Differential (Click to cross reference) abdominal muscle paralysis acid maltase deficiency acid maltase deficiency, adult activities of daily living scale adult polyglucosan body disease alpha glucosidase aminoacidopathies amyotrophic lateral sclerosis amyotrophic lateral sclerosis, differential diagnosis amyotrophic lateral sclerosis, misdiagnosis aneurysm anterior horn cell disease aspartate aminotransferase asymptomatic autonomic dysfunction axonal degeneration Babinski sign bladder dysfunction brainstem, atrophy bright tongue sign bulbar palsy calf hypertrophy cardiomegaly cardiomyopathy CAT scan, abnormal children chromosomal abnormality chromosome 11 Clinical Pathologic Conference(C.P.C.) compartment syndrome congenital myopathy congestive heart failure consanguinity creatine phosphokinase(CPK)elevated cultured skin fibroblasts degenerative diseases of CNS delay in diagnosis dementia developmental retardation diaphragmatic paralysis differential diagnosis difficulty climbing stairs distal muscle atrophy distal muscle weakness dysarthria dysphagia dyspnea efficacy electrocardiogram, abnormal electromyogram electron microscopy encephalopathy encephalopathy, anoxic encephalopathy, neonatal enzyme treatment enzyme, defect enzyme, muscle disease exercise exercise intolerance exercise-related muscle strength increase exome sequencing facial weakness falling familial fatigue fibrillations floppy infant gait disorder gait, spastic gaze palsy, vertical gene gene mutation gene therapy genetic diagnosis, prenatal genetic neurologic disorders genetic testing glycogen debranching enzyme deficiency glycogen storage disease Gowers maneuver hammertoes hepatomegaly heralding manifestation high arched feet hip flexor weakness histochemistry of muscle hyperreflexia hypoglycemia hypotension, systemic hypotonia hypotonia, infants hypoxia hypoxic encephalopathy iatrogenic neurologic disorders imbalance inborn errors of metabolism, screening inclusion bodies intellectual deterioration intrinsic hand muscles, wasting of ischemic exercise test Jewish laughing laughing, pathologic leg weakness, bilateral leukocytes leukodystrophy leukoencephalopathy limb-girdle weakness lipid storage disorder of CNS lipid storage myopathy low back pain lysosomal storage disease lysosomes, abnoral McArdle's disease McArdle's disease, adult onset memory, defect of recent memory, impairment of misdiagnosis molecular genetics mortality motor neuron disease MRI MRI, abnormal MRI, muscle mucopolysaccharidoses muscle atrophy, progressive muscle atrophy, static muscle biopsy muscle cramp muscle hypertrophy muscle pain muscle phosphofructokinase deficiency muscle phosphorylase deficiency muscle stiffness muscle strength, testing muscle wasting, diffuse muscle weakness muscle weakness, insidious onset of muscle weakness, proximal muscular dystrophy myelomalacia myeloneuropathy myelopathy myoglobinuria myopathy myopathy, distal, vacuolar myopathy, genetic myopathy, metabolic myopathy, necrotizing myopathy, vacuolar myositis myotonia congenita myotonic discharges neck weakness nerve biopsy nerve conduction studies neurogenic bladder neurologic disease neurologic disease, diagnoses of neurologic evaluation neuropathy neuropathy, sensory newborn, evaluation of next-generation sequencing Niemann-Pick disease night blindness orthopnea pain pain, arm pain, back pain, foot paraparesis paraparesis, spastic paraspinal muscle paraspinal muscle weakness PAS positive patient in waiting phosphorylase b kinase deficiency polyglucosan body polyglucosan body disease polymerase chain reaction Pompe's disease of glycogen storage preclinical prenatal diagnosis by amniocentesis prevention of neurologic disorders prognosis progressive neurologic disorder proximal muscle atrophy pseudobulbar palsy pseudomyotonia psychological testing pulmonary function tests pulmonary hypertension pyramidal tract radiculopathy renal failure respiratory failure review article RFLPs Romberg's sign scissors gait screening second wind phenomena seizure sensory loss short stature spasticity sphingolipodoses spinal muscular atrophy spinocerebellar degeneration subarachnoid hemorrhage tongue, enlarged tongue, weakness treatment of neurologic disorder urinary incontinence urine, dark vital capacity walking, difficulty with weakness weakness, generalized weakness, progressive weakness, proximal wheelchair white matter disease winging of scapula workup

Showing articles 150 to 157 of 157 << Previous Chronic Hexosaminidase A & B Deficiency et al. , Ann Neurol 2:156977., Goldie,W.D., 1977 Diagnosis of Fabry's Disease by Tear-Galactosidase A-Correspondence NEJM 290:57 1974., , 1974 Niemann-Pick Disease Correspondence NEJM 289:590, Dacremont,G.,et al, 1973 Tay-Sachs Disease-The Use of Tears for the Detection of Heterozygotes NEJM 289:1072, Carmody,P.,et al, 1973 Abnormal Head Size, In Neurology In Pediatrics (Ed) , 1970 Year Book Med. Publishers, p. 61., Bray,P.F., 1970 Prenatal Genetic Diagnosis NEJM 283:1370, Milunsky,A.,et al, 1970 Hysterical Hemiplegia and Hemianesthesia Postgrad Med 31:339-345, Magee,K.R., 1962 Cerebellar Ataxia in Children Handout & References., Gilbert,J.J., 1850 Showing articles 150 to 157 of 157 << Previous