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《所有・所属》…『の』,…のものである,…に属する・《材料・要素》…『でできた』,から成る・《部分》…『の』[『中の』] ・《数量・単位・種類を表す名詞に付いて》…の・《原因・動機》…『で』,のために(because of) ・《主格関係》…『の』,による,によって・《目的格関係》…『を』,の・《同格関係》…『という』・《関係・関連》…『についての』[『の』],の点で・《抽象名詞などと共に》…の[性質をもつ] ・《『It is』+『形』+『of』+『名』+『to』 doの形で,ofの後の名詞を意味上の主語として》・《分離》…『から』・《起原・出所》…『から』[『の』](out of) ・《『名』+『of』+『a』(『an』)+『名』の形で》…のような・《『名』+『of』+『mine』(『yours, his』など独立所有格)の形で》…の…・《時》(1)《副詞句を作って》…に《形容詞句を作って》…の・《時刻》《米》…前(to,《米》before)
(特定の事に関する,または特殊の性質の)文書資料の集成 / (研究用に収集した)資料
OLD French古[代]フランス語

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Description of a novel TUBA1A mutation in Arg-390 associated with asymmetrical polymicrogyria and mid-hindbrain dysgenesis.

Zanni G, Colafati GS, Barresi S, Randisi F, Talamanca LF, Genovese E, Bellacchio E, Bartuli A, Bernardi B, Bertini E.SourceUnit of Neuromuscular and Neurodegenerative Disorders, Laboratory of Molecular Medicine, Bambino Gesù Children's Hospital, IRCCS, Piazza S. Onofrio, 400165 Rome, Italy.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.Eur J Paediatr Neurol.2013 Jul;17(4):361-5. doi: 10.1016/j.ejpn.2012.12.006. Epub 2013 Jan 11.
Mutations of TUBA1A gene were first identified as causing a distinctive neuroradiologic phenotype characterized by cortical abnormalities ranging from classical lissencephaly to perisylvian pachygyria with dysgenetic corpus callosum, brainstem and cerebellum. We describe the clinical and neuroradiol
PMID 23317684

Hosseinzadeh K, Luo J, Borhani A, Hill L.SourceDepartment of Radiology, Presbyterian South Tower, University of Pittsburgh Medical Center, 200 Lothrop Street, Suite 3950, Pittsburgh, PA, 15213, USA, hosseinzadehk@upmc.edu.
Insights into imaging.Insights Imaging.2013 Jun;4(3):357-67. doi: 10.1007/s13244-013-0244-x. Epub 2013 Apr 13.
OBJECTIVE: This manuscript reviews congenital anomalies and imaging findings associated with non-visualisation of the cavum septi pellucidi (CSP) found on prenatal sonogram.BACKGROUND: Observation of a normal cavum septi pellucidi (CSP) is an important landmark in the second and third trimester pren
PMID 23584847

Late diagnosis of fetal central nervous system anomalies following a normal second trimester anatomy scan.

Yinon Y, Katorza E, Nassie DI, Ben-Meir E, Gindes L, Hoffmann C, Lipitz S, Achiron R, Weisz B.SourceDepartment of Obstetrics and Gynecology, Sheba Medical Center, Tel-Aviv University, Israel.
Prenatal diagnosis.Prenat Diagn.2013 May 24. doi: 10.1002/pd.4163. [Epub ahead of print]
OBJECTIVE: The aim of this study was to describe the nature of central nervous system (CNS) anomalies diagnosed during the third trimester following a normal anatomy scan at 21-24 weeks of gestation.METHODS: Retrospective cohort study of all pregnant women referred to the fetal medicine unit at Sh
PMID 23712473

Magnetic Resonance Imaging and Clinical Findings in a Miniature Schnauzer with Hypodipsic Hypernatremia

Shimokawa Miyama Takako,Iwamoto Emiko,Umeki Saori [他],NAKAICHI Munekazu,OKUDA Masaru,MIZUNO Takuya
Journal of
… A 6-month-old miniature Schnauzer presented with hypernatremia and clinical signs of vomiting, diarrhea, inappetence, and lethargy. … Endocrinological investigations and urinalysis excluded the possibility of diabetes insipidus and hyperaldosteronism. … Magnetic resonance imaging revealed dysgenesis of the corpus callosum and other forebrain structures. …
NAID 130000134306

Asymptomatic Huge Congenital Arachnoid Cyst Successfully Treated by Endoscopic Surgery

TSUTSUMI Satoshi,KONDO Akihide,YASUMOTO Yukimasa,ITO Masanori
Neurologia medico-chirurgica 48(9), 405-408, 2008-09-15
… A female neonate was the first child of a 30-year-old mother, with unremarkable medical history. … Prenatal ultrasonography performed at 36 weeks of gestation suggested intracranial mass lesion. … The baby was delivered by cesarean section at 41 weeks of gestation because of bradycardia and asphyxia. …
NAID 110006937255