeys BL; Freyer C; Palmieri F; Wredenberg A; Okazaki Y; Wedell A
Article: JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. 2015;74(11):1061-1070
Antemortem Prediction of Braak Stage
Carlson JOE; Gatz M; Pedersen NL; Graff C; Nennesmo I; Lindstrom A-K; Gerritsen L
Article: ACTA NEUROPATHOLOGICA COMMUNICATIONS. 2015;3:40
Visualization of regional tau deposits using ³H-THK5117 in Alzheimer brain tissue
Lemoine L; Saint-Aubert L; Marutle A; Antoni G; Eriksson JP; Ghetti B; Okamura N; Nennesmo I; Gillberg P-G; Nordberg A
Article: ANNALS OF THE RHEUMATIC DISEASES. 2015;74(1):204-210
Validation of a score tool for measurement of histological severity in juvenile dermatomyositis and association with clinical severity of disease
Varsani H; Charman SC; Li CK; Marie SKN; Amato AA; Banwell B; Bove KE; Corse AM; Emslie-Smith AM; Jacques TS; Lundberg IE; Minetti C; Nennesmo I; Rushing EJ; Sallum AME; Sewry C; Pilkington CA; Holton JL; Wedderburn LR
Article: ALZHEIMERS & DEMENTIA. 2015;11(1):40-50
Resolution of inflammation is altered in Alzheimer's disease
Wang X; Zhu M; Hjorth E; Cortes-Toro V; Eyjolfsdottir H; Graff C; Nennesmo I; Palmblad J; Eriksdotter M; Sambamurti K; Fitzgerald JM; Serhan CN; Granholm A-C; Schultzberg M
Article: BRAIN PATHOLOGY. 2014;24(4):317-333
Neuropathologic Assessment of Dementia Markers in Identical and Fraternal Twins
Iacono D; Volkman I; Nennesmo I; Pedersen NL; Fratiglioni L; Johansson B; Karlsson D; Winblad B; Gatz M
Article: ANNALS OF THE RHEUMATIC DISEASES. 2014;73(5):913-920
Anakinra treatment in patients with refractory inflammatory myopathies and possible predictive response biomarkers: a mechanistic study with 12 months follow-up
Zong M; Dorph C; Dastmalchi M; Alexanderson H; Pieper J; Amoudruz P; Helmers SB; Nennesmo I; Malmstrom V; Lundberg IE
Article: JOURNAL OF ALZHEIMERS DISEASE. 2014;39(4):787-797
Alteration of Thioredoxin and Glutaredoxin in the Progression of Alzheimer's Disease
Arodin L; Lamparter H; Karlsson H; Nennesmo I; Bjoernstedt M; Schroder J; Fernandes AP
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2013;21(11):1260-1265
Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration
Chiang H-H; Forsell C; Lilius L; Oijerstedt L; Thordardottir S; Shanmugarajan K; Westerlund M; Nennesmo I; Thonberg H; Graff C
Article: NEUROMUSCULAR DISORDERS. 2013;23(11):945-951
193rd ENMC International workshop Pathology diagnosis of idiopathic inflammatory myopathies 30 November 2 December 2012, Naarden, The Netherlands
De Bleecker JL; Lundberg IE; de Visser M
Article: JOURNAL OF NEUROINFLAMMATION. 2013;10:90
³H-Deprenyl and ³H-PIB autoradiography show different laminar distributions of astroglia and fibrillar β-amyloid in Alzheimer brain
Marutle A; Gillberg P-G; Bergfors A; Yu W; Ni R; Nennesmo I; Voytenko L; Nordberg A
Article: HUMAN MUTATION. 2013;34(2):363-373
A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
van der Zee J; Gijselinck I; Dillen L; Van Langenhove T; Theuns J; Engelborghs S; Philtjens S; Vandenbulcke M; Sleegers K; Sieben A; Baumer V; Maes G; Corsmit E; Borroni B; Padovani A; Archetti S; Perneczky R; Diehl-Schmid J; de Mendonca A; Miltenberger-Miltenyi G; Pereira S; Pimentel J; Nacmias B; Bagnoli S; Sorbi S; Graff C; Chiang H-H; Westerlund M; Sanchez-Valle R; Llado A; Gelpi E; Santana I; Almeida MR; Santiago B; Frisoni G; Zanetti O; Bonvicini C; Synofzik M; Maetzler W; vom Hagen JM; Schoels L; Heneka MT; Jessen F; Matej R; Parobkova E; Kovacs GG; Stroebel T; Sarafov S; Tournev I; Jordanova A; Danek A; Arzberger T; Fabrizi GM; Testi S; Salmon E; Santens P; Martin J-J; Cras P; Vandenberghe R; De Deyn PP; Cruts M; Van Broeckhoven C
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2012;20(8):897-904
Mutations in the mitochondrial tRNA^Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy
Tuppen HAL; Naess K; Kennaway NG; Al-Dosary M; Lesko N; Yarham JW; Bruhn H; Wibom R; Nennesmo I; Weleber RG; Blakely EL; Taylor RW; McFarland R
Article: EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY. 2012;16(4):379-389
Phenotypic and genotypic variability in Alpers syndrome
Sofou K; Moslemi A-R; Kollberg G; Bjarnadottir I; Oldfors A; Nennesmo I; Holme E; Tulinius M; Darin N
Article: JIMD REPORTS. 2012;4:67-73
Complete Deletion of a POLG1 Allele in a Patient with Alpers Syndrome.
