251 related articles for article (PubMed ID: 7330503)
1. [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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. [A family with progressive neural muscular atrophy--with special reference to relation with allied diseases (author's transl)].
Hayashi Y; Tomita M; Shimizu K; Takamiya M; Watanabe H
Rinsho Shinkeigaku; 1978 Oct; 18(10):593-600. PubMed ID: 709963
[No Abstract] [Full Text] [Related]
8. 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]
9. 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]
10. Mild early onset axonal Charcot-Marie-Tooth disease not linked to other axonal Charcot-Marie-Tooth loci.
Kochanski A; Kennerson M; Kawulak M; Ryniewicz B; Rowinska-Marcinska K; Walizada G; Nowakowski A; Hausmanowa-Petrusewicz I; Nicholson GA
Neurology; 2005 Feb; 64(3):533-5. PubMed ID: 15699389
[TBL] [Abstract][Full Text] [Related]
11. [Polymorphism of Charcot-Marie-Tooth neural amyotrophy in uniovular twins].
Popov'ian MD; Dubinskaia EE; Ageeva TS
Zh Nevropatol Psikhiatr Im S S Korsakova; 1977; 77(10):1446-8. PubMed ID: 563155
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. 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]
16. 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]
17. Peroneal muscular atrophy (Charcot-Marie-Tooth disease): a review of three cases.
Turton RL; McCracken JW
J Am Osteopath Assoc; 1970 Oct; 70(2):138-45. PubMed ID: 5202533
[No Abstract] [Full Text] [Related]
18. Neurophysiology and molecular genetics of Charcot-Marie-Tooth type 1 neuropathy in Croatian children: follow-up study.
Barisić N; Mihatov I
Croat Med J; 2000 Sep; 41(3):306-13. PubMed ID: 10962051
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. Variability in nerve biopsy findings in a kinship with dominantly inherited Charcot-Marie-Tooth disease.
Van Weerden TW; Houthoff HJ; Sie O; Minderhoud JM
Muscle Nerve; 1982 Mar; 5(3):185-96. PubMed ID: 7088015
[No Abstract] [Full Text] [Related]
[Next] [New Search]
