Publications by authors named "Shahnaz Bibi"

Claim this Profile
D
Diagnosis of HLH: two siblings, two distinct genetic causes.
Claire Escaron, Elizabeth Ralph, Shahnaz Bibi, Johannes Visser, Maurizio Aricò

Clin Exp Immunol· April 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Haematopoietic Stem Cell Transplantation for DNA Ligase 1 Deficiency.
Juliana M F Silva, Alison Jones, Keith Sibson, Shahnaz Bibi, Penny Jeggo

J Clin Immunol· January 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel Gain-of-Function Mutation in Stat1 Sumoylation Site Leads to CMC/CID Phenotype Responsive to Ruxolitinib.
Tariq Al Shehri, Kimberly Gilmour, Florian Gothe, Sam Loughlin, Shahnaz Bibi

J Clin Immunol· November 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel IL2RG Mutation Causes Leaky TLOWB+NK+ SCID With Nodular Regenerative Hyperplasia and Normal IL-15 STAT5 Phosphorylation.
João F Neves, Catarina Martins, Ana I Cordeiro, Conceição Neves, Vicent Plagnol, Shahnaz Bibi

J Pediatr Hematol Oncol· May 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
One hundred percent survival after transplantation of 34 patients with Wiskott-Aldrich syndrome over 20 years.
Reem Ahmed Elfeky, Juliana M Furtado-Silva, Robert Chiesa, Kanchan Rao, Persis Amrolia, Shahnaz Bibi

J Allergy Clin Immunol· November 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mitochondrial Genetic Diversity and Phylogeography of Mus musculus castaneus in Northern Punjab, Pakistan.
Shahnaz Bibi, Muhammad Sajid Nadeem, Andrew Stephen Wiewel, Mirza Azhar Beg, Khalid Hameed

Zoolog Sci· December 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome Sequencing.
Karin R Engelhardt, Yaobo Xu, Angela Grainger, Mila G C Germani Batacchi, David J Swan, Shahnaz Bibi

J Clin Immunol· January 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
X
X-linked Inhibitor of Apoptosis Complicated by Granulomatous Lymphocytic Interstitial Lung Disease (GLILD) and Granulomatous Hepatitis.
Cathal L Steele, Matthew Doré, Sandra Ammann, Maurice Loughrey, Angeles Montero, Shahnaz Bibi

J Clin Immunol· October 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease.
Turkan Patiroglu, H Haluk Akar, Kimberly Gilmour, Ekrem Unal, M Akif Ozdemir, Shahnaz Bibi

Clin Immunol· July 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Atypical severe combined immunodeficiency caused by a novel homozygous mutation in Rag1 gene in a girl who presented with pyoderma gangrenosum: a case report and literature review.
Turkan Patiroglu, H Haluk Akar, Kimberly Gilmour, M Akif Ozdemir, Shahnaz Bibi

J Clin Immunol· October 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The many faces of Artemis-deficient combined immunodeficiency - Two patients with DCLRE1C mutations and a systematic literature review of genotype-phenotype correlation.
Pamela P Lee, Lisa Woodbine, Kimberly C Gilmour, Shahnaz Bibi, Catherine M Cale

Clin Immunol· December 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis