Works matching AU Parvaneh, Nima

Results: 89
    1

    Severe combined immunodeficiency: A cohort of 40 patients.

    Published in:
    Pediatric Allergy & Immunology, 2008, v. 19, n. 4, p. 303, doi. 10.1111/j.1399-3038.2007.00647.x
    By:
    • Yeganeh, Mehdi;
    • Heidarzade, Marzieh;
    • Pourpak, Zahra;
    • Parvaneh, Nima;
    • Rezaei, Nima;
    • Gharagozlou, Mohammad;
    • Movahedi, Masoud;
    • Shabestari, Mahnaz Sadeghi;
    • Mamishi, Setareh;
    • Aghamohammadi, Asghar;
    • Moin, Mostafa
    Publication type:
    Article
    2
    3
    4
    5
    6
    7

    DOCK8 deficiency in six Iranian patients.

    Published in:
    Clinical Case Reports, 2016, v. 4, n. 6, p. 593, doi. 10.1002/ccr3.574
    By:
    • Saghafi, Shiva;
    • Pourpak, Zahra;
    • Nussbaumer, Franziska;
    • Fazlollahi, Mohammad Reza;
    • Houshmand, Massoud;
    • Hamidieh, Amir Ali;
    • Bemanian, Mohammad Hassan;
    • Nabavi, Mohammad;
    • Parvaneh, Nima;
    • Grimbacher, Bodo;
    • Moin, Mostafa;
    • Glocker, Cristina
    Publication type:
    Article
    8
    9

    IL-12Rβ1 Deficiency in Two of Fifty Children with Severe Tuberculosis from Iran, Morocco, and Turkey.

    Published in:
    PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0018524
    By:
    • Boisson-Dupuis, Stéphanie;
    • El Baghdadi, Jamila;
    • Parvaneh, Nima;
    • Bousfiha, Aziz;
    • Bustamante, Jacinta;
    • Feinberg, Jacqueline;
    • Samarina, Arina;
    • Grant, Audrey V.;
    • Janniere, Lucile;
    • El Hafidi, Naima;
    • Hassani, Amal;
    • Nolan, Daniel;
    • Najib, Jilali;
    • Camcioglu, Yildiz;
    • Hatipoglu, Nevin;
    • Aydogmus, Cigdem;
    • Tanir, Gonul;
    • Aytekin, Caner;
    • Keser, Melike;
    • Somer, Ayper
    Publication type:
    Article
    10

    LPS-Responsive Beige-Like Anchor Gene Mutation Associated With Possible Bronchiolitis Obliterans Organizing Pneumonia Associated With Hypogammaglobulinemia and Normal IgM Phenotype and Low Number of B Cells.

    Published in:
    Acta Medica Iranica, 2016, v. 54, n. 10, p. 620
    By:
    • Shokri, Sima;
    • Nabavi, Mohammad;
    • Hirschmugl, Tatjana;
    • Aghamohammadi, Asghar;
    • Arshi, Saba;
    • Bemanian, Mohamad Hassan;
    • Fallahpour, Morteza;
    • Molatefi, Rasool;
    • Rekabi, Mahsa;
    • Eslami, Narges;
    • Ahmadian, Javad;
    • Darabi, Kian;
    • Sedighi, Gholam Reza;
    • Monajemzadeh, Maryam;
    • Modaresi, Mohammadreza;
    • Parvaneh, Nima;
    • Boztug, Kaan;
    • Rezaei, Nima
    Publication type:
    Article
    11
    12
    13

    Visceral leishmaniasis in two patients with IL-12p40 and IL-12Rβ1 deficiencies.

    Published in:
    2017
    By:
    • Parvaneh, Nima;
    • Barlogis, Vincent;
    • Alborzi, Abdolvahab;
    • Deswarte, Caroline;
    • Boisson‐Dupuis, Stéphanie;
    • Migaud, Mélanie;
    • Farnaria, Catherine;
    • Markle, Janet;
    • Parvaneh, Leila;
    • Casanova, Jean‐Laurent;
    • Bustamante, Jacinta;
    • Boisson-Dupuis, Stéphanie;
    • Migaud, Mélanie;
    • Casanova, Jean-Laurent
    Publication type:
    journal article
    14
    15

    Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signaling.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39272-0
    By:
    • Nunes-Santos, Cristiane J.;
    • Kuehn, HyeSun;
    • Boast, Brigette;
    • Hwang, SuJin;
    • Kuhns, Douglas B.;
    • Stoddard, Jennifer;
    • Niemela, Julie E.;
    • Fink, Danielle L.;
    • Pittaluga, Stefania;
    • Abu-Asab, Mones;
    • Davies, John S.;
    • Barr, Valarie A.;
    • Kawai, Tomoki;
    • Delmonte, Ottavia M.;
    • Bosticardo, Marita;
    • Garofalo, Mary;
    • Carneiro-Sampaio, Magda;
    • Somech, Raz;
    • Gharagozlou, Mohammad;
    • Parvaneh, Nima
    Publication type:
    Article
    16
    17
    18
    19
    20

    Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel AIRE gene pathogenic variants.

    Published in:
    Orphanet Journal of Rare Diseases, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s13023-021-02170-z
    By:
    • Setoodeh, Aria;
    • Panjeh-Shahi, Samareh;
    • Bahmani, Fariba;
    • Vand-Rajabpour, Fatemeh;
    • Jalilian, Nazanin;
    • Sayarifard, Fatemeh;
    • Abbasi, Farzaneh;
    • Sayarifard, Azadeh;
    • Rostami, Parastoo;
    • Parvaneh, Nima;
    • Akhavan-Niaki, Haleh;
    • Ahmadifard, Mohamadreza;
    • Tabrizi, Mina
    Publication type:
    Article
    21

    Mortality and Morbidity in Common Variable Immunodeficiency.

    Published in:
    Journal of Tropical Pediatrics, 2007, v. 53, n. 1, p. 32
    By:
    • Asghar Aghamohammadi;
    • Nima Pouladi;
    • Nima Parvaneh;
    • Mehdi Yeganeh;
    • Masoud Movahedi;
    • Mohamad Gharagolou;
    • Zahra Pourpak;
    • Nima Rezaei;
    • Ali Salavati;
    • Sina Abdollahzade;
    • Mostafa Moin
    Publication type:
    Article
    22

    Gastrointestinal Manifestations in Patients with Common Variable Immunodeficiency.

    Published in:
    Digestive Diseases & Sciences, 2007, v. 52, n. 11, p. 2977, doi. 10.1007/s10620-006-9736-6
    By:
    • Ahmad Khodadad;
    • Nima Parvaneh;
    • Nima Rezaei;
    • Fatemeh Mahjoob;
    • Mohammad Bashashati;
    • Masoud Movahedi;
    • Mohammad Fazlollahi;
    • Fariborz Zandieh;
    • Zahra Roohi;
    • Sina Abdollahzade;
    • Ali Salavati;
    • Ali Kouhi;
    • Bahram Talebpour;
    • Nasser Daryani
    Publication type:
    Article
    23
    24

    Clinical and immunological characteristics of 69 leukocyte adhesion deficiency‐I patients.

    Published in:
    Pediatric Allergy & Immunology, 2023, v. 34, n. 7, p. 1, doi. 10.1111/pai.13990
    By:
    • Fazlollahi, Mohammad Reza;
    • Hamidieh, Amir Ali;
    • Moradi, Leila;
    • Shokouhi Shoormati, Raheleh;
    • Sabetkish, Nastaran;
    • Esmaeili, Behnaz;
    • Badalzadeh, Mohsen;
    • Alizadeh, Zahra;
    • Shamlou, Somayeh;
    • Movahedi, Masoud;
    • Mahloujirad, Maryam;
    • Razaghian, Anahita;
    • Arshi, Saba;
    • Gharagozlou, Mohammad;
    • Kalantari, Arash;
    • Bemanian, Mohammad Hassan;
    • Safari, Mojgan;
    • Heidarzadeh Arani, Marzieh;
    • Nabavi, Mohammad;
    • Parvaneh, Nima
    Publication type:
    Article
    25
    26
    27
    28
    29
    30
    31
    32
    33
    34

    An Overview on Hyper IgE Syndrome Patients Detected in Immunology, Asthma and Allergy Research Institute (2012-2015).

    Published in:
    Iranian Journal of Allergy, Asthma & Immunology, 2018, v. 17, p. 40
    By:
    • Saghafi, Shiva;
    • Fazlollahi, Mohammad Reza;
    • Houshmand, Massoud;
    • Movahedi, Massoud;
    • Ali Hamidieh, Amir;
    • Kalantari, Arash;
    • Zandieh, Fariborz;
    • Bemanian, Mohammad Hassan;
    • Nabavi, Mohammad;
    • Parvaneh, Nima;
    • Mahloojirad, Maryam;
    • Glocker, Cristina;
    • Buchta, Mary;
    • Nussbaumer, Franziska;
    • Pourpak, Zahra;
    • Grimbacher, Bodo;
    • Moin, Mostafa
    Publication type:
    Article
    35

    Health-Related Quality of Life in Primary Antibody Deficiency.

