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P G Barth

Showing results (141-150 of 177) with videos related to

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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.
Archives of Neurology|October 1, 1979
X-linked recessive congenital muscle fiber hypotrophy with central nuclei: abnormalities of growth and adenylate cyclase in muscle tissue culturesV Askanas, W K Engel, N B Reddy, et al.
European Journal of Pediatrics|November 1, 1985
A milder variant of Zellweger syndromeP G Barth, R B Schutgens, J A Bakkeren, et al.
Neuropediatrics|June 1, 1992
Leigh syndrome associated with a deficiency of the pyruvate dehydrogenase complex: results of treatment with a ketogenic dietF A Wijburg, P G Barth, L A Bindoff, et al.
Neuropediatrics|March 1, 2002
Neonatal diffusion-weighted MR imaging: relation with histopathology or follow-up MR examinationA M Roelants-van Rijn, P G Nikkels, F Groenendaal, et al.
Annals of Neurology|July 1, 1992
L-2-hydroxyglutaric acidemia: a novel inherited neurometabolic diseaseP G Barth, G F Hoffmann, J Jaeken, et al.
Journal of the Neurological Sciences|April 1, 1995
Immunophenotyping of congenital myopathies: disorganization of sarcomeric, cytoskeletal and extracellular matrix proteinsP F van der Ven, P H Jap, H J ter Laak, et al.
Pediatrics|December 1, 1991
Glutaryl-coenzyme A dehydrogenase deficiency: a distinct encephalopathyG F Hoffmann, F K Trefz, P G Barth, et al.
Neuropathology and Applied Neurobiology|November 26, 2016
Deregulated expression of EZH2 in congenital brainstem disconnectionP G Barth, E Aronica, S Fox, et al.
Pageof 18

Showing results (141-150 of 177) with videos related to

Sort By:
Pageof 18
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.
Archives of Neurology|October 1, 1979
X-linked recessive congenital muscle fiber hypotrophy with central nuclei: abnormalities of growth and adenylate cyclase in muscle tissue culturesV Askanas, W K Engel, N B Reddy, et al.
European Journal of Pediatrics|November 1, 1985
A milder variant of Zellweger syndromeP G Barth, R B Schutgens, J A Bakkeren, et al.
Neuropediatrics|June 1, 1992
Leigh syndrome associated with a deficiency of the pyruvate dehydrogenase complex: results of treatment with a ketogenic dietF A Wijburg, P G Barth, L A Bindoff, et al.
Neuropediatrics|March 1, 2002
Neonatal diffusion-weighted MR imaging: relation with histopathology or follow-up MR examinationA M Roelants-van Rijn, P G Nikkels, F Groenendaal, et al.
Annals of Neurology|July 1, 1992
L-2-hydroxyglutaric acidemia: a novel inherited neurometabolic diseaseP G Barth, G F Hoffmann, J Jaeken, et al.
Journal of the Neurological Sciences|April 1, 1995
Immunophenotyping of congenital myopathies: disorganization of sarcomeric, cytoskeletal and extracellular matrix proteinsP F van der Ven, P H Jap, H J ter Laak, et al.
Pediatrics|December 1, 1991
Glutaryl-coenzyme A dehydrogenase deficiency: a distinct encephalopathyG F Hoffmann, F K Trefz, P G Barth, et al.
Neuropathology and Applied Neurobiology|November 26, 2016
Deregulated expression of EZH2 in congenital brainstem disconnectionP G Barth, E Aronica, S Fox, et al.
Pageof 18