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F Hanefeld

Showing results (191-200 of 197) with videos related to

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Pediatrics|December 1, 1991
Glutaryl-coenzyme A dehydrogenase deficiency: a distinct encephalopathyG F Hoffmann, F K Trefz, P G Barth, et al.
International Journal of Cancer|September 29, 2000
C-MYC expression in medulloblastoma and its prognostic valueJ Herms, I Neidt, B Lüscher, et al.
Annals of Neurology|October 18, 2001
Autosomal dominant glut-1 deficiency syndrome and familial epilepsyK Brockmann, D Wang, C G Korenke, et al.
Journal of Medical Genetics|May 15, 2003
Mutation analysis in the MECP2 gene and genetic counselling for Rett syndromeH Gill, J P Cheadle, J Maynard, et al.
Journal of the Neurological Sciences|December 14, 2002
Filamin C accumulation is a strong but nonspecific immunohistochemical marker of core formation in muscleC G Bönnemann, T G Thompson, P F M van der Ven, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 1999
Mutations in the nebulin gene associated with autosomal recessive nemaline myopathyK Pelin, P Hilpelä, K Donner, et al.
Journal of Neurology|December 14, 2004
Escalating immunotherapy of multiple sclerosis--new aspects and practical applicationP Rieckmann, K V Toyka, C Bassetti, et al.
Pageof 20

Showing results (191-200 of 197) with videos related to

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 197 results.
Pediatrics|December 1, 1991
Glutaryl-coenzyme A dehydrogenase deficiency: a distinct encephalopathyG F Hoffmann, F K Trefz, P G Barth, et al.
International Journal of Cancer|September 29, 2000
C-MYC expression in medulloblastoma and its prognostic valueJ Herms, I Neidt, B Lüscher, et al.
Annals of Neurology|October 18, 2001
Autosomal dominant glut-1 deficiency syndrome and familial epilepsyK Brockmann, D Wang, C G Korenke, et al.
Journal of Medical Genetics|May 15, 2003
Mutation analysis in the MECP2 gene and genetic counselling for Rett syndromeH Gill, J P Cheadle, J Maynard, et al.
Journal of the Neurological Sciences|December 14, 2002
Filamin C accumulation is a strong but nonspecific immunohistochemical marker of core formation in muscleC G Bönnemann, T G Thompson, P F M van der Ven, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 1999
Mutations in the nebulin gene associated with autosomal recessive nemaline myopathyK Pelin, P Hilpelä, K Donner, et al.
Journal of Neurology|December 14, 2004
Escalating immunotherapy of multiple sclerosis--new aspects and practical applicationP Rieckmann, K V Toyka, C Bassetti, et al.
Pageof 20