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P G Barth

Showing results (121-130 of 177) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1989
Familial NADH: Q1 oxidoreductase (complex I) deficiency: variable expression and possible treatmentF A Wijburg, P G Barth, W Ruitenbeek, 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.
Human Mutation|January 1, 1995
Two intronic mutations in the adrenoleukodystrophy geneS Kemp, M J Ligtenberg, B M van Geel, 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.
Clinical Neurology and Neurosurgery|June 1, 1993
Delay in diagnosis of X-linked adrenoleukodystrophyB M van Geel, J Assies, E B Haverkort, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophyS Kemp, P A Mooyer, P A Bolhuis, et al.
Pageof 18

Showing results (121-130 of 177) with videos related to

Sort By:
Pageof 18
Journal of Inherited Metabolic Disease|January 1, 1989
Familial NADH: Q1 oxidoreductase (complex I) deficiency: variable expression and possible treatmentF A Wijburg, P G Barth, W Ruitenbeek, 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.
Human Mutation|January 1, 1995
Two intronic mutations in the adrenoleukodystrophy geneS Kemp, M J Ligtenberg, B M van Geel, 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.
Clinical Neurology and Neurosurgery|June 1, 1993
Delay in diagnosis of X-linked adrenoleukodystrophyB M van Geel, J Assies, E B Haverkort, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophyS Kemp, P A Mooyer, P A Bolhuis, et al.
Pageof 18