Results 141 to 150 of about 6,329 (224)

Glucose-6-phosphate dehydrogenase deficiency as a cause for nonimmune hydrops fetalis and severe fetal anemia: A systematic review. [PDF]

Mol Genet Genomic Med
Iyer NS, Mossayebi MH, Gao TJ, Haizler-Cohen L, Di Mascio D, McLaren RA, Al-Kouatly HB.   +6 more
europepmc   +1 more source

OP12.06: Perinatal mortality rate according to the location of fluid collection sites in non‐immune hydrops fetalis [PDF]

, 2015
Pardis Hosseinzadeh, Jimmy Espinoza, Andy Ness, Victoria Berger, E Werner, Bahram Salmanian, Z. Heidari‐Bateni, Michael A. Belfort, Alireza A. Shamshirsaz   +8 more
openalex   +1 more source

Spontaneous resolution of nonimmune hydrops fetalis in a fetus with TP63 gene mutation and LZTR1 gene variants. [PDF]

Clin Case Rep, 2021
Hurni Y, Marangoni M, Garofalo G, Cassart M, Tomasi L, Vandernoot I, Smits G, Gounongbé C.   +7 more
europepmc   +1 more source

Emergency Cesarean Section in a Dichorionic Diamniotic Twin Pregnancy With Hydrops Fetalis: A Report of a Critical Case. [PDF]

Cureus
Ahmad S, Karotkar S, Meshram RJ, Lohiya S, Rawat A.   +4 more
europepmc   +1 more source

Prenatal hydrops fetalis associated with infantile free sialic acid storage disease due to a novel homozygous deletion in the SLC17A5 gene. [PDF]

Cold Spring Harb Mol Case Stud, 2021
Hasnain A, Burnett S, Agatep R, Spriggs E, Chodirker B, Mhanni AAA.   +5 more
europepmc   +1 more source

Cystic hygroma and thymic aplasia innonimmune hydrops fetalis: A case report

, 2006
S. Bounyasong
openalex   +2 more sources

Antenatal Hydrops Fetalis with Umbilical Vein Varix and Thrombosis - Ultrasound Imaging: A Rare Case. [PDF]

J Med Ultrasound
Suryadevara M, Gupta R, Mishra GV, Nagendra V, Bhansali PJ.   +4 more
europepmc   +1 more source

Use of High-Performance Liquid Chromatography for Prenatal Diagnosis of a-Thalassemia (Hemoglobin Bart's) Hydrops Fetalis in Fetal Cord Blood Sample [PDF]

, 2015
Jayalakshmi Balakrishna, Men‐Jean Lee, Vijay Shah   +2 more
openalex   +1 more source

Hydrops fetalis caused by a complex congenital heart defect with concurrent hypoplasia of pulmonary blood vessels and lungs visualized by micro-CT in a French Bulldog. [PDF]

BMC Vet Res
Szaluś-Jordanow O, Barszcz K, Mądry W, Buczyński M, Czopowicz M, Gierulski A, Moroz-Fik A, Mickiewicz M, Grzegorczyk M, Jaroszewicz J.   +9 more
europepmc   +1 more source

Case Report: Whole Exome Sequencing Revealed Two Novel Mutations of PIEZO1 Implicated in Nonimmune Hydrops Fetalis. [PDF]

Front Genet, 2021
Chen Y, Jiang Y, Chen B, Qian Y, Liu J, Yang M, Zhao B, Luo Q.   +7 more
europepmc   +1 more source