Differential (Click to cross reference) abdominal distention areflexia ataxia basal ganglia, lesion, bilateral brainstem, lesion of cachexia cerebellar atrophy, secondary cerebellar degeneration cerebral cortical atrophy children chronic progressive external ophthalmoplegia Clinical Pathologic Conference(C.P.C.) coenzyme Q10 deficiency consanguinity corpus callosum, lesion of cranial neuropathy, multiple creatine phosphokinase(CPK)elevated cyst, parenchymal cytochrome c oxidase cytochrome c oxidase, deficiency deafness deep gray nuclei diarrhea extraocular muscle lesion eye movement, disorders of familial fever gait disorder gastrointestinal disease, neurologic complications gastrointestinal motility gastroparesis gaze palsy gene mutation gene therapy genetic counselling genetic neurologic disorders hearing loss hepatomegaly heralding manifestation intestinal pseudoobstruction Kearns-Sayre syndrome Leber's hereditary optic neuropathy Leigh's disease leukocyte enzyme abnormality leukodystrophy leukoencephalopathy MELAS syndrome MERRF syndrome microangiopathy, brain middle cerebellar peduncle, lesion middle cerebellar peduncle, lesion, bilateral misdiagnosis mitochondrial disease mitochondrial encephalomyopathy MNGIE syndrome MRI MRI pattern MRI, abnormal MRI, contrast enhanced MRI, diffusion weighted muscle biopsy muscle weakness, proximal myopathy myopathy, mitochondrial nausea and vomiting neurologic complications of, systemic disease neurologic disease, diagnoses of neurologic symptoms neuropathology neuropathy neuropathy, ataxia, retinitis pigmentosa neuropathy, peripheral ocular motility, disorders of ophthalmoplegia ophthalmoplegia, progressive external pain, abdominal pigmentary retinopathy polyneuropathy prognosis progressive neurologic disorder ptosis ragged-red fibers retina, abnormal retinal degeneration retinal lesion review article sensorineural hearing loss short stature succinate dehydrogenase deficiency symmetric brain lesions systemic illness thalamus, lesion of-bilateral treatment of neurologic disorder upgaze, paralysis of visceral neuropathy weakness weakness, generalized weakness, progressive weaning from respirator, failure to weight loss white matter disease white matter disease, pattern

Showing articles 200 to 203 of 203 << Previous Neuropathy & Mitochondrial Myopathy Ann Neurol 7:262-268, Peyronnard,M.J.,et al, 1980 Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification Neurol 29:1057-1061, Markesbery,Wm.R., 1979 A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission Arch Neurol 36:553-556, Barron,S.A.,et al, 1979 The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973 Showing articles 200 to 203 of 203 << Previous