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A F Hahn

Showing results (31-40 of 78) with videos related to

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Brain : a Journal of Neurology|October 1, 1990
X-linked dominant hereditary motor and sensory neuropathyA F Hahn, W F Brown, W J Koopman, et al.
Annals of Neurology|July 1, 1982
A variant form of metachromatic leukodystrophy without arylsulfatase deficiencyA F Hahn, B A Gordon, G G Hinton, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1991
Neuromyotonia in hereditary motor neuropathyA F Hahn, A W Parkes, C F Bolton, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1984
Polyneuropathy in critically ill patientsC F Bolton, J J Gilbert, A F Hahn, et al.
Acta Neuropathologica|January 1, 1981
The AB-variant of metachromatic leukodystrophy (postulated activator protein deficiency). Light and electron microscopic findings in a sural nerve biopsyA F Hahn, B A Gordon, J J Gilbert, et al.
Human Mutation|January 1, 1996
Novel mutations in the connexin 32 gene associated with X-linked Charcot-Marie tooth diseaseC C Tan, P J Ainsworth, A F Hahn, et al.
Acta Neuropathologica|January 1, 1989
Neuropathy in IgM lambda paraproteinemia. Immunoreactivity to neural proteins and chondroitin sulfateW C Yee, A F Hahn, S A Hearn, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1987
Treatment of experimental allergic neuritis with prednisoloneT E Feasby, J J Gilbert, A F Hahn, et al.
Neurology|March 1, 1990
Central lesions in chronic inflammatory demyelinating polyneuropathy: an MRI studyT E Feasby, A F Hahn, W J Koopman, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|July 1, 1988
Demyelination and axonal degeneration in Lewis rat experimental allergic neuritis depend on the myelin dosageA F Hahn, T E Feasby, A Steele, et al.
Pageof 8

Showing results (31-40 of 78) with videos related to

Sort By:
Pageof 8
Brain : a Journal of Neurology|October 1, 1990
X-linked dominant hereditary motor and sensory neuropathyA F Hahn, W F Brown, W J Koopman, et al.
Annals of Neurology|July 1, 1982
A variant form of metachromatic leukodystrophy without arylsulfatase deficiencyA F Hahn, B A Gordon, G G Hinton, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 1, 1991
Neuromyotonia in hereditary motor neuropathyA F Hahn, A W Parkes, C F Bolton, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1984
Polyneuropathy in critically ill patientsC F Bolton, J J Gilbert, A F Hahn, et al.
Acta Neuropathologica|January 1, 1981
The AB-variant of metachromatic leukodystrophy (postulated activator protein deficiency). Light and electron microscopic findings in a sural nerve biopsyA F Hahn, B A Gordon, J J Gilbert, et al.
Human Mutation|January 1, 1996
Novel mutations in the connexin 32 gene associated with X-linked Charcot-Marie tooth diseaseC C Tan, P J Ainsworth, A F Hahn, et al.
Acta Neuropathologica|January 1, 1989
Neuropathy in IgM lambda paraproteinemia. Immunoreactivity to neural proteins and chondroitin sulfateW C Yee, A F Hahn, S A Hearn, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1987
Treatment of experimental allergic neuritis with prednisoloneT E Feasby, J J Gilbert, A F Hahn, et al.
Neurology|March 1, 1990
Central lesions in chronic inflammatory demyelinating polyneuropathy: an MRI studyT E Feasby, A F Hahn, W J Koopman, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|July 1, 1988
Demyelination and axonal degeneration in Lewis rat experimental allergic neuritis depend on the myelin dosageA F Hahn, T E Feasby, A Steele, et al.
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