Results 81 to 90 of about 312,696 (257)

Avaliação da concentração de ferro orgânico em uma população de grávidas An assessment of organic iron concentration in pregnant women

Revista de Saúde Pública, 1983
Objetivou-se conhecer as alterações da concentração de hemoglobina (Hb), hematócrito (Ht), ferro sérico (FS), capacidade total de ligação de ferro (CTLF) e saturação de transferrina (ST) durante a gestação normal em mulheres não anêmicas (H > 11,0g/dl ...
Sophia Cornbluth Szarfarc, Arnaldo Augusto F. de Siqueira, Ignez Salas Martins   +2 more
doaj   +1 more source

Inactive matriptase-2 mutants found in IRIDA patients still repress hepcidin in a transfection assay despite having lost their serine protease activity. [PDF]

, 2012
L'article final de l'éditeur contient 9 pages. Le manuscrit accepté contient 32 pages.International audienceMutations of the TMPRSS6 gene, which encodes Matriptase-2, are responsible for iron-refractory iron-deficiency anemia.
Aguilar-Martinez, Patricia, Beaumont, Carole, Donadieu, Jean, Grandchamp, Bernard, Guillem, Flavia, Isidor, Bertrand, Kannengiesser, Caroline, Lenoir, Anne, Matak, Pavle, Méchinaud, Françoise, Nicolas, Gaël, Oudin, Claire, Vaulont, Sophie   +12 more
core   +3 more sources

Application of Hematological Indices for the Differential Diagnosis of Beta Thalassemia Trait and Iron Deficiency Anemia

Journal of Bahria University Medical and Dental College, 2017
Objective: To apply various hematological indices for the differential diagnosis of ß-Thalassemia trait (ß-TT) and iron deficiency anemia (IDA). Methodology: This retrospective descriptive study was conducted at Dar-ul-Sehat Hospital, Gulistan -e- Johar,
Sajid Abbas, Shaista Khurrum, Tahira Zamir   +2 more
doaj  

Bernard‐Soulier Syndrome: Identification of a Novel GP1BB Variant in a Mauritanian Patient

Molecular Genetics &Genomic Medicine, Volume 14, Issue 1, January 2026.
This study identifies a new mutation of the GP1BB gene responsible for Bernard‐Soulier syndrome in a Mauritanian patient. Genetic analysis reveals a nucleotide duplication resulting in a severe platelet adhesion defect. This work highlights the importance of molecular diagnosis and therapeutic strategies to improve the management of affected patients ...
Mohamed Lemine Salem, Ektelbenina Zein, Ghaber Sidi Mohamed   +2 more
wiley   +1 more source

Comparison between Automated Hematology Analyzer and Peripheral Blood Smear Examination for Assessment of Morphological Types of Anemia

GAIMS Journal of Medical Sciences
Background Anemia represents a major healthcare burden in developing country like India. Since decades peripheral blood smear has been used for diagnosis of anemia. Cell counter has been introduced with increasing efficacy and a decreasing cost all over
Raina Goti, Pragnesh H Shah, Jay Raval
doaj   +1 more source

Iron Refractory Iron Deficiency Anemia in Dizygotic Twins Due to a Novel Gene Mutation in Addition to Polymorphisms Associated With High Susceptibility to Develop Ferropenic Anemia

Journal of Investigative Medicine High Impact Case Reports, 2017
Iron refractory iron deficiency anemia (IRIDA) is an autosomal recessive ferropenic anemia. Its hypochromic microcytic pattern is associated with low transferrin saturation, normal-high ferritin, and inappropriately high hepcidin level.
Joana Pinto MM, Gustavo Nobre de Jesus MM, Mónica Palma Anselmo MM, Lúcia Gonçalves MSc, Daniela Brás BSc, João Madeira Lopes MD, João Meneses MD, Rui Victorino MD PhD, Paula Faustino PhD   +8 more
doaj   +1 more source

Anemia em crianças menores de dois anos atendidas nas unidades básicas de saúde no Estado de São Paulo, Brasil Anaemia in children under two years in basic health care units in the State of S. Paulo, Brazil

Revista de Saúde Pública, 1994
Foi realizado estudo com o objetivo de verificar a prevalência da anemia em crianças atendidas nas unidades básicas de saúde do Estado de São Paulo, Brasil.
Marco A. A. Torres, Kazue Sato, Suzana de Souza Queiroz   +2 more
doaj   +1 more source

Diagnosis and Treatment of Iron Deficiency and Iron Deficiency Anemia in Children and Adolescents: Recommendations of the Polish Pediatric Society, the Polish Society of Pediatric Oncology and Hematology, the Polish Society of Neonatology, and the Polish Society of Family Medicine

Nutrients
Background/Objectives. Iron deficiency is one of the most common nutritional deficiencies worldwide and is the leading cause of anemia in the pediatric population (microcytic, hypochromic anemia due to iron deficiency).
R. Chaber, Ewa Helwich, Ryszard Lauterbach, Agnieszka Mastalerz-Migas, Michał Matysiak, J. Peregud-Pogorzelski, J. Styczyński, T. Szczepański, T. Jackowska   +8 more
semanticscholar   +1 more source

Anaemia and cognitive function among Chinese elderly in Old Folks Homes [PDF]

, 2005
The relationship between anaemia and cognitive function was evaluated among 35 Chinese elderly (24 men and 11 women) aged 60 to 85 years (mean age 70.1 ± 6.7 years) from five old folks homes in Klang Valley. They were interviewed to obtain information on
Junara Mohd Alim,, Lee X.K,, Mokhtar Abu Bakar,, Nor Aini Umar,, Siti Balkis Budin,, Suzana Shahar,   +5 more
core  

Concentrations of Cysteinyl Leukotrienes in Various Biological Fluids of Children with Bronchial Asthma, Atopic Dermatitis and Food Protein Induced Enterocolitis [PDF]

, 2019
Clinical manifestation of food allergy is characterized by polymorphic cutaneous, respiratory and gastrointestinal syndromes. Leukotrienes occupy a key place in the pathogenesis of a wide range of inflammatory diseases, including bronchial asthma ...
Haiduchyk, H. (Halyna), Shadrin, O. (Oleg)   +1 more
core   +3 more sources