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Carola Hedberg

Showing results (1-10 of 67) with videos related to

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Molecular Aspects of Medicine|August 18, 2015
Polyglucosan storage myopathiesCarola Hedberg-Oldfors, Anders Oldfors
European Journal of Human Genetics : EJHG|October 3, 2013
B3GALNT2 is a gene associated with congenital muscular dystrophy with brain malformationsCarola Hedberg, Anders Oldfors, Niklas Darin
Neurology. Genetics|August 2, 2018
Carey-Fineman-Ziter syndrome with mutations in the myomaker gene and muscle fiber hypertrophyCarola Hedberg-Oldfors, Christopher Lindberg, Anders Oldfors
Neuromuscular Disorders : NMD|June 19, 2017
Muscle pathology in Vici syndrome-A case study with a novel mutation in EPG5 and a summary of the literatureCarola Hedberg-Oldfors, Niklas Darin, Anders Oldfors
Endocrine-Related Cancer|December 17, 2008
Molecular classification of spontaneous endometrial adenocarcinomas in BDII ratsEmma Samuelson, Carola Hedberg, Staffan Nilsson, et al.
Brain : a Journal of Neurology|November 16, 2013
Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domainCarola Hedberg, Atle Melberg, Kathe Dahlbom, et al.
American Journal of Medical Genetics. Part A|February 12, 2016
Novel myopathy in a newborn with Shwachman-Diamond syndrome and review of neonatal presentationAlexandra Topa, Mar Tulinius, Anders Oldfors, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 29, 2024
Abnormal expression of myosin heavy chains in early postnatal stages of spinal muscular atrophy type I at single fibre levelCarola Hedberg-Oldfors, Elizabeth Jennions, Kittichate Visuttijai, et al.
Cancer Cell International|June 29, 2011
SKY analysis revealed recurrent numerical and structural chromosome changes in BDII rat endometrial carcinomasEva Falck, Carola Hedberg, Karin Klinga-Levan, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 17, 2021
The phenotypic variability and natural history of NARS2 associated diseaseKalliopi Sofou, Gittan Kollberg, Carola Hedberg-Oldfors, et al.
Pageof 7

Showing results (1-10 of 67) with videos related to

Sort By:
Pageof 7
Molecular Aspects of Medicine|August 18, 2015
Polyglucosan storage myopathiesCarola Hedberg-Oldfors, Anders Oldfors
European Journal of Human Genetics : EJHG|October 3, 2013
B3GALNT2 is a gene associated with congenital muscular dystrophy with brain malformationsCarola Hedberg, Anders Oldfors, Niklas Darin
Neurology. Genetics|August 2, 2018
Carey-Fineman-Ziter syndrome with mutations in the myomaker gene and muscle fiber hypertrophyCarola Hedberg-Oldfors, Christopher Lindberg, Anders Oldfors
Neuromuscular Disorders : NMD|June 19, 2017
Muscle pathology in Vici syndrome-A case study with a novel mutation in EPG5 and a summary of the literatureCarola Hedberg-Oldfors, Niklas Darin, Anders Oldfors
Endocrine-Related Cancer|December 17, 2008
Molecular classification of spontaneous endometrial adenocarcinomas in BDII ratsEmma Samuelson, Carola Hedberg, Staffan Nilsson, et al.
Brain : a Journal of Neurology|November 16, 2013
Hereditary myopathy with early respiratory failure is caused by mutations in the titin FN3 119 domainCarola Hedberg, Atle Melberg, Kathe Dahlbom, et al.
American Journal of Medical Genetics. Part A|February 12, 2016
Novel myopathy in a newborn with Shwachman-Diamond syndrome and review of neonatal presentationAlexandra Topa, Mar Tulinius, Anders Oldfors, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 29, 2024
Abnormal expression of myosin heavy chains in early postnatal stages of spinal muscular atrophy type I at single fibre levelCarola Hedberg-Oldfors, Elizabeth Jennions, Kittichate Visuttijai, et al.
Cancer Cell International|June 29, 2011
SKY analysis revealed recurrent numerical and structural chromosome changes in BDII rat endometrial carcinomasEva Falck, Carola Hedberg, Karin Klinga-Levan, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 17, 2021
The phenotypic variability and natural history of NARS2 associated diseaseKalliopi Sofou, Gittan Kollberg, Carola Hedberg-Oldfors, et al.
Pageof 7