Gunnar Sjöberg

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Articles

Article: ANESTHESIA AND ANALGESIA. 2024;139(4):781-788
Validation of a Novel Method for Noninvasive Mixed Venous Oxygen Saturation Monitoring in Anesthetized Children
Svedmyr A; Steiner K; Andersson A; Sjoberg G; Hallback M; Wallin M; Lonnqvist P-A; Karlsson J
Article: ACTA PAEDIATRICA. 2024;113(4):812-817
Mind the gap-missing device on the shelf? Retrospective experience with 5/7 Occlutech duct Occluder
Steiner K; Sjoberg G; Karsenty C; Bianco L; Bautista-Rodriguez C; Fraisse A
Article: FRONTIERS IN CARDIOVASCULAR MEDICINE. 2024;11:1349166
Longitudinal ECG changes in tetralogy of Fallot and association with surgical repair
Bhat M; Malm T; Sjoberg G; Nordenstam F; Hanseus K; Rosenkvist C-J; Liuba P
Article: FRONTIERS IN CARDIOVASCULAR MEDICINE. 2024;11:1408543
Same-day discharge after percutaneous closure of persistent foramen ovale using intracardiac echocardiography and the Gore Septal Occluder
Steiner K; Sjoberg G; Damlin A; Settergren M; Verouhis D
Article: JACC-CARDIOVASCULAR INTERVENTIONS. 2023;16(4):444-453
Transcatheter Intervention for Coarctation of the Aorta A Nordic Population-Based Registry With Long-Term Follow-Up
Eriksson P; Pihkala J; Jensen AS; Dohlen G; Liuba P; Wahlander H; Sjoberg G; Hlebowicz J; Furenas E; Leirgul E; Settergren M; Vithessonthi K; Nielsen N-E; Christersson C; Sondergaard L; Sinisalo J; Nielsen-Kudsk JE; Dellborg M; Larsen SH
Article: ORPHANET JOURNAL OF RARE DISEASES. 2022;17(1):358
Rare clinical phenotype of filaminopathy presenting as restrictive cardiomyopathy and myopathy in childhood
Muravyev A; Vershinina T; Tesner P; Sjoberg G; Fomicheva Y; Cajbikova NN; Kozyreva A; Zhuk S; Mamaeva E; Tarnovskaya S; Jornholt J; Sokolnikova P; Pervunina T; Vasichkina E; Sejersen T; Kostareva A
Article: CARDIOLOGY IN THE YOUNG. 2022;32(6):861-868
Vitamin D, liver-related biomarkers, and distribution of fat and lean mass in young patients with Fontan circulation
Hansson L; Sandberg C; Ohlund I; Lind T; Bergdahl MS; Wiklund U; Hedlund ER; Sjoberg G; Rydberg A
Article: JOURNAL OF THE AMERICAN HEART ASSOCIATION. 2022;11(7):e022929
Impact of Left Ventricular Morphology on Adverse Outcomes Following Stage 1 Palliation for Hypoplastic Left Heart Syndrome: 20 Years of National Data From Sweden
Fricke K; Mellander M; Hanseus K; Tran P-K; Synnergren M; Ramgren JJ; Rydberg A; Sunnegardh J; Dalen M; Sjoberg G; Weismann CG; Liuba P
Article: PEDIATRIC CARDIOLOGY. 2022;43(2):449-456
Calf Muscle Oxygenation is Impaired and May Decline with Age in Young Patients with Total Cavopulmonary Connection
Bergdahl MS; Crenshaw AG; Hedlund ER; Sjoberg G; Rydberg A; Sandberg C
Article: ACTA PAEDIATRICA. 2021;110(11):3105-3115
Sudden cardiac death in childhood hypertrophic cardiomyopathy is best predicted by a combination of electrocardiogram risk-score and HCMRisk-Kids score
Ostman-Smith I; Sjoberg G; Dahlqvist JA; Larsson P; Fernlund E
Article: JOURNAL OF CLINICAL MEDICINE. 2020;10(1):E122-122
