Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Fazle Raziq"'
Publikováno v:
Gomal Journal of Medical Sciences, Vol 17, Iss 3, Pp 75-80 (2019)
Background: Falciparum malaria is a common disease in our area. Apart from its classical presentation, at times it may present with refractory anemia or pancytopenia. The aim of this study was to determine the refractory anemia and pancytopenia as co
Externí odkaz:
https://doaj.org/article/5cf2e4eb186348e3ae878d331400778c
Publikováno v:
Khyber Medical University Journal, Vol 12, Iss 1 (2020)
OBJECTIVE: To determine the diagnostic importance of immunohistochemistry (IHC) in classifying acute lymphoblastic leukemia (ALL) in a tertiary care center. METHODS: This cross-sectional descriptive study was done from January-2017 to December-2018 a
Externí odkaz:
https://doaj.org/article/61274d8243034ff5a4109167ae4c336f
Autor:
Arshi Naz, Muhammad Younus Jamal, Samina Amanat, Ikram Din ujjan, Akber Najmuddin, Humayun Patel, Fazle Raziq, Nisar Ahmed, Ayisha Imran, Tahir Sultan Shamsi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-7 (2017)
Abstract Background Autosomal recessive bleeding disorders (ARBDs) include deficiencies of clotting factors I, II, V, VII, X, XI, XIII, vitamin K dependent clotting factors, combined factor V & VIII, Von Willebrand Disease (vWD) type 3, Glanzmann’s
Externí odkaz:
https://doaj.org/article/d98164047c44450b892d10d2d7f3382d
Autor:
Yasar Mehmood Yousafzai, Jawad Ahmed, Fazle Raziq, Amanda Smith, Sandra Chudleigh, Allyson Doig, Darren O'Brien, Nicola Williams, Mike Leach, Mhairi Copland, Chris Halsey
Publikováno v:
Blood Advances, Vol 1, Iss , Pp 36-38 (2017)
Externí odkaz:
https://doaj.org/article/f5bb2e025a5a488babd14c093014d3b5
Autor:
Ismail Jalil, Muhammad Arshad, Zara Rafaque, Fazle Raziq, Robina Wazir, Sajid Malik, Javid Iqbal Dasti
Publikováno v:
Asian Pacific Journal of Tropical Biomedicine, Vol 6, Iss 7, Pp 609-613 (2016)
Objective: To study the seroprevalence of hepatitis B virus (HBV) and hepatitis delta virus (HDV) infections in patients visiting outpatient department of a major tertiary care hospital in Khyber Pakhtunkhwa region of Pakistan. Methods: Blood samples
Externí odkaz:
https://doaj.org/article/5118de1ad68b4353827e9ffe07f544cb
Publikováno v:
Khyber Medical University Journal, Vol 5, Iss 2 (2013)
OBJECTIVE: To determine the effect of malarial infection on hemoglobin,total leukocyte count (TLC) and platelet count of patients coming to atertiary care hospital.METHODOLOGY: This descriptive hospital based study was conductedin the Department of P
Externí odkaz:
https://doaj.org/article/9855beb74808453a9b4e2b170724552f
Publikováno v:
Gomal Journal of Medical Sciences, Vol 8, Iss 2 (2010)
Background: Being a B-cell malignancy, multiple myeloma is characterized by clonal expansion and accumulation of abnormal plasma cells in the bone marrow compartment. This study was conducted to determine the frequency and hematological presentation
Externí odkaz:
https://doaj.org/article/aa9c1eb5629b47d7a4d0082cf28fb36a
Publikováno v:
Gomal Journal of Medical Sciences, Vol 5, Iss 1 (2007)
Background: Many patients with cancer are complicated by disseminated intravascular coagulation. This study was aimed to determine the level of Fibrinogen Degradation Products and D-Dimers at various stages in patients suffering from breast carcinoma
Externí odkaz:
https://doaj.org/article/055da85f13554662bd2cd83dfd49a385
Publikováno v:
Gomal Journal of Medical Sciences, Vol 17, Iss 3, Pp 75-80 (2019)
Background: Falciparum malaria is a common disease in our area. Apart from its classical presentation, at times it may present with refractory anemia or pancytopenia. The aim of this study was to determine the refractory anemia and pancytopenia as co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e5b61ac149a47e3fbafe19bc27e9e36
https://doi.org/10.46903/gjms/17.03.2027
https://doi.org/10.46903/gjms/17.03.2027
Autor:
Nazish Saqlain, Shehla Tariq, Shahtaj Masood, Arijit Biswas, Fazle Raziq, Hamideh Yadegari, Tahir Shamsi, Anna Pavlova, Arshi Naz, Ulrich Budde, Shariq Ahmed, Samina Amanat, Johannes Oldenburg
Publikováno v:
Haemophilia. 25:1035-1044
INTRODUCTION Type 3 von Willebrand disease (VWD), a severe autosomal recessive hereditary bleeding disorder, is described by the virtual absence of von Willebrand factor (VWF). In consanguineous populations, for example Pakistan, the disease is repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb87bf64b32235b4f43cd4cb4a6ebd40
https://doi.org/10.1111/hae.13841
https://doi.org/10.1111/hae.13841