Umehara F - Search Results

1

Hereditary motor and sensory neuropathy with minifascicle formation in a patient with 46XY pure gonadal dysgenesis: a new clinical entity.

Sugie K, Futamura N, Suzumura A, Tate G, Umehara F. Sugie K, et al. Among authors: umehara f. Ann Neurol. 2002 Mar;51(3):385-8. doi: 10.1002/ana.10150. Ann Neurol. 2002. PMID: 11891836

2

Minifascicular neuropathy: a new concept of the human disease caused by desert hedgehog gene mutation.

Umehara F, Tate G, Itoh K, Osame M. Umehara F, et al. Cell Mol Biol (Noisy-le-grand). 2002 Mar;48(2):187-9. Cell Mol Biol (Noisy-le-grand). 2002. PMID: 11990454 Review.

3

Motor-sensory neuropathy without minifascicles in a patient with 46XY gonadal dysgenesis.

Malandrini A, Gambelli S, Muglia M, Berti G, Gaudiano C, Patitucci A, Sugie K, Umehara F, Quattrone A, Dotti MT, Federico A. Malandrini A, et al. Among authors: umehara f. Brain Dev. 2008 Apr;30(4):291-4. doi: 10.1016/j.braindev.2007.07.010. Epub 2007 Sep 4. Brain Dev. 2008. PMID: 17768021

4

Chronic severe axonal polyneuropathy associated with hyperthyroidism and multivitamin deficiency.

Sugie K, Umehara F, Kataoka H, Kumazawa A, Ueno S. Sugie K, et al. Among authors: umehara f. Neuro Endocrinol Lett. 2012;33(8):757-60. Neuro Endocrinol Lett. 2012. PMID: 23391976

5

A novel mutation of desert hedgehog in a patient with 46,XY partial gonadal dysgenesis accompanied by minifascicular neuropathy.

Umehara F, Tate G, Itoh K, Yamaguchi N, Douchi T, Mitsuya T, Osame M. Umehara F, et al. Am J Hum Genet. 2000 Nov;67(5):1302-5. doi: 10.1016/S0002-9297(07)62958-9. Epub 2000 Oct 2. Am J Hum Genet. 2000. PMID: 11017805 Free PMC article.

6

Motor-sensory neuropathy with minifascicle formation in a woman with normal karyotype.

Malandrini A, Gambelli S, Muglia M, Berti G, Patitucci A, Sugie K, Umehara F, Quattrone A, Dotti MT, Federico A. Malandrini A, et al. Among authors: umehara f. Neurology. 2005 Sep 13;65(5):776. doi: 10.1212/01.wnl.0000174516.41417.b9. Neurology. 2005. PMID: 16157924 No abstract available.

7

Hereditary motor and sensory neuropathy with myelin folding and juvenile onset glaucoma.

Kiwaki T, Umehara F, Takashima H, Nakagawa M, Kamimura K, Kashio N, Sakamoto Y, Unoki K, Nobuhara Y, Michizono K, Watanabe O, Arimura H, Osame M. Kiwaki T, et al. Among authors: umehara f. Neurology. 2000 Aug 8;55(3):392-7. doi: 10.1212/wnl.55.3.392. Neurology. 2000. PMID: 10932274

8

Neurologic manifestations of Kanzaki disease.

Umehara F, Matsumuro K, Kurono Y, Arimura K, Osame M, Kanzaki T. Umehara F, et al. Neurology. 2004 May 11;62(9):1604-6. doi: 10.1212/01.wnl.0000123116.96441.34. Neurology. 2004. PMID: 15136691

9

Polyneuropathy with minifascicle formation in a patient with 46XY mixed gonadal dysgenesis.

Umehara F, Yamaguchi N, Kodama D, Takenaga S, Kiwaki T, Sonoda Y, Arimura Y, Yamada H, Arimura K, Osame M. Umehara F, et al. Acta Neuropathol. 1999 Sep;98(3):309-12. doi: 10.1007/s004010051085. Acta Neuropathol. 1999. PMID: 10483790

10

Werner's syndrome associated with spastic paraparesis and peripheral neuropathy.

Umehara F, Abe M, Nakagawa M, Izumo S, Arimura K, Matsumuro K, Osame M. Umehara F, et al. Neurology. 1993 Jun;43(6):1252-4. doi: 10.1212/wnl.43.6.1252. Neurology. 1993. PMID: 8170578

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

116 results

Search Page

Filters