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Items: 1 to 20 of 372

1.

[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
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 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
4.

[An autopsy case of neuronal type Charcot-Marie-Tooth disease (HMSN type II) with nerve deafness and psychiatric symptoms].

Yoshimura I, Yoshimura N, Hanazono T, Usutani S, Muramoto Y, Fukushima Y.

No To Shinkei. 1992 Jun;44(6):571-8. Japanese.

PMID:
1389565
5.

[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
6.

[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
7.
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.

[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
10.

[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
11.

[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
12.

[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
13.

Peroneal muscular atrophy with pyramidal features.

Harding AE, Thomas PK.

J Neurol Neurosurg Psychiatry. 1984 Feb;47(2):168-72.

14.

[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
15.

[Progressive cerebellar ataxia and distal amyotrophy of Charcot-Marie-Tooth type with hyperglutamataemia:two sibling cases].

Tanji H, Takeda A, Tateyama M, Mochizuki H, Itoyama Y.

Rinsho Shinkeigaku. 1995 Jul;35(7):793-7. Japanese.

PMID:
8777805
16.

[A case of motor and sensory polyneuropathy with retinitis pigmentosa and diffuse idiopathic skeletal hyperostosis].

Osoegawa M, Araki E, Arakawa K, Okayama A, Yamada T, Ohnishi A, Kira J.

Rinsho Shinkeigaku. 1999 May;39(5):542-5. Japanese.

PMID:
10424146
17.
18.

[A case of motor neuropathy with pyramidal sign due to prolonged administration of high dose of pancuronium bromide (Myoblock)].

Miyoshi T, Ohnishi A, Yamaguchi Y.

Rinsho Shinkeigaku. 1993 Jun;33(6):620-4. Japanese.

PMID:
8403681
19.

[A case with hereditary motor and sensory neuropathy with multiple cranial nerves involvement].

Nakamura N, Oka N, Nakamura S, Akiguchi I, Kashii S.

Rinsho Shinkeigaku. 1995 May;35(5):516-20. Japanese.

PMID:
7664521
20.

[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

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