Ikuti
Saba Shahid
Saba Shahid
National Institute of Blood Diseases and Bone Marrow Transplantation
Email yang diverifikasi di nibd.edu.pk
Judul
Dikutip oleh
Dikutip oleh
Tahun
A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan
A Abid, S Khaliq, S Shahid, A Lanewala, M Mubarak, S Hashmi, J Kazi, ...
Gene 502 (2), 133-137, 2012
592012
Genomic profile of a patient with triple negative essential thrombocythemia, unresponsive to therapy: A case report and literature review.
TS Uzma Zaidi, Saba Shahid, Naveen Fatima, Shariq Ahmed, Gull Sufaida ...
J Adv Res. 4 (8), 375-378, 2017
13*2017
Alpha thalassemia deletions found in suspected cases of beta thalassemia major in Pakistani population.
TS Saba Shahid, Mohammad Nadeem, Danish Zahid, Jawwad Hassan, Saqib Ansari
Pak J. Med Sci. 2 (33), 411-416, 2017
12*2017
Synthesis, immunomodulation and cytotoxic effects of vanadium (IV) complexes
U Ashiq, R Ara Jamal, M Ahmed Mesaik, M Mahroof-Tahir, S Shahid, ...
Medicinal Chemistry 10 (3), 287-299, 2014
112014
Association of the ACE-II genotype with the risk of nephrotic syndrome in Pakistani children
S Shahid, A Abid, QS Mehdi, S Firasat, A Lanewala, AAS Naqvi, S Khaliq
Gene 493 (1), 165-168, 2012
112012
Unique molecular alteration patterns in von Hippel-Lindau (VHL) gene in a cohort of sporadic renal cell carcinoma patients from Pakistan
S Khaliq, S Ajaz, S Firasat, S Shahid, AS Hasan, G Sultan, R Mohsin, ...
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 763, 45-52, 2014
82014
Identification of LIPH gene mutation in a consanguineous family segregating the woolly hair/hypotrichosis phenotype
SH Shah, A Abid, S Shahid, S Khaliq
JPMA-Journal of the Pakistan Medical Association 61 (11), 1060, 2011
32011
Co-occurrence of oncogenic driver mutations (SF3B1, RUNX1 and CSF3R) with distinct prognostic Implication in a lower risk myelodysplastic syndrome patient.
TS Aisha Jamal , Nida Anwar , Saba Shahid , Shariq Ahmed
Merit Res J Med Sci. 4 (5), 192-196, 2017
2017
A spectrum of novel NPHS1 and NPHS2 gene mutations in Pediatric Nephrotic syndrome patients from Pakistan
A Abid, S Khalique, S Shahid, A Lanewala, M Mubarak, S Hashmi, ...
PEDIATRIC NEPHROLOGY 28 (8), 1461-1461, 2013
2013
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