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Neurology in Clinical Practice: an algorithmic approachNeuroweb.us - Differential diagnosis in neurology with algorithms produced by Deleu Dirk
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Neurology in Clinical Practice: an algorithmic approach | neuroweb.us Reviews
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Neuroweb.us - Differential diagnosis in neurology with algorithms produced by Deleu Dirk
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Selection of major neurological syndromes and neurological tests. Bilateral hilar lymph nodes with neurological disease. Chorea, choreoathetosis and ballism. Electrolyte abnormalities in neurology. Encephalopaty - Acute with episodic muscle rigidity. Encephalopathy - Chronic (progressive dementia plus syndrome). Forearm ischemic exercise screening test. Generalized weakness - Acute. Generalized weakness - Subacute/Chronic. Headache - Acute new onset. Headache - Exertional, cough and sexual.
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Autosomal dominant cerebellar ataxia. Autosomal dominant nocturnal frontal lobe epilepsy. Adult polyglucosan body disease. Brainstem auditory evoked potential. Cerebral autosomal dominant arteropathy with subcortical infarcts and leucoencephalopathy. Compound muscle action potential. Debrancher enzyme deficiency type III. Distal myopathy with rimmed vacuoles. Early onset ataxia with retained reflexes. Friedreich ataxia with retained reflexes. Familial ataxia with vitamin E deficiency.
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Neurologie - Dr. Ghervan Ovidiu - Neuroweb
Neurofiziologie: EEG,EMG,PE. Proiect neurologie - Dr. Ghervan Ovidiu, medic primar neurolog.
神経内科だより: 2011年06月 アーカイブ
2011年06月 アーカイブ. 2011年06月03日. 当科で原因遺伝子が発見された脊髄小脳変性症である 眼球運動失行と低アルブミン血症を伴う早発型失調症(Early onset Ataxia with Ocular motor apraxia and Hypoalbuminemia:EAOH) の遺伝子型と臨床型の相関についての報告です 横関明男先生による解説です どうぞご一読ください. Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia. Yokoseki A, Ishihara T, Koyama A, Shiga A, Yamada M, Suzuki C, Sekijima Y, Maruta K, Tsuchiya M, Date H, Sato T, Tada M, Ikeuchi T, Tsuji S, Nishizawa M, Onodera O. 本邦でFriedreich失調症と診断してきた症例は，Friedreich失調症の症状に...
Neurology in Clinical Practice: an algorithmic approach
Why on-line neurological algorithms? O provide the reader a quick, updated and reliable insight in the potential differential diagnosis of commonly (and less commonly) encountered neurological syndromes in adolescence and adulthood. Neurological disorders occurring in childhood are beyond the scope of this webpage. He chapters are divided in common recognizable neurological signs, symptoms and syndrome chapters, which implicates that a basic knowledge and interpretation of neurological history and synthe...
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