Results 151 to 160 of about 22,512 (233)

Endocrinopathies and growth in a UK cohort of children with transfusion dependent thalassaemia. [PDF]

Br J Haematol
Sethuraman C, Yo WK, Shone J, Gevers E, Kaya B, Willemsen RH.   +5 more
europepmc   +1 more source

CRISPR‐Cas9 and precision editing technologies linking functional genomics to clinical translation in genetic diseases

Clinical and Translational Medicine, Volume 16, Issue 9, September 2026.
CRISPR‐Cas9 and precision editing technologies enable a variant‐mechanism‐driven framework for genetic disease research and therapeutic development. Pathogenic variants are first interpreted according to mutation type, coding or regulatory consequence, tissue context, and disease mechanism.
Zijing Wen, Jianming Su
wiley   +1 more source

Incidence and determinants of red cell alloimmunization and autoimmunization in paediatric thalassaemia: A North Indian cohort study. [PDF]

Vox Sang
Paliwal A, Arora S, Radhakrishnan N, Dua S, Pokhrel A, Singh A, Khan A.   +6 more
europepmc   +1 more source

Thalassaemia genes in Baghdad, Iraq

, 1996
315-319To estimate the prevalence of thalassaemia genes in Baghdad, a study was made of 502 randomly selected pregnant women attending a major maternity care clinic in the city.
Yahya, H.I.
core  

Effects of Zinc Supplementation on Glycemic Control, Insulin Resistance, Inflammation and Oxidative Stress in Diabetes: A Systematic Review and Meta‐Analysis of Randomized Controlled Trials

Endocrinology, Diabetes &Metabolism, Volume 9, Issue 5, September 2026.
Zinc supplementation in diabetes is associated with improved insulin sensitivity, lipid profile, antioxidant status and reduced inflammation, without significant effects on glycemic indices. Overall, evidence from randomized trials supports zinc as a beneficial metabolic adjunct with moderate‐to‐high certainty. ABSTRACT Objectives Diabetes mellitus (DM)
Jessica Paola Loaiza‐Giraldo, Florencia Amigo‐Fierro, Camila Ignacia Cancino‐Castro, Matias Donoso‐Emig, Murtaja Satea, Ignacia Farías‐Quinteros, Alejandro Bruna‐Mejias, Pablo Nova‐Baeza, Mathias Orellana‐Donoso, Héctor Gutiérrez‐Espinoza, Gloria Cifuentes‐Suazo, Juan Sanchis‐Gimeno, Maria Piagkou, Vitor E. Valenti, Jose E. Leon‐Rojas, Juan José Valenzuela‐Fuenzalida   +15 more
wiley   +1 more source

Systematic review of economic evaluations in thalassaemia screening programmes globally: developing guidance for low- and middle-income (LMIC) settings. [PDF]

BMJ Open
Massey K, Phommasone K, Mehta A, Lee VQY, Ashley EA, Mayxay M, Painter C.   +6 more
europepmc   +1 more source

Septal Release: A Targeted Surgical Strategy for Recurrent Epistaxis

Eye &ENT Research, Volume 3, Issue 3, Page 163-167, September 2026.
ABSTRACT Background Recurrent epistaxis is a common pediatric condition that is typically managed with conservative therapies, but a subset of patients require surgical intervention after treatment failure. We seek to describe the efficacy of septal release for refractory pediatric epistaxis patients. Objective To compare outcomes of septal release for
Alexandra Welschmeyer, Daniel Karasik, Christopher L. Crafton, Eve Tranchito, Sarah Ridge, Cyrus C. Rabbani, Jay Shah   +6 more
wiley   +1 more source

Neutrophil extracellular traps induced by activated platelets as a cause of neutrophil-platelet aggregation in β-thalassaemia/haemoglobin E patients. [PDF]

Br J Haematol
Thubthed R, Praneetponkang R, Sittipaisankul P, Thiengtavor C, Chumpuchanaphai S, Paiboonsukwong K, Fucharoen S, Pattanapanyasat K, Vadolas J, Smith DR, Svasti S, Chaichompoo P.   +11 more
europepmc   +1 more source

Sickle Cell Disease and Kidney Injury: Circulating Uromodulin Allows Early Tissue Specific Diagnosis and Monitoring of Treatment

American Journal of Hematology, Volume 101, Issue 9, Page 2430-2434, September 2026.
Ferras Alashkar, Robert Hable, Denise Zwanziger, Friederike Poppenborg, Raina Yamamoto, Hans Christian Reinhardt, Alexander Röth, Victor Herbst, Yara Bestmann, Marco Kai, Jürgen E. Scherberich   +10 more
wiley   +1 more source

Inherited microcytic anemias due to disorders of iron and heme metabolism: An updated clinical review

HemaSphere, Volume 10, Issue 9, September 2026.
Abstract Microcytic anemia is among the most common hematological abnormalities in clinical practice and is usually attributable to iron deficiency, thalassemia traits, or anemia of inflammation. A small but clinically important subset of patients, however, has inherited disorders of iron metabolism or heme synthesis presenting with persistent ...
Alexandros Makis, Ioanna Saougou, Eleftheria Hatzimichael   +2 more
wiley   +1 more source