Right Heart Structure, Geometry and Function Assessed by Echocardiography in 6-Year-Old Children Born Extremely Preterm-A Population-Based Cohort Study
Mohlkert L-A; Hallberg J; Broberg O; Sjoberg G; Rydberg A; Liuba P; Fellman V; Domellof M; Norman M; Pegelow Halvorsen C
Journal article: EUROPEAN HEART JOURNAL. 2020;41(Supplement_2):ehaa946.2193
Transcatheter interventions of coarctation of the aorta (CoA): a multinational population-based registry – procedural complications
Eriksson P; Pikhala J; Jensen AS; Dohlen G; Liuba P; Wahlander H; Sjoberg G; Hlebowicz J; Furenas E; Dellborg M; Settergren M; Kudsk JEN; Sondergaard L; Sinisalo J; Holm S
Article: CARDIOLOGY IN THE YOUNG. 2020;30(8):1138-1143
Impaired knee extension muscle strength in adolescents but not in children with Fontan circulation
Sandberg C; Frisk E; Hansson L; Isberg A; Rylander Hedlund E; Sjoberg G; Rydberg A
Article: JOURNAL OF CARDIAC SURGERY. 2020;35(4):868-874
Long-term results of aortic arch reconstruction with branch pulmonary artery homograft patches
Lewis MJ; Johansson Ramgren J; Hallbergson A; Liuba P; Sjoberg G; Malm T
Article: ACTA PAEDIATRICA. 2020;109(4):746-753
Lung function and pulmonary vascular resistance are not associated in 6-year-old children born extremely preterm
Mohlkert L-A; Sjoberg G; Rydberg A; Halvorsen CP; Tufvesson E; Hallberg J; Domellof M; Norman M
Article: CARDIOLOGY IN THE YOUNG. 2020;30(3):303-312
Risk factors for adverse events within one year after atrial septal closure in children: a retrospective follow-up study
Tanghoj G; Liuba P; Sjoberg G; Naumburg E
Article: CONGENITAL HEART DISEASE. 2020;15(5):287-299
Atrial Septal Defect in Children: The Incidence and Risk Factors for Diagnosis
Tanghoj G; Lindam A; Liuba P; Sjoberg G; Naumburg E
Article: CARDIOLOGY. 2020;145(11):746-756
Genetic Spectrum of Left Ventricular Non-Compaction in Paediatric Patients
Vershinina T; Fomicheva Y; Muravyev A; Jorholt J; Kozyreva A; Kiselev A; Gordeev M; Vasichkina E; Segrushichev A; Pervunina T; Sjoberg G; Skyttner-Rahmani S; Sejersen T; Kostareva A
Article: PLOS ONE. 2020;15(3):e0229227
Infantile restrictive cardiomyopathy: cTnI-R170G/W impair the interplay of sarcomeric proteins and the integrity of thin filaments
Cimiotti D; Fujita-Becker S; Moehner D; Smolina N; Budde H; Wies A; Morgenstern L; Gudkova A; Sejersen T; Sjoeberg G; Muegge A; Nowaczyk MM; Reusch P; Pfitzer G; Stehle R; Schroder RR; Mannherz HG; Kostareva A; Jaquet K
Article: CARDIOLOGY IN THE YOUNG. 2019;29(7):922-929
Physical exercise may improve sleep quality in children and adolescents with Fontan circulation
Hedlund ER; Villard L; Lundell B; Sjobere G
Article: CARDIOLOGY IN THE YOUNG. 2019;29(5):626-636
Adverse events within 1 year after surgical and percutaneous closure of atrial septal defects in preterm children
Tanghoj G; Liuba P; Sjoeberg G; Rydberg A; Naumburg E
Article: FRONTIERS IN GENETICS. 2019;10:608
Truncating Variant in Myof Gene Is Associated With Limb-Girdle Type Muscular Dystrophy and Cardiomyopathy
