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Items: 1 to 20 of 940

1.
2.

[A case of hereditary motor and sensory neuropathy with pyramidal tract sign, optic nerve atrophy and mental retardation].

Adachi T, Imaoka K, Shirasawa A, Yamaguchi S, Kobayashi S.

Rinsho Shinkeigaku. 1998 Dec;38(12):1037-41. Review. Japanese.

PMID:
10349345
3.

[A family of hereditary motor and sensory neuropathy type I with a mutation (Arg98-->His) in myelin Po--report on a second Japanese family].

Ohnishi A, Kashiwada E, Hashimoto T, Yamamoto T, Murai Y, Ohashi H, Ikegami T, Hayasaka K, Sudo K, Yamamori S.

J UOEH. 1996 Mar 1;18(1):19-29. Japanese.

PMID:
8851708
4.

[A case of hereditary motor and sensory neuropathy type I with optic atrophy, neural deafness and pyramidal tract signs].

Saito T, Nishioka M, Ogino M, Endo K, Kowa H.

Rinsho Shinkeigaku. 1993 May;33(5):519-24. Review. Japanese.

PMID:
8365058
5.

[A 62-year-old man with familial parkinsonism with the onset at 24 years of the age].

Takubo H, Kondo T, Mori H, Miyake T, Suda K, Yokochi M, Imai H, Mizuno Y.

No To Shinkei. 1996 Jun;48(6):587-97. Japanese.

PMID:
8703564
6.

[A case of hereditary motor and sensory neuropathy of neuronal type with retardation of motor development].

Nakano S, Ohnishi A, Yamamoto T, Oishi T, Murai Y.

Rinsho Shinkeigaku. 1990 Apr;30(4):448-51. Japanese.

PMID:
2387117
7.

[A case of hereditary motor and sensory neuropathy type I with a new type of peripheral myelin protein (PMP)-22 mutation].

Ohnishi A, Yoshimura T, Kanehisa Y, Fukushima Y.

Rinsho Shinkeigaku. 1995 Jul;35(7):788-92. Japanese.

PMID:
8777804
8.

[A family of X-linked motor and sensory neuropathy with a new type of connexin32 mutation].

Ohnishi A, Yoshimura T, Takazawa A, Hashimoto T, Yamamoto T, Fukushima Y.

Rinsho Shinkeigaku. 1995 Aug;35(8):843-9. Japanese.

PMID:
8665724
9.

[An autopsy case with lower motor neuron disease showing a transient-appearance of anti-GM1 antibody and an improvement of conduction block after gamma-globulin administration].

Kikuchi H, Kawano Y, Dohura K, Kawamura T, Taniwaki T, Yamada T, Kato M, Iwaki T, Kira J.

No To Shinkei. 1999 May;51(5):455-64. Japanese.

PMID:
10396755
10.

[A 54-year-old man with progressive proximal muscle atrophy and gynecomastia].

Anno M, Gotoh K, Hirasawa E, Mori H, Nakajima Y, Mizuno Y.

No To Shinkei. 1995 Jan;47(1):87-96. Japanese.

PMID:
7669408
11.

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

Takamure M, Nakamuro T, Sugie K, Suzumura A, Takayanagi T.

Rinsho Shinkeigaku. 2000 May;40(5):433-8. Japanese.

PMID:
11002724
12.

[A case of hereditary motor and sensory neuropathy (HMSN type 2) with bilateral recurrent nerve palsy].

Kamei H, Nishimaru K, Abe H, Irie M, Ohnishi A.

Rinsho Shinkeigaku. 1993 Sep;33(9):957-60. Japanese.

PMID:
8299275
13.

[A 78-year-old man with young onset parkinsonism and sudden death].

Miyasaka H, Mori H, Saikawa T, Shirai T, Kondo T, Imai H, Mizuno Y.

No To Shinkei. 1996 May;48(5):487-95. Japanese.

PMID:
8672309
14.

[A familial Charcot-Marie-Tooth disease type 1B (CMTD1B) manifesting a new mutation of myelin P0 gene].

Mitsui Y, Matsui T, Nakamura Y, Takahashi M, Yoshikawa H, Hayasaka K.

Rinsho Shinkeigaku. 1994 Nov;34(11):1162-7. Review. Japanese.

PMID:
7537189
15.

[Familial idiopathic vitamin E deficiency associated with cerebellar atrophy].

Aoki K, Washimi Y, Fujimori N, Maruyama K, Yanagisawa N.

Rinsho Shinkeigaku. 1990 Sep;30(9):966-71. Japanese.

PMID:
2265507
17.

[Familial juvenile parkinsonism with dementia and autonomic failure--a case report].

Nitta E, Ishikawa A, Ishiguro H, Baba H, Fukuhara N.

Rinsho Shinkeigaku. 1993 Jan;33(1):74-7. Japanese.

PMID:
8334779
18.
19.

[A case of hereditary motor and sensory neuropathy with vocal cords palsy and diaphragmatic weakness].

Fukuda H, Kitani M, Imaoka K.

Rinsho Shinkeigaku. 1993 Feb;33(2):175-81. Japanese.

PMID:
8319389
20.

[A family of hereditary motor and sensory neuropathy type I with a new type of myelin P0 mutation].

Ohnishi A, Ohnari K, Hashimoto T, Hayasaka K, Yoshimura T, Fukushima Y.

Rinsho Shinkeigaku. 1994 Jun;34(6):546-51. Japanese.

PMID:
7525134

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