Naess K; Barbaro M; Bruhn H; Wibom R; Nennesmo I; von Döbeln U; Larsson N-G; Nemeth A; Lesko N
Article: INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE. 2012;5(2):201-207
Imaging astrocytosis with PET in Creutzfeldt-Jakob disease: case report with histopathological findings
Engler H; Nennesmo I; Kumlien E; Gambini JP; Lundberg PO; Savitcheva I; Langstrom B
Article: BMC RESEARCH NOTES. 2011;4:476
Mutation screening of patients with Alzheimer disease identifies APP locus duplication in a Swedish patient.
Thonberg H; Fallström M; Björkström J; Schoumans J; Nennesmo I; Graff C
Article: BRAIN. 2011;134(Pt 4):1116-1126
Reduced C-afferent fibre density affects perceived pleasantness and empathy for touch
Morrison I; Loken LS; Minde J; Wessberg J; Perini I; Nennesmo I; Olausson H
Article: BRAIN. 2011;134(Pt 1):301-317
Positron emission tomography imaging and clinical progression in relation to molecular pathology in the first Pittsburgh Compound B positron emission tomography patient with Alzheimer's disease
Kadir A; Marutle A; Gonzalez D; Scholl M; Almkvist O; Mousavi M; Mustafiz T; Darreh-Shori T; Nennesmo I; Nordberg A
Article: CLINICAL PHYSIOLOGY AND FUNCTIONAL IMAGING. 2011;31(1):18-25
Higher proportion of fast-twitch (type II) muscle fibres in idiopathic inflammatory myopathies - evident in chronic but not in untreated newly diagnosed patients
Loell I; Helmers SB; Dastmalchi M; Alexanderson H; Munters LA; Nennesmo I; Lindroos E; Borg K; Lundberg IE; Esbjornsson M
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2010;18(11):1202-1208
The PSEN1 I143T mutation in a Swedish family with Alzheimer's disease: clinical report and quantification of Aβ in different brain regions
Keller L; Welander H; Chiang H-H; Tjernberg LO; Nennesmo I; Wallin AK; Graff C
Article: MUSCLE & NERVE. 2010;41(6):751-757
BEDSIDE DIAGNOSIS OF RIPPLING MUSCLE DISEASE IN CAV3 p.A46T MUTATION CARRIERS
Sundblom J; Stalberg E; Osterdahl M; Rucker F; Montelius M; Kalimo H; Nennesmo I; Islander G; Smits A; Dahl N; Melberg A
Article: NEUROMUSCULAR DISORDERS. 2010;20(3):198-203
Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion
Lesko N; Naess K; Wibom R; Solaroli N; Nennesmo I; von Doebeln U; Karlsson A; Larsson N-G
Article: ACTA MYOLOGICA. 2009;28(3):91-93
Severe phenotype of a patient with autosomal recessive centronuclear myopathy due to a BIN1 mutation.
