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Journal of the Neurological Sciences
|
July 1, 1995
Familial spastic paraplegia with mental impairment and thin corpus callosum
A Nakamura, K Izumi, F Umehara, et al.
Journal of Neuropathology and Experimental Neurology
|
November 1, 1994
Apoptosis of T lymphocytes in the spinal cord lesions in HTLV-I-associated myelopathy: a possible mechanism to control viral infection in the central nervous system
F Umehara, A Nakamura, S Izumo, et al.
Acta Neuropathologica
|
January 1, 1993
Dominantly inherited motor and sensory neuropathy with excessive myelin folding complex
F Umehara, S Takenaga, M Nakagawa, et al.
Medical Hypotheses
|
December 1, 1993
An autoaggressive process against bystander tissues in HTLV-I-infected individuals: a possible pathomechanism of HAM/TSP
S Ijichi, S Izumo, N Eiraku, et al.
Journal of the Neurological Sciences
|
November 1, 1995
Deletion in chromosome 17p11.2 including the peripheral myelin protein-22 (PMP-22) gene in hereditary neuropathy with liability to pressure palsies
F Umehara, T Kiwaki, H Yoshikawa, et al.
Acta Neuropathologica
|
September 14, 1999
Polyneuropathy with minifascicle formation in a patient with 46XY mixed gonadal dysgenesis
F Umehara, N Yamaguchi, D Kodama, et al.
Neurology
|
September 15, 2005
Motor-sensory neuropathy with minifascicle formation in a woman with normal karyotype
A Malandrini, S Gambelli, M Muglia, et al.
Acta Neuropathologica
|
August 31, 2000
Histopathological analysis of four autopsy cases of HTLV-I-associated myelopathy/tropical spastic paraparesis: inflammatory changes occur simultaneously in the entire central nervous system
M M Aye, E Matsuoka, T Moritoyo, et al.
Neurology
|
April 24, 1999
A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths
M Nakagawa, M Suehara, A Saito, et al.
Acta Neurologica Scandinavica
|
January 25, 2003
Gap junction protein beta 1 (GJB1) mutations and central nervous system symptoms in X-linked Charcot-Marie-Tooth disease
H Takashima, M Nakagawa, F Umehara, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 75) with videos related to
Sort By:
Page
of 8
Journal of the Neurological Sciences
|
July 1, 1995
Familial spastic paraplegia with mental impairment and thin corpus callosum
A Nakamura, K Izumi, F Umehara, et al.
Journal of Neuropathology and Experimental Neurology
|
November 1, 1994
Apoptosis of T lymphocytes in the spinal cord lesions in HTLV-I-associated myelopathy: a possible mechanism to control viral infection in the central nervous system
F Umehara, A Nakamura, S Izumo, et al.
Acta Neuropathologica
|
January 1, 1993
Dominantly inherited motor and sensory neuropathy with excessive myelin folding complex
F Umehara, S Takenaga, M Nakagawa, et al.
Medical Hypotheses
|
December 1, 1993
An autoaggressive process against bystander tissues in HTLV-I-infected individuals: a possible pathomechanism of HAM/TSP
S Ijichi, S Izumo, N Eiraku, et al.
Journal of the Neurological Sciences
|
November 1, 1995
Deletion in chromosome 17p11.2 including the peripheral myelin protein-22 (PMP-22) gene in hereditary neuropathy with liability to pressure palsies
F Umehara, T Kiwaki, H Yoshikawa, et al.
Acta Neuropathologica
|
September 14, 1999
Polyneuropathy with minifascicle formation in a patient with 46XY mixed gonadal dysgenesis
F Umehara, N Yamaguchi, D Kodama, et al.
Neurology
|
September 15, 2005
Motor-sensory neuropathy with minifascicle formation in a woman with normal karyotype
A Malandrini, S Gambelli, M Muglia, et al.
Acta Neuropathologica
|
August 31, 2000
Histopathological analysis of four autopsy cases of HTLV-I-associated myelopathy/tropical spastic paraparesis: inflammatory changes occur simultaneously in the entire central nervous system
M M Aye, E Matsuoka, T Moritoyo, et al.
Neurology
|
April 24, 1999
A novel MPZ gene mutation in dominantly inherited neuropathy with focally folded myelin sheaths
M Nakagawa, M Suehara, A Saito, et al.
Acta Neurologica Scandinavica
|
January 25, 2003
Gap junction protein beta 1 (GJB1) mutations and central nervous system symptoms in X-linked Charcot-Marie-Tooth disease
H Takashima, M Nakagawa, F Umehara, et al.
Page
of 8