Results 191 to 200 of about 139,693 (301)

Loss of Function SPTA1 Variants Causes Neonatal Liver Failure and Fetal Anemia [PDF]

open access: bronze
John Brewin   +11 more
openalex   +1 more source

ANÁLISE HEMATOLÓGICA DA TRANSFUSÃO INTRAUTERINA NO TRATAMENTO DA ANEMIA FETAL: UMA REVISÃO SISTEMÁTICA

open access: diamond, 2020
B.F. Gambarra   +5 more
openalex   +1 more source

World Postpartum Haemorrhage Day: Renewing the Global Call to End Deaths From Postpartum Haemorrhage

open access: yes
BJOG: An International Journal of Obstetrics &Gynaecology, EarlyView.
PPH Roadmap Advocacy Working Group   +25 more
wiley   +1 more source

Characteristics of Women, Intrapartum Interventions, and Maternal and Neonatal Outcomes Among Users of Intrapartum Water Immersion: The UK POOL Cohort Study

open access: yesBirth, EarlyView.
ABSTRACT Background The POOL study explored intrapartum water immersion and associated maternal and neonatal outcomes at 26 UK sites 2015–2022. Methods Retrospective and prospective data captured in electronic maternity and neonatal UK National Health Service (NHS) information systems. Analysis—(a) proportions of women using and factors associated with
Julia Sanders   +15 more
wiley   +1 more source

OP23.10: Best timing for sequential intrauterine transfusion in fetal alloimmune anemia [PDF]

open access: bronze, 2017
T. Rosa Vega   +6 more
openalex   +1 more source

Short‐term risks and benefits of hydroxyurea (hydroxycarbamide)‐induced transfusion independence in patients with beta‐thalassaemia syndromes

open access: yesBritish Journal of Haematology, EarlyView.
Clinical outcomes of hydroxyurea (hydroxycarbamide)‐induced transfusion independence in patients with β‐thalassaemia syndromes.
B. R. Sevanthini   +11 more
wiley   +1 more source

Fetal thrombocytopenia in pregnancies complicated by fetal anemia due to red-cell alloimmunization: cohort study and meta-analysis. [PDF]

open access: yesJ Perinatol, 2019
Rosenbloom JI   +6 more
europepmc   +1 more source

Genetic Landscape of Robin Sequence: A Systematic Review

open access: yesClinical Genetics, EarlyView.
This systematic review summarizes the genetic landscape of Robin sequence (RS), highlighting key differences between isolated and non‐isolated forms and emphasizing the role of up‐to‐date genetic testing for diagnosis and clinical management. ABSTRACT Robin sequence (RS) is a congenital condition characterized by micrognathia, glossoptosis, and upper ...
Shirley van de Velde   +8 more
wiley   +1 more source

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