Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H H Goebel

Showing results (241-250 of 323) with videos related to

Pageof 33
Sort By:
Der Nervenarzt|November 11, 1999
[Indications for simultaneous origin of a German and American family with type II hereditary amyloid neuropathy]S Seddigh, N Dahmen, H H Goebel, et al.
Journal of Child Neurology|January 1, 1997
Infantile intranuclear rod myopathyH H Goebel, A Piirsoo, I Warlo, et al.
European Journal of Pediatrics|January 1, 1985
A case of lipogranulomatosis Farber: some clinical and ultrastructural aspectsU Burck, H W Moser, H H Goebel, et al.
Medizinische Klinik (Munich, Germany : 1983)|April 10, 1987
[Rhabdomyolysis caused by carnitine palmitoyltransferase deficiency]M Weber, H H Goebel, E Wandel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1982
The forearm ischaemic work test--hazardous to McArdle patients?H M Meinck, H H Goebel, K W Rumpf, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|December 1, 1987
[Leigh's subacute necrotizing encephalomyelopathy due to decreased activity of the pyruvate dehydrogenase complex]H Siemes, H H Goebel, R C Sengers, et al.
Neuropediatrics|August 1, 1981
Neuromyopathy and vitamin E deficiency in manU Burck, H H Goebel, H D Kuhlendahl, et al.
Brain & Development|January 1, 1992
A mild juvenile variant of type IV glycogenosisE Reusche, F Aksu, H H Goebel, et al.
Prenatal Diagnosis|April 1, 1989
Probable exclusion of juvenile neuronal ceroid lipofuscinosis in a fetus at risk: an interim reportA Kohlschütter, R Rauskolb, H H Goebel, et al.
Acta Neuropathologica|January 1, 1973
Biological characteristics of peripheral nerve tumors induced with ethylnitrosoureaH Cravioto, J F Weiss, E de C Weiss, et al.
Pageof 33

Showing results (241-250 of 323) with videos related to

Sort By:
Pageof 33
Der Nervenarzt|November 11, 1999
[Indications for simultaneous origin of a German and American family with type II hereditary amyloid neuropathy]S Seddigh, N Dahmen, H H Goebel, et al.
Journal of Child Neurology|January 1, 1997
Infantile intranuclear rod myopathyH H Goebel, A Piirsoo, I Warlo, et al.
European Journal of Pediatrics|January 1, 1985
A case of lipogranulomatosis Farber: some clinical and ultrastructural aspectsU Burck, H W Moser, H H Goebel, et al.
Medizinische Klinik (Munich, Germany : 1983)|April 10, 1987
[Rhabdomyolysis caused by carnitine palmitoyltransferase deficiency]M Weber, H H Goebel, E Wandel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1982
The forearm ischaemic work test--hazardous to McArdle patients?H M Meinck, H H Goebel, K W Rumpf, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|December 1, 1987
[Leigh's subacute necrotizing encephalomyelopathy due to decreased activity of the pyruvate dehydrogenase complex]H Siemes, H H Goebel, R C Sengers, et al.
Neuropediatrics|August 1, 1981
Neuromyopathy and vitamin E deficiency in manU Burck, H H Goebel, H D Kuhlendahl, et al.
Brain & Development|January 1, 1992
A mild juvenile variant of type IV glycogenosisE Reusche, F Aksu, H H Goebel, et al.
Prenatal Diagnosis|April 1, 1989
Probable exclusion of juvenile neuronal ceroid lipofuscinosis in a fetus at risk: an interim reportA Kohlschütter, R Rauskolb, H H Goebel, et al.
Acta Neuropathologica|January 1, 1973
Biological characteristics of peripheral nerve tumors induced with ethylnitrosoureaH Cravioto, J F Weiss, E de C Weiss, et al.
Pageof 33