Progressive multifocal leukoencephalopathy in a 15-year-old boy with X-linked hyper-IgM syndrome: a case report
Saeedeh Delavari, Ali Pourvali, Mehran Akbari, Shiva Vajdian et autres
0 citationsJournal of Medical Case Reports
Nima Parvaneh
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235Publications signalées
6252Citations signalées
2Affiliations récentes
Institutions déclarées
Domaines associés
Immunodeficiency and Autoimmune DisordersBlood disorders and treatmentsImmune Cell Function and InteractionAutoimmune and Inflammatory Disorders ResearchPlatelet Disorders and Treatments
Publications récentes
ER proteostasis failure in HYOU1 deficiency alters B cells, neutrophils, and interferon signalling
Aida Idani, Sabrina Bibi‐Triki, Tristan Stemmelen, Mirjana Radosavljevic et autres
0 citationsJournal of Human Immunity
Familial pulmonary alveolar proteinosis and type I interferonopathy by mutation of STAT2 (TIMS2)
Conor Gruber, Meredith Ramba, Bineeta Debnath, Lorenzo Cuollo et autres
0 citationsThe Journal of Experimental Medicine
Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosis
Diana Olguín Calderón, Laura E. Kilpatrick, Clément Conil, Quentin Philippot et autres
1 citationThe Journal of Experimental Medicine
TLR7 F507S gain-of-function mutation presenting with early-onset SLE and hypertriglyceridemia: Response to JAK inhibition
Nima Parvaneh, H Karami, Leila Shahbaznejad, Zahra Rezaei et autres
3 citationsJournal of Human Immunity
Genotypes truncating the intracellular tail of human pre-TCRα: From amorphic to isomorphic
Marie Materna, Christian Beetz, Christian A. Ganoza, Caroline Deswarte et autres
1 citationJournal of Human Immunity
The neurologic face of X-linked lymphoproliferative syndrome type 1: a systematic review
Erta Rajabi, Saber Gharagozlou, Kousha Farhadi, Moeinadin Safavi et autres
0 citationsOrphanet Journal of Rare Diseases
Thrombocytopenia in patients with inborn errors of immunity
Saba Fekrvand, Maryam Mohtashami, Negin Sanadgol, Helia Salehi et autres
0 citationsBMC Immunology
Exploring the Landscape of Food Allergies in Pediatric Atopic Dermatitis: A Cross-Sectional Study in Iran
Mohadese Mahdavi, Saber Gharagozlou, Masoud Movahedi, Nima Parvaneh et autres
0 citationsIndian Journal of Dermatology
Neonatal diabetes mellitus is a significant feature of COXPD ‐24 caused by recessive NARS2 variants
Russell Donis, Matthew N. Wakeling, Nicola Jeffery, Molly Govier et autres
3 citationsDiabetic Medicine
Pyoderma Gangrenosum as the First Sign of GATA2-Deficiency Associated Childhood Myelodysplastic Syndrome, Case Report and Review of Literature
Moienadin Safavi, Zahra Naderi, Alieh Safari Sharari, Nima Parvaneh et autres
0 citationsInnovative Journal of Pediatrics
Complete Complement Factor I (CFI) deficiency: a systematic review of forty-nine patients including three novel cases
Erta Rajabi, Mahsa Choroom Kheirabadi, Nasrin Alipour Olyaei, Anne Molitor et autres
2 citationsBMC Immunology
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