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P G Barth

Showing results (61-70 of 177) with videos related to

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Acta Neuropathologica|August 1, 1996
Histopathology of an infantile-onset spongiform leukoencephalopathy with a discrepantly mild clinical courseM S van der Knaap, P G Barth, G F Vrensen, et al.
Neuromuscular Disorders : NMD|January 1, 1994
Cultured human muscle cells and respiratory chain deficienciesN H Herzberg, P A Bolhuis, C van den Bogert, et al.
Brain : a Journal of Neurology|October 1, 1995
Non-decussating retinal-fugal fibre syndrome. An inborn achiasmatic malformation associated with visuotopic misrouting, visual evoked potential ipsilateral asymmetry and nystagmusP Apkarian, L J Bour, P G Barth, et al.
European Journal of Pediatrics|April 1, 1995
The Hoyeraal-Hreidarsson syndrome: the fourth case of a separate entity with prenatal growth retardation, progressive pancytopenia and cerebellar hypoplasiaC M Aalfs, H van den Berg, P G Barth, et al.
Pediatric Radiology|January 1, 1995
Subependymal germinolytic cysts in Zellweger syndromeI M Russel, L van Sonderen, H L van Straaten, et al.
Neuropediatrics|May 28, 2008
Congenital brainstem disconnection associated with a syrinx of the brainstemP G Barth, L S de Vries, P G J Nikkels, et al.
Neuropediatrics|February 1, 1987
The heterogeneity of the Pena-Shokeir syndromeG Hageman, J Willemse, B A van Ketel, et al.
Neuropediatrics|November 1, 1988
Gliomatosis cerebri in a newbornP G Barth, F C Stam, W Hack, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 27, 1993
[Pelizaeus-Merzbacher disease]J C Koetsveld-Baart, I E Glaudemans-van Gelderen, J Valk, et al.
American Journal of Human Genetics|March 1, 1991
Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28P A Bolhuis, G W Hensels, T J Hulsebos, et al.
Pageof 18

Showing results (61-70 of 177) with videos related to

Sort By:
Pageof 18
Acta Neuropathologica|August 1, 1996
Histopathology of an infantile-onset spongiform leukoencephalopathy with a discrepantly mild clinical courseM S van der Knaap, P G Barth, G F Vrensen, et al.
Neuromuscular Disorders : NMD|January 1, 1994
Cultured human muscle cells and respiratory chain deficienciesN H Herzberg, P A Bolhuis, C van den Bogert, et al.
Brain : a Journal of Neurology|October 1, 1995
Non-decussating retinal-fugal fibre syndrome. An inborn achiasmatic malformation associated with visuotopic misrouting, visual evoked potential ipsilateral asymmetry and nystagmusP Apkarian, L J Bour, P G Barth, et al.
European Journal of Pediatrics|April 1, 1995
The Hoyeraal-Hreidarsson syndrome: the fourth case of a separate entity with prenatal growth retardation, progressive pancytopenia and cerebellar hypoplasiaC M Aalfs, H van den Berg, P G Barth, et al.
Pediatric Radiology|January 1, 1995
Subependymal germinolytic cysts in Zellweger syndromeI M Russel, L van Sonderen, H L van Straaten, et al.
Neuropediatrics|May 28, 2008
Congenital brainstem disconnection associated with a syrinx of the brainstemP G Barth, L S de Vries, P G J Nikkels, et al.
Neuropediatrics|February 1, 1987
The heterogeneity of the Pena-Shokeir syndromeG Hageman, J Willemse, B A van Ketel, et al.
Neuropediatrics|November 1, 1988
Gliomatosis cerebri in a newbornP G Barth, F C Stam, W Hack, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 27, 1993
[Pelizaeus-Merzbacher disease]J C Koetsveld-Baart, I E Glaudemans-van Gelderen, J Valk, et al.
American Journal of Human Genetics|March 1, 1991
Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28P A Bolhuis, G W Hensels, T J Hulsebos, et al.
Pageof 18