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P G Barth

Showing results (171-180 of 177) with videos related to

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Journal of the Neurological Sciences|December 1, 1983
An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytesP G Barth, H R Scholte, J A Berden, et al.
American Journal of Human Genetics|October 23, 1997
The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathiesP D'Adamo, L Fassone, A Gedeon, et al.
Annals of Neurology|June 9, 1999
Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex IR H Triepels, L P van den Heuvel, J L Loeffen, et al.
Neurology|June 15, 2007
Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the familiesA J van der Kooi, W S Frankhuizen, P G Barth, et al.
Journal of Medical Genetics|May 17, 2005
POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndromeJ van Reeuwijk, M Janssen, C van den Elzen, et al.
Journal of Neurology|September 19, 2000
Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophyH B Ginjaar, A J van der Kooi, H Ceelie, et al.
Brain : a Journal of Neurology|October 1, 1996
The clinical spectrum of limb girdle muscular dystrophy. A survey in The NetherlandsA J van der Kooi, P G Barth, H F Busch, et al.
Pageof 18

Showing results (171-180 of 177) with videos related to

Sort By:
Pageof 18
You have reached the last page of results.This site can display upto 177 results.
Journal of the Neurological Sciences|December 1, 1983
An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytesP G Barth, H R Scholte, J A Berden, et al.
American Journal of Human Genetics|October 23, 1997
The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathiesP D'Adamo, L Fassone, A Gedeon, et al.
Annals of Neurology|June 9, 1999
Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex IR H Triepels, L P van den Heuvel, J L Loeffen, et al.
Neurology|June 15, 2007
Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the familiesA J van der Kooi, W S Frankhuizen, P G Barth, et al.
Journal of Medical Genetics|May 17, 2005
POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndromeJ van Reeuwijk, M Janssen, C van den Elzen, et al.
Journal of Neurology|September 19, 2000
Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophyH B Ginjaar, A J van der Kooi, H Ceelie, et al.
Brain : a Journal of Neurology|October 1, 1996
The clinical spectrum of limb girdle muscular dystrophy. A survey in The NetherlandsA J van der Kooi, P G Barth, H F Busch, et al.
Pageof 18