Kiselev A; Vaz R; Knyazeva A; Sergushichev A; Dmitrieva R; Khudiakov A; Jorholt J; Smolina N; Sukhareva K; Fomicheva Y; Mikhaylov E; Mitrofanova L; Predeusu A; Sjoberg G; Rudenko D; Sejersen T; Lindstrand A; Kostareva A
Article: FRONTIERS IN CARDIOVASCULAR MEDICINE. 2019;6:185
Predictors of the Need for an Atrial Septal Defect Closure at Very Young Age
Tanghoj G; Liuba P; Sjoberg G; Naumburg E
Article: HUMAN MUTATION. 2018;39(9):1161-1172
De novo mutations in FLNC leading to early-onset restrictive cardiomyopathy and congenital myopathy
Kiselev A; Vaz R; Knyazeva A; Khudiakov A; Tarnovskaya S; Liu J; Sergushichev A; Kazakov S; Frishman D; Smolina N; Pervunina T; Jorholt J; Sjoberg G; Vershinina T; Rudenko D; Arner A; Sejersen T; Lindstrand A; Kostareva A
Article: CARDIOLOGY IN THE YOUNG. 2018;28(9):1115-1122
Impaired lung function in children and adolescents with Fontan circulation may improve after endurance training
Hedlund ER; Ljungberg H; Soderstrom L; Lundell B; Sjoberg G
Article: CARDIOLOGY IN THE YOUNG. 2018;28(3):438-446
Can endurance training improve physical capacity and quality of life in young Fontan patients?
Hedlund ER; Lundell B; Soderstrom L; Sjoberg G
Article: JOURNAL OF THE AMERICAN HEART ASSOCIATION. 2018;7(2):e007742
The Preterm Heart in Childhood: Left Ventricular Structure, Geometry, and Function Assessed by Echocardiography in 6-Year-Old Survivors of Periviable Births
Mohlkert L-A; Hallberg J; Broberg O; Rydberg A; Halvorsen CP; Liuba P; Fellman V; Domellof M; Sjoberg G; Norman M
Article: FRONTIERS IN GENETICS. 2018;9:684
Time- and Ventricular-Specific Expression Profiles of Genes Encoding Z-Disk Proteins in Pressure Overload Model of Left Ventricular Hypertrophy
Knyazeva A; Krutikov A; Golovkin A; Mishanin A; Pavlov G; Smolina N; Hushkina A; Sejersen T; Sjoberg G; Galagudza M; Kostareva A
Journal article: EUROPEAN HEART JOURNAL. 2017;38(suppl_1):ehx502.p1606
P1606Mutation in MYOF gene is associated with ventricular arrhythmias and limb girdle muscle phenotype
Kiselev A; Dmitrieva R; Smolina N; Khudiakov A; Sergushichev A; Mikhailov E; Mitrophanova L; Rudenko D; Jornholt J; Sjoberg G; Sejersen T; Kostareva A
Journal article: EUROPEAN HEART JOURNAL. 2017;38(suppl_1):ehx493.p5404
P5404Hotspot mutation in FLNC gene as a cause of restrictive cardiomyopathy associated with congenital myopathy development
Kiselev A; Knyazeva A; Sergushichev A; Hudiakov A; Pervunina T; Vershinina T; Nikitina I; Rudenko D; Vasichkina E; Jornholt J; Sjoberg G; Sejersen T; Kostareva A
Article: PEDIATRIC RESEARCH. 2017;81(2):299-306
Preterm arteries in childhood: dimensions, intima-media thickness, and elasticity of the aorta, coronaries, and carotids in 6-y-old children born extremely preterm
Mohlkert L-A; Hallberg J; Broberg O; Hellstroem M; Halvorsen CP; Sjoberg G; Bonamy A-KE; Liuba P; Fellman V; Domelloef M; Norman M
Article: OPEN HEART. 2017;4(2):e000658
Predictors of risk for sudden death in childhood hypertrophic cardiomyopathy: the importance of the ECG risk score.
