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Analysis of pattern of ABO Blood groups in pediatric diabetic patients–An observational study
LIAQUAT MEDICAL RESEARCH JOURNAL 2022
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Hemostatic and thrombotic parameters in acure leukemia-A comparison of pre and post remission induction phase
LIAQUAT MEDICAL RESEARCH JOURNAL 2022
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COVID-19 and humoral immune response in convalescent plasma donors in Pakistani cohort.
LIAQUAT MEDICAL RESEARCH JOURNAL 2022
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Usefulness of convalescent plasma transfusion for the treatment of severely ill COVID-19 patients in Pakistan
BMC INFECTIOUS DISEASES 2021
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Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population
THROMBOSIS JOURNAL 2019
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Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population (vol 15, 24, 2017)
THROMBOSIS JOURNAL 2019
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Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population
THROMBOSIS JOURNAL 2017
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Identification of Molecular Defects in ITGA2B and ITGB3 Genes and Phenotypic Correlation in Pakistani Patients with Glanzmann Thrombasthenia
BLOOD, THE JOURNAL OF THE AMERICAN SOCIETY OF HEMATOLOGY 2015
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Characterization of Phenotypic Expression of Inherited Fibrinogen Coagulopathy in Pakistani Index Patients
BLOOD, THE JOURNAL OF THE AMERICAN SOCIETY OF HEMATOLOGY 2015
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Identification of Novel Mutations with Molecular Modelling of Missense Mutations of Congenital Afibrinogenemia Patients in Pakistan
BLOOD, THE JOURNAL OF THE AMERICAN SOCIETY OF HEMATOLOGY 2015
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A New Genetic Alteration in Fibrinogen Gene with a Direful Phenotype: A Tie-in in a Newborn
International Society of Thrombosis and Haemostasis,2020 Virtual Congress, | 12 Jul 2020
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Correlation of Hemorrhagic Complications with Novel Mutations in FGA And FGG: In Punjabi Congenital Afibrinogenemia Patients
XXVI Congress of International Society of Thrombosis and Hemostasis | 08 Jul 2017
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Characterization of phenotypic expression of inherited fibrinogen coagulopathy in Pakistani index patients
THE 62ND ANNUAL MEETING OF THESCIENTIFIC AND STANDARDIZATION COMMITTEE OF THEINTERNATIONAL SOCIETY ON THROMBOSIS ANDHAEMOSTASIS | 25 May 2016
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Characterization of phenotypic expression of inherited fibrinogen coagulopathy in Pakistani index patients
18th Pakistan Society of Haematology Annual Conference 2016 | 05 May 2016
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Molecular modelling of identified six novel missense mutations in pakistani congenital afibrinogenemia patients
JOURNAL OF THROMBOSIS AND HAEMOSTASIS | 01 Jan 2016
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12 NOVEL MUTATIONS IDENTIFIED IN PATIENTS OF CONGENITAL AFIBRINOGENEMIA IN PAKISTAN.
60TH ANNUAL MEETING OF THE SCIENTIFIC AND STANDARDIZATION COMMITTEE OF THE INTERNATIONAL SOCIETY ON THROMBOSIS AND HAEMOSTASIS | 23 Jun 2014
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Identification of novel mutations in fibrinogen gene alpha (FGA) and frequency of mutations in Pakistani population
JOURNAL OF THROMBOSIS AND HAEMOSTASIS | 01 Jan 2014