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P G Barth

Showing results (131-140 of 177) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1996
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblastsP G Barth, C Van den Bogert, P A Bolhuis, et al.
Neurology|February 1, 1995
The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2): compiled data from 10 pedigreesP G Barth, G Blennow, H G Lenard, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Macrocephaly: an important indication for organic acid analysisG F Hoffmann, F K Trefz, P G Barth, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Vitamin C treatment in Menkes' disease: failure to affect biochemical and clinical parametersC J de Groot, F A Wijburg, P G Barth, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
The inborn errors of peroxisomal beta-oxidation: a reviewR J Wanders, C W van Roermund, R B Schutgens, et al.
Heart (British Cardiac Society)|March 20, 1998
The heart in limb girdle muscular dystrophyA J van der Kooi, W G de Voogt, P G Barth, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Pathobiochemical implications of hyperdopaminuria in patients with aromatic L-amino acid decarboxylase deficiencyN G Abeling, C Bräutigam, G F Hoffmann, et al.
Biochemical and Biophysical Research Communications|August 27, 1999
Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patientsN Shimozawa, Z Zhang, Y Suzuki, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
L-2-hydroxyglutaric acidaemia: clinical and biochemical findings in 12 patients and preliminary report on L-2-hydroxyacid dehydrogenaseP G Barth, G F Hoffmann, J Jaeken, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 16, 2003
Audit of prenatal and postnatal diagnosis of isolated open spina bifida in three university hospitals in The NetherlandsM A G Olde Scholtenhuis, T E Cohen-Overbeek, M Offringa, et al.
Pageof 18

Showing results (131-140 of 177) with videos related to

Sort By:
Pageof 18
Journal of Inherited Metabolic Disease|January 1, 1996
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblastsP G Barth, C Van den Bogert, P A Bolhuis, et al.
Neurology|February 1, 1995
The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2): compiled data from 10 pedigreesP G Barth, G Blennow, H G Lenard, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Macrocephaly: an important indication for organic acid analysisG F Hoffmann, F K Trefz, P G Barth, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Vitamin C treatment in Menkes' disease: failure to affect biochemical and clinical parametersC J de Groot, F A Wijburg, P G Barth, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
The inborn errors of peroxisomal beta-oxidation: a reviewR J Wanders, C W van Roermund, R B Schutgens, et al.
Heart (British Cardiac Society)|March 20, 1998
The heart in limb girdle muscular dystrophyA J van der Kooi, W G de Voogt, P G Barth, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Pathobiochemical implications of hyperdopaminuria in patients with aromatic L-amino acid decarboxylase deficiencyN G Abeling, C Bräutigam, G F Hoffmann, et al.
Biochemical and Biophysical Research Communications|August 27, 1999
Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patientsN Shimozawa, Z Zhang, Y Suzuki, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
L-2-hydroxyglutaric acidaemia: clinical and biochemical findings in 12 patients and preliminary report on L-2-hydroxyacid dehydrogenaseP G Barth, G F Hoffmann, J Jaeken, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 16, 2003
Audit of prenatal and postnatal diagnosis of isolated open spina bifida in three university hospitals in The NetherlandsM A G Olde Scholtenhuis, T E Cohen-Overbeek, M Offringa, et al.
Pageof 18