Gunnar Sjöberg

Om mig
Publikationer
Forskningsbidrag
Populärvetenskap och samverkan

Om mig

Forskare och överläkare på Barnhjärtcentrum med speciell inriktning mot
interventionell barnkardiologi och kardiogenetik. FOU-ansvarig inom enheten
för barnkardiologi och ledamot av FOU grupp inom ME/OO HBM2.

Forskningsbeskrivning

Med min bakgrund inom molekylärbiologisk grundforskning på muskelceller var
det naturligt att som kliniker intressera mig för patientgruppen barn med
ärftliga hjärtmuskelsjukdomar (kardiomyopatier). Min forskning har därför
rört genetiska och molekylära aspekter på dessa sjukdomar och
laboratorieverksamheten har tidigare varit på CMM följt av Bioclinicum här
på KI med ett nära samarbete med Almazov Medical Center i St Petersburg.
Som interventionell barnkardiolog har forskning inom även detta fält på
senare år tagit plats med studier av öppetstående ductus arteriosus och
förmaksseptumdefekter framför allt hos för tidigt födda barn. Som
huvudhandledare för Eva Rylander Hedlund också slutfört ett
doktorandprojekt med studier av fysisk aktivitet hos barn med
enkammarhjärta.

Artiklar

Article: ACTA PAEDIATRICA, INTERNATIONAL JOURNAL OF PAEDIATRICS. 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: 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, INTERNATIONAL JOURNAL OF PAEDIATRICS. 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, INTERNATIONAL JOURNAL OF PAEDIATRICS. 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: 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: 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(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, INTERNATIONAL JOURNAL OF PAEDIATRICS. 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
Journal article: KARDIOLOGIIA. 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: 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
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 AND 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: THE 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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Alla övriga publikationer

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 (CVR). 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 (CVR). 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 (CVR). 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 (CVR). 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 (CVR). 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: ADVANCES IN EXPERIMENTAL MEDICINE AND BIOLOGY. 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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Swedish Heart-Lung Foundation
1 January 2020 - 31 December 2022

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