60 related articles for article (PubMed ID: 1013449)
1. [Familial myopathies (D.M.). Electroclinical study].
Pérez Maiquez F
Rev Clin Esp; 1976 Oct; 143(2):125-33. PubMed ID: 1013449
[No Abstract] [Full Text] [Related]
2. [Familial atrophic myotonia].
Neĭmark EZ; Tokar' ZM; Vasil'eva AF; Pecherskaia IE
Vrach Delo; 1974; 0(7):99-103. PubMed ID: 4421221
[No Abstract] [Full Text] [Related]
3. [Myotonic dystrophy].
Nesterov LN; Sushcheva GP; Viatkina SIa; Nesterova IM
Zh Nevropatol Psikhiatr Im S S Korsakova; 1983; 83(11):1636-41. PubMed ID: 6232784
[TBL] [Abstract][Full Text] [Related]
4. [Various clinical and genetic aspects of atrophic myotony].
Hariga J; Matthys E; Mechler L; Jonckheer M
Acta Neurol Psychiatr Belg; 1969 Mar; 69(3):215-33. PubMed ID: 4982079
[No Abstract] [Full Text] [Related]
5. Myotonic dystrophy: limited electromyographic abnormalities in 2 definite cases.
Sun SF; Streib EW
Clin Genet; 1983 Feb; 23(2):111-4. PubMed ID: 6839522
[TBL] [Abstract][Full Text] [Related]
6. [Myotonic dystrophy severity (Steinert's disease) (author's transl)].
Turpin JC; Morice J
Sem Hop; 1980 Feb 18-25; 56(7-8):335-40. PubMed ID: 6246628
[TBL] [Abstract][Full Text] [Related]
7. [Myotonic dystrophy in the neonate (author's transl)].
Messer J; Brochard A; Willard D; Jesel M
Acta Paediatr Belg; 1973; 27(4):263-72. PubMed ID: 4589108
[No Abstract] [Full Text] [Related]
8. [An unstable mutation as cause of myotonic dystrophy].
Brunner HG; Höweler CJ; Smeets HJ; Wieringa B
Ned Tijdschr Geneeskd; 1993 Nov; 137(48):2468-72. PubMed ID: 8272119
[No Abstract] [Full Text] [Related]
9. [Steinert's disease in childhood. Study of a family].
Franchini F; Galluzzi F; Ciampolini M; Di Maria M
Riv Clin Pediatr; 1969; 82():253-8. PubMed ID: 5405479
[No Abstract] [Full Text] [Related]
10. [Clinical study of 8 families with various members affected with myotonic dystrophy of Curshmann Steinert's type. Genetic considerations].
Morales Asin F; Mostacero Miguel E; García Alvarez F; Olascoaga Urtaza J; Domínguez Arranz M; Morales Asin J; López del Val J
Rev Clin Esp; 1980 Jul; 157(5):319-23. PubMed ID: 7403606
[No Abstract] [Full Text] [Related]
11. [Genetic heterogeneity of myotonic dystrophy].
Kliuchikov VN; Kopshitser IZ
Zh Nevropatol Psikhiatr Im S S Korsakova; 1983; 83(11):1641-5. PubMed ID: 6675361
[TBL] [Abstract][Full Text] [Related]
12. Dystrophia myotonica in a Nigerian family.
Dada TO
East Afr Med J; 1973 Apr; 50(4):213-28. PubMed ID: 4730256
[No Abstract] [Full Text] [Related]
13. [Myotonic dystrophia. A report of three patients in Cuba].
Lozada-Mengana Y; Alvarez-Valiente H; Aguilera-Pacheco O
Rev Neurol; 2001 Aug 16-31; 33(4):398-400. PubMed ID: 11708269
[No Abstract] [Full Text] [Related]
14. Myotonic dystrophy: its occurrence in childhood.
Gordon N; Hilson D
Br J Clin Pract; 1967 Nov; 21(11):537-40. PubMed ID: 4169454
[No Abstract] [Full Text] [Related]
15. Five years experience of predictive testing for myotonic dystrophy using linked DNA markers.
Reardon W; Floyd JL; Myring J; Lazarou LP; Meredith AL; Harper PS
Am J Med Genet; 1992 Aug; 43(6):1006-11. PubMed ID: 1415325
[TBL] [Abstract][Full Text] [Related]
16. Myotonic disorder without myotonia?
Carter GT; Weiss MD; Bird TD
Muscle Nerve; 2009 Dec; 40(6):1071-2; author reply 1072. PubMed ID: 19722253
[No Abstract] [Full Text] [Related]
17. [Congenital myotonic dystrophy].
Oliván Gonzalvo G; Alonso Gregorio M; López Moreno MJ; Domínguez Arranz MM; Olivares López JL; Pérez González JM
An Esp Pediatr; 1990 May; 32(5):460-3. PubMed ID: 2400164
[No Abstract] [Full Text] [Related]
18. Myotonic dystrophy in childhood.
Lanzi G; Besana D; Ottolini A; Venco A
Acta Neurol Belg; 1982; 82(3):150-8. PubMed ID: 7113652
[TBL] [Abstract][Full Text] [Related]
19. Familial left ventricular hypertrabeculation in myotonic dystrophy type 1.
Finsterer J; Stöllberger C; Kopsa W
Herz; 2003 Aug; 28(5):466-70. PubMed ID: 12928748
[TBL] [Abstract][Full Text] [Related]
20. "Shake hands"; diagnosing a floppy infant--myotonic dystrophy and the congenital subtype: a difficult perinatal diagnosis.
Verrijn Stuart AA; Huisman M; van Straaten HL; Bakker JC; Arabin B
J Perinat Med; 2000; 28(6):497-501. PubMed ID: 11155437
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
