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humans (232) 232
male (132) 132
female (106) 106
myopathies, nemaline - complications (103) 103
clinical neurology (102) 102
index medicus (85) 85
nemaline myopathy (75) 75
adult (72) 72
muscle, skeletal - pathology (63) 63
myopathy (62) 62
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myopathies, nemaline - pathology (60) 60
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congenital myopathy (35) 35
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myopathies, nemaline - physiopathology (26) 26
respiratory insufficiency - etiology (25) 25
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muscles (23) 23
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muscles - pathology (21) 21
electromyography (20) 20
gene (20) 20
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muscular diseases - complications (19) 19
muscle fibers, skeletal - pathology (18) 18
aged (17) 17
congenital myopathies (17) 17
dna mutational analysis (17) 17
muscular diseases - pathology (17) 17
myopathies, structural, congenital - pathology (17) 17
research (17) 17
dilated cardiomyopathy (16) 16
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malignant hyperthermia (16) 16
muscle (16) 16
muscle diseases (16) 16
muscle proteins - genetics (16) 16
muscle, skeletal - metabolism (16) 16
neuromuscular diseases (16) 16
muscle weakness - etiology (15) 15
muscle, skeletal - ultrastructure (15) 15
myopathies, structural, congenital - genetics (15) 15
skeletal-muscle (15) 15
actins - genetics (14) 14
animals (14) 14
health aspects (14) 14
hiv infections - complications (14) 14
mutation - genetics (14) 14
rod myopathy (14) 14
age of onset (13) 13
genetics & heredity (13) 13
muscular dystrophy (13) 13
myopathies, structural, congenital - complications (13) 13
myopathy, central core - genetics (13) 13
review (13) 13
acta1 (12) 12
cardiomyopathy (12) 12
magnetic resonance imaging (12) 12
medicine & public health (12) 12
muscle, skeletal - physiopathology (12) 12
myopathies, nemaline - therapy (12) 12
pedigree (12) 12
pregnancy (12) 12
ryanodine receptor calcium release channel - genetics (12) 12
abridged index medicus (11) 11
duchenne muscular-dystrophy (11) 11
fiber-type disproportion (11) 11
follow-up studies (11) 11
medicine (11) 11
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respiratory insufficiency - therapy (11) 11
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young adult (11) 11
children (10) 10
congenital diseases (10) 10
hypertrophic cardiomyopathy (10) 10
immunohistochemistry (10) 10
microscopy, electron (10) 10
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myopathies, nemaline - etiology (10) 10
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Journal Article
Medicine (United States), ISSN 0025-7974, 2016, Volume 95, Issue 4, p. e2527
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2015, Volume 53, Issue 6, pp. 473 - 477
Journal Article
Journal Article
Journal of Craniofacial Surgery, ISSN 1049-2275, 01/2017, Volume 28, Issue 3, pp. e258 - e260
Nemaline myopathy (NM) is a rare congenital muscular disease characterized by the presence of rod (nemaline) bodies visualized on muscle biopsy. The disease is... 
Nemaline myopathy | Nemaline bodies | Craniofacial dysmorphism | SURGERY | nemaline myopathy | ADOLESCENTS | MUSCULAR-DYSTROPHY | nemaline bodies | CONGENITAL MYOPATHIES | MYOTONIC-DYSTROPHY | CHILDREN | Child, Preschool | Male | Craniofacial Abnormalities - etiology | Myopathies, Nemaline - complications | Craniofacial Abnormalities - diagnosis | Humans
Journal Article
Journal Article
Journal Article
REVISTA DE NEUROLOGIA, ISSN 0210-0010, 2017, Volume 64, Issue s01, pp. S89 - S94
Journal Article
Neurology, ISSN 0028-3878, 01/2016, Volume 86, Issue 1, pp. e4 - e9
A 64-year-old man was referred with a 5-month history of progressive muscle weakness. He first noted a stooped posture and gait difficulties, followed by... 
INFECTION | ONSET NEMALINE MYOPATHY | ROD MYOPATHY | CLINICAL NEUROLOGY | Myopathies, Nemaline - complications | Muscle Weakness - diagnosis | Paraspinal Muscles - pathology | Humans | Middle Aged | Muscle Weakness - complications | Male | Electromyography | Myopathies, Nemaline - diagnosis
Journal Article
Acta neuropathologica communications, ISSN 2051-5960, 2014, Volume 2, Issue 1, pp. 44 - 44
Journal Article