Nima Parvaneh
Overview
Explore the profile of Nima Parvaneh including associated specialties, affiliations and a list of published articles.
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Articles
142
Citations
1946
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0
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Recent Articles
1.
Sharafian S, Barjouei Fard G, Atabakzadeh M, Movahedi M, Parvaneh N, Shariat M, et al.
Iran J Allergy Asthma Immunol
. 2025 Feb;
23(6):746-752.
PMID: 39985499
Asthma is a prevalent chronic inflammatory disorder in children, and poor therapeutic response in asthmatic children could result from various factors related to the doctor, patient, disease, and treatment. This...
2.
Bosticardo M, Dobbs K, Delmonte O, Martins A, Pala F, Kawai T, et al.
Sci Immunol
. 2025 Jan;
10(103):eadq1697.
PMID: 39792639
Human recombination-activating gene (RAG) deficiency can manifest with distinct clinical and immunological phenotypes. By applying a multiomics approach to a large group of -mutated patients, we aimed at characterizing the...
3.
Hosseinpour S, Pazouki R, Ashrafi M, Bemanalizadeh M, Ghahvechi Akbari M, Rezaei S, et al.
Iran J Child Neurol
. 2024 Oct;
18(4):33-45.
PMID: 39478947
Objectives: Acute Flaccid Paralysis (AFP) in children can stem from a diverse array of potential diagnoses. Materials & Methods: This retrospective study sought to diagnose children referred to a referral...
4.
Buso H, Adam E, Arkwright P, Bhattad S, Hamidieh A, Behfar M, et al.
J Clin Immunol
. 2024 Oct;
45(1):35.
PMID: 39470951
C1q deficiency is a rare inborn error of immunity characterized by increased susceptibility to infections and autoimmune manifestations mimicking SLE, with an associated morbidity and mortality. Because C1q is synthesized...
5.
Ashari K, Parvaneh N, Mirnia K, Ayati M, Saeedi M, Salehzadeh F, et al.
Pediatr Rheumatol Online J
. 2024 Oct;
22(1):90.
PMID: 39425177
Background: Gain of function (GOF) mutations in NOD-like receptor family CARD-containing 4 protein (NLRC4) gene induce a wide spectrum of autoinflammatory phenotypes. Currently, we categorize them into four groups: familial...
6.
Molitor A, Lederle A, Radosavljevic M, Sapuru V, Zavorka Thomas M, Yang J, et al.
Sci Adv
. 2024 Sep;
10(37):eado5545.
PMID: 39270020
Inositol 1,4,5-trisphosphate (IP3) receptor type 1 (), (), and () encode the IP3 receptor (IP3R), a key player in intracellular calcium release. In four unrelated patients, we report that an...
7.
Movahedi M, Movahedi M, Parvaneh N, Abolhassani H, Mahdavi M, Mosavikhorshidi M, et al.
Iran J Allergy Asthma Immunol
. 2024 Jun;
23(2):158-167.
PMID: 38822511
Patients with inborn errors of immunity (IEI) are among the high-risk groups regarding COVID-19. Receiving booster doses (third and fourth) in addition to the standard doses is recommended in these...
8.
Neehus A, Carey B, Landekic M, Panikulam P, Deutsch G, Ogishi M, et al.
Cell
. 2024 May;
187(13):3460.
PMID: 38776920
No abstract available.
9.
Kogl T, Chang H, Staniek J, Chiang S, Thoulass G, Lao J, et al.
J Exp Med
. 2024 May;
221(7).
PMID: 38771261
No abstract available.
10.
Kogl T, Chang H, Staniek J, Chiang S, Thoulass G, Lao J, et al.
J Exp Med
. 2024 May;
221(7).
PMID: 38722309
SYNTAXIN-11 (STX11) is a SNARE protein that mediates the fusion of cytotoxic granules with the plasma membrane at the immunological synapses of CD8 T or NK cells. Autosomal recessive inheritance...