Giant Filiform Polyposis, A Rare Entity in a Patient of Ulcerative Colitis: A Case Report

Por Ali, Zafar, Iltaf, Salma
Publicado no Cureus (2019)

Unusual Presentation of a Rare Tumor: Histiocytic Sarcoma Presenting as a Finger Growth

Por Ali, Zafar, Hanif, Faiza
Publicado no Cureus (2019)

Angiofibroma of Soft Tissue: A Newly Described Entity; A Case Report and Review of Literature

Por Ali, Zafar, Anwar, Fatima
Publicado no Cureus (2019)

Transient ST Segment Elevation in Two Patients with COVID-19 and a Normal Transthoracic Echocardiogram

Por Asif, Talal, Ali, Zafar
Publicado no Eur J Case Rep Intern Med (2020)

An Investigation of Fractional Bagley–Torvik Equation

Por Azhar Ali Zafar, Grzegorz Kudra, Jan Awrejcewicz
Publicado em 2019-12-01

Prevalence of NAFLD in Healthy and Young Male Individuals

Por Niaz, Asif, Ali, Zafar, Nayyar, Shaista, Fatima, Naureen
Publicado em 2011

Isavuconazole: A Promising Salvage Therapy for Invasive Mucormycosis

Por Shafiq, Muhammad, Ali, Zafar, Ukani, Rehman, Brewer, Joseph
Publicado no Cureus (2018)

Investigation of Entropy in Two-Dimensional Peristaltic Flow with Temperature Dependent Viscosity, Thermal and Electrical Conductivity

Por Qasim, Muhammad, Ali, Zafar, Farooq, Umer, Lu, Dianchen
Publicado no Entropy (Basel) (2020)

The study of gene GJB2/DFNB1 causing deafness in humans by linkage analysis from district Peshawar

Por Ali, Zafar, Babar, Masroor Ellahi, Ahmad, Jamil, Shah, Sajjad Ali
Publicado em 2012

Incidental primary papillary mucinous adenocarcinoma of the renal pelvis in a case of non-functioning kidney due to chronic pyelonephritis and pelvic calculus

Por Shantilal Mohanlalji Sisodia, Wasif Ali Zafar Ali Khan, Shweta Prakash Bhavsar
Publicado em 2012-01-01

Ruptured Sinus of Valsalva Aneurysm Causing Aorto–Atrial Fistula and Acute Heart Failure: A Rare Encounter

Por Ali, Zafar, Asif, Talal, Sheehy, Justin P, Jacob, Dany, Baweja, Paramdeep
Publicado no Eur J Case Rep Intern Med (2020)

Adenoid cystic carcinoma of Bartholin's gland: Report of a case and review of literature

Por Sisodia, Shantilal M., Khan, Wasif Ali Zafar Ali, Ansari, Sameer A.H., Mahajan, Vinod
Publicado em 2013

Comparison of a clinical-laboratory algorithm, 4t and heparin-induced thrombocytopenia expert probability scores in the diagnosis of heparin-induced thrombocytopenia in the critica...

Por Younis, Moustafa, Ya’qoub, Lina, Ali, Zafar, Grover, Punita, Ya’acoub, Rawan, Hamarshi, Majdi S
Publicado no Am J Blood Res (2019)

Molecular investigation of mental retardation locus gene PRSS12 by linkage analysis

Por Ali, Zafar, Babar, Masroor Ellahi, Ahmad, Jamil, Yousaf, Muhammad Zubair, Asif, Muhammad, Shah, Sajjad Ali
Publicado em 2011

Fatty acids characterization, oxidative perspectives and consumer acceptability of oil extracted from pre-treated chia (Salvia hispanica L.) seeds

Por Imran, Muhammad, Nadeem, Muhammad, Manzoor, Muhammad Faisal, Javed, Amna, Ali, Zafar, Akhtar, Muhammad Nadeem, Ali, Muhammad, Hussain, Yasir
Publicado no Lipids Health Dis (2016)

Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features

Por Ali, Zafar, Zulfiqar, Shumaila, Klar, Joakim, Wikström, Johan, Ullah, Farid, Khan, Ayaz, Abdullah, Uzma, Baig, Shahid, Dahl, Niklas
Publicado no BMC Med Genet (2017)

Is TLE1 Expression Limited to Synovial Sarcoma? Our Experience at Shifa International Hospital, Pakistan

Por Ali, Zafar, Haroon Khan, Asna, Rehman, Usama, Faisal, Muhammad, Ahmad, Imran N, Mamoon, Nadira, Nasir, Humaira, Hameed, Zujajah
Publicado no Cureus (2019)

A missense variant in ITPR1 provides evidence for autosomal recessive SCA29 with asymptomatic cerebellar hypoplasia in carriers

Por Klar, Joakim, Ali, Zafar, Farooq, Muhammad, Khan, Kamal, Wikström, Johan, Iqbal, Maria, Zulfiqar, Shumaila, Faryal, Sanam, Baig, Shahid Mahmood, Dahl, Niklas
Publicado no Eur J Hum Genet (2017)

An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 consanguineous families from Pakistan

Por Rasool, Sajida, Baig, Jamshaid Mahmood, Moawia, Abubakar, Ahmad, Ilyas, Iqbal, Maria, Waseem, Syeda Seema, Asif, Maria, Abdullah, Uzma, Makhdoom, Ehtisham Ul Haq, Kaygusuz, Emrah, Zakaria, Muhammad, Ramzan, Shafaq, Haque, Saif ul, Mir, Asif, Anjum, Iram, Fiaz, Mehak, Ali, Zafar, Tariq, Muhammad, Saba, Neelam, Hussain, Wajid, Budde, Birgit, Irshad, Saba, Noegel, Angelika Anna, Höning, Stefan, Baig, Shahid Mahmood, Nürnberg, Peter, Hussain, Muhammad Sajid
Publicado no Mol Genet Genomic Med (2020)

Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy

Por Martin, Carol-Anne, Ahmad, Ilyas, Klingseisen, Anna, Hussain, Muhammad Sajid, Bicknell, Louise S, Leitch, Andrea, Nürnberg, Gudrun, Toliat, Mohammad Reza, Murray, Jennie E, Hunt, David, Khan, Fawad, Ali, Zafar, Tinschert, Sigrid, Ding, James, Keith, Charlotte, Harley, Margaret E, Heyn, Patricia, Müller, Rolf, Hoffmann, Ingrid, Cormier-Daire, Valérie, Dollfus, Hélène, Dupuis, Lucie, Bashamboo, Anu, McElreavey, Kenneth, Kariminejad, Ariana, Mendoza-Londono, Roberto, Moore, Anthony T, Saggar, Anand, Schlechter, Catie, Weleber, Richard, Thiele, Holger, Altmüller, Janine, Höhne, Wolfgang, Hurles, Matthew E, Noegel, Angelika Anna, Baig, Shahid Mahmood, Nürnberg, Peter, Jackson, Andrew P
Publicado no Nat Genet (2014)