Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Shahida Mohsin"'
Publikováno v:
Journal of the Pakistan Medical Association, Vol 73, Iss 12 (2023)
Objectives: To detect mutation in cases having haemoglobin A2 level 7percent on high performance liquid chromatography. Method: The cross-sectional, descriptive study was conducted from July 2017 to December 2018 at the Department of Haematology an
Externí odkaz:
https://doaj.org/article/7750a9e95ed9432baf2c27cf47923506
Autor:
Muhammad Bilal Ghafoor, Faiza Yasmeen, Abdul Wadood Khalid, Ghulam Mustafa, Shagufta Khaliq, Shahida Mohsin
Publikováno v:
Journal of the Pakistan Medical Association, Vol 72, Iss 3 (2022)
Objective: To observe vitamin K epoxide reductase complex subunit 1-1639 G>A polymorphism in patients resistant to warfarin therapy, and to calculate the allele frequency of the polymorphism in local patients. Method: The cross-sectional case-contr
Externí odkaz:
https://doaj.org/article/e6901505146b43b584e9e75da0258f59
Publikováno v:
Journal of the Pakistan Medical Association, Vol 71, Iss 5 (2021)
Objective: This study was aimed to evaluate the influence of these genetic modifiers (HBB gene cluster: rs7482144; BCL11A: rs766432; HBS1L-MYB: rs9399137) on the HbF levels in Thalassemia major and thalassemia intermedia. Methods: The cohort study co
Externí odkaz:
https://doaj.org/article/0bf009e23363433c90edb81a8e877de3
Publikováno v:
Biomedical Papers, Vol 161, Iss 2, Pp 158-163 (2017)
Background: Fanconi anemia is a rare autosomal recessive disorder of genetic instability. It is both molecularly and clinically, a heterogeneous disorder. Its incidence is 1 in 129,000 births and relatively high in some ethnic groups. Sixteen genes h
Externí odkaz:
https://doaj.org/article/a1bd360f7c17415fa5255b0f1a864892
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 26, Iss 1, Pp 19-25 (2015)
Patients on hemodialysis (HD) are usually anemic because of defective erythropoeisis. Hepcidin is a polypeptide that regulates iron homeostasis and could serve as an indicator of functional iron deficiency in patients with end-stage renal disease (ES
Externí odkaz:
https://doaj.org/article/fb5dfb0623e643baac169473484dd228
Publikováno v:
Journal of Applied Hematology, Vol 5, Iss 1, Pp 10-14 (2014)
Background: Stored platelet concentrates (PC) are in increasing demand for transfusion to patients with thrombocytopenia or disordered platelet function with active bleeding. Platelets are difficult to preserve in vitro for longer period of time. Dif
Externí odkaz:
https://doaj.org/article/6250731e6d674b61b221d4de6147f18c
Publikováno v:
Turkish Journal of Hematology, Vol 34, Iss 3, Pp 278-279 (2017)
Externí odkaz:
https://doaj.org/article/96ea258a25f24c65818bbb9924161819
Autor:
Shahida Mohsin
Publikováno v:
Journal of Rawalpindi Medical College, Vol 17, Iss 2 (2013)
Background: To determine the frequency and specificities of red blood cells -antibodies in multi-transfused cancer patients. Methods: From total of 150 patients, 24 patients were diagnosed with haematological and 126 with non-haematological malignanc
Externí odkaz:
https://doaj.org/article/6b5a570751954b5284488a8864e674de
Autor:
Shahida Mohsin
Publikováno v:
Journal of Rawalpindi Medical College, Vol 16, Iss 1 (2012)
Background: To describe the clinical presentation and complications of von Willebrand disease(vWD). Methods: In this descriptive study, out of 426 patients,visiting the hemophilia welfare society Lahore, 57 cases of vWD, diagnosed on the basis of cli
Externí odkaz:
https://doaj.org/article/91af15b139594b8eb0bf88dfe6fcb460
Publikováno v:
Journal of the Pakistan Medical Association. :1-13
Objective To evaluate the influence of certain genetic modifiers on foetal haemoglobin levels in thalassemia major and thalassemia intermedia. Methods The cohort study was conducted from November 2018 to August 2019, at Department of Haematology, Uni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5c7d070cda7868cbfc4239ab2f95d71
https://doi.org/10.47391/jpma.1351
https://doi.org/10.47391/jpma.1351