Östman-Smith I; Sjöberg G; Rydberg A; Larsson P; Fernlund E
Article: ACTA PAEDIATRICA. 2016;105(11):1322-1328
Reduced physical exercise and health-related quality of life after Fontan palliation
Hedlund ER; Lundell B; Villard L; Sjoberg G
Article: PLOS ONE. 2016;11(9):e0163362
Genetic Spectrum of Idiopathic Restrictive Cardiomyopathy Uncovered by Next-Generation Sequencing
Kostareva A; Kiselev A; Gudkova A; Frishman G; Ruepp A; Frishman D; Smolina N; Tarnovskaya S; Nilsson D; Zlotina A; Khodyuchenko T; Vershinina T; Pervunina T; Klyushina A; Kozlenok A; Sjoberg G; Golovljova I; Sejersen T; Shlyakhto E
Journal article: KARDIOLOGIYA. 2016;17(4):278-286
Genetic variants of cardiomyopathies with the neuromuscular phenotype
Kostareva AA; Pervunina TM; Moiseeva OM; Vershinina TL; Gudkova AY; Romanova EI; Kozlova SN; Rudenko DI; Sejersen T; Sjoberg G; Shlyakhto EV
Article: MOLECULAR GENETICS AND METABOLISM. 2015;115(2-3):118-127
Various lamin A/C mutations alter expression profile of mesenchymal stem cells in mutation specific manner
Malashicheva A; Bogdanova M; Zabirnyk A; Smolina N; Ignatieva E; Freilikhman O; Fedorov A; Dmitrieva R; Sjoberg G; Sejersen T; Kostareva A
Article: BIOMED RESEARCH INTERNATIONAL. 2015;2015:594751-12
Primary Murine Myotubes as a Model for Investigating Muscular Dystrophy
Smolina N; Kostareva A; Bruton J; Karpushev A; Sjoberg G; Sejersen T
Journal article: ARCHIVES OF DISEASE IN CHILDHOOD. 2014;99(Suppl 2):a116
PS-012 Left Heart Structure And Function In 6-year-old Children Born Extremely Preterm
Mohlkert L; Broberg O; Hellström M; Halvorsen CP; Hallberg J; Sjöberg G; Bonamy AE; Fellman V; Domellöf M; Norman M
Article: CELL CALCIUM. 2014;56(4):269-275
Aggregate-prone desmin mutations impair mitochondrial calcium uptake in primary myotubes
Smolina N; Bruton J; Sjoberg G; Kostareva A; Sejersen T
Article: CONGENITAL HEART DISEASE. 2014;9(5):391-396
Variants in the NOTCH1 Gene in Patients with Aortic Coarctation
Freylikhman O; Tatarinova T; Smolina N; Zhuk S; Klyushina A; Kiselev A; Moiseeva O; Sjoberg G; Malashicheva A; Kostareva A
Article: PEDIATRIC CARDIOLOGY. 2013;34(2):467-470
Diagnostic Challenge in Desmin Cardiomyopathy With Transformation of Clinical Phenotypes
Gudkova A; Kostareva A; Sjoberg G; Smolina N; Turalchuk M; Kuznetsova I; Rybakova M; Edstrom L; Shlyakhto E; Sejersen T
Journal article: ARCHIVES OF DISEASE IN CHILDHOOD. 2012;97(Suppl 2):a326-A327
1139 Right Heart Dimensions and Function at 6 Years-Of-Age Using 2D- and 3D-Echocardiography
Mohlkert L; Halvorsen C; Sjöberg G; Hallberg J; Norman M
Article: ACTA MYOLOGICA. 2011;30(1):42-45
Desmin A213V substitution represents a rare polymorphism but not a mutation and is more prevalent in patients with heart dilation of various origins.
