BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

285 related articles for article (PubMed ID: 8777804)

  • 1. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A case of Charcot-Marie-Tooth disease 1 B with Val 146Phe mutation of myelin protein zero showing a severe clinical phenotype].
    Ohnishi A; Aoki A; Yamamoto T; Tsuji S
    Rinsho Shinkeigaku; 2000 Mar; 40(3):268-70. PubMed ID: 10885340
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 18(1):19-29. PubMed ID: 8851708
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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. PubMed ID: 7537189
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Molecular pathology of Charcot-Marie-Tooth disease type 1A: abnormal expression of PMP-22].
    Yoshikawa H; Nishimura T; Yanagihara T
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1441-3. PubMed ID: 8752424
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year study.
    Bird TD; Kraft GH; Lipe HP; Kenney KL; Sumi SM
    Ann Neurol; 1997 Apr; 41(4):463-9. PubMed ID: 9124803
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Charcot-Marie-Tooth type X: A novel mutation in the Cx32 gene with central conduction slowing.
    Seeman P; Mazanec R; Ctvrtecková M; Smilková D
    Int J Mol Med; 2001 Oct; 8(4):461-8. PubMed ID: 11562788
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A.
    Valentijn LJ; Baas F; Wolterman RA; Hoogendijk JE; van den Bosch NH; Zorn I; Gabreëls-Festen AW; de Visser M; Bolhuis PA
    Nat Genet; 1992 Dec; 2(4):288-91. PubMed ID: 1303281
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Peripheral nerve abnormalities of mutant (PMA) mouse--myelinated fiber counts of sciatic, peroneal, sural and tibial nerves].
    Ohnishi A; Kuroiwa Y; Esaki K
    No To Shinkei; 1986 Mar; 38(3):289-93. PubMed ID: 3707778
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Phenotypic heterogeneity in Japanese Charcot-Marie-Tooth disease type 1A patients with PMP-22 gene duplication].
    Yamamoto M; Sobue G; Yasuda T; Yamamoto K; Kumazawa K; Mitsuma T
    Rinsho Shinkeigaku; 1995 Oct; 35(10):1085-91. PubMed ID: 8821490
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Clinical, pathologic and molecular genetic studies of patients with hereditary motor and sensory neuropathy (HMSN)].
    Ohnishi A
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1438-40. PubMed ID: 8752423
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication.
    Timmerman V; Nelis E; Van Hul W; Nieuwenhuijsen BW; Chen KL; Wang S; Ben Othman K; Cullen B; Leach RJ; Hanemann CO
    Nat Genet; 1992 Jun; 1(3):171-5. PubMed ID: 1303230
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A.
    Valentijn LJ; Bolhuis PA; Zorn I; Hoogendijk JE; van den Bosch N; Hensels GW; Stanton VP; Housman DE; Fischbeck KH; Ross DA
    Nat Genet; 1992 Jun; 1(3):166-70. PubMed ID: 1303229
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Peroneal muscular atrophy with autosomal dominant inheritance.
    McLeod JG; Low PA
    Clin Exp Neurol; 1977; 14():142-53. PubMed ID: 616594
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A.
    Patel PI; Roa BB; Welcher AA; Schoener-Scott R; Trask BJ; Pentao L; Snipes GJ; Garcia CA; Francke U; Shooter EM; Lupski JR; Suter U
    Nat Genet; 1992 Jun; 1(3):159-65. PubMed ID: 1303228
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.