Post-Surgical Loco Regional Recurrence Of Breast Carcinoma In Iraq
مجلة كلية الطب, 2007 Background : From the standpoint of mortality &morbidity, cancer is by far the most important clinical problem that concerns the breast today .The age adjusted incidence of new cases has been increasing steadily with increase in the incidence among the ...
Ali M. Al-saiegh
doaj
Speech Disorder in Iraqi Patients with Stroke
ABSTRACT Language is an essential part of life, by which we can communicate with each other about thoughts, feelings, send messages, and communicate with each other, etc. Language, a core intellectual ability, is supported by complex neural and psychological mechanisms. These papers are divided into three chapters.
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Spectrum of Congenital Heart Diseases in Iraqi Patients. [PDF]
Eurasian J MedAl-Hamash SM +3 more
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Acid sphingomyelinase deficiency: Phenotypic, biochemical, and molecular heterogeneity in a series of 47 Iraqi patients from a single center. [PDF]
Mol Genet Metab RepFarhan R +7 more
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Association between CNR1 gene polymorphisms and susceptibility to diabetic nephropathy in Iraqi patients with T2DM. [PDF]
J Med Life, 2023 Aljorani RH +2 more
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Awareness, Willingness, and Concerns about Clinical Trial Participation among Iraqi Patients: A Cross-Sectional Study. [PDF]
Glob HeartDakhil ZA +10 more
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The influence of ABCB1 rs4148738 (C>T) polymorphism on rivaroxaban exposure and bleeding risk in Iraqi patients with non-valvular atrial fibrillation. [PDF]
Qatar Med JJalel HK, Hamid MO, Ibadi MH.
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Interleukin-15 and Tumor Necrosis Factor-α in Iraqi Patients with Alopecia Areata. [PDF]
Dermatol Res Pract, 2023 Kamil ZA, Abdullah GA, Zalzala HH.
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Association of socioeconomic and demographic determinants with clinical outcomes in Iraqi patients with diabetes: A cross-sectional study. [PDF]
PLOS Glob Public HealthMohammed SI +3 more
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Growth Failure in Thalassemia Major Patients in Samples of Iraqi Patients
Medicina Moderna - Modern MedicineIntroduction: Thalassemia, a hereditary autosomal recessive blood disorder, arises from genetic abnormalities leading to a diminished synthesis rate of one of the globin chains constituting hemoglobin. The integration of transfusion and chelation therapies has significantly elongated the lifespan of individuals diagnosed with thalassemia.
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