Mejaddam AY; Nennesmo I; Sejersen T
Article: JOURNAL OF IMMUNOLOGY. 2009;183(7):4792-4799
T Cell Infiltrates in the Muscles of Patients with Dermatomyositis and Polymyositis Are Dominated by CD28^null T Cells
Fasth AER; Dastmalchi M; Rahbar A; Salomonsson S; Pandya JM; Lindroos E; Nennesmo I; Malmberg K-J; Soderberg-Naucler C; Trollmo C; Lundberg IE; Malmstrom V
Article: PLOS GENETICS. 2009;5(5):e1000499
Sensory Ataxic Neuropathy in Golden Retriever Dogs Is Caused by a Deletion in the Mitochondrial tRNA^Tyr Gene
Baranowska I; Jaderlund KH; Nennesmo I; Holmqvist E; Heidrich N; Larsson N-G; Andersson G; Wagner EGH; Hedhammar A; Wibom R; Andersson L
Article: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. 2009;80(2):188-195
A novel NGFB point mutation: a phenotype study of heterozygous patients
Minde J; Andersson T; Fulford M; Aguirre M; Nennesmo I; Remahl IN; Svensson O; Holmberg M; Toolanen G; Solders G
Article: EUROPEAN JOURNAL OF NEUROLOGY. 2009;16(1):48-53
Impairment of short-term memory and Korsakoff syndrome are common in AIDS patients with cytomegalovirus encephalitis
Pirskanen-Matell R; Grutzmeier S; Nennesmo I; Sandstrom E; Ehrnst A
Article: ANNALS OF THE RHEUMATIC DISEASES. 2008;67(12):1670-1677
A high incidence of disease flares in an open pilot study of infliximab in patients with refractory inflammatory myopathies
Dastmalchi M; Grundtman C; Alexanderson H; Mavragani CP; Einarsdottir H; Helmers SB; Elvin K; Crow MK; Nennesmo I; Lundberg IE
Article: ALZHEIMERS & DEMENTIA. 2008;4(6):414-420
Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family
Chiang H-H; Rosvall L; Brohede J; Axelman K; Bjork BF; Nennesmo I; Robins T; Graff C
Article: JOURNAL OF INTERNAL MEDICINE. 2008;264(4):388-400
Central nervous system involvement in severe congenital neutropenia:: neurological and neuropsychological abnormalities associated with specific HAX1 mutations
Carlsson G; van't Hooft I; Melin M; Entesarian M; Laurencikas E; Nennesmo I; Trebinska A; Grzybowska E; Palmblad J; Dahl N; Nordenskjold M; Fadeel B; Henter J-I
Article: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS. 2007;363(4):989-993
VEGF reduces astrogliosis and preserves neuromuscular junctions in ALS transgenic mice
Zheng C; Skold MK; Li J; Nennesmo I; Fadeel B; Henter J-I
Article: ARTHRITIS & RHEUMATOLOGY. 2007;57(7):1192-1201
International consensus on a proposed score system for muscle biopsy evaluation in patients with juvenile dermatomyositis: A tool for potential use in clinical trials
Wedderburn LR; Varsani H; Li CKC; Newton KR; Amato AA; Banwell B; Bove KE; Corse AM; Emslie-Smith A; Harding B; Hoogendijk J; Lundberg IE; Marie S; Minetti C; Nennesmo I; Rushing EJ; Sewry C; Charman SC; Pilkington CA; Holton JL
Article: ANNALS OF THE RHEUMATIC DISEASES. 2007;66(10):1276-1283
Limited effects of high-dose intravenous immunoglobulin (IVIG) treatment on molecular expression in muscle tissue of patients with inflammatory myopathies
Helmers SB; Dastmalchi M; Alexanderson H; Nennesmo I; Esbjornsson M; Lindvall B; Lundberg IE
Article: EXPERIMENTAL NEUROLOGY. 2006;202(2):373-380
Apolipoprotein E deficiency increased microglial activation/CCR3 expression and hippocampal damage in kainic acid exposed mice
Duan R-S; Chen Z; Dou Y-C; Quezada HC; Nennesmo I; Adem A; Winblad B; Zhu J
Article: ANNALS OF THE RHEUMATIC DISEASES. 2006;65(12):1565-1571