Kostareva A; Sjoberg G; Gudkova A; Smolina N; Semernin E; Shlyakhto E; Sejersen T
Article: PEDIATRIC BLOOD & CANCER. 2010;54(4):579-584
Exercise echocardiography in asymptomatic survivors of childhood cancer treated with anthracyclines: a prospective follow-up study.
Sieswerda E; Kremer LCM; Vidmar S; De Bruin ML; Smibert E; Sjöberg G; Cheung MMH; Weintraub RG
Article: JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY. 2008;29(1):25-36
Mice expressing L345P mutant desmin exhibit morphological and functional changes of skeletal and cardiac mitochondria
Kostareva A; Sjoberg G; Bruton J; Zhang S-J; Balogh J; Gudkova A; Hedberg B; Edstrom L; Westerblad H; Sejersen T
Article: JOURNAL OF HEART AND LUNG TRANSPLANTATION. 2007;26(3):293-295
X-linked cardiomyopathy presenting as contracted endocardial fibroelastosis.
Sjoberg G; Chow CW; Cooper S; Weintraub RG
Article: ACTA MYOLOGICA. 2006;25(3):109-115
Desmin mutations in a St. Petersburg cohort of cardiomyopathies.
Kostareva A; Gudkova A; Sjoberg G; Kiselev I; Moiseeva O; Karelkina E; Goldfarb L; Schlyakhto E; Sejersen T
Article: HUMAN MUTATION. 2006;27(9):906-913
Variable pathogenic potentials of mutations located in the desmin alpha-helical domain
Goudeau B; Rodrigues-Lima F; Fischer D; Casteras-Simon M; Sambuughin N; de Visser M; Laforet P; Ferrer X; Chapon F; Sjoberg G; Kostareva A; Sejersen T; Dalakas MC; Goldfarb LG; Vicart P
Article: EXPERIMENTAL CELL RESEARCH. 2006;312(9):1554-1565
Forced expression of desmin and desmin mutants in cultured cells:: Impact of myopathic missense mutations in the central coiled-coil domain on network formation
Baer H; Kostareva A; Sjoeberg G; Sejersen T; Katus HA; Herrmann H
Article: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 2005;102(42):15099-15104
Severe muscle disease-causing desmin mutations interfere with in vitro filament assembly at distinct stages
Bär H; Mücke N; Kostareva A; Sjöberg G; Aebi U; Herrmann H
Journal article: EUROPEAN JOURNAL OF HEART FAILURE, SUPPLEMENT. 2005;4(1):25
107 Desmin mutations in patients with cardiomyopathies
Kostareva A; Sjoberg G; Gudkova A; Kiselev I; Schlyakhto E; Sejersen T
Journal article: EUROPEAN JOURNAL OF HEART FAILURE, SUPPLEMENT. 2003;2(1):15-16
113 Morphological features of cardiomyopathy in L345P desmin transgenic mice
Kostareva A; Sjoberg G; Amineva KH; Gudkova A; Sejersen T; Shlyakhto E
Article: ACTA NEUROPATHOLOGICA. 2002;104(5):493-504
Cytoskeletal derangements in hereditary myopathy with a desmin L345P mutation
Carlsson L; Fischer C; Sjöberg G; Robson RM; Sejersen T; Thornell LE
Article: HUMAN MOLECULAR GENETICS. 1999;8(12):2191-2198
A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filament formation
Sjöberg G; Saavedra-Matiz CA; Rosen DR; Wijsman EM; Borg K; Horowitz SH; Sejersen T
