Results 181 to 190 of about 4,949,451 (244)

Frequency of Zinc Deficiency Among Thalassemia Major Patients: A Comparative Cross-Sectional Study. [PDF]

Cureus
Hayat U, Zaidi U, Munzir S, Dildar S, Sharif Z, Farzana T, Nizamuddin M, Shamsi T.   +7 more
europepmc   +1 more source

Clinical Image-Vertebral artery beading in a child with Beta Thalassemia major. [PDF]

Oxf Med Case Reports
Chalipat S, Kulkarni V, Krishna J, Mathew A, Mane S.   +4 more
europepmc   +1 more source

Abatacept improves posttransplant survival and reduces endothelial injury syndromes in β-thalassemia major. [PDF]

Blood Adv
Khandelwal P, Ibrahimova A, Lane A, Grimley M, Davies SM, Jodele S.   +5 more
europepmc   +1 more source

How Far Can we Go? Managing Moyamoya Syndrome in a 3-Year-Old With Thalassemia Major: A Rare Pediatric Case From Nepal. [PDF]

Clin Case Rep
Parajuli K, Jha A, Neupane A, Gupta S, Timsina N, Bhagat S, Gupta RB, Sah A, Katwal A.   +8 more
europepmc   +1 more source

Compound Heterozygous Hemoglobin E-Beta (HbE-β)-Thalassemia Presenting With Chipmunk or Rodent Facies, and a Severe Thalassemia Major Phenotype. [PDF]

Cureus
Dutta A, Banik A, Das D, Dutta TS.
europepmc   +1 more source

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Cholelithiasis in Thalassemia Major

Radiology, 1970
Abstract In a study of patients with thalassemia major by oral cholecystography, the incidence of cholelithiasis is determined. Six of 26 patients aged ten years and older have biliary calculi; in addition, gallstones have been demonstrated during life or at autopsy in 7 of 35 who have died. The association of gallstones with thalassemia, less frequent
K W, Dewey, H, Grossman, V C, Canale
openaire   +2 more sources

Cholelithiasis in thalassemia major

European Journal of Haematology, 2008
AbstractObjectives:  Aim of this study was to evaluate prevalence and characteristics of cholelithiasis in a large population of patients with thalassemia major (TM).Methods:  Data from 858 consecutive patients with transfusion‐dependent thalassemia at five major Italian centers were analyzed.
Origa R, Galanello R, Perseu L, Tavazzi D, Domenica Cappellini M, Terenzani L, Forni GL, Quarta G, Boetti T, PIGA, Antonio Giulio   +9 more
openaire   +6 more sources

Heterogeneity of Thalassemia Major

Archives of Pediatrics & Adolescent Medicine, 1963
Previous communications1,2concerning A2hemoglobin in parents of subjects with thalassemia major reported normal levels in a small minority. Fetal hemoglobin percentage was determined in some of these individuals and was noted to be unexpectedly high in all but one.
J A, WOLFF, V G, IGNATOV
openaire   +2 more sources

Cardiovascular MRI in thalassemia major

Annals of the New York Academy of Sciences, 2010
MRI assessment of myocardial iron and function has revolutionized the treatment of thalassemia major patients. While knowledge of somatic iron stores is vital for iron chelation management, it does not adequately monitor cardiac risk. MRI monitoring of cardiac T2* allows preclinical recognition of myocardial iron, stratifies prospective cardiac risk ...
John C, Wood, Leila, Noetzli
openaire   +2 more sources