Signs of inflammation in both symptomatic and asymptomatic muscles from patients with polymyositis and dermatomyositis
Dorph C; Englund P; Nennesmo I; Lundberg IE
Article: JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. 2006;65(8):758-768
POLG1 mutations associated with progressive encephalopathy in childhood
Kollberg G; Moslemi A-R; Darin N; Nennesmo I; Bjamadottir I; Uvebrant P; Holme E; Melberg A; Tulinius M; Oldfors A
Article: NEUROBIOLOGY OF AGING. 2005;26(5):597-606
Human monoclonal antibodies against amyloid-beta from healthy adults
Geylis V; Kourilov V; Meiner Z; Nennesmo I; Bogdanovic N; Steinitz M
Article: DEVELOPMENTAL NEUROBIOLOGY. 2005;62(2):207-218
Increased microglial activation and astrogliosis after intranasal administration of kainic acid in C57BL/6 mice
Chen ZG; Duan RS; Quezada HC; Mix E; Nennesmo I; Adem A; Winblad B; Zhu J
Article: JOURNAL OF NEUROIMMUNOLOGY. 2005;159(1-2):165-176
Dendritic cells in the cerebrospinal fluid and peripheral nerves in Guillain-Barre syndrome and chronic inflammatory demyelinating polyradiculoneuropathy
Press R; Nennesmo I; Kouwenhoven M; Huang YM; Link H; Pashenkov M
Article: EXPERIMENTAL NEUROLOGY. 2004;190(2):486-494
Anti-cytokine autoantibodies in experimental autoimmune neuritis in Lewis rats
Zhu W; Mix E; Nennesmo I; Adem A; Zhu J
Article: MUSCLE & NERVE. 2004;30(6):752-760
Familial insensitivity to pain (HSAN V) and a mutation in the NGFB gene.: A neurophysiological and pathological study
Minde J; Toolanen G; Andersson T; Nennesmo I; Remahl IN; Svensson O; Solders G
Article: ANNALS OF NEUROLOGY. 2004;56(4):564-567
Vascular endothelial growth factor prolongs survival in a transgenic mouse model of ALS
Zheng CY; Nennesmo I; Fadeel B; Henter JI
Article: ACTA RADIOLOGICA. 2004;45(5):547-555
Detection of small implanted tumors growing during repeated magnetic resonance imaging of the rabbit liver:: Application of an interpretation model
Thorstensen Ö; Isberg B; Jorulf H; Svahn U; Westman L; Venizelos N; Nennesmo I
Article: NEUROBIOLOGY OF DISEASE. 2004;16(3):630-637
CCR5 deficiency does not prevent P0 peptide 180-199 immunized mice from experimental autoimmune neuritis
Duan RS; Chen ZG; Bao L; Quezada HC; Nennesmo I; Winblad B; Zhu J
Article: JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. 2004;63(2):120-128
Increased susceptibility to experimental autoimmune neuritis after upregulation of the autoreactive T cell response to peripheral myelin antigen in apolipoprotein E-deficient mice
Yu S; Duan RS; Chen ZG; Quezada HC; Bao L; Nennesmo I; Zhu SW; Winblad B; Ljunggren HG; Zhu J
Article: JOURNAL OF AFFECTIVE DISORDERS. 2003;76(1-3):55-68
Alterations of mitochondrial function and correlations with personality traits in selected major depressive disorder patients
Gardner A; Johansson A; Wibom R; Nennesmo I; von Döbeln U; Hagenfeldt L; Hällström T
Article: MUSCLE & NERVE. 2003;27(4):442-448
CBA/J mice infected with Trypanosoma cruzi:: An experimental model for inflammatory myopathies
Andersson J; Englund P; Sunnemark D; Dahlstedt A; Westerblad H; Nennesmo I; Örn A; Lundberg IE
Article: ACTA PSYCHIATRICA SCANDINAVICA. 2003;107(3):233-239
Alterations of rCBF and mitochondrial dysfunction in major depressive disorder:: a case report
Gardner A; Pagani M; Wibom R; Nennesmo I; Jacobsson H; Hällström T
Article: EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING. 2003;30(1):85-95
Multitracer study with positron emission tomography in Creutzfeldt-Jakob disease.
