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Ieke B Ginjaar

Showing results (1-10 of 16) with videos related to

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Journal of Medical Genetics|January 13, 2016
The importance of genetic diagnosis for Duchenne muscular dystrophyAnnemieke Aartsma-Rus, Ieke B Ginjaar, Kate Bushby
Neurology|December 29, 2005
Dystrophin analysis in carriers of Duchenne and Becker muscular dystrophyEdo M Hoogerwaard, Ieke B Ginjaar, Egbert Bakker, et al.
Muscle & Nerve|June 14, 2006
CAV3 gene mutation analysis in patients with idiopathic hyper-CK-emiaJaap C Reijneveld, Ieke B Ginjaar, Wendy S Frankhuizen, et al.
Pediatric Neurology|July 22, 2014
Clinical experience with long-term acetazolamide treatment in children with nondystrophic myotonias: a three-case reportJoekie M Markhorst, Bas C Stunnenberg, Ieke B Ginjaar, et al.
Neuromuscular Disorders : NMD|May 5, 2009
Rapid and cost effective detection of small mutations in the DMD gene by high resolution melting curve analysisRowida Almomani, Nienke van der Stoep, Egbert Bakker, et al.
Pediatric Neurology|April 17, 2004
Novel mutations in three patients with LGMD2C with phenotypic differencesSascha Vermeer, Aad Verrips, Michèl A A P Willemsen, et al.
Journal of Child Neurology|May 17, 2014
What can we learn from assisted bicycle training in a girl with dystrophinopathy? A case studyJilske Huijben, Merel Jansen, Ieke B Ginjaar, et al.
Journal of Neuromuscular Diseases|January 2, 2021
Elucidation of the Genetic Cause in Dutch Limb Girdle Muscular Dystrophy Families: A 27-Year's JourneyL Ten Dam, M de Visser, Ieke B Ginjaar, et al.
Neuromuscular Disorders : NMD|April 24, 2013
ANO5 mutations in the Dutch limb girdle muscular dystrophy populationAnneke J van der Kooi, Leroy Ten Dam, Wendy S Frankhuizen, et al.
Muscle & Nerve|March 13, 2014
Cardiac involvement in Dutch patients with sarcoglycanopathy: a cross-sectional cohort and follow-up studySteven M Schade van Westrum, Lukas R C Dekker, Willem G de Voogt, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Journal of Medical Genetics|January 13, 2016
The importance of genetic diagnosis for Duchenne muscular dystrophyAnnemieke Aartsma-Rus, Ieke B Ginjaar, Kate Bushby
Neurology|December 29, 2005
Dystrophin analysis in carriers of Duchenne and Becker muscular dystrophyEdo M Hoogerwaard, Ieke B Ginjaar, Egbert Bakker, et al.
Muscle & Nerve|June 14, 2006
CAV3 gene mutation analysis in patients with idiopathic hyper-CK-emiaJaap C Reijneveld, Ieke B Ginjaar, Wendy S Frankhuizen, et al.
Pediatric Neurology|July 22, 2014
Clinical experience with long-term acetazolamide treatment in children with nondystrophic myotonias: a three-case reportJoekie M Markhorst, Bas C Stunnenberg, Ieke B Ginjaar, et al.
Neuromuscular Disorders : NMD|May 5, 2009
Rapid and cost effective detection of small mutations in the DMD gene by high resolution melting curve analysisRowida Almomani, Nienke van der Stoep, Egbert Bakker, et al.
Pediatric Neurology|April 17, 2004
Novel mutations in three patients with LGMD2C with phenotypic differencesSascha Vermeer, Aad Verrips, Michèl A A P Willemsen, et al.
Journal of Child Neurology|May 17, 2014
What can we learn from assisted bicycle training in a girl with dystrophinopathy? A case studyJilske Huijben, Merel Jansen, Ieke B Ginjaar, et al.
Journal of Neuromuscular Diseases|January 2, 2021
Elucidation of the Genetic Cause in Dutch Limb Girdle Muscular Dystrophy Families: A 27-Year's JourneyL Ten Dam, M de Visser, Ieke B Ginjaar, et al.
Neuromuscular Disorders : NMD|April 24, 2013
ANO5 mutations in the Dutch limb girdle muscular dystrophy populationAnneke J van der Kooi, Leroy Ten Dam, Wendy S Frankhuizen, et al.
Muscle & Nerve|March 13, 2014
Cardiac involvement in Dutch patients with sarcoglycanopathy: a cross-sectional cohort and follow-up studySteven M Schade van Westrum, Lukas R C Dekker, Willem G de Voogt, et al.
Pageof 2