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44. [Contribution to the clinical and genetic study of dystrophia myotonica (Steinert) and of myotonia congenita (Thomsen). Description of 8 families afflicted with Steinert's disease and of a recent case of Thomsen's disease]. DUMAINE L; LOZERON P J Genet Hum; 1961 Dec; 10():221-96. PubMed ID: 13888352 [No Abstract] [Full Text] [Related]
45. [Auricular flutter preceding by several years the discovery of Steinert's disease. 3 cases]. Rey JL; Tribouilloy C; Marek A; Slama MA; Cimino L; Bernasconi P; Quiret JC; Lesbre JP Ann Cardiol Angeiol (Paris); 1989 May; 38(5):255-9. PubMed ID: 2660734 [TBL] [Abstract][Full Text] [Related]
46. [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]
47. [Direct genotypic analysis of myotonic dystrophy: detection of an unstable DNA fragment in carriers]. Cobo AM; Martorell L; López de Munain A; Basauri B; Martínez JM; Johnson K; Baiget M Med Clin (Barc); 1993 Mar; 100(10):361-4. PubMed ID: 8097270 [TBL] [Abstract][Full Text] [Related]
48. Asperger syndrome associated with Steinert's myotonic dystrophy. Blondis TA; Cook E; Koza-Taylor P; Finn T Dev Med Child Neurol; 1996 Sep; 38(9):840-7. PubMed ID: 8810716 [TBL] [Abstract][Full Text] [Related]
49. "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]
54. [Megacolon in a case of Steinert's myotonic dystrophy]. Argentino C; Cruccu G; Prencipe M Riv Neurol; 1980; 50(1):20-5. PubMed ID: 7466200 [TBL] [Abstract][Full Text] [Related]
55. Should we perform systematic electrophysiological study in Steinert's disease? Fayssoil A J Cardiothorac Surg; 2008 Oct; 3():56. PubMed ID: 18928563 [TBL] [Abstract][Full Text] [Related]
56. [Neonatal Steinert's disease. Comments on a case and determination of the pregnancy aspects which are predictive of neonatal death]. Ferreira O; Morvan J; Bernard AM; Verjut JP; Cleophax JP J Gynecol Obstet Biol Reprod (Paris); 1989; 18(3):349-54. PubMed ID: 2661648 [TBL] [Abstract][Full Text] [Related]
57. [Curschmann-Steinert's myotonic dystrophy]. Morales Asin F; Rey del Corral P; Clavel Escribano M; Domínguez Zorita M Arch Neurobiol (Madr); 1969; 32(2):233-49. PubMed ID: 5810839 [No Abstract] [Full Text] [Related]
58. Skin features in myotonic dystrophy type 1: an observational study. Campanati A; Giannoni M; Buratti L; Cagnetti C; Giuliodori K; Ganzetti G; Silvestrini M; Provinciali L; Offidani A Neuromuscul Disord; 2015 May; 25(5):409-13. PubMed ID: 25813338 [TBL] [Abstract][Full Text] [Related]
59. [Intergenerational study of the mutation that causes Myotonic Dystrophy Type 1 in Costa Rica]. Morales Montero F; Cuenca Berger P; Brian Gago R; Sittenfeld M; del Valle G Rev Neurol; 2003 Jan 1-15; 36(1):20-5. PubMed ID: 12577208 [TBL] [Abstract][Full Text] [Related]