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27. [Congenital myotonic dystrophy]. Krause W; Kirchner M; Schmidt A; Clausner B Z Geburtshilfe Perinatol; 1984; 188(2):94-9. PubMed ID: 6375183 [TBL] [Abstract][Full Text] [Related]
28. Peripheral microcirculatory lesions in myotonic dystrophy. A light and an electron microscopic study on digital biopsies. Scelsi R; Poggi P; Nappi G; Sandrini G Acta Neurol (Napoli); 1978; 33(2):137-48. PubMed ID: 207159 [No Abstract] [Full Text] [Related]
29. Expression of MBNL and CELF mRNA transcripts in muscles with myotonic dystrophy. Nezu Y; Kino Y; Sasagawa N; Nishino I; Ishiura S Neuromuscul Disord; 2007 Apr; 17(4):306-12. PubMed ID: 17331722 [TBL] [Abstract][Full Text] [Related]
30. Hyperproliferation of synapses on spinal motor neurons of Duchenne muscular dystrophy and myotonic dystrophy patients. Nagao M; Kato S; Hayashi H; Misawa H Acta Neuropathol; 2003 Dec; 106(6):557-60. PubMed ID: 12920538 [TBL] [Abstract][Full Text] [Related]
31. [True muscle hypertrophy of the unilateral calf in congenital myotonic dystrophy--a case report]. Anegawa T; Namamura M; Hara K; Yamamoto K Rinsho Shinkeigaku; 1993 Oct; 33(10):1100-2. PubMed ID: 8293616 [TBL] [Abstract][Full Text] [Related]
32. Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy. Vattemi G; Tomelleri G; Filosto M; Savio C; Rizzuto N; Tonin P Neuropathol Appl Neurobiol; 2005 Feb; 31(1):45-52. PubMed ID: 15634230 [TBL] [Abstract][Full Text] [Related]
33. Myotonic dystrophy: relative sensitivity of symptoms signs and abnormal investigations. Avaria M; Patterson V Ulster Med J; 1994 Oct; 63(2):151-4. PubMed ID: 8650827 [TBL] [Abstract][Full Text] [Related]
34. [MyoD mRNA expression in skeletal muscle of patients with myotonic dystrophy]. Zhao XP; Pu CQ; Duan F; Liu JX; Mao YL; Luo P Zhonghua Yi Xue Za Zhi; 2009 Feb; 89(7):466-8. PubMed ID: 19567095 [TBL] [Abstract][Full Text] [Related]
35. [Pathology of the heart in myotonic dystrophy]. Hizawa K Rinsho Shinkeigaku; 1983 Dec; 23(12):1082-5. PubMed ID: 6677414 [No Abstract] [Full Text] [Related]
36. New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2). Sallinen R; Vihola A; Bachinski LL; Huoponen K; Haapasalo H; Hackman P; Zhang S; Sirito M; Kalimo H; Meola G; Horelli-Kuitunen N; Wessman M; Krahe R; Udd B Neuromuscul Disord; 2004 Apr; 14(4):274-83. PubMed ID: 15019706 [TBL] [Abstract][Full Text] [Related]
37. Bite force and handgrip force in patients with molecular diagnosis of myotonic dystrophy. Guimaraes AS; Carlsson GE; Marie SK J Oral Rehabil; 2007 Mar; 34(3):195-200. PubMed ID: 17302947 [TBL] [Abstract][Full Text] [Related]
38. [A study on abnormality of water and sodium metabolism in patients with myotonic dystrophy]. Sakamoto M; Nishimura Y; Oki Y; Hishida A; Honda N Rinsho Shinkeigaku; 1986 Jun; 26(6):619-24. PubMed ID: 3769311 [No Abstract] [Full Text] [Related]