H B Ginjaar - JoVE Visualize

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Nederlands Tijdschrift Voor Geneeskunde|December 5, 2000

[The heartache of muscular dystrophy]E M Hoogerwaard, H B Ginjaar, A A Wilde, et al.

Journal of Neuromuscular Diseases|November 19, 2016

Prolonged Ambulation in Duchenne Patients with a Mutation Amenable to Exon 44 SkippingJ C van den Bergen, H B Ginjaar, E H Niks, et al.

Muscle & Nerve|May 8, 1998

Limb girdle muscular dystrophy: a pathological and immunohistochemical reevaluationA J van der Kooi, H B Ginjaar, H F Busch, et al.

Neuropediatrics|January 24, 2006

Molybdenum cofactor deficiency presenting as neonatal hyperekplexia: a clinical, biochemical and genetic studyA Macaya, L Brunso, N Fernández-Castillo, et al.

Neuromuscular Disorders : NMD|July 19, 2003

Somatic mosaicism of a point mutation in the dystrophin gene in a patient presenting with an asymmetrical muscle weakness and contracturesA T J M Helderman-van den Enden, H B Ginjaar, A L J Kneppers, et al.

FEBS Letters|August 24, 1992

Construction of dystrophin fusion proteins to raise targeted antibodies to different epitopesH B Ginjaar, H B van Paassen, J T den Dunnen, et al.

European Journal of Neurology|March 28, 2013

Long-term follow-up study on patients with Miyoshi phenotype of distal muscular dystrophyW H J P Linssen, W G de Voogt, M Krahn, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|February 13, 2009

Redefining the clinical phenotypes of non-dystrophic myotonic syndromesJ Trip, G Drost, H B Ginjaar, et al.

Nucleic Acids Research|July 25, 1989

High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridizationL A Blonden, J T den Dunnen, H M van Paassen, et al.

Clinical Genetics|November 13, 2010

Duchenne/Becker muscular dystrophy in the family: have potential carriers been tested at a molecular level?A T J M Helderman-van den Enden, J C van den Bergen, M H Breuning, et al.

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Showing results (11-20 of 39) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|December 5, 2000

[The heartache of muscular dystrophy]E M Hoogerwaard, H B Ginjaar, A A Wilde, et al.

Journal of Neuromuscular Diseases|November 19, 2016

Prolonged Ambulation in Duchenne Patients with a Mutation Amenable to Exon 44 SkippingJ C van den Bergen, H B Ginjaar, E H Niks, et al.

Muscle & Nerve|May 8, 1998

Limb girdle muscular dystrophy: a pathological and immunohistochemical reevaluationA J van der Kooi, H B Ginjaar, H F Busch, et al.

Neuropediatrics|January 24, 2006

Molybdenum cofactor deficiency presenting as neonatal hyperekplexia: a clinical, biochemical and genetic studyA Macaya, L Brunso, N Fernández-Castillo, et al.

Neuromuscular Disorders : NMD|July 19, 2003

Somatic mosaicism of a point mutation in the dystrophin gene in a patient presenting with an asymmetrical muscle weakness and contracturesA T J M Helderman-van den Enden, H B Ginjaar, A L J Kneppers, et al.

FEBS Letters|August 24, 1992

Construction of dystrophin fusion proteins to raise targeted antibodies to different epitopesH B Ginjaar, H B van Paassen, J T den Dunnen, et al.

European Journal of Neurology|March 28, 2013

Long-term follow-up study on patients with Miyoshi phenotype of distal muscular dystrophyW H J P Linssen, W G de Voogt, M Krahn, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|February 13, 2009

Redefining the clinical phenotypes of non-dystrophic myotonic syndromesJ Trip, G Drost, H B Ginjaar, et al.

Nucleic Acids Research|July 25, 1989

High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridizationL A Blonden, J T den Dunnen, H M van Paassen, et al.

Clinical Genetics|November 13, 2010

Duchenne/Becker muscular dystrophy in the family: have potential carriers been tested at a molecular level?A T J M Helderman-van den Enden, J C van den Bergen, M H Breuning, et al.

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