Noninfectious Complications in B-Lymphopenic Common Variable Immunodeficiency von Pashangzadeh, S, Delavari, S, Moeini Shad, T, Salami, F, Rasouli, S E, Yazdani, R, Mahdaviani, S A, Nabavi, M, Aleyasin, S, Ahanchian, H, Jabbari-Azad, F, Chavoshzadeh, Z, Nazari, F, Momen, T, Sherkat, R, Abolnezhadian, F, Esmaeilzadeh, H, Fallahpour, M, Arshi, S, Bemanian, M H, Shokri, S, Ebrahimi, S S, Abolmolouki, M, Farid, A S, Rezaei, A, Esmaeili, M, Kalantari, A, Sadeghi-Shabestari, M, Shirkani, A, Behniafard, N, Khalili, A, Eslamian, M H, Cheraghi, T, Shafie, A, Tavakol, M, Khoshkhui, M, Iranparast, S, Shamshiri, M, Shahri, M A, Khazaei, R, Asadi, M, Babaha, F, Aghamohammadi, A, Rezaei, N, Abolhassani, H

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Reduced-intensity conditioning hematopoietic SCT for pediatric patients with LAD-1: clinical efficacy and importance of chimerism von Hamidieh, A A, Pourpak, Z, Hosseinzadeh, M, Fazlollahi, M R, Alimoghaddam, K, Movahedi, M, Hosseini, A, Chavoshzadeh, Z, Jalili, M, Arshi, S, Moin, M, Ghavamzadeh, A

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Spectrum of Phenotypes Associated with Mutations in LRBA von Alkhairy, Omar K., Abolhassani, Hassan, Rezaei, Nima, Fang, Mingyan, Andersen, Kasper Krogh, Chavoshzadeh, Zahra, Mohammadzadeh, Iraj, El-Rajab, Mariam A., Massaad, Michel, Chou, Janet, Aghamohammadi, Asghar, Geha, Raif S., Hammarström, Lennart

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Association of HAX1 Deficiency with Neurological Disorder von Rezaei, N., Chavoshzadeh, Z., Alaei, O.R., Sandrock, I., Klein, C.

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Laryngeal foreign body aspiration misdiagnosed as asthma: two case reports and a review of the literature von Chavoshzadeh, Z, Golnabi, A, Rezaei, N, Mehdizadeh, M

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Clinical, immunologic, molecular analyses and outcomes of iranian patients with LRBA deficiency: A longitudinal study von Azizi, Gholamreza, Abolhassani, Hassan, Mahdaviani, Seyed Alireza, Chavoshzadeh, Zahra, Eshghi, Peyman, Yazdani, Reza, Kiaee, Fatemeh, Shaghaghi, Mohammadreza, Mohammadi, Javad, Rezaei, Nima, Hammarström, Lennart, Aghamohammadi, Asghar

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JAGN1 mutation with distinct clinical features; two case reports and literature review von Hojabri, Mahsa, Farsi, Yeganeh, Jamee, Mahnaz, Abolhassani, Hassan, Khani, Hedieh Haji Khodaverdi, Karimi, Abdollah, Mesdaghi, Mehrnaz, Chavoshzadeh, Zahra, Sharafian, Samin

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Global systematic review of primary immunodeficiency registries von Abolhassani, H, Azizi, G, Sharifi, L, Yazdani, R, Mohsenzadegan, M, Delavari, S, Sohani, M, Shirmast, P, Zahra, Mahdaviani, SA, Kalantari, A, Tavakol, M, Jabbari-Azad, F, Ahanchian, H, Momen, T, Sherkat, R, Sadeghi-Shabestari, M, Aleyasin, S, Esmaeilzadeh, H, Al-Herz, W, Bousfiha, AA, Condino-Neto, A, Seppanen, M, Sullivan, KE, Hammarstrom, L, Modell, V, Modell, F, Quinn, J, Orange, JS, Aghamohammadi, A

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Is the Atopy Patch Test Reliable in the Evaluation of Food Allergy-Related Atopic Dermatitis? von Mansouri, Mahboubeh, Rafiee, Elham, Darougar, Sepideh, Mesdaghi, Mehrnaz, Chavoshzadeh, Zahra

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Clinical, immunological, and genetic features in 780 patients with autoimmune lymphoproliferative syndrome (ALPS) and ALPS‐like diseases: A systematic review von Hafezi, Nasim, Zaki‐Dizaji, Majid, Nirouei, Matineh, Asadi, Gelayol, Sharifinejad, Niusha, Jamee, Mahnaz, Erfan Rasouli, Seyed, Hamedifar, Haleh, Sabzevari, Araz, Chavoshzadeh, Zahra, Yazdani, Reza, Abolhassani, Hassan, Aghamohammadi, Asghar, Azizi, Gholamreza

