250 related articles for article (PubMed ID: 7139106)
1. 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]
2. Hereditary angioneurotic edema and Charcot-Marie-Tooth disease in the same family.
Fernandez PG; Day JH; Simpson NE; Zachariah PK
Can Med Assoc J; 1978 Sep; 119(5):455-8. PubMed ID: 688147
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [Charcot-Marie-Tooth disease. Report of a family (author's transl)].
Alonso ME; Figueroa HH; Zermeño F; Escobar A; Flores T
Rev Invest Clin; 1981; 33(3):303-7. PubMed ID: 7330503
[No Abstract] [Full Text] [Related]
5. Pathogenesis of pes cavus in Charcot-Marie-Tooth disease.
Sabir M; Lyttle D
Clin Orthop Relat Res; 1983 May; (175):173-8. PubMed ID: 6839584
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Homozygous expression of a dominant gene for Charcot-Marie-Tooth neuropathy.
Killian JM; Kloepfer HW
Ann Neurol; 1979 Jun; 5(6):515-22. PubMed ID: 475348
[TBL] [Abstract][Full Text] [Related]
8. Recessive inheritance in a neuronal motor neuropathy form of peroneal muscular atrophy.
Frajman M; Brilla E; Gutiérrez A; Hun L
Rev Invest Clin; 1983; 35(4):305-8. PubMed ID: 6672928
[No Abstract] [Full Text] [Related]
9. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy.
McLeod JG; Low PA; Morgan JA
Proc Aust Assoc Neurol; 1975; 12():23-5. PubMed ID: 1215391
[TBL] [Abstract][Full Text] [Related]
10. Palmoplantar keratoderma and Charcot-Marie-Tooth disease.
Rabbiosi G; Borroni G; Pinelli P; Cosi V
Arch Dermatol; 1980 Jul; 116(7):789-90. PubMed ID: 6446889
[TBL] [Abstract][Full Text] [Related]
11. Recessively inherited Charcot-Marie-Tooth syndrome in identical twins.
Beighton PH
Birth Defects Orig Artic Ser; 1971 Feb; 7(2):105. PubMed ID: 5173114
[No Abstract] [Full Text] [Related]
12. 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]
13. [Peroneal muscular atrophy associated with intellectual impairment and pyramidal signs].
Sobue G; Ibi T; Matsuoka Y; Takahashi A
Rinsho Shinkeigaku; 1985 Jul; 25(7):818-25. PubMed ID: 4075646
[No Abstract] [Full Text] [Related]
14. [Charcot-Marie-Tooth disease. Peroneal muscular atrophy].
Hagen T; Jensen D; Dietrichson P; Heiberg A
Tidsskr Nor Laegeforen; 1990 Oct; 110(24):3110-5. PubMed ID: 2237866
[TBL] [Abstract][Full Text] [Related]
15. [Charcot-Marie-Tooth disease. Genetical, clinical and electrodiagnostic study of 2 families].
Krstić S; Vidaković Z; Ignjatović M
Srp Arh Celok Lek; 1975 Sep; 103(9):769-77. PubMed ID: 1228922
[No Abstract] [Full Text] [Related]
16. Hypertrophic interstitial neuropathy of Déjérine-Sottas.
Beighton PH
Birth Defects Orig Artic Ser; 1971 Feb; 7(2):103-4. PubMed ID: 5173113
[No Abstract] [Full Text] [Related]
17. [Usefulness Of electromyographic examination of families of patients affected with hypertrophic sensory-motor neuropathy (Charcot-Marie-Tooth disease). Preliminary results].
Fardin P; Micaglio GF; Angelini C; Negrin P; Siciliano G
Riv Neurobiol; 1984; 30(2-3):222-8. PubMed ID: 6544478
[No Abstract] [Full Text] [Related]
18. Variation of phenotype in Charcot-Marie-Tooth disease.
Baker RS; Upton AR
Neuropadiatrie; 1979 Aug; 10(3):290-5. PubMed ID: 583067
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Peroneal musclar atrophy (of Charcot-Marie-Tooth) in two African brothers.
Billinghurst JR
Afr J Med Med Sci; 1976 Dec; 5(4):269-72. PubMed ID: 829740
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
