Wikipedia preview

出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/02/15 22:09:11」(JST)

UpToDate Contents

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. 新生児の持続性肺高血圧症 persistent pulmonary hypertension of the newborn
2. 肺発達異常の放射線学的所見 radiographic appearance of developmental anomalies of the lung
3. 胎児サーベイランスのための臍動脈ドップラー超音波検査 doppler ultrasound of the umbilical artery for fetal surveillance
4. 先天性心疾患における心房性不整脈（房室ブロックを含む） atrial arrhythmias including av block in congenital heart disease
5. 新生児における胸水の病因、臨床症状、診断および評価 etiology clinical manifestations diagnosis and evaluation of pleural effusions in the neonate

Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract.

Kohl S1, Chen J2, Vivante A3, Hwang DY4, Shril S2, Dworschak GC5, Van Der Ven A2, Sanna-Cherchi S6, Bauer SB7, Lee RS7, Soliman NA8, Kehinde EO9, Reutter HM10, Tasic V11, Hildebrandt F12.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.Nephrol Dial Transplant.2016 Aug;31(8):1280-3. doi: 10.1093/ndt/gfv447. Epub 2016 Jan 29.
BACKGROUND: Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause of chronic kidney diseases in children and young adults, accounting for ∼50% of cases. These anomalies represent maldevelopment of the genitourinary system and can be genetically explained in only 10
PMID 26908769

Corrigendum: Assisted reproduction causes placental maldevelopment and dysfunction linked to reduced fetal weight in mice.

Clinical and genetic characteristics of Leber congenital amaurosis with novel mutations in known genes based on a Chinese eastern coast Han population.

Wang S1, Zhang Q1, Zhang X1, Wang Z1, Zhao P2.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie.Graefes Arch Clin Exp Ophthalmol.2016 Jul 16. [Epub ahead of print]
PURPOSE: To study the genotype-phenotype characteristics of Leber congenital amaurosis (LCA) in the Chinese eastern coast Han population.METHODS: Children with strictly defined LCA with novel mutations of known LCA genes identified by targeted next-generation sequencing (NGS) and a prediction of pat
PMID 27422788

Directed Differentiation of Patient-Specific Induced Pluripotent Stem Cells Identifies the Transcriptional Repression and Epigenetic Modification of NKX2-5, HAND1, and NOTCH1 in Hypoplastic Left Heart Syndrome