WordNet

write by means of a keyboard with types; "type the acceptance letter, please" (同)typewrite
a small metal block bearing a raised character on one end; produces a printed character when inked and pressed on paper; "he dropped a case of type, so they made him pick them up"
(biology) the taxonomic group whose characteristics are used to define the next higher taxon
a subdivision of a particular kind of thing; "what type of sculpture do you prefer?"
all of the tokens of the same symbol; "the word `element contains five different types of character"
printed characters; "small type is hard to read"
identify as belonging to a certain type; "Such people can practically be typed" (同)typecast
writing done with a typewriter (同)typewriting

PrepTutorEJDIC

〈C〉(…の)『型』,タイプ,類型,種類(kind)《+of+名》 / 〈C〉(その種類の特質を最もよく表している)『典型』,手本,模範《+of+名》 / 〈U〉《集合的に》活字;〈C〉(1個の)活字 / 〈U〉(印刷された)字体,活字 / 〈C〉(貨幣・メダルなどの)模様,図柄 / 〈C〉血液型(blood group) / …‘を'タイプに打つ / (…として)…‘を'分類する《+名+as+名(doing)》 / …‘の'型を決める / タイプライターを打つ

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1. 遺伝性運動失調の概要 overview of the hereditary ataxias
2. 症候性（二次性）ミオクローヌス symptomatic secondary myoclonus
3. ミオクローヌスの分類および評価 classification and evaluation of myoclonus
4. 先天性代謝異常：疫学、病因、および臨床的特徴 inborn errors of metabolism epidemiology pathogenesis and clinical features
5. 律動眼振 jerk nystagmus

Gowda VK1,2, Srinivasan VM3, Benakappa N3, Benakappa A3.
Indian journal of pediatrics.Indian J Pediatr.2017 Jan 31. doi: 10.1007/s12098-016-2286-9. [Epub ahead of print]
PMID 28138907

Multigene panel next generation sequencing in a patient with cherry red macular spot: Identification of two novel mutations in NEU1 gene causing sialidosis type I associated with mild to unspecific biochemical and enzymatic findings.

Mütze U1, Bürger F2, Hoffmann J3, Tegetmeyer H4, Heichel J5, Nickel P6, Lemke JR7, Syrbe S1, Beblo S6.
Molecular genetics and metabolism reports.Mol Genet Metab Rep.2016 Dec 1;10:1-4. eCollection 2017.
PMID 27942463

Measurement of Elevated Concentrations of Urine Keratan Sulfate by UPLC-MSMS in Lysosomal Storage Disorders (LSDs): Comparison of Urine Keratan Sulfate Levels in MPS IVA Versus Other LSDs.

Clinical and Serial MRI Findings of a Sialidosis Type I Patient with a Novel Missense Mutation in the NEU1 Gene

Sekijima Yoshiki,Nakamura Katsuya,Kishida Dai,Narita Aya,Adachi Kaori,Ohno Kosaku,Nanba Eiji,Ikeda Shu-ichi
Internal Medicine 52(1), 119-124, 2013
… The case of a Japanese sialidosis type I patient with a novel NEU1 gene mutation is described. … The p.D135N mutation is a novel mutation that is considered to be associated with the mild clinical phenotype of sialidosis. …
NAID 130003365573

Naganawa Yasunori,Itoh Kohji,Shimmoto Michie [他],TAKIGUCHI Kyoko,DOI Hirofumi,NISHIZAWA Yuzuru,KOBAYASHI Takayoshi,KAMEI Sachiko,LUKONG Kiven E.,PSHEZHETSKY Alexey V.,SAKURABA Hitoshi
Journal of human genetics 45(4), 241-249, 2000-07-01
NAID 10011570484