    Published in:
    Iranian Journal of Allergy, Asthma & Immunology, 2011, v. 10, n. 1, p. 47
    By:
    • Aghamohammadi, Asghar;
    • Montazeri, Ali;
    • Abolhassani, Hassan;
    • Saroukhani, Sepideh;
    • Pourjabbar, Sarvenaz;
    • Tavassoli, Mahmoud;
    • Darabi, Behzad;
    • Imanzadeh, Amir;
    • Parvaneh, Nima;
    • Rezaei, Nima
    Publication type:
    Article
    36
    37
    38
    39
    40
    41

    Inherited and acquired immunodeficiencies underlying tuberculosis in childhood.

    Published in:
    Immunological Reviews, 2015, v. 264, n. 1, p. 103, doi. 10.1111/imr.12272
    By:
    • Boisson‐Dupuis, Stéphanie;
    • Bustamante, Jacinta;
    • El‐Baghdadi, Jamila;
    • Camcioglu, Yildiz;
    • Parvaneh, Nima;
    • El Azbaoui, Safaa;
    • Agader, Aomar;
    • Hassani, Amal;
    • El Hafidi, Naima;
    • Mrani, Nidal Alaoui;
    • Jouhadi, Zineb;
    • Ailal, Fatima;
    • Najib, Jilali;
    • Reisli, Ismail;
    • Zamani, Adil;
    • Yosunkaya, Sebnem;
    • Gulle‐Girit, Saniye;
    • Yildiran, Alisan;
    • Cipe, Funda Erol;
    • Torun, Selda Hancerli
    Publication type:
    Article
    42
    43
    44

    Novel CYBA mutation in a family with BCGitis.

    Published in:
    Acta Microbiologica et Immunologica Hungarica, 2020, v. 67, n. 1, p. 56, doi. 10.1556/030.66.2019.043
    By:
    • Rayzan, Elham;
    • Pouladfar, Gholamreza;
    • Parvaneh, Nima;
    • Shahrooei, Mohammad;
    • Aryan, Zahra;
    • Rezaei, Nima
    Publication type:
    Article
    45
    46
    47

    Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects.

    Published in:
    Expert Review of Clinical Immunology, 2016, v. 12, n. 4, p. 479, doi. 10.1586/1744666X.2016.1139451
    By:
    • Abolhassani, Hassan;
    • Vitali, Massimiliano;
    • Lougaris, Vassilios;
    • Giliani, Silvia;
    • Parvaneh, Nima;
    • Parvaneh, Leila;
    • Mirminachi, Babak;
    • Cheraghi, Taher;
    • Khazaei, Hosseinali;
    • Mahdaviani, Seyed Alireza;
    • Kiaei, Fatemeh;
    • Tavakolinia, Naiimeh;
    • Mohammadi, Javad;
    • Negahdari, Babak;
    • Rezaei, Nima;
    • Hammarstrom, Lennart;
    • Plebani, Alessandro;
    • Aghamohammadi, Asghar
    Publication type:
    Article
    48

    Long-term evaluation of a historical cohort of Iranian common variable immunodeficiency patients.

    Published in:
    Expert Review of Clinical Immunology, 2014, v. 10, n. 10, p. 1405, doi. 10.1586/1744666X.2014.958469
    By:
    • Aghamohammadi, Asghar;
    • Abolhassani, Hassan;
    • Latif, AmirHossein;
    • Tabassomi, Firouzeh;
    • Shokuhfar, Tahaamin;
    • Torabi Sagvand, Babak;
    • Shahinpour, Shervin;
    • Mirminachi, Babak;
    • Parvaneh, Nima;
    • Movahedi, Masoud;
    • Gharagozlou, Mohammad;
    • Sherkat, Roya;
    • Amin, Reza;
    • Aleyasin, Soheila;
    • Faridhosseini, Reza;
    • Jabbari-Azad, Farahzad;
    • Cheraghi, Taher;
    • Eslamian, Mohamad Hosein;
    • Khalili, Abbas;
    • Kalantari, Najmoddin
    Publication type:
    Article
    49
    50