Results 121 to 130 of about 31,854 (258)
Isolation of a polymorphic DNA sequence pJSB11 (D19S16) from the human chromosome 19cen-q13.2 region linked to the myotonic dystrophy (DM) gene [PDF]
, 1987 Jan Schepens +4 more
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Coincidence of neurofibromatosis and myotonic dystrophy in a kindred. [PDF]
, 1981 Kazushi Ichikawa +3 more
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Partial Syndrome of Myotonic Dystrophy: Clinical Presentation and Follow-up [PDF]
, 1989 Jean Mathieu +4 more
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CONGENITAL MYOTONIC DYSTROPHY – CASE REPORT
Zdravniški Vestnik, 2001 Background. Myotonic dystrophy is inherited as an autosomal dominant trait. It is characterized by myotonia, myopathy of voluntary and involuntary muscles, frontal baldness in men, cardiac conduction abnormalities, catharacts, intellectual deterioration ...
David Neubauer +4 more
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Cognitive and personality function in myotonic muscular dystrophy. [PDF]
, 1984 Roger A. Brumback, Helen W. Wilson
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Electron Spin Resonance Studies of Erythrocytes from Patients with Myotonic Muscular Dystrophy
, 1974 D. Allan Butterfield +3 more
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Aberrant Myokine Signaling in Congenital Myotonic Dystrophy
Cell Reports, 2017 Summary: Myotonic dystrophy types 1 (DM1) and 2 (DM2) are dominantly inherited neuromuscular disorders caused by a toxic gain of function of expanded CUG and CCUG repeats, respectively.
Masayuki Nakamori +8 more
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Noninvasive assessment of left ventricular function in myotonic muscular dystrophy.
, 1978 Achille Venco +4 more
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