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P G Barth

Showing results (111-120 of 177) with videos related to

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Neuromuscular Disorders : NMD|July 1, 1995
Abnormal expression of intermediate filament proteins in X-linked myotubular myopathy is not reproduced in vitroP F Van der Ven, P H Jap, P G Barth, 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.
Journal of Medical Genetics|September 1, 1995
The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studiesC Wallgren-Pettersson, A Clarke, F Samson, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Progressive generalized brain atrophy and infantile spasms associated with cytochrome c oxidase deficiencyH D Bakker, C Van den Bogert, J G Drewes, et al.
Ultrastructural Pathology|September 1, 1983
Ultrastructure of the liver in th cerebrohepatorenal syndrome of ZellwegerW J Mooi, K P Dingemans, M A van den Bergh Weerman, et al.
American Journal of Human Genetics|October 30, 1998
X chromosome inactivation in carriers of Barth syndromeK H Orstavik, R E Orstavik, A K Naumova, et al.
European Journal of Pediatrics|July 1, 1994
Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcificationsJ F Samson, P G Barth, J I de Vries, et al.
European Journal of Pediatrics|September 15, 1999
Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha geneW Lissens, P Vreken, P G Barth, et al.
Journal of Medical Genetics|October 22, 2003
PTEN hamartoma tumour syndrome: variability of an entityJ H M Merks, L S de Vries, X-P Zhou, et al.
Journal of Neuropathology and Experimental Neurology|September 1, 1993
Ependymal abnormalities in lissencephaly/pachygyriaH B Sarnat, H Z Darwish, P G Barth, et al.
Pageof 18

Showing results (111-120 of 177) with videos related to

Sort By:
Pageof 18
Neuromuscular Disorders : NMD|July 1, 1995
Abnormal expression of intermediate filament proteins in X-linked myotubular myopathy is not reproduced in vitroP F Van der Ven, P H Jap, P G Barth, 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.
Journal of Medical Genetics|September 1, 1995
The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studiesC Wallgren-Pettersson, A Clarke, F Samson, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
Progressive generalized brain atrophy and infantile spasms associated with cytochrome c oxidase deficiencyH D Bakker, C Van den Bogert, J G Drewes, et al.
Ultrastructural Pathology|September 1, 1983
Ultrastructure of the liver in th cerebrohepatorenal syndrome of ZellwegerW J Mooi, K P Dingemans, M A van den Bergh Weerman, et al.
American Journal of Human Genetics|October 30, 1998
X chromosome inactivation in carriers of Barth syndromeK H Orstavik, R E Orstavik, A K Naumova, et al.
European Journal of Pediatrics|July 1, 1994
Familial mitochondrial encephalopathy with fetal ultrasonographic ventriculomegaly and intracerebral calcificationsJ F Samson, P G Barth, J I de Vries, et al.
European Journal of Pediatrics|September 15, 1999
Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha geneW Lissens, P Vreken, P G Barth, et al.
Journal of Medical Genetics|October 22, 2003
PTEN hamartoma tumour syndrome: variability of an entityJ H M Merks, L S de Vries, X-P Zhou, et al.
Journal of Neuropathology and Experimental Neurology|September 1, 1993
Ependymal abnormalities in lissencephaly/pachygyriaH B Sarnat, H Z Darwish, P G Barth, et al.
Pageof 18