Results 101 to 110 of about 247,564 (312)

Preliminares del estudio de la meniscocitemia en Colombia, s. a.

Revista de la Facultad de Medicina, 1943
Otros nombres de la enfermedad: Anemia Falciforme; Drepanocitemia; "Sickle Cell Anemia" y "Sickle Cell 'I'rait" en Estados Unidos. La MENISCOCITEMIA es una enfermedad sanguínea caracterizada por la aparición de eritrocitos en forma de hoz, granos de ...
Benjamín Mera
doaj  

Semi-Blind and l1 Robust System Identification for Anemia Management [PDF]

arXiv, 2020
Chronic diseases such as cancer, diabetes, heart diseases, chronic kidney disease (CKD) require a drug management system that ensures a stable and robust output of the patient's condition in response to drug dosage. In the case of CKD, the patients suffer from the deficiency of red blood cell count and external human recombinant erythropoietin (EPO) is
arxiv  

Spleen histology in children with sickle cell disease and hereditary spherocytosis: Hints on the disease pathophysiology [PDF]

, 2016
open2Hereditary spherocytosis (HS) and sickle cell disease (SCD) are associated with splenomegaly and spleen dysfunction in pediatric patients. Scant data exist on possible correlations between spleen morphology and function in HS and SCD.
Alaggio Rita, Colombatti Raffaella, De Vito Rita, Fuligni Fabio, Gamba Piergiorgio, Ichino Martina, Pizzi Marco, Sabattini Elena, Sainati Laura, Santoro Luisa, Zucchetta Pietro   +10 more
core   +1 more source

PERIPHERAL BLOOD PICTURE OF SICKLE CELL ANEMIA

Gomal Journal of Medical Sciences, 2018
Laboratory diagnosis of sickle cell anemia involves phenotypic testing for the presence of the sickle haemoglobin and genetic analysis. Phenotypic tests include sickling test and sickle solubility test. Sickle cell anemia can be diagnosed by the presence
Zahid Ullah
doaj  

Comprehensive neuropsychological evaluation of children and adolescents with sickle cell anemia: a hospital-based sample

Revista Brasileira de Hematologia e Hemoterapia
Background: Individuals with sickle cell anemia may suffer symptomatic or silent cerebral infarcts leading to neurocognitive complications. This study investigated the cognitive and intellectual performance of children and adolescents with sickle cell ...
Samantha Nunes, Nayara Argollo, Marivania Mota, Camilo Vieira, Eduardo Pondé de Sena   +4 more
doaj   +1 more source

AAPT Diagnostic Criteria for Chronic Sickle Cell Disease Pain [PDF]

, 2017
Pain in sickle cell disease (SCD) is associated with increased morbidity, mortality, and high health care costs. Although episodic acute pain is the hallmark of this disorder, there is an increasing awareness that chronic pain is part of the pain ...
Aguilar, Ameringer, Ballas, Ballas, Ballas, Barakat, Bediako, Brandow, Brandow, Bruehl, Campbell, Campbell, Carlton Dampier, Carroll, Carroll, Carroll, Crawford, Dampier, Dampier, Dampier, Dampier, Dampier, Dampier, Darbari, Darbari, Darbari, DeBaun, Deepika S. Darbari, Dworkin, Dyson, Edwards, Fillingim, Fillingim, Franck, Gil, Gil, Hassell, Hoff, Houston-Yu, Igbineweka, Jonassaint, Kathryn Hassell, Kato, Kauf, Koshy, Levenson, Lewandowski, Long, Mahadeo, Maixner, Mathur, McClish, Milner, Minniti, Minniti, Myrvik, Niebanck, Palermo, Palermo, Palermo, Paul, Platt, Powars, Raphael, Savitt, Schwartz, Serarslan, Serjeant, Shapiro, Sil, Smith, Smith, Sogutlu, Steinberg, Taylor, Tonya M. Palermo, Tsao, Turk, Valrie, Vance, Vardeh, Walco, Walco, Wallen, Wally Smith, Wilkie, William Zempsky, Wison Schaeffer, Yawn, Zempsky   +89 more
core   +3 more sources

Distal renal tubular acidosis in sickle cell anemia

Saudi Journal of Kidney Diseases and Transplantation, 2018
We report a rare case of two young male siblings with sickle cell anemia who presented with bilateral lower limb deformities, failure to thrive, polyuria, and polydipsia.
Anjali Bharani, Rani Manchanda, Ritesh Kumar Singh, Swati Prashant   +3 more
doaj   +1 more source

Pulmonary hypertension in adolescents with sickle cell disease [PDF]

, 2016
Sickle cell disease consists of a group of disorders that have a similar mutation in at least one of the beta-globin chains of hemoglobin. This results in a change of the hemoglobin to sickle shaped cells when in the deoxygenated state.
Akinyemi, Katherine
core   +1 more source

Comorbidity, Pain, Utilization, and Psychosocial Outcomes in Older versus Younger Sickle Cell Adults: The PiSCES Project [PDF]

, 2017
Background. Patients with SCD now usually live well into adulthood. Whereas transitions into adulthood are now often studied, little is published about aging beyond the transition period. We therefore studied age-associated SCD differences in utilization,
Aisiku, Imoigele P., Bovbjerg, Viktor E., Levenson, James L., McClish, Donna K., Roberts, John D., Roseff, Susan D., Smith, Wally R.   +6 more
core   +4 more sources

Hydroxyurea treatment does not increase blood viscosity and improves red blood cell rheology in sickle cell anemia

Haematologica, 2015
The presence of sickle hemoglobin (HbS) in red blood cells (RBC) of patients with sickle cell anemia (SCA) is at the origin of their rheological abnormalities.
Nathalie Lemonne, K. Charlot, Xavier Waltz, S. Ballas, Y. Lamarre, Ketty Lee, R. Hierso, Catherine Connes, M. Etienne‐Julan, M. Romana, P. Connes   +10 more
semanticscholar   +1 more source