Differential (Click to cross reference) acetazolamide acid maltase deficiency advances in neurology adverse drug reaction airway obstruction alopecia alveolar hypoventilation Alzheimer's disease Alzheimer's disease, familial amniocentesis amyloidosis amyotrophic lateral sclerosis amyotrophic lateral sclerosis, epidemiology of amyotrophic lateral sclerosis, familial amyotrophic lateral sclerosis, guamian type of anasarca anesthesia, general anterior interosseous neuropathy antiarrhythmic drugs antibodies to voltage-gated calcium channels anticoagulant, treatment anticoagulant, treatment in CVD anticonvulsants anticonvulsants, untoward effects of antihistamines arrhythmia, cardiac arthrogryposis multiplex aspiration aspirin asymptomatic ataxia ataxia, paroxysmal atelectasis atrial fibrillation atrioventricular block audiogram auditory evoked brainstem potentials autoimmune disease automatic implantable cardioverter-defibrillator axonopathy, distal baldness basal ganglia, calcification of 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potentials exercise exercise electrocardiography eye closure facial appearance, abnormal facial nerve palsy facial nerve palsy, bilateral facial nerve, lesion of facial weakness facial weakness, bilateral falling false negative familial familial hemiplegic migraine Fazio-Londe's disease floppy infant fluorescein angiography fragile-X syndrome Friedreich's ataxia frontal balding F-wave response gene gene mutation genetic counselling genetic diagnosis genetic diagnosis, prenatal genetic linkage genetic neurologic disorders genetic screening genetic testing glioma glucose tolerance test, abnormal Gowers maneuver gray matter Guillain Barre syndrome Guyon's canal hammertoes hand weakness hearing loss heart block heart block, complete heavy metal intoxication high arched feet high arched palate hip dysplasia hip pain histochemistry histochemistry of muscle H-reflex testing huntingtin Huntington's chorea hydrocephalus hydrops fetalis hypercapnia hyperinsulinism hyperkalemic periodic paralysis hyperostosis hyperparathyroidism hypersomnia hypokalemia hypokalemic periodic paralysis hypotonia hypotonia, causes of hypotonia, infants hypoxic encephalopathy inclusion bodies inclusion bodies, eosinophilic cytoplasmic inclusion body myositis INR values intellectual deficit intelligence quotient iris, abnormal kaliuresis Kearns-Sayre syndrome klippel feil syndrome Kugelberg-Welander syndrome lid abnormalities lid closure, weakness of lid retraction, lower life expectancy lordosis malignancy screen malignant hyperpyrexia manic-depressive median neuropathy Melkersson's syndrome mental retardation metabolic acidosis mexiletine microcephaly micrognathia migraine mitochondrial disease mitochondrial encephalomyopathy mitral valve prolapse modafinil molecular genetics mononeuropathy mortality motor neuron disease MRI MRI, abnormal MRI, functional MRI, muscle MRS muscle atrophy, progressive muscle biopsy muscle cramp muscle diseases, characteristics of muscle hypertrophy muscle pain muscle stiffness muscle wasting, diffuse muscle weakness muscle weakness, proximal muscle, metabolic disorders of muscular dystrophy muscular dystrophy, Becker muscular dystrophy, cardiovascular changes with muscular dystrophy, classification muscular dystrophy, congenital muscular dystrophy, Duchenne muscular dystrophy, facioscapulohumeral muscular dystrophy, limb-girdle myasthenia gravis myasthenic crisis myasthenic syndrome myocarditis myoglobinuria myopathy myopathy, carcinomatous myopathy, distal myopathy, drug-induced myopathy, mitochondrial myopathy, myofibrillar myopathy, proximal myopathy, thyroid disease causing myositis myotonia myotonia congenita myotonia dystrophica myotonia dystrophica, classification myotonia dystrophica, type 2 myotonia, causes of myotonia, treatment of myotonic discharges neck weakness neoplasm, metastatic to CNS neoplasm, primary intracerebral neoplasm, primary intracranial neoplasm, primary of CNS nerve biopsy nerve conduction studies nerve conduction 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stiff man syndrome sudden death taurine temporalis muscle wasting temporalis muscle weakness temporomandibular joint, dislocation term infant testicular atrophy thoracic outlet syndromes thyrotoxicosis tocainide torticollis transient ischemic attack treatment of neurologic disorder tricresylphosphate trinucleotide repeats tubular aggregates, muscle twins ulnar neuropathy ultrasonography ventricular tachycardia viral infection, CNS visual evoked response weakness weakness, progressive weakness, proximal weaning from respirator, failure to Werdnig-Hoffman disease wheelchair white matter disease white matter disease, periventricular winging of scapula workup X-linked bulbospinal neuronopathy

Showing articles 500 to 507 of 507 << Previous Mental Deficiency Associated with Muscular Dystrophy Brain 89:769, Rosman,N.P.,et al, 1966 The Muscular Dystrophies NEJM 273:537, 5961965., Zundel,W.,et al, 1965 Seronegative Ocular Syphilis & Neurosyphilis, Neuro-Ophthalmology Symposium, U. of Miami (Ed) , St. Louis:C. V. Mosby Co. , 1965, p. 1, Smith,J.L., 1965 Muscular Dystrophy Am J Med 35:632, Pearson,C.M., 1963 Angiokeratoma Corporis Diffusum Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962 Neuro CPC of MGH Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958 Causalgia of the Face, Two Cases Successfully Treated by Sympathectomy BMJ 1:804-805, Bingham,J.A.W., 1947 Five Types of Dystrophy Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850 Showing articles 500 to 507 of 507 << Previous