WordNet

holding office; "the in party"
to or toward the inside of; "come in"; "smash in the door" (同)inwards, inward
currently fashionable; "the in thing to do"; "large shoulder pads are in"
directed or bound inward; "took the in bus"; "the in basket"
showing favoritism
being or affecting only a part; not total; "a partial description of the suspect"; "partial collapse"; "a partial eclipse"; "a partial monopoly"; "partial immunity"
(of diseases) arising from an unknown cause; "idiopathic epilepsy"
the earliest state of immaturity (同)babyhood
the early stage of growth or development (同)babyhood, early_childhood
a disorder of the central nervous system characterized by loss of consciousness and convulsions

PrepTutorEJDIC

《具体的な場所,位置》 / …『の中に』(『で』) / …『において』,…で / 《intoの代りに移動を表す動詞と共に》…『の中へ』 / (乗り物)『に乗って』 / …『の状熊に』(『で』) / …『に従事して』,に属して / …『を身につけて』,に覆われて / 《『in』do『ing』の形で》…『するときに』,する際に(when) / 《時間》 / …『して』,…『が経過したあと』 / …『の間に』 / …『については』,…の点では / 《方法・手段・材料》…『で』 / 《人を目的語にして,性質・能力があることを示して》…の中に / …の目的で,のつもりで,として / 《比率割合》…のうちで,につき / 《過去分詞に伴って》…に[…されて] / 『中へ』(に) / 『在宅して』,帰って / (乗り物などが)『到着して』,(時期・季節が)来て / 出回って,流行して / 《俗》流行の,当世風の / 《話》特定の人々にのみ理解される
(また『part』)『一部分の』,部分的な;不完全な / 不公平な,偏った / 《補語にのみ用いて》(…が)特に好きで《+『to』+『名』》
特発性疾患の(病気の原因があいまいな,また不明な場合)
(人の)『幼年時代』,乳幼時
てんかん

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Community-based epidemiological study of epilepsy in the Qena governorate in Upper Egypt, a door-to-door survey.

Fawi G1, Khedr EM2, El-Fetoh NA2, Thabit MN3, Abbass MA4, Zaki AF4.
Epilepsy research.Epilepsy Res.2015 Jul;113:68-75. doi: 10.1016/j.eplepsyres.2015.03.010. Epub 2015 Apr 7.
BACKGROUND: The aim of this study is to estimate the epidemiological features of epilepsy in a representative governorate of Upper Egypt.MATERIALS AND METHODS: A door-to-door community-based survey study was performed using a sample of 10 areas among various districts of the Qena governorate in Uppe
PMID 25986192

Novel compound heterozygous mutations in TBC1D24 cause familial malignant migrating partial seizures of infancy.

Milh M1, Falace A, Villeneuve N, Vanni N, Cacciagli P, Assereto S, Nabbout R, Benfenati F, Zara F, Chabrol B, Villard L, Fassio A.
Human mutation.Hum Mutat.2013 Jun;34(6):869-72. doi: 10.1002/humu.22318. Epub 2013 Apr 12.
Early-onset epileptic encephalopathies (EOEEs) are a group of rare devastating epileptic syndromes of infancy characterized by severe drug-resistant seizures and electroencephalographic abnormalities. The current study aims to determine the genetic etiology of a familial form of EOEE fulfilling the
PMID 23526554

Helbig I1, Lowenstein DH.
Current opinion in neurology.Curr Opin Neurol.2013 Apr;26(2):179-85. doi: 10.1097/WCO.0b013e32835ee6ff.
PURPOSE OF REVIEW: We aim to review the most recent advances in the field of epilepsy genetics with particular focus on the progress in gene discovery in monogenic epilepsies, identification of risk genes in complex genetic epilepsies and recent findings in the field of epilepsy pharmacogenomics.REC
PMID 23429546