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H H Goebel

Showing results (301-310 of 323) with videos related to

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Neurology|December 30, 2004
T2-hyperintense cerebellar cortex in Marinesco-Sjögren syndromeI Harting, A Blaschek, N I Wolf, et al.
Neuropediatrics|May 1, 1988
Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosisT Voit, O Krogmann, H G Lenard, et al.
Neurology|January 5, 2002
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutationM Vorgerd, K Ricker, F Ziemssen, et al.
Annals of the New York Academy of Sciences|March 27, 1995
X-linked dilated cardiomyopathy. Novel mutation of the dystrophin geneW M Franz, M Cremer, R Herrmann, et al.
Journal of Medical Genetics|November 10, 2000
Desmin splice variants causing cardiac and skeletal myopathyK Y Park, M C Dalakas, H H Goebel, et al.
Annals of Neurology|February 5, 1998
Localization of the giant axonal neuropathy gene to chromosome 16q24K M Flanigan, T O Crawford, J W Griffin, et al.
Acta Neuropathologica|January 1, 1987
Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorderA Bardosi, W Creutzfeldt, S DiMauro, et al.
American Journal of Medical Genetics|October 27, 1998
Megalencephaly, mega corpus callosum, and complete lack of motor development: a previously undescribed syndromeG Göhlich-Ratmann, M Baethmann, P Lorenz, et al.
Deutsche Medizinische Wochenschrift (1946)|May 29, 1981
[Myoglobinuric renal failure in hyperosmolar diabetic coma (author's transl)]K W Rumpf, H Kaiser, H J Gröne, et al.
Journal of the Neurological Sciences|January 1, 1997
Progressive cerebellar ataxia, proximal neurogenic weakness and ocular motor disturbances: hexosaminidase A deficiency with late clinical onset in four siblingsE Hund, A Grau, W Fogel, et al.
Pageof 33

Showing results (301-310 of 323) with videos related to

Sort By:
Pageof 33
Neurology|December 30, 2004
T2-hyperintense cerebellar cortex in Marinesco-Sjögren syndromeI Harting, A Blaschek, N I Wolf, et al.
Neuropediatrics|May 1, 1988
Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosisT Voit, O Krogmann, H G Lenard, et al.
Neurology|January 5, 2002
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutationM Vorgerd, K Ricker, F Ziemssen, et al.
Annals of the New York Academy of Sciences|March 27, 1995
X-linked dilated cardiomyopathy. Novel mutation of the dystrophin geneW M Franz, M Cremer, R Herrmann, et al.
Journal of Medical Genetics|November 10, 2000
Desmin splice variants causing cardiac and skeletal myopathyK Y Park, M C Dalakas, H H Goebel, et al.
Annals of Neurology|February 5, 1998
Localization of the giant axonal neuropathy gene to chromosome 16q24K M Flanigan, T O Crawford, J W Griffin, et al.
Acta Neuropathologica|January 1, 1987
Myo-, neuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorderA Bardosi, W Creutzfeldt, S DiMauro, et al.
American Journal of Medical Genetics|October 27, 1998
Megalencephaly, mega corpus callosum, and complete lack of motor development: a previously undescribed syndromeG Göhlich-Ratmann, M Baethmann, P Lorenz, et al.
Deutsche Medizinische Wochenschrift (1946)|May 29, 1981
[Myoglobinuric renal failure in hyperosmolar diabetic coma (author's transl)]K W Rumpf, H Kaiser, H J Gröne, et al.
Journal of the Neurological Sciences|January 1, 1997
Progressive cerebellar ataxia, proximal neurogenic weakness and ocular motor disturbances: hexosaminidase A deficiency with late clinical onset in four siblingsE Hund, A Grau, W Fogel, et al.
Pageof 33