Results 231 to 240 of about 27,264 (283)
Some of the next articles are maybe not open access.
Prenatal Diagnosis, 2021
Nonimmune hydrops fetalis (NIHF) has varied etiology. We assessed the etiological spectrum and evaluated the utility of fetal whole exome sequencing (fWES) for the diagnosis of NIHF.
Alec Reginald Errol Correa +7 more
semanticscholar +1 more source
Nonimmune hydrops fetalis (NIHF) has varied etiology. We assessed the etiological spectrum and evaluated the utility of fetal whole exome sequencing (fWES) for the diagnosis of NIHF.
Alec Reginald Errol Correa +7 more
semanticscholar +1 more source
The many etiologies of nonimmune hydrops fetalis diagnosed by exome sequencing
Prenatal Diagnosis, 2021To explain the importance of identifying an etiology for the pathological finding of nonimmune hydrops fetalis (NIHF) and to explore the impact of exome sequencing in recurrent NIHF.
T. Wagner +9 more
semanticscholar +1 more source
Outcomes of allogeneic transplantation for hemoglobin Bart’s hydrops fetalis syndrome in Hong Kong
Pediatric Transplantation, 2021Hemoglobin Bart's hydrops fetalis syndrome (BHFS) was once considered a fatal condition universally. Medical advances over the past three decades have resulted in increasing numbers of BHFS survivors.
W. Y. Chan +6 more
semanticscholar +1 more source
Hemoglobin, 2021
α0-Thalassemia (α0-thal) Chiang Rai (– –CR; NC_000016.10: g.144215_188843del) was identified as a novel 44.6 kb deletional type of α-thalassemia (α-thal), removing all α-like globin genes.
Chedtapak Ruengdit +3 more
semanticscholar +1 more source
α0-Thalassemia (α0-thal) Chiang Rai (– –CR; NC_000016.10: g.144215_188843del) was identified as a novel 44.6 kb deletional type of α-thalassemia (α-thal), removing all α-like globin genes.
Chedtapak Ruengdit +3 more
semanticscholar +1 more source
Clinics in Perinatology, 2000
Although most NIH fetuses have poor prognosis, it is imperative to attempt to identify the underlying cause to present parents with the best estimate for prognosis and future outcomes. Identification of a disorder with a good prognosis may prevent unnecessary termination of pregnancy and give a chance for therapy. Identification of a disorder with poor
R, Bukowski, G R, Saade
openaire +2 more sources
Although most NIH fetuses have poor prognosis, it is imperative to attempt to identify the underlying cause to present parents with the best estimate for prognosis and future outcomes. Identification of a disorder with a good prognosis may prevent unnecessary termination of pregnancy and give a chance for therapy. Identification of a disorder with poor
R, Bukowski, G R, Saade
openaire +2 more sources
Nonimmunologic hydrops fetalis
American Journal of Obstetrics and Gynecology, 1984Twenty cases of nonimmunologic hydrops fetalis were reviewed. The incidence of nonimmunologic hydrops fetalis was 1/2,029 (20 cases in 40,588 deliveries). The diverse etiologies of nonimmunologic hydrops fetalis are demonstrated. The incidence of erythroblastosis fetalis caused by Rh isoimmunization declined markedly.
Seung Soon Im +4 more
openaire +3 more sources
Pediatrics In Review, 1987
Hydrops fetalis or fetal hydrops is defined as a generalized abnormal accumulation of serous fluid in the entire body including abnormal collection in tissues and body cavities. It is not a specific disease but the end result of many fetal conditions.
Barbara McGillivray, Judith G. Hall
openaire +3 more sources
Hydrops fetalis or fetal hydrops is defined as a generalized abnormal accumulation of serous fluid in the entire body including abnormal collection in tissues and body cavities. It is not a specific disease but the end result of many fetal conditions.
Barbara McGillivray, Judith G. Hall
openaire +3 more sources
Nonimmune hydrops fetalis and congenital disorders of glycosylation: A systematic literature review
Journal of Inherited Metabolic Disease, 2020Numerous etiologies may lead to nonimmune hydrops fetalis (NIHF) including congenital disorders of glycosylation (CDG). Recognition of CDG in NIHF is challenging. This study reviews prenatal and neonatal characteristics of CDG presenting with NIHF.
Mona M Makhamreh +4 more
semanticscholar +1 more source
Outcomes of haemoglobin Bart’s hydrops fetalis following intrauterine transfusion in Ontario, Canada
Archives of Disease in Childhood, 2020Objectives With improved access to intrauterine transfusion (IUT), more fetuses with haemoglobin Bart’s hydrops fetalis (HBHF; homozygous α0-thalassaemia) will survive.
Hui Jue Zhang +13 more
semanticscholar +1 more source
Nonimmune hydrops fetalis: Genetic analysis and clinical outcome
Prenatal Diagnosis, 2020To investigate the genetic causes and clinical outcomes of nonimmune hydrops fetalis (NIHF).
Q. Deng +8 more
semanticscholar +1 more source