Engler H; Lundberg PO; Ekbom K; Nennesmo I; Nilsson A; Bergström M; Tsukada H; Hartvig P; Långström B
Article: DIABETES. 2002;51(12):3376-3383
Marked heterogeneity of human skeletal muscle lipolysis at rest
Hagström-Toft E; Qvisth V; Nennesmo I; Rydén M; Bolinder H; Enoksson S; Bolinder J; Arner P
Article: EXPERIMENTAL NEUROLOGY. 2002;177(1):314-320
CD4 and CD8 T cells, but not B cells, are critical to the control of murine experimental autoimmune neuritis
Zhu Y; Bao L; Zhu SW; Chen ZG; van der Meide P; Nennesmo I; Winblad B; Ljunggren HG; Zhu J
Article: NEUROPHARMACOLOGY. 2002;42(5):731-739
Suppression of experimental autoimmune neuritis by ABR-215062 is associated with altered Th1/Th2 balance and inhibited migration of inflammatory cells into the peripheral nerve tissue
Zou LP; Abbas N; Volkmann I; Nennesmo I; Levi M; Wahren B; Winblad B; Hedlund G; Zhu J
Article: ARTHRITIS & RHEUMATOLOGY. 2002;46(4):1044-1055
Interleukin-1α expression in capillaries and major histocompatibility complex class I expression in type II muscle fibers from polymyositis and dermatomyositis patients -: Important pathogenic features independent of inflammatory cell clusters in muscle tissue
Englund P; Nennesmo I; Klareskog L; Lundberg IE
Article: BRAIN RESEARCH. 2002;931(2):135-145
Excitotoxic neurodegeneration induced by intranasal administration of kainic acid in C57BL/6 mice
Chen ZG; Ljunggren HG; Bogdanovic N; Nennesmo I; Winblad B; Zhu J
Article: RHEUMATOLOGY. 2001;40(12):1346-1354
Increased endothelial expression of HLA-DQ and interleukin 1α in extra-articular rheumatoid arthritis.: Results from immunohistochemical studies of skeletal muscle
Turesson C; Englund P; Jacobsson LTH; Sturfelt G; Truedsson L; Nennesmo I; Lundberg IE
Article: AMERICAN JOURNAL OF PATHOLOGY. 2001;159(4):1263-1273
Skeletal muscle fibers express major histocompatibility complex class II antigens independently of inflammatory infiltrates in inflammatory myopathies
Englund P; Lindroos E; Nennesmo I; Klareskog L; Lundberg IE
Article: EUROPEAN JOURNAL OF HAEMATOLOGY. 2001;67(3):189-193
Antibody reactivities to skeletal muscle proteins in a patient with λ light chain secreting multiple myeloma, generalised amyloidosis and rhabdomyolysis
Sundblad A; Porwit A; Ostad M; Nennesmo I; Holm G; Ösby E; Borg K; Björkholm M
Article: JOURNAL OF RHEUMATOLOGY. 2001;28(7):1591-1599
Percutaneous conchotome muscle biopsy. A useful diagnostic and assessment tool
Dorph C; Nennesmo I; Lundberg IE
Article: ANNALS OF THE RHEUMATIC DISEASES. 2001;60(4):423-426
MRI guided muscle biopsy confirmed polymyositis diagnosis in a patient with interstitial lung disease
Lampa J; Nennesmo I; Einarsdottir H; Lundberg I
Article: ACTA NEUROLOGICA SCANDINAVICA. 2001;103(2):131-135
Report of a patient with inclusion body myositis and CD8⁺ chronic lymphocytic leukaemia -: post-mortem analysis of muscle and brain
Arnardottir S; Ansved T; Nennesmo I; Borg K
Article: ACTA NEUROPATHOLOGICA. 2000;100(6):709-711
Amyloid in a multiple sclerosis lesion is clearly of Aλ type
Schröder R; Nennesmo I; Linke RP
Article: JOURNAL OF NEUROSCIENCE RESEARCH. 2000;62(5):717-721
P0 protein peptide 180-199 together with pertussis toxin induces experimental autoimmune neuritis in resistant C57BL/6 mice
Zou LP; Ljunggren HG; Levi M; Nennesmo I; Wahren B; Mix E; Winblad B; Schalling M; Zhu J
Article: PEDIATRIC TRANSPLANTATION. 2000;4(3):211-214
Fatal deterioration of neurological disease after orthotopic liver transplantation for valproic acid-induced liver damage.
