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F Umehara

Showing results (71-80 of 75) with videos related to

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Neurology|August 12, 2004
SET binding factor 2 (SBF2) mutation causes CMT4B with juvenile onset glaucomaR Hirano, H Takashima, F Umehara, et al.
Neurology|August 10, 2000
Hereditary motor and sensory neuropathy with myelin folding and juvenile onset glaucomaT Kiwaki, F Umehara, H Takashima, et al.
Journal of the Neurological Sciences|March 20, 1997
Autosomal dominant early onset dementia and leukoencephalopathy in a Japanese family: clinical, neuroimaging and genetic studiesY Utatsu, H Takashima, K Michizono, et al.
Neurology|June 14, 2006
Early clinical signs and imaging findings in Gerstmann-Sträussler-Scheinker syndrome (Pro102Leu)H Arata, H Takashima, R Hirano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 19, 2005
Age associated axonal features in HNPP with 17p11.2 deletion in JapanH Koike, M Hirayama, M Yamamoto, et al.
Pageof 8

Showing results (71-80 of 75) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 75 results.
Neurology|August 12, 2004
SET binding factor 2 (SBF2) mutation causes CMT4B with juvenile onset glaucomaR Hirano, H Takashima, F Umehara, et al.
Neurology|August 10, 2000
Hereditary motor and sensory neuropathy with myelin folding and juvenile onset glaucomaT Kiwaki, F Umehara, H Takashima, et al.
Journal of the Neurological Sciences|March 20, 1997
Autosomal dominant early onset dementia and leukoencephalopathy in a Japanese family: clinical, neuroimaging and genetic studiesY Utatsu, H Takashima, K Michizono, et al.
Neurology|June 14, 2006
Early clinical signs and imaging findings in Gerstmann-Sträussler-Scheinker syndrome (Pro102Leu)H Arata, H Takashima, R Hirano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 19, 2005
Age associated axonal features in HNPP with 17p11.2 deletion in JapanH Koike, M Hirayama, M Yamamoto, et al.
Pageof 8