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P G Barth

Showing results (71-80 of 177) with videos related to

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Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1985
Neuropathological findings in a case of combined deficiency of sulphite oxidase and xanthine dehydrogenaseP G Barth, F A Beemer, B P Cats, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 19, 2000
[Sensitive and specific screening for detection of spina bifida by echography in the second trimester; systematic review and meta-analysis]J M Vos, M Offringa, C M Bilardo, et al.
Neuropediatrics|November 1, 1989
Schilder's diffuse sclerosis: case study with three years' follow-up and neuro-imagingP G Barth, M M Derix, M C de Krom, et al.
Neurology|January 1, 1996
Peripheral nerve abnormalities in adrenomyeloneuropathy: a clinical and electrodiagnostic studyB M van Geel, J H Koelman, P G Barth, et al.
Developmental Medicine and Child Neurology|August 1, 1990
Diagnostic features and clinical signs of 21 patients with lissencephaly type 1J F de Rijk-van Andel, W F Arts, P G Barth, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Clinical effects of serine medication in non-ketotic hyperglycinaemia due to deficiency of P-protein of the glycine cleavage complexF A Wijburg, C J de Groot, R B Schutgens, et al.
Neurology|January 5, 2002
Late onset white matter disease in peroxisome biogenesis disorderP G Barth, J Gootjes, H Bode, et al.
Journal of Computer Assisted Tomography|March 1, 1995
Central cortico-subcortical involvement: a distinct pattern of brain damage caused by perinatal and postnatal asphyxia in term infantsR P Rademakers, M S van der Knaap, B Verbeeten, et al.
Neuropadiatrie|May 1, 1980
Congenital muscular dystrophy and cerebral dysgenesis in a Dutch familyJ B Krijgsman, P G Barth, F C Stam, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)P G Barth, R J Wanders, P Vreken, et al.
Pageof 18

Showing results (71-80 of 177) with videos related to

Sort By:
Pageof 18
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1985
Neuropathological findings in a case of combined deficiency of sulphite oxidase and xanthine dehydrogenaseP G Barth, F A Beemer, B P Cats, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 19, 2000
[Sensitive and specific screening for detection of spina bifida by echography in the second trimester; systematic review and meta-analysis]J M Vos, M Offringa, C M Bilardo, et al.
Neuropediatrics|November 1, 1989
Schilder's diffuse sclerosis: case study with three years' follow-up and neuro-imagingP G Barth, M M Derix, M C de Krom, et al.
Neurology|January 1, 1996
Peripheral nerve abnormalities in adrenomyeloneuropathy: a clinical and electrodiagnostic studyB M van Geel, J H Koelman, P G Barth, et al.
Developmental Medicine and Child Neurology|August 1, 1990
Diagnostic features and clinical signs of 21 patients with lissencephaly type 1J F de Rijk-van Andel, W F Arts, P G Barth, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Clinical effects of serine medication in non-ketotic hyperglycinaemia due to deficiency of P-protein of the glycine cleavage complexF A Wijburg, C J de Groot, R B Schutgens, et al.
Neurology|January 5, 2002
Late onset white matter disease in peroxisome biogenesis disorderP G Barth, J Gootjes, H Bode, et al.
Journal of Computer Assisted Tomography|March 1, 1995
Central cortico-subcortical involvement: a distinct pattern of brain damage caused by perinatal and postnatal asphyxia in term infantsR P Rademakers, M S van der Knaap, B Verbeeten, et al.
Neuropadiatrie|May 1, 1980
Congenital muscular dystrophy and cerebral dysgenesis in a Dutch familyJ B Krijgsman, P G Barth, F C Stam, et al.
Journal of Inherited Metabolic Disease|July 17, 1999
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)P G Barth, R J Wanders, P Vreken, et al.
Pageof 18