Results 241 to 250 of about 1,827,024 (396)

Safety of a trial of labor after cesarean in kidney and liver transplant recipients: A multicenter cohort study

International Journal of Gynecology &Obstetrics, Volume 170, Issue 1, Page 471-477, July 2025.
Abstract Objective To evaluate the trends, safety, and feasibility of a trial of labor after cesarean (TOLAC) among kidney and liver transplant recipients. Methods This was a retrospective cohort study using the Transplant Pregnancy Registry International.
Anjali Walia, Ophelia Yin, Lisa A. Coscia, Serban Constantinescu, Monika Sarkar, Michael J. Moritz, Yalda Afshar, Roxanna A. Irani   +7 more
wiley   +1 more source

Crosstalk Between Sickle Cell Disease and Ferroptosis. [PDF]

Int J Mol Sci
Russo A, Patanè GT, Calderaro A, Barreca D, Tellone E, Putaggio S.   +5 more
europepmc   +1 more source

Neonatal screening for sickle cell diseases in Camberwell: results and recommendations of a two year pilot study. [PDF]

, 1986
M E Horn, Moira Dick, B‐M Frost, L. R. Davis, A. J. Bellingham, Catherine Stroud, John Studd   +6 more
openalex   +1 more source

Epithelial Atg5 Deficiency Intensifies Caspase‐11 Activation, Fueling Extracellular mtDNA Release to Activate cGAS–STING–NLRP3 Axis in Macrophages During Pseudomonas Infection

MedComm, Volume 6, Issue 7, July 2025.
This work illuminates the essential role of epithelial ATG5 in defending against P. aeruginosa. Atg5 deficiency impairs bacterial clearance and aggravates inflammation via AKT/PI3K/NF‐κB, inflammasome activation, and pyroptosis. Mechanistically, impaired mitophagy intensifies mitochondrial damage.
Junyi Wang, Lei Zhang, Yingying Liu, Yao Liu, Anying Xiong, Qin Ran, Xiang He, Vincent Kam Wai Wong, Colin Combs, Guoping Li, Min Wu   +10 more
wiley   +1 more source

Serum urate concentrations in homozygous sickle cell disease [PDF]

, 1981
Karel De Ceulaer, AG Morgan, E Choo-Kang, W. A. Wilson, GR Serjeant   +4 more
openalex   +1 more source

Barriers to Hematopoietic Stem Cell Transplant Among Caregivers and Adolescents With Sickle Cell Disease

Pediatric Blood &Cancer, Volume 72, Issue 7, July 2025.
ABSTRACT Background Hematopoietic stem cell transplantation (HSCT) is a curative treatment for sickle cell disease (SCD). However, barriers exist that prevent access to this treatment modality. Methods An IRB‐approved mixed‐method survey of barriers to HSCT in SCD was given to parents, caregivers, and adolescents obtaining care at the Children's of ...
Chibuzo Ilonze, Alexandria Broadnax, Hilary Haines, Jeffrey Lebensburger, Frederick Goldman   +4 more
wiley   +1 more source

Dynamics of neutrophil phenotype and function in sickle cell disease. [PDF]

Front Immunol
Gaartman AE, de Ligt LA, Beuger BM, Tool ATJ, Veldthuis M, Kuijpers TW, van Zwieten R, Biemond BJ, van Bruggen R, Nur E.   +9 more
europepmc   +1 more source

Causes of death in sickle-cell disease in Jamaica. [PDF]

, 1982
A N Thomas, C. W. Pattison, G. R. Serjeant   +2 more
openalex   +1 more source

Sickle Cell Story Club: Implementation of a Clinic‐Based Literacy Promotion Program

Pediatric Blood &Cancer, Volume 72, Issue 7, July 2025.
ABSTRACT Background Literacy promotion is central to child development, particularly for children with sickle cell disease (SCD) given patterns of neurocognitive involvement. Book ownership programs offer a unique strategy within pediatric healthcare. This study aimed to evaluate the implementation of a literacy promotion program within an outpatient ...
Julia E. LaMotte, Jillian R. Bouck, Kristen Pogue, Lauren Fancher, Olivia Coughlin, Seethal A. Jacob   +5 more
wiley   +1 more source

Optimization of hydroxyurea in sickle cell disease in Brazil. [PDF]

Hematol Transfus Cell Ther
Lobo C, Silva-Pinto AC, Cançado RD.
europepmc   +1 more source