P G Barth|R A Hirasing - JoVE Visualize

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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 Neuropathology and Experimental Neurology|September 1, 1993

Ependymal abnormalities in lissencephaly/pachygyriaH B Sarnat, H Z Darwish, P G Barth, et al.

Neuropediatrics|July 13, 1999

Pontocerebellar hypoplasia associated with respiratory-chain defectsT J de Koning, L S de Vries, F Groenendaal, et al.

Neurology|December 11, 2002

Biochemical markers predicting survival in peroxisome biogenesis disordersJ Gootjes, P A W Mooijer, C Dekker, et al.

Neuropediatrics|June 1, 1993

Molybdenum-cofactor deficiency: an easily missed cause of neonatal convulsionsH M Slot, W C Overweg-Plandsoen, H D Bakker, et al.

Tijdschrift Voor Kindergeneeskunde|October 1, 1989

[X-linked adrenoleukodystrophy and other peroxisomal diseases caused by a failing peroxisomal beta-oxidation system: clinical expression, diagnosis and treatment]R J Wanders, P G Barth, R B Schutgens, et al.

Neurology|April 1, 1997

A new leukoencephalopathy with vanishing white matterM S van der Knaap, P G Barth, F J Gabreëls, et al.

European Journal of Pediatrics|July 1, 1985

Cerebral gigantism (Sotos syndrome). Compiled data of 22 cases. Analysis of clinical features, growth and plasma somatomedinJ M Wit, F A Beemer, P G Barth, et al.

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Showing results (171-180 of 224) with videos related to

Sort By:

Pageof 23

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 Neuropathology and Experimental Neurology|September 1, 1993

Ependymal abnormalities in lissencephaly/pachygyriaH B Sarnat, H Z Darwish, P G Barth, et al.

Neuropediatrics|July 13, 1999

Pontocerebellar hypoplasia associated with respiratory-chain defectsT J de Koning, L S de Vries, F Groenendaal, et al.

Neurology|December 11, 2002

Biochemical markers predicting survival in peroxisome biogenesis disordersJ Gootjes, P A W Mooijer, C Dekker, et al.

Neuropediatrics|June 1, 1993

Molybdenum-cofactor deficiency: an easily missed cause of neonatal convulsionsH M Slot, W C Overweg-Plandsoen, H D Bakker, et al.

Tijdschrift Voor Kindergeneeskunde|October 1, 1989

[X-linked adrenoleukodystrophy and other peroxisomal diseases caused by a failing peroxisomal beta-oxidation system: clinical expression, diagnosis and treatment]R J Wanders, P G Barth, R B Schutgens, et al.

Neurology|April 1, 1997

A new leukoencephalopathy with vanishing white matterM S van der Knaap, P G Barth, F J Gabreëls, et al.

European Journal of Pediatrics|July 1, 1985

Cerebral gigantism (Sotos syndrome). Compiled data of 22 cases. Analysis of clinical features, growth and plasma somatomedinJ M Wit, F A Beemer, P G Barth, et al.

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