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[Whole exome sequencing analysis of compound heterozygous variants of CDAN1 gene in a Chinese family with non-immune hydrops fetalis].
Wang Y, Li Q, Sun X, Li S, He J, Zhang M, Huang L, He W. Wang Y, et al. Nan Fang Yi Ke Da Xue Xue Bao. 2021 Dec 20;41(12):1899-1903. doi: 10.12122/j.issn.1673-4254.2021.12.21. Nan Fang Yi Ke Da Xue Xue Bao. 2021. PMID: 35012925 Free PMC article. Chinese.
OBJECTIVE: To study the clinical characteristics and genetic variants in a family with non-immune hydrops fetalis. METHODS: Peripheral blood samples were collected from a pregnant woman with suspected non-immune hydrops fetalis of the fetus for routine blood analysi …
OBJECTIVE: To study the clinical characteristics and genetic variants in a family with non-immune hydrops fetalis. METHODS: Periphera …
Case Report: Treatment of Extremely Preterm Infants With Birthweight Below 300 g: Case Series.
Shitara Y, Kakiuchi S, Mukai T, Kashima K, Kato M, Takahashi N. Shitara Y, et al. Front Pediatr. 2021 Dec 6;9:758683. doi: 10.3389/fped.2021.758683. eCollection 2021. Front Pediatr. 2021. PMID: 34938697 Free PMC article.
The infant in case 2 managed to survive through severe prematurity secondary to hydrops fetalis. However, complications followed soon as tracheal granulation tissue was formed with neurodevelopmental impairment. ...
The infant in case 2 managed to survive through severe prematurity secondary to hydrops fetalis. However, complications followed soon …
Placental transcriptome sequencing combined with bioinformatics predicts potential genes and circular RNAs associated with hemoglobin Bart's hydrops fetalis syndrome.
Deng L, Lu Y, Yang D, Yang F, Ruan H, Wei C, Lai K, Pang L. Deng L, et al. J Obstet Gynaecol Res. 2021 Dec 21. doi: 10.1111/jog.15126. Online ahead of print. J Obstet Gynaecol Res. 2021. PMID: 34935248
AIM: Hemoglobin Bart's hydrops fetalis syndrome (BHFS) is the most severe form of alpha-thalassemia. ...
AIM: Hemoglobin Bart's hydrops fetalis syndrome (BHFS) is the most severe form of alpha-thalassemia. ...
Conservative Management of Presumed Fetal Anemia Secondary to Maternal Chemotherapy for Acute Myeloid Leukemia.
Nowik CM, Gerrie AS, Wong J. Nowik CM, et al. AJP Rep. 2021 Dec 15;11(4):e137-e141. doi: 10.1055/s-0041-1740561. eCollection 2021 Oct. AJP Rep. 2021. PMID: 34925954 Free PMC article.
To our knowledge, we present the first case of presumed severe fetal anemia related to in utero exposure to chemotherapy that was managed conservatively with close sonographic monitoring, including serial measurement of MCA PSV. This case suggests that in the absence of hydrops …
To our knowledge, we present the first case of presumed severe fetal anemia related to in utero exposure to chemotherapy that was managed co …
Rh Incompatibility.
Costumbrado J, Mansour T, Ghassemzadeh S. Costumbrado J, et al. 2021 Dec 14. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan–. 2021 Dec 14. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan–. PMID: 29083656 Free Books & Documents.
This is of particular concern if an Rh-negative mother is carrying an Rh-positive fetus, which can result in consequences along the spectrum of HDN ranging from self-limited hemolytic anemia to severe hydrops fetalis....
This is of particular concern if an Rh-negative mother is carrying an Rh-positive fetus, which can result in consequences along the spectrum …
Omenn Syndrome due to RAG1 Mutation Presenting With Nonimmune Hydrops Fetalis in Two Siblings.
Valeri L, Lugli L, Iughetti L, Soresina A, Giliani S, Porta F, Berardi A. Valeri L, et al. Pediatrics. 2022 Jan 1;149(1):e2021052411. doi: 10.1542/peds.2021-052411. Pediatrics. 2022. PMID: 34889447
We report 2 siblings affected by OS due to a homozygous frameshift mutation (NM_000448.3:c.519delT, p.E174Sfs*26) in the RAG1 gene presenting with nonimmune hydrops fetalis (NIHF). To the best of our knowledge, this is the first reported association between OS and NIHF. .. …
We report 2 siblings affected by OS due to a homozygous frameshift mutation (NM_000448.3:c.519delT, p.E174Sfs*26) in the RAG1 gene presentin …
Biallelic ANGPT2 loss-of-function causes severe early-onset non-immune hydrops fetalis.
Smeland MF, Brouillard P, Prescott T, Boon LM, Hvingel B, Nordbakken CV, Nystad M, Holla ØL, Vikkula M. Smeland MF, et al. J Med Genet. 2021 Dec 7:jmedgenet-2021-108179. doi: 10.1136/jmedgenet-2021-108179. Online ahead of print. J Med Genet. 2021. PMID: 34876502 Free article.
BACKGROUND: Hydrops fetalis, a pathological fluid accumulation in two or more body compartments, is aetiologically heterogeneous. We investigated a consanguineous family with recurrent pregnancy loss due to severe early-onset non-immune hydrops fetalis. METHODS AND …
BACKGROUND: Hydrops fetalis, a pathological fluid accumulation in two or more body compartments, is aetiologically heterogeneous. We …
4,280 results