Article: PEDIATRIC RESEARCH. 1998;43(3):386-392
Pediatric rhabdomyosarcomas express the intermediate filament nestin
Kobayashi M; Sjöberg G; Söderhäll S; Lendahl U; Sandstedt B; Sejersen T
Article: DIFFERENTIATION. 1997;61(3):151-159
Distribution of nestin in the developing mouse limb bud in vivo and in micro-mass cultures of cells isolated from limb buds
Wroblewski J; Engstrom M; EdwallArvidsson C; Sjoberg G; Sejersen T; Lendahl U
Article: NEUROMUSCULAR DISORDERS. 1997;7(1):39-54
Tenascin-C expression correlates with macrophage invasion in Duchenne muscular dystrophy and in myositis
Gullberg D; Velling T; Sjoberg G; Salmivirta K; Gaggero B; Tiger CF; Edstrom L; Sejersen T
Article: EXPERIMENTAL CELL RESEARCH. 1995;220(1):112-123
ANALYSIS OF FIBRONECTIN AND VITRONECTIN RECEPTORS ON HUMAN FETAL SKELETAL-MUSCLE CELLS UPON DIFFERENTIATION
GULLBERG D; SJOBERG G; VELLING T; SEJERSEN T
Article: DEVELOPMENTAL DYNAMICS. 1995;204(1):57-65
UP-REGULATION OF A NOVEL INTEGRIN ALPHA-CHAIN (ALPHA(MT)) ON HUMAN FETAL MYOTUBES
GULLBERG D; VELLING T; SJOBERG G; SEJERSEN T
Journal article: EXPERIMENTAL CELL RESEARCH. 1994;214(2):447-458
COLOCALIZATION OF NESTIN AND VIMENTIN/DESMIN IN SKELETAL-MUSCLE CELLS DEMONSTRATED BY 3-DIMENSIONAL FLUORESCENCE DIGITAL IMAGING MICROSCOPY
SJOBERG G; JIANG WQ; RINGERTZ NR; LENDAHL U; SEJERSEN T
Journal article: JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY. 1994;53(4):416-423
MYOFIBERS FROM DUCHENNE/BECKER MUSCULAR-DYSTROPHY AND MYOSITIS EXPRESS THE INTERMEDIATE FILAMENT NESTIN
SJOBERG G; EDSTROM L; LENDAHL U; SEJERSEN T
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All other publications

Conference publication: PEDIATRIC CARDIOLOGY. 2022;43(8):1938-1939
Same Day Discharge of Patients After Persistent Foramen Ovale (PFO) Closure with GORE®CARDIOFORM Septal Occluder (GSO)
Steiner K; Sjoberg G; Damlin A; Settergren M
Conference publication: EUROPEAN HEART JOURNAL. 2020;41:2193
Transcatheter interventions of coarctation of the aorta (CoA): a multinational population-based registry - procedural complications
Eriksson P; Pikhala J; Jensen AS; Dohlen G; Liuba P; Wahlander H; Sjoberg G; Hlebowicz J; Furenas E; Dellborg M; Settergren M; Kudsk JEN; Sondergaard L; Sinisalo J; Holm S
Conference publication: EUROPEAN HEART JOURNAL. 2020;41:2197
Transcatheter intervention of coarctation of the aorta (CoA): a multinational population-based registry - effect on hypertension
Eriksson P; Pihkala J; Jensen AS; Dohlen G; Liuba R; Wahlander H; Sjoberg G; Hlebowicz J; Furenas E; Dellborg M; Settergren M; Kudsk-Nielsen JE; Sondergaard L; Sinisalo J; Larsen SH
Meeting abstract: CARDIOVASCULAR RESEARCH. 2018;114:S19
New variant in CMYA5 gene is associated with early-onset restrictive cardiomyopathy and autism-spectrum disorder
