134 related articles for article (PubMed ID: 2591266)
1. [X-linked recessively inherited peroneal muscular atrophy].
Wang DS
Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1989 Jun; 22(3):139-40, 190. PubMed ID: 2591266
[TBL] [Abstract][Full Text] [Related]
2. X-linked dominant Charcot-Marie-Tooth neuropathy with 15 cases in a family genetic linkage study.
Ionasescu VV; Burns TL; Searby C; Ionasescu R
Muscle Nerve; 1988 Nov; 11(11):1154-6. PubMed ID: 3226432
[TBL] [Abstract][Full Text] [Related]
3. Hereditary motor-sensory neuropathies. Charcot-Marie-Tooth syndrome.
Bird TD
Neurol Clin; 1989 Feb; 7(1):9-23. PubMed ID: 2646524
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. [A family of scapula-back type of x-linked recessive muscular dystrophy].
Ji XW
Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1989 Jun; 22(3):136-8, 190. PubMed ID: 2591265
[TBL] [Abstract][Full Text] [Related]
6. Heterogeneity of Charcot-Marie-Tooth disease suggested by a linkage study.
Micaglio G; Fardin P; Battilana M; Lombardi A; Mostacciuolo ML; Danieli GA; Angelini C
Adv Neurol; 1988; 48():209-19. PubMed ID: 3334783
[No Abstract] [Full Text] [Related]
7. 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]
8. 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]
9. Screening of dominantly inherited Charcot-Marie-Tooth neuropathies.
Ionasescu VV; Ionasescu R; Searby C
Muscle Nerve; 1993 Nov; 16(11):1232-8. PubMed ID: 8413376
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [DNA diagnosis of X-linked recessive bulbospinal muscular atrophy by androgen receptor gene mutations].
Doyu M; Sobue G; Mukai E; Takahashi A; Mitsuma T
Rinsho Shinkeigaku; 1992 Mar; 32(3):336-9. PubMed ID: 1628462
[TBL] [Abstract][Full Text] [Related]
12. [Estimation of the probability of heterozygosity in Duchenne-type progressive muscular dystrophy].
Guízar Vázquez J; Navarrete Cadena C; Rico R; Mora G; Zavala C
Bol Med Hosp Infant Mex; 1981; 38(1):23-33. PubMed ID: 7284070
[TBL] [Abstract][Full Text] [Related]
13. [X chromosome-linked bulbospinal neuronopathy in adults].
Mozolevskiĭ IuV
Zh Nevropatol Psikhiatr Im S S Korsakova; 1989; 89(3):121-3. PubMed ID: 2728735
[TBL] [Abstract][Full Text] [Related]
14. [An autopsy case of X-linked recessive bulbar-spinal muscular atrophy].
Hirayama M; Hashizume Y; Takagi T; Higo H; Ito M
Rinsho Shinkeigaku; 1988 Oct; 28(10):1131-6. PubMed ID: 3064949
[No Abstract] [Full Text] [Related]
15. X-linked recessive bulbospinal neuronopathy.
Phanthumchinda K
J Med Assoc Thai; 1992 Jun; 75(6):369-73. PubMed ID: 1487685
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of X-linked spinal and bulbar muscular atrophy in a Greek family.
Yapijakis C; Kapaki E; Boussiou M; Vassilopoulos D; Papageorgiou C
Prenat Diagn; 1996 Mar; 16(3):262-5. PubMed ID: 8710782
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Linkage in a family with X-linked Charcot-Marie-Tooth disease.
Haites N; Fairweather N; Clark C; Kelly KF; Simpson S; Johnston AW
Clin Genet; 1989 Jun; 35(6):399-403. PubMed ID: 2567643
[TBL] [Abstract][Full Text] [Related]
19. DNA probes in Charcot-Marie-Tooth neuropathy.
Nicholson GA; Griffiths LR; McLeod JG
Aust Paediatr J; 1988; 24 Suppl 1():90-1. PubMed ID: 3202739
[TBL] [Abstract][Full Text] [Related]
20. Charcot-Marie-Tooth's disease with severe trophic and sensory disorders. Study of a case following along a half a century with anatomical studies.
Barraquer-Bordas L; Navarro C; Salisachs P
Acta Neurol Latinoam; 1981; 27(3-4):177-89. PubMed ID: 6965173
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
