P G Barth|R A Hirasing - JoVE Visualize

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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.

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, 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.

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.

Acta Neuropathologica|January 1, 1995

Congenital muscular dystrophy and severe central nervous system atrophy in two siblingsQ H Leyten, P G Barth, F J Gabreëls, et al.

Neuromuscular Disorders : NMD|July 23, 1998

Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch familiesP G Barth, R J Wanders, W Ruitenbeek, et al.

Pageof 23

Showing results (181-190 of 224) with videos related to

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Pageof 23

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.

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, 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.

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.

Acta Neuropathologica|January 1, 1995

Congenital muscular dystrophy and severe central nervous system atrophy in two siblingsQ H Leyten, P G Barth, F J Gabreëls, et al.

Neuromuscular Disorders : NMD|July 23, 1998

Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch familiesP G Barth, R J Wanders, W Ruitenbeek, et al.

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