Results 31 to 40 of about 4,456 (190)

Hemoglobin Kansas found by electrophoretic diagnosis in Brazil Hemoglobina Kansas diagnosticada através de eletroforese no Brasil

Revista Brasileira de Hematologia e Hemoterapia, 2002
Some hemoglobin variants with abnormal oxygen affinity have been reported so far from various regions of the world. They can be classified by their oxygen affinity and 15 variants with low oxygen affinity have been reported.
Claudia R. Bonini-Domingos, Patrícia H.O. Calderan, Fátima A.M. Siqueira, Paulo C. Naoum   +3 more
doaj   +1 more source

A comparative study of norethisterone and combined oral contraceptive pill in the treatment of dysfunctional uterine bleeding

CHRISMED Journal of Health and Research, 2019
Background: A significant percentage of women in India suffer from dysfunctional uterine bleeding (DUB), which has a negative impact on physical and social life.
Sayantan Sen, Tapan Kumar Mandal, Arijit Dutta, Himel Mondal, Tufan Khalua   +4 more
doaj   +1 more source

ABNORMAL HEMOGLOBINS: LABORATORY METHODS

Hemoglobin, 2001
Laboratory methods allowing the detection and characterization of hemoglobin variants are reviewed. Protein chemistry techniques such as isoelectrofocusing, electrophoreses under various experimental conditions, cation exchange and reversed phase high performance liquid chromatography, are the most frequently used for the detection of variants.
Josiane Bardakdjian-Michau, Frederic Galactéros, Henri Wajcman, Danielle Promé, Christian Godart, Didier Hurtrel, Mireille Mathis, Claude Préhu, Jean Riou   +8 more
core   +3 more sources

Spectrum of hemoglobin variants in Eastern Indian population; a study of 14,145 cases [PDF]

Al Ameen Journal of Medical Sciences, 2013
Background: Inherited disorders of hemoglobin are extremely common in Indian population ranging from near structurally normal hemoglobins to severe transfusion dependant hemoglobinopathies.
Suprio Ray Chaudhury, Himansu Roy, Nirmal Kumar Bhattacharyya, Palash Kumar Mondal, Pranab Kumar Biswas, Sumit Roy   +5 more
doaj  

Hemoglobin S identification in blood donors: A cross section of prevalence

Hematology, Transfusion and Cell Therapy, 2022
Introduction: In Brazil, the sickle cell trait (SCT) has an average prevalence of 4% in the general population and 6–10% among Afro-descendants. Although SCT is highly prevalent, a large segment of the population ignores their status.
Fernanda Lima Kroger, Ianka Cristina Ernesto, Marina Schuffner Silva, Olivia Franco dos Santos, Renato Lourenço de Medeiros, Daniela de Oliveira Werneck Rodrigues   +5 more
doaj   +1 more source

DRUGS, ANESTHESIA AND ABNORMAL HEMOGLOBINS*

Annals of the New York Academy of Sciences, 1968
G. Stamatoyannopoulos, A. G. Motulsky
core   +3 more sources

Rastreamento de hemoglobinas variantes e talassemias com associação de métodos de diagnóstico Tracking of variant hemoglobins and thalassemias by association of diagnosis methodologies

Revista Brasileira de Hematologia e Hemoterapia, 2008
O diagnóstico neonatal de hemoglobinopatias permite a melhoria na qualidade de vida do doente com a implementação de medidas profiláticas, acompanhamento clínico e aconselhamento genético.
Luciane M. S. Melo, Fátima A. M. Siqueira, Agnes C. F. Conte, Claudia R. Bonini Domingos   +3 more
doaj   +1 more source

Prevalence of Beta-Thalassemia Trait and Abnormal Hemoglobins in the Province of Adiyaman, Turkey

, 2012
Background/Aims: Thalassemia is one of the most common hereditary disorders in Turkey. The aim of this study was to determine the prevalence of the beta-thalassemia trait and abnormal hemoglobins in the province of Adiyaman in Turkey.
Tuncdemir, Aygul, Bayram, Suleyman, Rencuzogullari, Eyup, Onderci, Muhittin, Mutalip, Abdullah, Koc, Tuba, Kucuk, Meral Urhan, Atakur, Selman, Faruk, Muslum, Aslan, Sinan, Sevgiler, Yusuf, Genc, Ahmet, Korkmaz, Deniz Tastemir   +12 more
core   +1 more source

HB D Los Angeles in a Brazilian family Hb D Los Angeles em família brasileira

Revista Brasileira de Hematologia e Hemoterapia, 2001
Inherited disorders of hemoglobin, the most common monogenic disease, are now well understood at the molecular level, knowledge, which has led to considerable improvements in their control and management.
Guilherme G. Leoneli, Silma M.A. Melo, Marco A. Zago, Wilson A. Silva Jr., Cláudia R. Bonini-Domingos   +4 more
doaj   +1 more source

Neonatal Screening for Sickle Cell Disease in Congo

Anemia, 2022
Introduction. Sickle cell disease is an autosomal recessive inherited disorder due to the mutation of a gene coding for the globin beta chain. The aim of this study is to update the epidemiological data on hemoglobinoses, in particular sickle cell ...
Alexis Elira Dokekias, Lethso Thibaut Ocko Gokaba, Josué Simo Louokdom, Lydie Ngolet Ocini, Firmine Olivia Galiba Atipo Tsiba, Coreillia Irène Ondzotto Ibatta, Quentin Ngoma Kouandzi, Serge Talomg Tamekue, Jayne Chelsea Bango, Jade Vanessa Nziengui Mboumba, Simon Charles Kobawila   +10 more
doaj   +1 more source