These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
372 related items for PubMed ID: 10349345
1. [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. PubMed ID: 10349345 [Abstract] [Full Text] [Related]
2. [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. PubMed ID: 8365058 [Abstract] [Full Text] [Related]
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. PubMed ID: 2387117 [Abstract] [Full Text] [Related]
4. [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. PubMed ID: 8665724 [Abstract] [Full Text] [Related]
5. [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. PubMed ID: 8299275 [Abstract] [Full Text] [Related]
6. [An unusual case of peroneal muscular atrophy with rigidity, polyneuropathy, mental retardation, and diabetes mellitus developed in familial Parkinson's disease]. Saito T, Hosoda M, Aoto K, Hasegawa H, Kowa H. Rinsho Shinkeigaku; 1995 Aug; 35(8):878-83. PubMed ID: 8665730 [Abstract] [Full Text] [Related]
7. [A family of hereditary motor and sensory neuropathy with spastic paraplegia (HMSN type V)]. Murayama T, Nagamatsu M, Sugimura K, Matsuoka Y, Takahashi A. Rinsho Shinkeigaku; 1989 Oct; 29(10):1272-7. PubMed ID: 2691166 [Abstract] [Full Text] [Related]
10. Hereditary motor and sensory neuropathy type I and motor neuron disease. An unusual association. La Pia S, Valiani R, Vitolo S, Galdiero S, Rossi V, Santangelo R, Barbieri F. Acta Neurol (Napoli); 1989 Aug; 11(4):226-32. PubMed ID: 2801256 [Abstract] [Full Text] [Related]
11. [A family of hereditary motor and sensory neuropathy with spastic paraplegia (HMSN type V) presenting with phenotypic uniformity including onset in early childhood]. Yamashita M, Yamamoto T, Oka N. No To Shinkei; 1999 Nov; 51(11):975-9. PubMed ID: 10586415 [Abstract] [Full Text] [Related]
12. [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. PubMed ID: 1389565 [Abstract] [Full Text] [Related]
13. [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. PubMed ID: 8777804 [Abstract] [Full Text] [Related]
14. [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. PubMed ID: 7525134 [Abstract] [Full Text] [Related]
15. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies. Vasilescu C. Rom J Neurol Psychiatry; 1993 Jun; 31(3-4):207-19. PubMed ID: 8011484 [Abstract] [Full Text] [Related]