Results 131 to 140 of about 5,241 (198)

Performance Evaluation of the Sysmex 'RBC Defect Workflow Optimisation' Flag for the Detection of Haemoglobinopathies and Iron Deficiency Anaemia. [PDF]

Int J Lab Hematol
Van Vlierberghe M, Louagie H, Ghys T, Degandt S.   +3 more
europepmc   +1 more source

Mapping Current and Emerging Laboratory Techniques for Haemoglobinopathy Carrier Detection and Prevention: A Narrative Review from the HELIOS Action. [PDF]

Int J Mol Sci
Mohd Yasin N, Chatzimatthaiou S, Perolla A, Blanco Alvarez A, Brito M, El-Kamah G, Xhetani M, Kountouris P, Stephanou C, Traeger-Synodinos J.   +9 more
europepmc   +1 more source

Haemoglobinopathies and health disparities: findings of a large-scale sample survey among indigenous populations in Odisha, India. [PDF]

BMJ Open
Bhattacharya H, Pradhan R, Singh S, Kavitha AK, Bhattacharya D, Kshatri JS, Kshatri JS, Pati S.   +7 more
europepmc   +1 more source

The Molecular Pathology of Non-Malignant Haematological Disease. [PDF]

Br J Biomed Sci
Blann AD, Dunn RG.
europepmc   +1 more source

Temporal patterns of haemoglobin phenotypes among Nigerian university students based on ten years of surveillance data. [PDF]

Sci Rep
Adeleke TO, Ughonu CP, Agelebe E, Adeleke OV, Dosumu TO, Ajala DE, Ayenigba B, Adegoke SA, Slusher TM, Boucher AA.   +9 more
europepmc   +1 more source

Hb Thessaloniki, a Novel, Hyperunstable, Alpha Globin Variant Detected in Northern Greece. [PDF]

Hematol Rep
Boutou E, Papandreou N, Mantzou G, Vlachaki E, Vyzantiadis A, Chassanidis C, Dimopoulou M, Balassopoulou A, Theodoridou S.   +8 more
europepmc   +1 more source

Haemoglobinopathies in Europe: health & migration policy perspectives

BACKGROUND: Major haemoglobinopathies (MH), such as thalassaemia syndromes (Thal) and sickle cell disorders (SCD), are genetic defects associated with chronic anaemia and other complications.
Petrova-Benedict, Roumyana, Aguilar Martinez, Patricia, Vives i Corrons, Joan Lluís, Eleftheriou, Androulla, Angastiniotis, Michael, Mañú Pereira, María del Mar, Gulbis, Beatrice   +6 more
core  

Frequency of haemoglobinopathies: a single-centre, cross-sectional study from Islamabad, Pakistan

, 2012
1257-1259Thalassaemia is the most frequent hereditary disorder in Pakistan, with an estimated 8-10 million carriers. This single-centre study reported the frequency of haemoglobinopathies among 504 consecutive cases visiting Islamabad Diagnostic Centre ...
Zaheer, H.A., Waheed, U., Satti, H.S., Farooq, N.   +3 more
core  

Haemoglobin D-Punjab haemoglobinopathy, the silent epidemic: A prospective hospital based study in Gujarat, India. [PDF]

Bioinformation
Anandani G, Goswami P, Bhankhodia V, Dholariya S, Thesiya Y, Dangar A.   +5 more
europepmc   +1 more source

Advances in Gene Therapy for Inherited Haemoglobinopathies. [PDF]

Hematol Rep
Gaspar AB, Gaspar HB.
europepmc   +1 more source