Results 151 to 160 of about 2,781 (251)

The Relevance of β-Thalassemia Heterozygosity in Pediatric Clinical Practice: Croatian Experience. [PDF]

Children (Basel)
Dordevic A, Ugrin M, Sutic IM, Roganovic J, Pavlovic S.   +4 more
europepmc   +1 more source

Prevalence of Low Bone Mineral Density Increases With Age in Sickle Cell Disease

eJHaem, Volume 7, Issue 3, June 2026.
ABSTRACT Introduction Skeletal complications are common in sickle cell disease (SCD). We previously showed that the prevalence of low areal bone mineral density (aBMD) increased with age in a pediatric SCD cohort, even after adjusting for short stature. Data on age‐related aBMD trends in young adults is lacking.
Jahnavi Gollamudi, Chengzhou Wu, Guolian Kang, Michael Sexton Lamonica, Pei‐Lin Chen, Ragha Srinivasan, Khalid El‐Bashir, Jane Hankins, Parul Rai, Clifford Takemoto, Hyacinth I. Hyacinth, Matthew R. Allen, Babette S. Zemel, Oyebimpe Adesina   +13 more
wiley   +1 more source

Development of an ELISA strip for the detection of α thalassemias

Haematologica, 2010
Luksana Makonkawkeyoon, Somphon Pharephan, Pannee Sirivatanapa, Wirote Tuntiwechapikul, Sanit Makonkawkeyoon   +4 more
doaj   +1 more source

Advancing Hematopoietic Stem Cell Transplantation (HSCT) in Africa: A Pathway to Curing Hematological Disorders. [PDF]

Health Sci Rep
Ogunniyi TJ, Abdulkareem RR, Emiola AR, Bamidele TR, Wazhi GB, Arinde PO, Yisa SS, Makanjuola O, Batisani K, Ilesanmi A.   +9 more
europepmc   +1 more source

Validation of Gazelle Microchip Electrophoresis for Premarital Hemoglobinopathy Screening in Türkiye

eJHaem, Volume 7, Issue 3, June 2026.
ABSTRACT Introduction Hemoglobinopathies, the most prevalent recessive monogenic disorders globally, encompass thalassemia syndromes and structural hemoglobin variants, affecting approximately 5% of the world's population as carriers, with around 315,000 affected births annually.
Duran Canatan, Serpil Delibaş, Emel Altunsoy, Elif Gözde Gökkaya, Sultan Aydın, Defne Ay Tuncel, Rucha Natu, Priyaleela Thota, Umut A. Gurkan   +8 more
wiley   +1 more source

Structural and clinical characterization of Hb Móstoles (HBA2:c.176A>G; p.His59Arg): a new unstable alpha-globin variant with thalassemic features. [PDF]

Am J Blood Res
Ferrer-Benito S, Ordoñez M, Bermejo A, Martínez JM, Ortega B, González FA, Villegas A, Benavente C, Ropero P.   +8 more
europepmc   +1 more source

Luspatercept in Transfusion‐Dependent Thalassemia With Red Blood Cell Antibodies: A Case Series

eJHaem, Volume 7, Issue 3, June 2026.
ABSTRACT Red blood cell (RBC) antibodies complicate transfusion support in transfusion‐dependent thalassemia (TDT), and data on luspatercept in this setting remain limited. We retrospectively reviewed seven adults with TDT and RBC antibodies treated with luspatercept at Srinagarind Hospital from January 2025 to January 2026.
Nattiya Teawtrakul
wiley   +1 more source

Co-Induction of ULK-1 and AHSP mRNAs in Erythroid Precursor Cells Isolated From a Sirolimus-Treated β-Thalassemia Patient: A Case Report Study. [PDF]

Br J Biomed Sci
Zurlo M, Finotti A, Gamberini MR, Gambari R.   +3 more
europepmc   +1 more source

Fungal‐Bacterial Interactions in Polymicrobial Infections: Hidden Threats

MicrobiologyOpen, Volume 15, Issue 3, June 2026.
ABSTRACT Polymicrobial infections involving fungi and bacteria represent a major and increasingly recognized clinical challenge, in which interkingdom interactions significantly amplify disease severity, antimicrobial resistance, and treatment failure. Rather than passive co‐existence, fungal–bacterial communities form highly coordinated systems driven
Mohammad Javad Roustaye Gourabi, Masoud Kargar, Atefeh Kamali, Javad Yasbolaghi Sharahi   +3 more
wiley   +1 more source

Epidemiological Profile of Haemoglobinopathies in Different Districts of West Bengal: A Retrospective Study. [PDF]

Niger Med J
Dhar O, Sharma A, Bhaumik S, Das AK.
europepmc   +1 more source