Kiselev A; Kornishina T; Sergushichev A; Smolina N; Klyushina A; Pervunina T; Bang ML; Sjoberg G; Sejersen T; Kostareva A
Meeting abstract: CARDIOVASCULAR RESEARCH. 2018;114:S22
Desmin mutations impair mitochondrial function by promoting mtDNA release
Smolina N; Khudiakov A; Sjoberg G; Sejersen T; Kostareva A
Conference publication: EUROPEAN HEART JOURNAL. 2017;38:344
Mutation in MYOF gene is associated with ventricular arrhythmias and limb girdle muscle phenotype
Kiselev A; Dmitrieva R; Smolina N; Khudiakov A; Sergushichev A; Mikhailov E; Mitrophanova L; Rudenko D; Jornholt J; Sjoberg G; Sejersen T; Kostareva A
Conference publication: EUROPEAN HEART JOURNAL. 2017;38:1145
Hotspot mutation in FLNC gene as a cause of restrictive cardiomyopathy associated with congenital myopathy development
Kiselev A; Knyazeva A; Sergushichev A; Hudiakov A; Pervunina T; Vershinina T; Nikitina I; Rudenko D; Vasichkina E; Jornholt J; Sjoberg G; Sejersen T; Kostareva A
Letter: INTERNATIONAL JOURNAL OF CARDIOLOGY. 2016;216:188-189
Progressive cardiac conduction disease associated with a DSP gene mutation
Kiselev A; Mikhaylov E; Parmon E; Sjoberg G; Sejersen T; Tarnovskaya S; Nugnyi P; Mitrofanova L; Lebedev D; Kostareva A
Letter: INTERNATIONAL JOURNAL OF CARDIOLOGY. 2015;184:272-273
Neonatal hypertrophic cardiomyopathy caused by double mutation in RAS pathway genes
Pervunina T; Vershinina T; Kiselev A; Nikitina I; Grekhov E; Mitrofanova L; Sjoberg G; Kostareva A
Meeting abstract: CARDIOVASCULAR RESEARCH. 2014;103:s104-s105
Genetic spectrum of idiopathic restrictive cardiomyopathy uncovered by new generation sequencing
Kostareva A; Gudkova A; Kiselev A; Zlotina A; Smolina N; Klyushina A; Hodyuchenko T; Sjoberg G; Sejersen T; Shlyakhto E
Meeting abstract: CARDIOVASCULAR RESEARCH. 2014;103:s73
Aggregate prone desmin mutations reduced mitochondrial calcium uptake in primary myotubes upon electrical stimulation
Smolina N; Bruton J; Sjoberg G; Kostareva A; Sejersen T
Conference publication: EUROPEAN HEART JOURNAL. 2014;35:534
Genetic spectrum of idiopathic restrictive cardiomyopathy uncovered by NGS
Kostareva A; Gudkova A; Kiselev A; Zlotina A; Klyushina A; Hodyuchenko T; Smolina N; Sjoberg G; Sejersen T; Shlyakhto E
Conference publication: EUROPEAN HEART JOURNAL. 2014;35:109
Aggregate prone desmin mutations reduced mitochondrial calcium uptake in primary myotubes upon electrical stimulation
Kostareva A; Smolina N; Bruton J; Sjoberg G; Sejersen T
Review: FRONTIERS IN BIOSCIENCE - SCHOLAR. 2013;5(1):325-340
Genetic spectrum of cardiomyopathies with neuromuscular phenotype.
Kostareva A; Sejersen T; Sjoberg G
Conference publication: CARDIOVASCULAR RESEARCH. 2010;87:S72
A213V desmin substitution represents a rare polymorphism rather than disease-causing mutation and is more prevalent in patients with heart dilation of various origins.
