S. Shahid

发表

Experience of using home-based fortified diet in rehabilitation of malnourished children at Indus Hospital, Karachi, Pakistan: an institution based retrospective chart review study

M. Mahesar, A. Rahim, S. Shahid, 2021, BMC Nutrition.

Association of the ACE-II genotype with the risk of nephrotic syndrome in Pakistani children.

S. Q. Mehdi, S. Khaliq, S. Naqvi, 2012, Gene.

High Risk Myelodyplastic Syndrome with Good Risk Cytogenetics and Somatic Oncogenic Driver Mutation

T. Shamsi, S. Waheed, Shariq Ahmed, 2018, National Journal of Health Sciences.

Clinical features and outcome of COVID‐19 positive children from a tertiary healthcare hospital in Karachi

S. Maqsood, M. Raza, S. Shahid, 2021, Journal of medical virology.

Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic Syndrome

S. Khaliq, S. Hashmi, A. Abid, 2018, Front. Genet..

Scleral-fixated intraocular lens implants—evolution of surgical techniques and future developments

B. Flores-Sánchez, L. Wickham, S. Shahid, 2021, Eye.

The Dawn of next generation DNA sequencing in myelodysplastic syndromes- experience from Pakistan

T. Shamsi, A. Naz, M. Shakeel, 2021, BMC genomics.

Homozygous CALR Mutation in Primary Myelofibrosis and Its Effect on Disease Phenotype: A Case Report and Review of the Literature

T. Shamsi, Shariq Ahmed, S. Shahid, 2019, Case reports in hematology.

Comparison of Clinical and Diagnostic Features of Pediatric Oncology Patients With or Without COVID-19 Infection: A Retrospective Chart Review

N. Rafiq, S. Maqsood, S. Shahid, 2021, Journal of pediatric hematology/oncology.

Genomic profile of a patient with triple negative essential thrombocythemia, unresponsive to therapy: A case report and literature review

T. Shamsi, Shariq Ahmed, M. Nadeem, 2017, Journal of advanced research.

Identification of LIPH gene mutation in a consanguineous family segregating the woolly hair/hypotrichosis phenotype.

S. Khaliq, A. Abid, S. Shahid, 2011, JPMA. The Journal of the Pakistan Medical Association.

A Novel Nonsense Mutation in FERMT3 Causes LAD-III in a Pakistani Family

Saima Siddiqui, T. Shamsi, Shariq Ahmed, 2019, Front. Genet..

A benign course of MDS with del 7q and ASXL1 mutation

T. Shamsi, Shariq Ahmed, M. Nadeem, 2018 .

ANALYSIS OF PRESCRIPTION PATTERN OF ANTIBIOTICS USED FOR THE MANAGEMENT OF URINARY TRACT INFECTION IN A KIDNEY CENTER

S. Ali, S. Shahid, Hassan, 2018 .

Primary hyperoxaluria: Comprehensive mutation screening of the disease causing genes and spectrum of disease‐associated pathogenic variants

M. Zafar, S. Khaliq, S. Hashmi, 2022, Clinical genetics.

Novel Genetic Variations in Acute Myeloid Leukemia in Pakistani Population

Saima Siddiqui, I. Khan, T. Shamsi, 2020, Frontiers in Genetics.

Case Report 2F

M. Borhany, T. Shamsi, S. Shahid, 2019 .

A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.

S. Q. Mehdi, S. Khaliq, J. Kazi, 2012, Gene.

Analysis of stochastic dynamics of tumor with drug interventions

S. Shahid, J. Hussain, Z. Bano, 2022, Chaos, Solitons & Fractals.

Upregulated type I interferon responses in asymptomatic COVID-19 infection are associated with improved clinical outcome

Safina Abdul Razzak, N. Ghanchi, Z. Hasan, 2021, Scientific Reports.

Unique molecular alteration patterns in von Hippel-Lindau (VHL) gene in a cohort of sporadic renal cell carcinoma patients from Pakistan.

S. Q. Mehdi, S. Khaliq, M. Mubarak, 2014, Mutation research.

Higher entropy observed in SARS-CoV-2 genomes from the first COVID-19 wave in Pakistan

Safina Abdul Razzak, N. Ghanchi, R. Hasan, 2021, PloS one.

A review of clinical profile, complications and antibiotic susceptibility pattern of extensively drug-resistant (XDR) Salmonella Typhi isolates in children in Karachi

Nida Ghouri, M. Mahesar, S. Shahid, 2020, BMC Infectious Diseases.

Clinical spectrum and outcomes of patients with different resistance patterns of Salmonella enterica

Nida Ghouri, M. Mahesar, M. Imran, 2021, Pakistan journal of medical sciences.

Alpha thalassemia deletions found in suspected cases of beta thalassemia major in Pakistani population

T. Shamsi, M. Nadeem, S. Shahid, 2017, Pakistan journal of medical sciences.

Transcriptomic profiling of disease severity in patients with COVID-19 reveals role of blood clotting and vasculature related genes

N. Ghanchi, Z. Hasan, B. Jamil, 2020, medRxiv.

SARS-CoV-2 genome analysis of strains in Pakistan reveals GH, S and L clade strains at the start of the pandemic

Safina Abdul Razzak, N. Ghanchi, R. Hasan, 2020, bioRxiv.

E cacy of Home-Based Forti ed Diet in Rehabilitation of Malnourished Children in Resource Restrained Country: An Institution Based Retrospective Study

S. Shahid, 2020 .

Effectiveness of home-based forti ed diet in the rehabilitation of malnourished children in resource restrained country: an institution based retrospective study

S. Shahid, 2020 .

Frequency of Nucleophosmin 1 Gene Mutation ( NPM 1 ) in Acute Myeloid Leukemia-A Single Center Experience

T. Shamsi, Shariq Ahmed, S. Shahid, 2018 .

Rare and heterogeneous manifestations of leucocyte adhesion deficiency type 1: report of two cases with diagnostic dilemmas and novel ITGB2 mutation

A. Abid, S. Shahid, S. Junejo, 2023, Allergy, Asthma & Clinical Immunology.

Unique molecular alteration patterns in von Hippel-Lindau (VHL) gene in a cohort of sporadic renal cell carcinoma patients from Pakistan.

S. Khaliq, M. Mubarak, A. Hashmi, 2014, Mutation research.

Lemierre’s syndrome in a child

S. Shahid, S. Akhtar, Anjum Naveed, 2021, Pakistan journal of medical sciences.

Synthesis, immunomodulation and cytotoxic effects of vanadium (IV) complexes.

U. Ashiq, K. Khan, S. Shahid, 2014, Medicinal chemistry (Shariqah (United Arab Emirates)).

Cholera outbreak in 2022 among children in Karachi: Study of cases attending to a Tertiary Care Hospital

S. Maqsood, Nazia Khursheed, S. Shahid, 2023, Pakistan journal of medical sciences.