Kayihan N; Nennesmo I; Ericzon BG; Németh A
Article: CYTOKINE. 2000;12(6):808-810
High inflammation and mild demyelination in the peripheral nervous system induced by an intraneural injection of rr interleukin-4
Deretzi G; Pelidou SH; Zou LP; Wei L; Nennesmo I; Zhu J
Article: JOURNAL OF RHEUMATOLOGY. 2000;27(4):940-948
Increased expression of interleukin 1α and MHC class I in muscle tissue of patients with chronic, inactive polymyositis and dermatomyositis
Nyberg P; Wikman AL; Nennesmo I; Lundberg I
Article: ACTA NEUROLOGICA SCANDINAVICA. 2000;101(1):47-52
Polyneuropathy in late Lyme borreliosis -: a clinical, neurophysiological and morphological description
Kindstrand E; Nilsson BY; Hovmark A; Nennesmo I; Pirskanen R; Solders G; Åsbrink E
Article: SCANDINAVIAN JOURNAL OF IMMUNOLOGY. 2000;51(1):29-35
Intranasal administration of recombinant mouse interleukin-12 increases inflammation and demyelination in chronic experimental autoimmune neuritis in Lewis rats
Pelidou SH; Zou LP; Deretzi G; Nennesmo I; Wei L; Mix E; van der Meide PH; Zhu J
Article: NEUROLOGY. 1999;53(9):2190-2192
Neuroimaging study in autosomal dominant cerebellar ataxia, deafness, and narcolepsy
Melberg A; Dahl N; Hetta J; Valind S; Nennesmo I; Lundberg PO; Raininko R
Article: AIDS. 1999;13(9):1071-1075
BK virus as the cause of meningoencephalitis, retinitis and nephritis in a patient with AIDS
Bratt G; Hammarin AL; Grandien M; Hedquist BG; Nennesmo I; Sundelin B; Seregard S
Article: JOURNAL OF AUTOIMMUNITY. 1999;12(2):81-89
Nasal administration of recombinant rat IL-4 ameliorates ongoing experimental autoimmune neuritis and inhibits demyelination
Deretzi G; Zou LP; Pelidou SH; Nennesmo I; Levi M; Wahren B; Mix E; Zhu J
Article: JOURNAL OF NEUROIMMUNOLOGY. 1999;94(1-2):196-203
Induction of experimental autoimmune neuritis in CD4^-8^- C57BL/6J mice
Zhu J; Nennesmo I; Deng GM; Levi M; Wahren B; Diab A; Mix E; Zhou JN; Ljunggren HG
Article: JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM. 1999;4(2):91-98
Lymphocytes in sural nerve biopsies from patients with plasma cell dyscrasia and polyneuropathy.
Solders G; Nennesmo I; Ernerudh J; Cruz M; Vrethem M
Article: OPHTHALMOLOGY. 1999;106(1):129-132
Identification of BK virus in a patient with Acquired Immune Deficiency Syndrome and bilateral atypical retinitis
Hedquist BG; Bratt G; Hammarin AL; Grandien M; Nennesmo I; Sundelin B; Seregard S
Article: ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA. 1998;77(9):939
Fatal brain edema not related to metastatic disease in a patient with choriocarcinoma
Flam F; Nennesmo I; Sjovall K; Hannerz J; Lindqvist M
Article: AMERICAN JOURNAL OF FORENSIC MEDICINE AND PATHOLOGY. 1997;18(4):384-390
Unexpected death in two young infants mimics SIDS - Autopsies demonstrate tumors of medulla and heart
Rajs J; Rasten-Almqvist P; Nennesmo I
Article: ACTA PAEDIATRICA. 1997;86(5):484-492
Treatment of adrenoleukodystrophy with bone marrow transplantation
Malm G; Ringden O; Anvret M; vonDobeln U; Hagenfeldt L; Isberg B; Knuutila S; Nennesmo I; Winiarski J; Marcus C
Article: JOURNAL OF PEDIATRICS. 1997;130(3):358-365
Neuropathologic findings and neurologic symptoms in twenty-three children with hemophagocytic lymphohistiocytosis
Henter JI; Nennesmo I
Article: ACTA NEUROPATHOLOGICA. 1997;93(2):205-209
Multiple sclerosis and amyloid deposits in the white matter of the brain
Nennesmo I; Bogdanovic N; Petren AL; Fredrikson S
Article: AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY. 1997;176(1):49-53
Tissue distribution of transplanted fetal liver cells in the human fetal recipient
Westgren M; Ek S; Bui TH; Jansson B; Kjaeldgaard A; Markling L; Nennesmo I; Seiger A; Sarby B; Thornstrom S; Ringden O
Article: ACTA NEUROLOGICA SCANDINAVICA. 1996;94(4):233-241
Monozygotic twins with MELAS-like syndrome lacking ragged red fibers and lactacidaemia.
Melberg A; Akerlund P; Raininko R; Silander HC; Wibom R; Khaled A; Nennesmo I; Lundberg PO; Olsson Y
Article: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 1996;93(18):9799-9804
Cholesterol homeostasis in human brain: Evidence for an age-dependent flux of 24S-hydroxycholesterol from the brain into the circulation
Lutjohann D; Breuer O; Ahlborg G; Nennesmo I; Siden A; Diczfalusy U; Bjorkhem I
Article: EUROPEAN UROLOGY. 1996;29(3):355-361
Morphological and X-ray microanalytical changes in mammalian tissue after overhydration with irrigating fluids
Hahn RG; Nennesmo I; Rajs J; Sundelin B; Wroblewski R; Zhang WB
Article: JOURNAL OF THE NEUROLOGICAL SCIENCES. 1995;134(1-2):119-129
Autosomal dominant cerebellar ataxia deafness and narcolepsy.
Melberg A; Hetta J; Dahl N; Nennesmo I; Bengtsson M; Wibom R; Grant C; Gustavson KH; Lundberg PO
Article: CLINICAL AND DIAGNOSTIC VIROLOGY. 1995;4(3):223-230
NO ASSOCIATION OF JC VIRUS WITH ALZHEIMERS-DISEASE OR ASTROCYTOMAS
BOGDANOVIC G; HAMMARIN AL; GRANDIEN M; WINBLAD B; BERGENHEIM AT; NENNESMO I; DALIANIS T
Visa fler

Alla övriga publikationer

Preprint: MEDRXIV. 2023;MEDRXIV
Creating the Pick's disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick's disease.
Valentino RR; Scotton WJ; Roemer SF; Lashley T; Heckman MG; Shoai M; Martinez-Carrasco A; Tamvaka N; Walton RL; Baker MC; Macpherson HL; Real R; Soto-Beasley AI; Mok K; Revesz T; Warner TT; Jaunmuktane Z; Boeve BF; Christopher EA; DeTure M; Duara R; Graff-Radford NR; Josephs KA; Knopman DS; Koga S; Murray ME; Lyons KE; Pahwa R; Parisi JE; Petersen RC; Whitwell J; Grinberg LT; Miller B; Schlereth A; Seeley WW; Spina S; Grossman M; Irwin DJ; Lee EB; Suh E; Trojanowski JQ; Van Deerlin VM; Wolk DA; Connors TR; Dooley PM; Frosch MP; Oakley DH; Aldecoa I; Balasa M; Gelpi E; Borrego-Écija S; de Eugenio Huélamo RM; Gascon-Bayarri J; Sánchez-Valle R; Sanz-Cartagena P; Piñol-Ripoll G; Molina-Porcel L; Bigio EH; Flanagan ME; Gefen T; Rogalski EJ; Weintraub S; Redding-Ochoa J; Chang K; Troncoso JC; Prokop S; Newell KL; Ghetti B; Jones M; Richardson A; Robinson AC; Roncaroli F; Snowden J; Allinson K; Green O; Rowe JB; Singh P; Beach TG; Serrano GE; Flowers XE; Goldman JE; Heaps AC; Leskinen SP; Teich AF; Black SE; Keith JL; Masellis M; Bodi I; King A; Sarraj S-A; Troakes C; Halliday GM; Hodges JR; Kril JJ; Kwok JB; Piguet O; Gearing M; Arzberger T; Roeber S; Attems J; Morris CM; Thomas AJ; Evers BM; White CL; Mechawar N; Sieben AA; Cras PP; De Vil BB; De Deyn PPPP; Duyckaerts C; Le Ber I; Seihean D; Turbant-Leclere S; MacKenzie IR; McLean C; Cykowski MD; Ervin JF; Wang S-HJ; Graff C; Nennesmo I; Nagra RM; Riehl J; Kovacs GG; Giaccone G; Nacmias B; Neumann M; Ang L-C; Finger EC; Blauwendraat C; Nalls MA; Singleton AB; Vitale D; Cunha C; Carvalho A; Wszolek ZK; Morris HR; Rademakers R; Hardy JA; Dickson DW; Rohrer JD; Ross OA
Editorial comment: NEUROLOGY-GENETICS. 2021;7(6):e636
Predominant Spastic Paraparesis Associated With the D178N Mutation in PRNP
Thams S; Paucar M; Wingard L; Thonberg H; Smith C; Nennesmo I; Svenningsson P
Editorial comment: MOLECULAR PSYCHIATRY. 2021;26(10):5471
Lack of fibrillar amyloid plaques but hypometabolism and astrogliosis in autosomal dominant variant AssPParc Alzheimer's disease
Lemoine L; Gillberg P-G; Bogdanovic N; Nennesmo I; Saint-Aubert L; Viitanen M; Graff C; Ingelsson M; Nordberg A
Other: CEREBELLUM AND ATAXIAS. 2017;4:5
An unusual cause of fatal rapid-onset ataxia plus syndrome.
