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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 11801400)

  • 21. Late onset axonal Charcot-Marie-Tooth phenotype caused by a novel myelin protein zero mutation.
    Bienfait HM; Faber CG; Baas F; Gabreëls-Festen AA; Koelman JH; Hoogendijk JE; Verschuuren JJ; Wokke JH; de Visser M
    J Neurol Neurosurg Psychiatry; 2006 Apr; 77(4):534-7. PubMed ID: 16543539
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Screening of the myelin protein zero gene in patients with Charcot-Marie-Tooth disease.
    Nowakowski A; Kochański A
    Acta Biochim Pol; 2004; 51(1):273-80. PubMed ID: 15094849
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A rat model of Charcot-Marie-Tooth disease 1A recapitulates disease variability and supplies biomarkers of axonal loss in patients.
    Fledrich R; Schlotter-Weigel B; Schnizer TJ; Wichert SP; Stassart RM; Meyer zu Hörste G; Klink A; Weiss BG; Haag U; Walter MC; Rautenstrauss B; Paulus W; Rossner MJ; Sereda MW
    Brain; 2012 Jan; 135(Pt 1):72-87. PubMed ID: 22189569
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Phenotypic variation of a novel nonsense mutation in the P0 intracellular domain.
    Senderek J; Ramaekers VT; Zerres K; Rudnik-Schöneborn S; Schröder JM; Bergmann C
    J Neurol Sci; 2001 Nov; 192(1-2):49-51. PubMed ID: 11701152
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Novel mutations in the Charcot-Marie-Tooth disease genes PMP22, MPZ, and GJB1.
    Huehne K; Benes V; Thiel C; Kraus C; Kress W; Hoeltzenbein M; Ploner CJ; Kotzian J; Reis A; Rott HD; Rautenstrauss BW
    Hum Mutat; 2003 Jan; 21(1):100. PubMed ID: 12497641
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Two families of Charcot-Marie-Tooth disease with Adie's pupil, axonal neuropahy and the Thr124Met mutation in the peripheral myelin protein zero gene].
    Misu K; Yoshihara T; Yamamoto M; Hattori N; Nagamatu M; Mukai E; Takegami T; Sobue G
    Rinsho Shinkeigaku; 2000 Feb; 40(2):149-54. PubMed ID: 10835936
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Myelin protein zero (MPZ) gene mutations in nonduplication type 1 Charcot-Marie-Tooth disease.
    Roa BB; Warner LE; Garcia CA; Russo D; Lovelace R; Chance PF; Lupski JR
    Hum Mutat; 1996; 7(1):36-45. PubMed ID: 8664899
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Pathology of a mouse mutation in peripheral myelin protein P0 is characteristic of a severe and early onset form of human Charcot-Marie-Tooth type 1B disorder.
    Rünker AE; Kobsar I; Fink T; Loers G; Tilling T; Putthoff P; Wessig C; Martini R; Schachner M
    J Cell Biol; 2004 May; 165(4):565-73. PubMed ID: 15148307
    [TBL] [Abstract][Full Text] [Related]  

  • 29. An axonal form of Charcot-Marie-Tooth disease showing distinctive features in association with mutations in the peripheral myelin protein zero gene (Thr124Met or Asp75Val).
    Misu K; Yoshihara T; Shikama Y; Awaki E; Yamamoto M; Hattori N; Hirayama M; Takegami T; Nakashima K; Sobue G
    J Neurol Neurosurg Psychiatry; 2000 Dec; 69(6):806-11. PubMed ID: 11080237
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Charcot-Marie-Tooth disease and related neuropathies: mutation distribution and genotype-phenotype correlation.
    Boerkoel CF; Takashima H; Garcia CA; Olney RK; Johnson J; Berry K; Russo P; Kennedy S; Teebi AS; Scavina M; Williams LL; Mancias P; Butler IJ; Krajewski K; Shy M; Lupski JR
    Ann Neurol; 2002 Feb; 51(2):190-201. PubMed ID: 11835375
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A novel MPZ mutation in Charcot-Marie-Tooth disease type 1B with focally folded myelin and multiple entrapment neuropathies.
    Iida M; Koike H; Ando T; Sugiura M; Yamamoto M; Tanaka F; Sobue G
    Neuromuscul Disord; 2012 Feb; 22(2):166-9. PubMed ID: 21940171
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Targeting the colony stimulating factor 1 receptor alleviates two forms of Charcot-Marie-Tooth disease in mice.
    Klein D; Patzkó Á; Schreiber D; van Hauwermeiren A; Baier M; Groh J; West BL; Martini R
    Brain; 2015 Nov; 138(Pt 11):3193-205. PubMed ID: 26297559
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype.
    De Jonghe P; Timmerman V; Ceuterick C; Nelis E; De Vriendt E; Löfgren A; Vercruyssen A; Verellen C; Van Maldergem L; Martin JJ; Van Broeckhoven C
    Brain; 1999 Feb; 122 ( Pt 2)():281-90. PubMed ID: 10071056
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Charcot-Marie-Tooth 1B caused by expansion of a familial myelin protein zero (MPZ) gene duplication.
    Speevak MD; Farrell SA
    Eur J Med Genet; 2013 Oct; 56(10):566-9. PubMed ID: 23811036
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B disease.
    Sindou P; Vallat JM; Chapon F; Archelos JJ; Tabaraud F; Anani T; Braund KG; Maisonobe T; Hauw JJ; Vandenberghe A
    Muscle Nerve; 1999 Jan; 22(1):99-104. PubMed ID: 9883862
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Charcot-Marie-Tooth disease due to the Thr124Met mutation in the myelin protein zero gene associated with multiple sclerosis.
    Rajabally YA; Abbott RJ
    J Peripher Nerv Syst; 2005 Dec; 10(4):388-9. PubMed ID: 16279991
    [No Abstract]   [Full Text] [Related]  

  • 37. Charcot-Marie-Tooth disease with intermediate conduction velocities caused by a novel mutation in the MPZ gene.
    Banchs I; Casasnovas C; Montero J; Volpini V; Martínez-Matos JA
    Muscle Nerve; 2010 Aug; 42(2):184-8. PubMed ID: 20544920
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [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]  

  • 39. Early onset Charcot-Marie-Tooth type 1B disease caused by a novel Leu190fs mutation in the myelin protein zero gene.
    Kochański A; Kabzińska D; Drac H; Ryniewicz B; Rowińska-Marcińska K; Hausmanowa-Petrusewicz I
    Eur J Paediatr Neurol; 2004; 8(4):221-4. PubMed ID: 15261887
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Charcot-Marie-Tooth disease and related inherited neuropathies.
    Murakami T; Garcia CA; Reiter LT; Lupski JR
    Medicine (Baltimore); 1996 Sep; 75(5):233-50. PubMed ID: 8862346
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.