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Differential
(Click to cross reference)
anxiety
arrhythmia, cardiac
calf hypertrophy
calpain III deficiency
cardiomyopathy
cardiovascular disease
children
chromosomal abnormality
chromosome 17
chromosome 7
congestive heart failure
contractures, joint
creatine phosphokinase(CPK)elevated
diamond on quadriceps
differential diagnosis
dystonia
dystrophin
dystrophin associated proteins
electron microscopy
epsilon sarcoglycan gene
exercise
familial
gene
gene mutation
genetic neurologic disorders
genetic testing
Gowers maneuver
limb-girdle weakness
misdiagnosis
molecular genetics
movement disorder
muscle biopsy
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, Duchenne
muscular dystrophy, dystrophin normal
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myoclonic dystonia
myoclonus
myoclonus, action
myoglobinuria
myopathy
neurologic disease, diagnoses of
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
respiratory failure
review article
rhabdomyolysis
sarcoglycan
sarcoglycanopathy
spastic dysphonia
speech disorder
toe walking
treatment of neurologic disorder
urine, dark
weakness, progressive
weakness, proximal
wheelchair
winging of scapula
workup
Showing articles 0 to 11 of 11

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

The Clinical Spectrum of Sarcoglycanopathies
Neurol 52:176-179, Angelini,C.,et al, 1999

Mutations in the Sarcoglycan Genes in Patients with Myopathy
NEJM 336:618-624, Duggan,D.J.,et al, 1997

The Muscular Dystrophies-Clarity or Chaos
NEJM 336 650-651, Dubowitz,V., 1997

Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
Neurol 48:1227-1234, Eymard,B.,et al, 1997

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996

Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
Ann Neurol 38:367-372, 3531995., Ljunggren,A.,et al, 1995

Abnormal Expression of Dystrophin-Associated Proteins in Fukuyama-Type Congenital Muscular Dystrophy
Lancet 341:521-522, Matsumura,K.,et al, 1993

Duchenne Muscular Dystrophy:Deficiency of Dystrophin-Associated Proteins in the Sarcolemma
Neurol 43:795-800, Ohlendieck,K.,et al, 1993



Showing articles 0 to 11 of 11