Sugie K - Search Results

1

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: sugie k. 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

2

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: sugie k. Neurology. 2005 Sep 13;65(5):776. doi: 10.1212/01.wnl.0000174516.41417.b9. Neurology. 2005. PMID: 16157924 No abstract available.

3

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. Ann Neurol. 2002 Mar;51(3):385-8. doi: 10.1002/ana.10150. Ann Neurol. 2002. PMID: 11891836

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. Neuro Endocrinol Lett. 2012;33(8):757-60. Neuro Endocrinol Lett. 2012. PMID: 23391976

5

[Merosin-positive congenital muscular dystrophy with early orthopaedic problems in relation to Ullrich's disease].

Chang S, Ishikawa T, Nonaka I, Tsukamoto H, Saito M, Ban K, Wada I, Sugie K, Nishino I. Chang S, et al. Among authors: sugie k. No To Hattatsu. 2003 Mar;35(2):159-64. No To Hattatsu. 2003. PMID: 12661101 Japanese.

6

Partial duplication of DHH causes minifascicular neuropathy: A novel mutation detection of DHH.

Sato NS, Maekawa R, Ishiura H, Mitsui J, Naruse H, Tokushige SI, Sugie K, Tate G, Shimizu J, Goto J, Tsuji S, Shiio Y. Sato NS, et al. Among authors: sugie k. Ann Clin Transl Neurol. 2017 May 22;4(6):415-421. doi: 10.1002/acn3.417. eCollection 2017 Jun. Ann Clin Transl Neurol. 2017. PMID: 28589169 Free PMC article.

7

[A case of acute multifocal motor neuropathy with conduction block after Campylobacter jejuni enteritis].

Sugie K, Murata K, Ikoma K, Suzumura A, Takayanagi T. Sugie K, et al. Rinsho Shinkeigaku. 1998 Jan;38(1):42-5. Rinsho Shinkeigaku. 1998. PMID: 9597909 Japanese.

8

[A patient of Charcot-Marie-tooth disease with rigid spine and respiratory failure].

Takamure M, Nakamuro T, Sugie K, Suzumura A, Takayanagi T. Takamure M, et al. Among authors: sugie k. Rinsho Shinkeigaku. 2000 May;40(5):433-8. Rinsho Shinkeigaku. 2000. PMID: 11002724 Japanese.

9

[A report of two siblings with both maternal dentato-rubro-pallido-luysian atrophy and paternal Ehlers-Danlos syndrome type III].

Sugie K, Nakamuro T, Harada N, Suzumura A, Takayanagi T. Sugie K, et al. Rinsho Shinkeigaku. 1998 Mar;38(3):233-7. Rinsho Shinkeigaku. 1998. PMID: 9711120 Japanese.

10

[A case of antiphospholipid antibody syndrome with cerebral infarction showing slowly progressive pure motor monoparesis in unilateral upper extremity].

Sugie K, Goto Y, Takamure M, Suzumura A, Takayanagi T. Sugie K, et al. No To Shinkei. 2000 Nov;52(11):1007-11. No To Shinkei. 2000. PMID: 11215263 Japanese.

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