Differential (Click to cross reference) acid maltase deficiency advances in neurology adverse drug reaction alpha-fetoprotein Alzheimer's disease amyloidosis amyotrophic lateral sclerosis amyotrophic lateral sclerosis, diagnosis of amyotrophic lateral sclerosis, differential diagnosis amyotrophic lateral sclerosis, epidemiology of amyotrophic lateral sclerosis, familial amyotrophic lateral sclerosis, guamian type of amyotrophic lateral sclerosis, misdiagnosis amyotrophic lateral sclerosis, work up anterior horn cell disease anterior tibial muscle weakness apraxia of eye movements areflexia arthrogryposis multiplex ataxia ataxia telangiectasia ataxia, cerebellar ataxia, truncal benign congenital hypotonia bone marrow biopsy Brugada syndrome bulbar palsy bulbar palsy, progressive cachexia CAG repeats calf hypertrophy carcinoembryonic antigen carcinoma central core disease cerebellar ataxia, children cerebellar ataxia, hereditary cerebellar degeneration Charcot-Marie-Tooth chest x-ray, abnormal children chorea choreoathetosis chromosomal abnormality chromosome 11 chromosome 5 chronic polyneuritis, children Clinical Pathologic Conference(C.P.C.) coma complications congenital heart disease congenital myopathy congestive heart failure constipation creatine phosphokinase(CPK)elevated degenerative diseases of CNS dementia denervation of muscle denervation potentials dentatorubral-pallidoluysian atrophy depression dermatomyositis developmental milestones developmental milestones, loss of developmental retardation diabetes mellitus diaphragmatic paralysis diaphragmatic paralysis, causes of differential diagnosis distal muscle atrophy distal muscle weakness DNA probes drooling dysarthria dysphagia dyspnea dystonia dystrophin efficacy electrocardiogram, abnormal electromyogram encephalopathy encephalopathy, anoxic encephalopathy, neonatal enzyme, muscle disease epidemiology of neurology eye movement, disorders of facial weakness, bilateral facioscapulohumeral syndrome familial fasciculation fatigue Fazio-Londe's disease fibrillations floppy infant foot drop fragile-X syndrome Friedreich's ataxia gait disorder gait, waddling gene gene mutation gene therapy genetic counselling genetic diagnosis, prenatal genetic linkage genetic neurologic disorders genetic screening genetic testing growth retardation Guillain Barre syndrome gynecomastia heavy metal intoxication history of neurology Hodgkin's disease huntingtin Huntington's chorea hypercapnia hypertension hypoglycemia hypoglycemic coma hyporeflexia hypotonia hypotonia, infants hypoxic encephalopathy immunodeficiency immunosuppression inclusion bodies inclusion bodies, eosinophilic cytoplasmic infant, evaluation of intestinal pseudoobstruction intrinsic hand muscles, wasting of Isaacs syndrome jaw closure weakness klippel feil syndrome Kugelberg-Welander syndrome leg weakness, bilateral leg weakness, unilateral leukemia lid closure, weakness of life expectancy liver disease lordosis lymphadenopathy lymphoma masseter muscle weakness mental retardation misdiagnosis molecular genetics monoclonal gammopathy monomelic amyotrophy mononeuropathy mortality motor neuron disease motor system movement disorder movement disorder, extrapyramidal MRI MRI, abnormal MRI, spinal cord multiple myeloma multiple system atrophy muscle atrophy, progressive muscle atrophy, static muscle biopsy muscle cramp muscle diseases, characteristics of muscle hypertrophy muscle pain muscle wasting, diffuse muscle weakness muscle weakness, proximal muscle, metabolic disorders of muscular dystrophy muscular dystrophy, Becker muscular dystrophy, Becker, carrier muscular dystrophy, cardiovascular changes with muscular dystrophy, differential diagnosis of muscular dystrophy, Duchenne muscular dystrophy, facioscapulohumeral muscular dystrophy, limb-girdle myasthenia gravis myasthenia gravis, distal weakness myasthenia gravis, limb-girdle myasthenic crisis myocardial injury myocytolysis myokymia myopathy myopathy, 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sudden death survival motor neuron gene telangiectases term infant testicular atrophy tongue, fasciculations of torticollis treatment of neurologic disorder tremor tremor, postural tricresylphosphate trinucleotide repeats tuberous sclerosis vitamin E vitamin E deficiency Waldenstrom's macroglobulinemia walking, difficulty with weakness weakness, generalized weakness, infant weakness, progressive weaning from respirator, failure to weight loss Werdnig-Hoffman disease West disease wheelchair whistle, inability to winging of scapula workup X-linked bulbospinal neuronopathy

Showing articles 50 to 64 of 64 << Previous Vitamin E Deficiency in Werdnig-Hoffmann Disease Ann Neurol 10:266-268, Shapira,Y.,et al, 1981 Use of the ECG in the Diagnosis of Childhood Spinal Muscular Atrophy Arch Neurol 36:317-318, Russman,B.S.,et al, 1979 Diaphragmatic Paralysis in Motor Neuron Disease Neurol 28:18, Parhad,I.M.,et al, 1978 Distal Chronic Spinal Muscular Atrophy Involving the Hands JNNP 41:653-658, O'Sullivan,D.J.,et al, 1978 Sparing of the Onufrowicz Nucleus in Sacral Anterior Horn Lesions Ann Neurol 4:245-249, Iwata,M.,et al, 1978 Chronic Neurogenic Quadriceps Amyotrophy Ann Neurol 2:528, Furukawa,T.,et al, 1977 Quadriceps Myopathy-Entity or Syndrome Arch Neurol 31:60, Boddie,H.,et al, 1974 Epidemiology of Motor-Neuron Diseases NEJM 288:1047, Bobwick,A.R.,et al, 1973 Infantile Spinal Muscular Atrophy Arch Neurol 25:276, Wilkins,R.,et al, 1971 Neurogenic Muscular Atrophy of Infancy with Prolonged Survival Brain 92:9, Munsat,T.,et al, 1969 Chronic Spinal Muscular Atrophy in Adults J Neurol Sci 9:527, Meadows,J.C.,et al, 1969 Chronic Spinal Muscular Atrophy in Adults J Neurol Sci 9:551, Meadows,J.C.,et al, 1969 Neurogenic Muscular Atrophy Simulating Facioscapulohumeral Muscular Dystrophy J Neurol Sci 9:389, Furukawa,T.,et al, 1969 Diseases of Muscles-Clinical Manifestations & Differential Diagnosis The New Physic 263, 1967, Oct., Boshes,L., 1967 Neuro CPC of MGH Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958 Showing articles 50 to 64 of 64 << Previous