Results 231 to 240 of about 1,827,024 (396)

616 ZINC DEFICIENCY IN CHILDREN WITH SICKLE CELL DISEASE (SCD) [PDF]

, 1978
Gungor Karayalcin, Philip Lanzkowsky
openalex   +1 more source

Medication Utilization Among Children With Sickle Cell Disease in the United States

Pediatric Blood &Cancer, Volume 72, Issue 8, August 2025.
ABSTRACT Background and Objective The medication management of children with sickle cell disease (SCD), especially since the release of the 2014 National Heart, Lung, and Blood Institute (NHLBI) SCD treatment guidelines, is not well described in the published literature.
Abiodun John Ologunowa, Kelly L. Matson, Jung Eun Lee, Meghan McCormick, Mary L. Greaney, Aisling R. Caffrey   +5 more
wiley   +1 more source

First record of Microlechia Turati, 1924 (Lepidoptera: Gelechiidae) from Australia with description of a new species

Austral Entomology, Volume 64, Issue 3, August 2025.
Abstract The genus Microlechia Turati, 1924, including a newly described species Microlechia zwicki sp. nov., is recorded for the first time in Australia. Detailed illustrations of the adult specimen and male genitalia of this new species are provided, alongside a discussion of how it could be diagnosed form related species within the genus. An updated
Oleksiy V. Bidzilya, Hossein Rajaei
wiley   +1 more source

Acute splenic sequestration and hypersplenism in the first five years in homozygous sickle cell disease. [PDF]

, 1981
J M Topley, D. W. O. Rogers, MC Stevens, G. R. Serjeant   +3 more
openalex   +1 more source

Elevated transpulmonary gradient and cardiac magnetic resonance-derived right ventricular remodeling predict poor outcomes in sickle cell disease

Haematologica, 2016
Kim-Lien Nguyen, Xin Tian, Shoaib Alam, Alem Mehari, Steve W. Leung, Catherine Seamon, Darlene Allen, Caterina P. Minniti, Vandana Sachdev, Andrew E. Arai, Gregory J. Kato   +10 more
doaj   +1 more source

Infections in sickle cell disease. [PDF]

Haematologica
Scourfield LEA, Nardo-Marino A, Williams TN, Rees DC.   +3 more
europepmc   +1 more source

Gall stones in Jamaican children with homozygous sickle cell disease. [PDF]

, 1989
David Webb, J S Darby, David Dunn, S I Terry, G. R. Serjeant   +4 more
openalex   +1 more source

Sickle-cell disease: a call to action [PDF]

, 2015
Piel, FB, Weatherall, DJ
core   +1 more source

Deciphering Pain Experience in Adult Patients With Sickle Cell Disease: A Network Analysis of Pain‐Related Factors in a Single French Sickle Cell Centre

European Journal of Pain, Volume 29, Issue 6, July 2025.
ABSTRACT Background Sickle cell disease (SCD) is the most prevalent inherited haemoglobinopathy characterised by chronic pain with acute painful episodes due to vaso‐occlusion. The effective management of pain by adults with SCD influences their health outcomes. Opioids remain essential for most pain syndromes, but non‐pharmacological interventions are
D. Oudin Doglioni, M. Couette, S. Forté, F. Galacteros, M.‐C. Gay   +4 more
wiley   +1 more source

S268: INTERIM ANALYSIS OF A PHASE 2 TRIAL TO ASSESS THE EFFICACY AND SAFETY OF CRIZANLIZUMAB IN SICKLE CELL DISEASE PATIENTS WITH PRIAPISM (SPARTAN)

HemaSphere, 2023
Alan Anderson, Fuad El Rassi, Michael R. Debaun, Modupe Idowu, Julie Kanter, Soheir Adam, Susanna Curtis, Darla Liles, Biree Andemariam, Morgan L. Mclemore, Robert Sheppard Nickel, Poornima Ramadas, Jincy Paulose, Dram Laine, Mahmudul Khan, Deepika Darbari, Arthur L. Burnett   +16 more
doaj   +1 more source