神経内科だより 2011年06月 アーカイブ
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神経内科だより 2011年06月 アーカイブDESCRIPTION
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 HypoalbuminemiaEAOH 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.CONTENT
This domain neuroweb.sblog.jp has the following on the site, "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 HypoalbuminemiaEAOH 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." We observed that the webpage also said " Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia." It also stated " 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."SEEK OTHER WEB SITES
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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