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26. [A genealogical study of Steinert's disease (author's transl)]. Robert JM; Pernod J J Genet Hum; 1976 Jun; 24(2):143-51. PubMed ID: 965951 [TBL] [Abstract][Full Text] [Related]
27. "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]
30. [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]
31. The expanding clinical and genetic spectrum of the myotonic dystrophies. Ricker K Acta Neurol Belg; 2000 Sep; 100(3):151-5. PubMed ID: 11098287 [TBL] [Abstract][Full Text] [Related]
32. An intergenerational contraction of the CTG repeat in Japanese myotonic dystrophy. Matsumura R; Namikawa T; Miki T; Kihira T; Yamagata H; Mano Y; Takayanagi T J Neurol Sci; 1996 Jul; 139(1):48-51. PubMed ID: 8836971 [TBL] [Abstract][Full Text] [Related]
33. [Regional clinico-genetic features of myotonias]. Khannanova FK Zh Nevropatol Psikhiatr Im S S Korsakova; 1986; 86(3):342-6. PubMed ID: 2939672 [TBL] [Abstract][Full Text] [Related]
34. [Neonatal Steinert's disease: apropos of 2 cases in 2 successive generations]. Bétrémieux P; Blin-Jezequel E; Lefrançois C; Le Marec B J Genet Hum; 1985 Jan; 33(1):21-30. PubMed ID: 3856628 [TBL] [Abstract][Full Text] [Related]
35. The coexistence of myasthenia gravis and myotonic dystrophy in one family. Maytal J; Spiro AJ; Sinnar S; Moshe SL Neuropediatrics; 1987 Feb; 18(1):8-10. PubMed ID: 3561710 [TBL] [Abstract][Full Text] [Related]
36. [From gene to disease; altered RNA processing as a cause of myotonic dystrophy type 1]. de Die-Smulders CE; Faber CG; Smeets HJ Ned Tijdschr Geneeskd; 2005 Sep; 149(37):2043-6. PubMed ID: 16184945 [TBL] [Abstract][Full Text] [Related]
37. Genetic epidemiology of myotonic dystrophy in Istria, Croatia. Medica I; Marković D; Peterlin B Acta Neurol Scand; 1997 Mar; 95(3):164-6. PubMed ID: 9088385 [TBL] [Abstract][Full Text] [Related]
38. Myotonic dystrophy in a female with myasthenia gravis. de los Angeles Avaria M; Kleinsteuber K; Novoa F; Faundez P; Carvallo P Pediatr Neurol; 2007 Jun; 36(6):421-3. PubMed ID: 17560508 [TBL] [Abstract][Full Text] [Related]
39. [Eugenic significance of linkage between the gene loci for dystrophia myotonica (Steiner's disease) and ABH-secretor]. Zimmerli O; Moser H; Lattke F; von Matt B; Gerber H Schweiz Med Wochenschr; 1977 Mar; 107(10):327-35. PubMed ID: 847432 [TBL] [Abstract][Full Text] [Related]
40. Mitochondrial DNA sequence analysis in congenital myotonic dystrophy. Thyagarajan D; Byrne E; Noer S; Lertrit P; Utthanophol P; Kapsa R; Marzuki S Ann Neurol; 1991 Nov; 30(5):724-7. PubMed ID: 1763896 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]