Differential (Click to cross reference) ankle reflex, absent areflexia arrhythmia, cardiac ataxia ataxia, cerebellar ataxia, progressive ataxic gait autosomal rcessive spastic ataxia of Charlevoix-Saguenay Babinski sign benign essential tremor Brown-Vialetto-Van Laere syndrome calf hypertrophy cardiomyopathy central core disease cerebellar atrophy, primary Charcot-Marie-Tooth children chromosomal abnormality chromosome 17 clubfoot as related to neurologic disease cognition consanguinity contractures, joint corpus callosum, thinning cranial neuropathy cranial neuropathy, multiple creatine phosphokinase(CPK)elevated developmental milestones, loss of differential diagnosis dislocated hip, congenital distal muscle atrophy distal muscle weakness diurnal variation dopa responsive dystonia dysarthria dystonia endemic area evoked potentials facial weakness failure to thrive falling familial fine motor function, impaired finger nose finger test foot deformity foot drop gait disorder gait, waddling gene gene mutation genetic counselling genetic neurologic disorders genetic testing hammertoes hand deformity hand weakness hearing loss high arched feet hyperreflexia hyporeflexia hypotonia hypotonia, infants imbalance incoordination intrinsic hand muscles, wasting of kyphoscoliosis, neurologic causes of L-dopa leg weakness, bilateral leprosy lordosis malignant hyperpyrexia microcephaly mitral valve prolapse molecular genetics MRI, abnormal muscle atrophy, static muscle biopsy muscle cramp muscle weakness muscle weakness, proximal muscular dystrophy muscular dystrophy, Becker myopathy nerve conduction studies nerve enlargement nerve hypertrophy neuropathy neuropathy, hereditary peripheral neuropathy, hypertrophic neuropathy, peripheral nystagmus pain, foot Parkinson disease past pointing pes cavus polymerase chain reaction polyneuropathy polyneuropathy, familial pons, lesion of prognosis progressive neurologic disorder pseudohypertrophy pyramidal tract dysfunction rash Red flags renal tubular acidosis review article riboflavin transporter deficiency Romberg's sign Samoa scoliosis scoliosis, neurologic association with sensory loss skin, biopsy skin, lesions in neurologic disorders steppage gait toe walking treatment of neurologic disorder tremor tremor, intention tripping visual evoked response walking walking frame walking, difficulty with weakness weakness, generalized weakness, progressive wheelchair wide based gait wrist drop

Showing articles 850 to 857 of 857 << Previous The Neurologist's Experience with Pheochromocytoma JAMA 197:100, Thomas,J.E.,et al, 1966 Giant-Cell Arteritis-An Acute Hand Syndrome J Bone & Joint Surg 45A:1269963., Bugg,E.I.,et al, 1963 Peripheral Entrapment Neuropathies 87, 1963, William & Wilkins Co. , Chpt. 15., Kopell,H.P.,et al, 1963 Diseases of the Basal Ganglia-Their Relation to Disorders of Movement Lancet 1099, 1960, Nov., Denny-Brown,D., 1960 Neurologic Manifestations of Chronic Carbon Monoxide Poisoning NEJM 261:1217-1220, Gilbert,G.J.,et al, 1959 Neurologic Manifestations of Chronic Pulmonary Insufficiency NEJM 257:579-590, Austen,F.K.,et al, 1957 Neurological & Psychiatric Signs Associated with SLE JAMA l60:455, Clark,E.,et al, 1956 Electric Shocks and Weakness of the Right Hand in a Young Man:Hirayama Disease , Witiw,C.D.&OToole,J.E., Showing articles 850 to 857 of 857 << Previous