Kmezic I; Weinberg J; Hauzenberger D; Hashim F; Kollia E; Klimkowska M; Nennesmo I; Paucar M
Other: CLINICAL CASE REPORTS. 2016;4(8):777-781
Case report: Intraneural perineurioma of the sciatic nerve in an adolescent - strategies for revealing the diagnosis.
Dahlin LB; Nennesmo I; Besjakov J; Ferencz I; Andersson GS; Backman C
Meeting abstract: NEUROMUSCULAR DISORDERS. 2015;25:S235
Late-onset limb-girdle muscular dystrophy caused by GMPPB-mutation
Balcin H; Palmio J; Nennesmo I; Solders G; Udd B
Letter: ACTA NEUROPATHOLOGICA. 2014;127(2):297-298
Neuropathological characterization of two siblings carrying the MAPT S305S mutation demonstrates features resembling argyrophilic grain disease
Ronnback A; Nennesmo I; Tuominen H; Grueninger F; Viitanen M; Graff C
Meeting abstract: FREE RADICAL BIOLOGY AND MEDICINE. 2012;53:S72
Redox proteins in the defense against dopamine induced cell death
Arodin L; Nennesmo I; Bjornstedt M; Fernandes AP
Corrigendum: EUROPEAN JOURNAL OF HUMAN GENETICS. 2012;20(8):910
Mutations in the mitochondrial tRNA^Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy (vol 20, pg 897, 2012)
Tuppen HAL; Naess K; Kennaway NG; Al-Dosary M; Lesko N; Yarham JW; Bruhn H; Wibom R; Nennesmo I; Weleber RG; Blakely EL; Taylor RW; McFarland R
Published conference paper: BIOCHIMICA ET BIOPHYSICA ACTA: INTERNATIONAL JOURNAL OF BIOCHEMISTRY AND BIOPHYSICS. 2009;1787(5):484-490
MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome
Naess K; Freyer C; Bruhn H; Wibom R; Malm G; Nennesmo I; von Dobeln U; Larsson N-G
Letter: ACTA NEUROPATHOLOGICA. 2005;110(3):315-316
Alzheimer pathology associated with POLG1 mutation, multiple mtDNA deletions, and APOE4/4:: premature ageing or just coincidence?
Melberg A; Nennesmo I; Moslemi AR; Kollberg G; Luoma P; Suomalainen A; Holme E; Oldfors A
Corrigendum: EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING. 2003;30(1):187
Multitracer study with positron emission tomography in Creutzfeldt-Jakob disease (vol 30, pg 187, 2003)
Engler H; Lundberg PO; Ekbom K; Nennesmo I; Nilsson A; Bergström M; Tsukada H; Hartvig P; Långström B
Letter: LANCET. 1999;354(9189):1559
Reappraisal of aluminosis and dementia.
Sjögren B; Ljunggren KG; Basun H; Frech W; Nennesmo I

Artiklar

Alla övriga publikationer

Nyheter från KI

Kalenderhändelser från KI