ルシー・レヴィ症候群
WordNet
- impose and collect; "levy a fine" (同)impose
- a charge imposed and collected
- the act of drafting into military service (同)levy en masse
- a pattern of symptoms indicative of some disease
- a complex of concurrent things; "every word has a syndrome of meanings"
- United States pathologist who discovered viruses that cause tumors (1879-1970) (同)Peyton_Rous, Francis Peyton Rous
PrepTutorEJDIC
- (…に)〈税金など〉‘を'強制的に課する《+『名』+『on』(『upon』)+『名』》;〈税金など〉‘を'取り立てる / 《文》(…に対して)〈戦争〉‘を'始める《+『upon』(『against』)+『名』》 / (税金などの)強制課税(取り立て);(兵士の)召集 / 取り立てた税金;召集兵,召集軍隊
- (疾患の徴候となる一群の)症徴候,症候群 / (事件・社会的状態などのパターンを示す)徴候形態
UpToDate Contents
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English Journal
- PIPs in neurological diseases.
- Waugh MG1.
- Biochimica et biophysica acta.Biochim Biophys Acta.2015 Aug;1851(8):1066-1082. doi: 10.1016/j.bbalip.2015.02.002. Epub 2015 Feb 11.
- Phosphoinositide (PIP) lipids regulate many aspects of cell function in the nervous system including receptor signalling, secretion, endocytosis, migration and survival. Levels of PIPs such as PI4P, PI(4,5)P2 and PI(3,4,5)P3 are normally tightly regulated by phosphoinositide kinases and phosphatases
- PMID 25680866
- Tryptophan to Glycine mutation in the position 116 leads to protein aggregation and decreases the stability of the LITAF protein.
- Kumar CV1, Swetha RG, Ramaiah S, Anbarasu A.
- Journal of biomolecular structure & dynamics.J Biomol Struct Dyn.2015 Aug;33(8):1695-709. doi: 10.1080/07391102.2014.968211. Epub 2014 Oct 13.
- Mutations in the gene-encoding vesicle lipopolysaccharide-induced tumor necrosis factor (LITAF) protein cause Charcot-Marie-Tooth type 1C (CMT1C) disease, a neurological disorder. The LITAF gene is mapped to chromosome number 16 and can be found at cytogenetic location 16p13 of the chromosome. CMT1C
- PMID 25245565
- Dynamic pedobarography and radiographic evaluation of surgically treated cavovarus foot deformity in children with Charcot-Marie-Tooth disease.
- Erickson S1, Hosseinzadeh P, Iwinski HJ, Muchow RC, Talwalkar VR, Walker JL, Milbrandt TA.
- Journal of pediatric orthopedics. Part B.J Pediatr Orthop B.2015 Jul;24(4):336-40. doi: 10.1097/BPB.0000000000000163.
- Pedobarography is a common tool for the evaluation of foot deformity. We describe our radiographic and pedobarographic outcomes of surgical treatment of cavovarus foot deformity in children with Charcot-Marie-Tooth disease. Nineteen patients for a total of 30 feet were included. Preoperative and pos
- PMID 25768680
Japanese Journal
- Roussay-Levy syndrome 様の臨床像を呈し, 腰椎神経根の肥厚を認めた Charcot-Marie-Tooth disease type 1B の一例
- 後藤 啓五,角田 由華,市川 由布子,藤掛 彰史,福岡 敬晃,徳井 啓介,丹羽 淳一,泉 雅之,中尾 直樹,衣斐 達,両角 佐織,祖父江 元,道勇 学
- 末梢神経 = Peripheral nerve 21(2), 355, 2010-12-01
- NAID 10027742613
- PMP22遺伝子の重複をみとめたRoussy-Levy症候群の1例
- Roussy-Levy syndrome is a phenotypic variant of Charcot-Marie-Tooth syndrome type 1A associated with a duplication on chromosome 17p11.2
Related Links
- Roussy-Lévy syndrome Synonyms Hereditary areflexic dystasia, Roussy Levy hereditary areflexic dystasia, Roussy-Levy Syndrome, Roussy-Levy disease, Roussy-Lévy syndrome Summary Charcot-Marie-Tooth disease is a... ] ...
- Important It is possible that the main title of the report Roussy Levy Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this ...
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- 英
- Roussy-Levy syndrome
- 同
- 遺伝性無反射性起立障害 hereditary areflexic dystasia, 筋萎縮を伴う遺伝性失調症 hereditary ataxia with muscular atrophy
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