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Brain : a Journal of Neurology
|
October 1, 1990
X-linked dominant hereditary motor and sensory neuropathy
A F Hahn, W F Brown, W J Koopman, et al.
Annals of Neurology
|
July 1, 1982
A variant form of metachromatic leukodystrophy without arylsulfatase deficiency
A F Hahn, B A Gordon, G G Hinton, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 1, 1991
Neuromyotonia in hereditary motor neuropathy
A F Hahn, A W Parkes, C F Bolton, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1984
Polyneuropathy in critically ill patients
C 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 biopsy
A 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 disease
C 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 sulfate
W 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 prednisolone
T E Feasby, J J Gilbert, A F Hahn, et al.
Neurology
|
March 1, 1990
Central lesions in chronic inflammatory demyelinating polyneuropathy: an MRI study
T 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 dosage
A F Hahn, T E Feasby, A Steele, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 78) with videos related to
Sort By:
Page
of 8
Brain : a Journal of Neurology
|
October 1, 1990
X-linked dominant hereditary motor and sensory neuropathy
A F Hahn, W F Brown, W J Koopman, et al.
Annals of Neurology
|
July 1, 1982
A variant form of metachromatic leukodystrophy without arylsulfatase deficiency
A F Hahn, B A Gordon, G G Hinton, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 1, 1991
Neuromyotonia in hereditary motor neuropathy
A F Hahn, A W Parkes, C F Bolton, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1984
Polyneuropathy in critically ill patients
C 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 biopsy
A 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 disease
C 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 sulfate
W 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 prednisolone
T E Feasby, J J Gilbert, A F Hahn, et al.
Neurology
|
March 1, 1990
Central lesions in chronic inflammatory demyelinating polyneuropathy: an MRI study
T 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 dosage
A F Hahn, T E Feasby, A Steele, et al.
Page
of 8