Results 91 to 100 of about 28,606 (278)

Effects of Daily Zinc, Daily Multiple Micronutrient Powder, or Therapeutic Zinc Supplementation for Diarrhea Prevention on Physical Growth, Anemia, and Micronutrient Status in Rural Laotian Children: A Randomized Controlled Trial. [PDF]

, 2019
ObjectivesTo evaluate the optimal zinc supplementation strategy for improving growth and hematologic and micronutrient status in young Laotian children.Study designIn total, 3407 children aged 6-23 months were randomized to receive either daily ...
Arnold, Charles D, Barffour, Maxwell A, Bounheuang, Bangone, Brown, Kenneth H, Chanhthavong, Bigphone, Hess, Sonja Y, Hinnouho, Guy-Marino, Kounnavong, Sengchanh, Ratsavong, Kethmany, Sengnam, Khanpaseuth, Sitthideth, Dalaphone, Wessells, K Ryan   +11 more
core  

Impact of multi-micronutrient fortified rice on hemoglobin, iron and vitamin A status of Cambodian schoolchildren : a double-blind cluster-randomized controlled trial [PDF]

, 2016
In Cambodia, micronutrient deficiencies remain a critical public health problem. Our objective was to evaluate the impact of multi-micronutrient fortified rice (MMFR) formulations, distributed through a World Food Program school-meals program (WFP-SMP ...
Berger, Jacques, Burja, K., Chamnan, C., Dijkhuizen, M.A., Fiorentino, Marion, Kuong, K., Parker, M., Perignon, Marlène, Wieringa, Franck   +8 more
core   +3 more sources

Estimation of the prevalence of Hemoglobinopathies in Erbil governorate, Kurdistan region of Iraq

, 2022
SarkarS Aziz, BahraK Hamad, HeroO Hamad, MuzhdaI Qader, EmanN Ali, RayanH Muhammed, Mudhir Sabir Shekha   +6 more
openalex   +1 more source

Prevalence of hemoglobinopathies using high-performance liquid chromatography as diagnostic tool in anemic patients of tertiary care center of Western India

Asian Journal of Transfusion Science
CONTEXT: Hemoglobinopathies are the most common heterogeneous group of monogenetic disorder in the world and its prevalence varies with geographical regions.
Virender Singh, Amit Kumar Biswas, Ajay Kumar Baranwal, Bhushan Asthana, Tejpal Dahiya   +4 more
doaj   +1 more source

Towards a proteomics meta-classification [PDF]

, 2004
that can serve as a foundation for more refined ontologies in the field of proteomics. Standard data sources classify proteins in terms of just one or two specific aspects.
Kumar, Anand, Smith, Barry
core   +1 more source

GENE THERAPY IN THALASSEMIA AND HEMOGLOBINOPATHIES

Mediterranean Journal of Hematology and Infectious Diseases, 2009
Sickle cell disease (SCD) and ß-thalassemia represent the most common hemoglobinopathies caused, respectively, by the alteration of structural features or deficient production of the ß-chain of the Hb molecule.
Laura Breda, Roberto Gambari, Stefano Rivella   +2 more
doaj   +1 more source

758. A Nonhuman Primate Transplantation Model to Evaluate Gene Editing Strategies Aimed at Inducing Fetal Hemoglobin Production for the Treatment of Hemoglobinopathies [PDF]

, 2016
Olivier Humbert, Hans‐Peter Kiem
openalex   +1 more source

A Small Key for a Heavy Door: Genetic Therapies for the Treatment of Hemoglobinopathies [PDF]

, 2021
Hidde A. Zittersteijn, Cornelis L. Harteveld, Stefanie Klaver-Flores, Arjan C. Lankester, Rob C. Hoeben, Frank J. T. Staal, Manuel A.F.V. Gonçalves   +6 more
openalex   +1 more source

Hemoglobinopathies [PDF]

Deutsches Ärzteblatt international, 2011
Michael R. DeBaun, Melissa Frei-Jones, Elliott Vichinsky   +2 more
  +4 more sources

A national register for surveillance of inherited disorders: beta thalassaemia in the United Kingdom [PDF]

, 2001
OBJECTIVE: To demonstrate the value of a national register for surveillance of services for an inherited disorder. METHODS: Data from the United Kingdom Thalassaemia Register and the United Kingdom Register of Prenatal Diagnosis for Haemoglobin Disorders
Darlison, M, Khan, M, King, A, Layton, M, Modell, B, Old, J, Petrou, M, Varnavides, L   +7 more
core   +1 more source