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 *

111 related articles for article (PubMed ID: 2519453)

  • 21. Pathogenesis of Charcot-Marie-Tooth disease. Gait analysis and electrophysiologic, genetic, histopathologic, and enzyme studies in a kinship.
    Sabir M; Lyttle D
    Clin Orthop Relat Res; 1984 Apr; (184):223-35. PubMed ID: 6705352
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Congenital pes cavus in a Charcot-Marie-tooth disease type 1A newborn.
    Fusco C; Frattini D; Scarano A; Giustina ED
    Pediatr Neurol; 2009 Jun; 40(6):461-4. PubMed ID: 19433282
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Neurofibromatosis type 1 associated with Charcot-Marie-Tooth type 1A.
    Koc F; Guzel AI
    J Dermatol; 2009 May; 36(5):306-11. PubMed ID: 19383003
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Malignant melanoma and Charcot-Marie-Tooth disease.
    Greene MH; Mead GD; Reimer RR; Bergfeld WF; Fraumeni JF
    Am J Med Genet; 1980; 5(1):69-71. PubMed ID: 7395902
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Anesthetic management for laparoscopic surgery in a patient with Charcot-Marie-Tooth disease].
    Niiyama Y; Kanaya N; Namiki A
    Masui; 2003 May; 52(5):524-6. PubMed ID: 12795137
    [TBL] [Abstract][Full Text] [Related]  

  • 26. X-linked Charcot-Marie-Tooth disease: molecular analysis of interfamilial variability.
    Niewiadomski LA; Kelly TE
    Am J Med Genet; 1996 Dec; 66(2):175-8. PubMed ID: 8958325
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Charcot-Marie-Tooth disease with Leber optic atrophy.
    McLeod JG; Low PA; Morgan JA
    Neurology; 1978 Feb; 28(2):179-84. PubMed ID: 563998
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafness.
    Joo IS; Ki CS; Joo SY; Huh K; Kim JW
    Neuromuscul Disord; 2004 May; 14(5):325-8. PubMed ID: 15099592
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A V38A mutation in X-linked Charcot-Marie-Tooth neuropathy with unusual clinical features.
    Karadima G; Panas M; Floroskufi P; Kalfakis N; Vassilopoulos D
    J Neurol; 2004 Feb; 251(2):222-3. PubMed ID: 14991359
    [No Abstract]   [Full Text] [Related]  

  • 30. Modafinil reduces fatigue in Charcot-Marie-Tooth disease type 1A: a case series.
    Carter GT; Han JJ; Mayadev A; Weiss MD
    Am J Hosp Palliat Care; 2006; 23(5):412-6. PubMed ID: 17060310
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Bilateral sudden sensorineural hearing loss caused by Charcot-Marie-Tooth disease.
    Papadakis CE; Hajiioannou JK; Kyrmizakis DE; Bizakis JG
    J Laryngol Otol; 2003 May; 117(5):399-401. PubMed ID: 12803792
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Clinical and genetic description of a family with Charcot-Marie-Tooth disease type 1B from a transmembrane MPZ mutation.
    Eggers SD; Keswani SC; Melli G; Cornblath DR
    Muscle Nerve; 2004 Jun; 29(6):867-9. PubMed ID: 15170620
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Identification of a new genetic entity in the form of an autosomal dominant axonal Charcot-Marie-Tooth disease associated with periodic paralyses and pyramidal syndrome].
    Chokri B; Salem M; Faycel H
    Tunis Med; 2005 Sep; 83(9):547-55. PubMed ID: 16383201
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Proximal Charcot-Marie-Tooth syndrome with duplication on chromosome 17p11.2.
    Auer-Grumbach M; Wagner K; Payer F; Hartung HP
    Ann N Y Acad Sci; 1999 Sep; 883():469-71. PubMed ID: 10586276
    [No Abstract]   [Full Text] [Related]  

  • 35. Charcot-Marie-Tooth disease.
    Martel J; Mierau D; Donat J
    J Manipulative Physiol Ther; 1995; 18(3):168-71. PubMed ID: 7790797
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Charcot-Marie-Tooth disease with sensorineural hearing loss--an autosomal dominant trait.
    Kousseff BG; Hadro TA; Treiber DL; Wollner T; Morris C
    Birth Defects Orig Artic Ser; 1982; 18(3B):223-8. PubMed ID: 7139106
    [No Abstract]   [Full Text] [Related]  

  • 37. Treatment of the cavus foot. Deformity in the pediatric patient with Charcot-Marie-Tooth.
    Olney B
    Foot Ankle Clin; 2000 Jun; 5(2):305-15. PubMed ID: 11232232
    [TBL] [Abstract][Full Text] [Related]  

  • 38. X-linked Charcot-Marie-Tooth disease with myokymia: report of a family.
    Chakravarty A; Ghosh B; Sengupta S; Mukhopadhyay S
    Neurol India; 2003 Sep; 51(3):385-7. PubMed ID: 14652447
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Myasthenia gravis and Charcot-Marie-Tooth disease type 1A: an unusual combination of diseases.
    Chen CM; Chang HS; Lyu RK; Tang LM; Chen ST
    Muscle Nerve; 1997 Nov; 20(11):1457-9. PubMed ID: 9342165
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Charcot-Marie-Tooth disease type II and dopa-sensitive Parkinson syndrome].
    Dupuis JM; Brucher JM
    Rev Neurol (Paris); 1994 Oct; 150(10):740-1. PubMed ID: 7792485
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.