Kostareva A; Malashicheva A; Sjoberg G; Gudkova A; Semernin E; Shlyakhto E; Sejersen T
Conference publication: EUROPEAN HEART JOURNAL. 2010;31:924-925
Desmin L345P transgenic mice exhibit morphological and biochemical features of amyloidosis of two distinct types
Klingstedt T; Kostareva A; Sjoberg G; Gudkova A; Nilsson P; Hammarstrom P; Sejersen T
Letter: INTERNATIONAL JOURNAL OF CARDIOLOGY. 2009;131(3):410-412
Deletion in TNNI3 gene is associated with restrictive cardiomyopathy
Kostareva A; Gudkova A; Sjoberg G; Morner S; Semernin E; Krutikov A; Shlyakhto E; Sejersen T
Published conference paper: CELL BIOLOGY AND TRANSLATIONAL MEDICINE, VOL 14: STEM CELLS IN LINEAGE SPECIFIC DIFFERENTIATION AND DISEASE. 2009;652:13-21
Standards of Care for Duchenne Muscular Dystrophy: Brief Treat-NMD Recommendations
Sejerson T; Bushby K
Conference publication: EUROPEAN JOURNAL OF CELL BIOLOGY. 2008;87(7):449-450
L345P desmin transgenic mice exhibit changes in mitochondrial Ca²⁺ handling
Kostareva A; Bruton J; Sjoberg G; Gudkova A; Westerblad H; Sejersen T
Conference publication: EUROPEAN HEART JOURNAL. 2007;28:795
L345P desmin transgenic mice exhibit changes in mitochondrial Ca²⁺ handling
Kostareva A; Bruton J; Sjoberg G; Gudkova A; Westerblad H; Sejersen T
Conference publication: EUROPEAN HEART JOURNAL. 2006;27:542
Deletion in the cardiac troponin I gene, resulting in premature stop codon, causes restrictive cardiomyopathy
Kostareva A; Gudkova A; Sjoberg G; Morner S; Semernin E; Krutikov A; Schlyakhto E; Sejersen TH
Review: LAKARTIDNINGEN. 2005;102(11):845-853
[Hereditary cardiomyopathies: a review. Mutation of structural proteins a common cause of hereditary cardiomyopathy].
Sjöberg G; Kostareva A; Sejersen T
Conference publication: EUROPEAN JOURNAL OF CELL BIOLOGY. 2005;84:97
Missense mutations of desmin corrupt filament formation at various stages of the assembly process
Bär H; Mücke N; Kostareva A; Sjöberg G; Aebi U; Herrmann H
Review: JOURNAL OF STRUCTURAL BIOLOGY. 2004;148(2):137-152
The biology of desmin filaments:: how do mutations affect their structure, assembly, and organisation?
Bär H; Strelkov SV; Sjöberg G; Aebi U; Herrmann H
Conference publication: NEUROMUSCULAR DISORDERS. 2004;14(8-9):594
Morphological features of cardiomyopathy in L345P desmin transgenic mice
Kostareva A; Sjöberg G; Gudkova A; Zhang S; Westerblad H; Sejersen T
Conference publication: EUROPEAN JOURNAL OF CELL BIOLOGY. 2004;83:39
Molecular analysis of mutations causing human desmin-related myopathy (DRM)
Bär H; Sjöberg G; Herrmann H
Meeting abstract: EUROPEAN HEART JOURNAL. 2003;24:695
Morphological features of cardiomyopathy in L345P desmin mutation
Kostareva A; Sjoberg G; Gudkova A; Rybakova M; Sejersen T; Shlyakhto E
Conference publication: NEUROMUSCULAR DISORDERS. 2003;13(7-8):629
Functional analyses of L345P desmin mutation associated with familial myopathy and cardiomyopathy
Kostareva A; Sjöberg G; Gudkova A; Sejersen T
Thesis / dissertation: 1997
Nestin : filament formation and expression in myogenesis and muscle disorders
Sjöberg, Gunnar
Conference publication: MOLECULAR BIOLOGY OF THE CELL. 1997;8:2272
Nestin forms obligate heteropolymers with desmin and vimentin in vivo.
Sjoberg G; Meng JJ; Sejersen T; Ip W
Published conference paper: ANNALS OF THE NEW YORK ACADEMY OF SCIENCES. 1996;785:353-355
Nestin distribution in the developing limb bud in vivo and in vitro
Wroblewski J; Engstrom M; EdwallArvidsson C; Sjoberg G; Sejersen T; Lendahl U
Conference publication: JOURNAL OF CELLULAR BIOCHEMISTRY. 1994;:511
INTERMEDIATE FILAMENT NESTIN EXPRESSION DURING MYOGENESIS AND IN MUSCLE DISORDERS
SEJERSEN T; LENDAHL U; SJOBERG G; EDSTROM L
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