Results 131 to 140 of about 283,076 (217)

The fetal hydrops-associated single-residue mutation L322P disrupts mechanical but not chemical activation of the PIEZO1 ion channel. [PDF]

Proc Natl Acad Sci U S A
Jiang J, Guo W, Chen X, He Q, Wang Y, Zhu X, Yan L, Qiao J, Xiao B.   +8 more
europepmc   +1 more source

Fetal Hydrops Associated With 47,XXX: A Case Report and Literature Review. [PDF]

Cureus
Sugai S, Haino K, Hayashi M, Nirei J, Yoshihara K, Nishijima K.   +5 more
europepmc   +1 more source

A novel homozygous intronic variant affecting splicing in the RYR1 gene contributes to fetal hydrops. [PDF]

Genes Dis
Hou W, Huang G, Wei H, Li W, Huang H, Qiu Y, Zhu H, Han H, Chen P, Zhang X.   +9 more
europepmc   +1 more source

The First Case Report of a Homozygous Consensus Acceptor Splice Variant in the NUP214 Gene Associated With Fetal Hydrops and Arthrogryposis Multiplex. [PDF]

Cureus
Tamhankar V, Patel SJ, Kachhadiya T, Vaniawala S, Patel J, Bhammar R, Patel S, Vaniawala S, Menon P, Tamhankar PM.   +9 more
europepmc   +1 more source

Recurrent fetal hydrops with maternal M alloimmunisation: not a benign condition. [PDF]

BMJ Case Rep, 2019
Yu M, Graham K, Pasalic L, Alahakoon TI.
europepmc   +1 more source

Staged biventricular repair in a premature neonate with critical aortic stenosis, severe mitral regurgitation, and fetal hydrops: a case report. [PDF]

Gen Thorac Cardiovasc Surg Cases
Teguri Y, Kido T, Miwa K, Kanaya T, Iwai S, Aoki H, Tsumura S.   +6 more
europepmc   +1 more source

Congenital yellow nail syndrome presenting with eyelid lymphedema and fetal hydrops. [PDF]

JAAD Case Rep, 2019
El Alami J, Galicier L, Huynh S, Frumholtz L, Bagot M, de Masson A, Vignes S, Bouaziz JD.   +7 more
europepmc   +1 more source

Radiofrequency thermal ablation of giant placental chorioangioma complicated with fetal hydrops: a case report and successful outcome. [PDF]

Case Rep Perinat Med
Le Vance J, Gurney L, Meher S, Negrine R, Hodgetts Morton V, Marton T, Morris RK.   +6 more
europepmc   +1 more source

Failure of NIPT to detect constitutional chromoanasynthesis involving chromosome 21 in a case of fetal hydrops-A case report. [PDF]

Clin Case Rep, 2019
Bone K, MacPherson MJ, Chernos J, Lauzon J.   +3 more
europepmc   +1 more source

The near disappearance of fetal hydrops in relation to current state-of-the-art management of red cell alloimmunization. [PDF]

Prenat Diagn, 2018
Zwiers C, Oepkes D, Lopriore E, Klumper FJ, de Haas M, van Kamp IL.   +5 more
europepmc   +1 more source