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Electromyography in congenital nemaline myopathy
Muscle & Nerve, 1989AbstractTo clarify the discrepancies between earlier reports of electromyography (EMG) in congenital nemaline myopathy (CNM), conventional electromyography was done on 13 patients with CNM, and results were compared with those of 18 earlier EMG examinations of the same patients.
C, Wallgren-Pettersson +2 more
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Genetics of congenital nemaline myopathy
Muscle & Nerve, 1980AbstractFamily patterns for 50 reported probands with congenital nemaline myopathy were compared with expected patterns derived from various possible genetic hypotheses. The disease had a high mortality in childhood but remained clinically stationary after this period. Some normal relatives showed nemaline rods on muscle biopsy. Chromosomes were normal
K, Kondo, T, Yuasa
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FATAL NEONATAL NEMALINE MYOPATHY
Acta Pathologica Japonica, 1982Nemaline myopathy was first reported in 1963 and has been considered to be a congenital, nonāprogressive myopathy with weakness since birth. However, severe forms leading to death in infancy have been rarely reported. Recently we necropsied a female infant with fatal neonatal nemaline myopathy who required mechanical ventilatory support immediately ...
T, Matsuo +4 more
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Respiratory failure in nemaline myopathy
Pediatric Neurology, 1997Four patients with nemaline myopathy, 1 with the severe infantile form and 3 with the benign congenital (classical) form, exhibited significant respiratory problems. In the patient with the severe infantile form, respiratory failure paralleled the generalized muscle weakness, whereas the 3 patients with the benign infantile form suddenly developed ...
M, Sasaki +3 more
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The American Journal of Cardiology, 1986
R S, Rosenson, G H, Mudge, M G, Sutton
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R S, Rosenson, G H, Mudge, M G, Sutton
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Nemaline body myopathy caused by a novel mutation in troponin T1 (TNNT1)
Muscle and Nerve, 2016Yakov Fellig +2 more
exaly