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Human PIK3R1 mutations disrupt lymphocyte differentiation to cause activated PI3Kδ syndrome 2 von Nguyen, Tina, Lau, Anthony, Bier, Julia, Cooke, Kristen C, Lenthall, Helen, Ruiz-Diaz, Stephanie, Avery, Danielle T, Brigden, Henry, Zahra, David, Sewell, William A, Droney, Luke, Okada, Satoshi, Asano, Takaki, Abolhassani, Hassan, Chavoshzadeh, Zahra, Abraham, Roshini S, Rajapakse, Nipunie, Klee, Eric W, Church, Joseph A, Williams, Andrew, Wong, Melanie, Burkhart, Christoph, Uzel, Gulbu, Croucher, David R, James, David E, Ma, Cindy S, Brink, Robert, Tangye, Stuart G, Deenick, Elissa K

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Necrosis of nasal cartilage due to mucormycosis in a patient with severe congenital neutropenia due to HAX1 deficiency von Fahimzad, A, Chavoshzadeh, Z, Abdollahpour, H, Klein, C, Rezaei, N

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The Autoimmune Manifestations in Patients with Genetic Defects in the B Cell Development and Differentiation Stages von Azizi, Gholamreza, Hesari, Mina Fattah, Sharifinejad, Niusha, Fayyaz, Farimah, Chavoshzadeh, Zahra, Mahdaviani, Seyed Alireza, Alan, Mahnaz Seifi, Jamee, Mahnaz, Tavakol, Marzieh, Sadri, Homa, Shahrestanaki, Ehsan, Nabavi, Mohammad, Ebrahimi, Sareh Sadat, Shirkani, Afshin, Vosughi Motlagh, Ahmad, Delavari, Samaneh, Rasouli, Seyed Erfan, Esmaeili, Marzie, Salami, Fereshte, Yazdani, Reza, Rezaei, Nima, Abolhassani, Hassan

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Demographic, clinical, immunological, and molecular features of iranian national cohort of patients with defect in DCLRE1C gene von Ghadimi, Soodeh, Jamee, Mahnaz, Abolhassani, Hassan, Parvaneh, Nima, Rezaei, Nima, Delavari, Samaneh, Sadeghi-Shabestari, Mahnaz, Tabatabaei, Sedigheh Rafiei, Fahimzad, Alireza, Armin, Shahnaz, Chavoshzadeh, Zahra, Sharafian, Samin

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Pulmonary complications in primary hypogammaglobulinemia: a survey by high resolution CT scan von Gharagozlou, M, Ebrahimi, F A, Farhoudi, A, Aghamohammadi, A, Bemanian, M-H, Chavoshzadeh, Z, Heidarzadeh, M, Mehdizadeh, M, Moin, M, Movahedi, M, Nabavi, M, Pourpak, Z, Rezaei, N

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Autoimmunity in monogenic combined immune deficiencies with associated or syndromic features von Sharifinejad, Niusha, Azizi, Gholamreza, Chavoshzadeh, Zahra, Mahdaviani, Seyed Alireza, Alan, Mahnaz Seifi, Tavakol, Marzieh, Sadri, Homa, Nabavi, Mohammad, Ebrahimi, Sareh Sadat, Shirkani, Afshin, Vosughi Motlagh, Ahmad, Safarirad, Molood, Aghamahdi, Fatemeh, Nazari, Farzad, Delavari, Samaneh, Jamee, Mahnaz, Fayyaz, Farimah, Samimisedeh, Parham, Matani, Rahman, Esmaeili, Marzie, Yazdani, Reza, Rezaei, Nima, Abolhassani, Hassan

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Novel Mutation Detection of an Inflammatory Molecule Elastase ii Gene Encoding Neutrophil Elastase in Kostmann Syndrome von Ahangari, G., Chavoshzadeh, Z., Lari, Z., Ramyar, A., Farhoudi, A.

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New Presentation of CD27 Deficiency; Coronary Ectasia and COVID-19 von Golchehre, Zahra, Sharafian, Samin, Momtazmanesh, Nader, Chavoshzadeh, Zahra, Karimi, Abdollah, Abolhassani, Hassan, Kazemi Aghdam, Maryam, Vahidshahi, Koroush, Hashemimoghaddam, Seyedehatefeh, Kosari, Farid, Khafafpour, Zahra, Shamsian, Bibi Shahin, Keramatipour, Mohammad

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Evaluation of Lymphocyte Transformation Test Results in Patients with Delayed Hypersensitivity Reactions following the Use of Anticonvulsant Drugs von Karami, Zahra, Mesdaghi, Mehrnaz, Karimzadeh, Parvaneh, Mansouri, Mahboubeh, Taghdiri, Mohammad Mehdi, Kayhanidoost, Zarrintaj, Jebelli, Bita, Shekarriz Foumani, Reza, Babaie, Delara, Chavoshzadeh, Zahra

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Autoimmune versus Non-autoimmune Cutaneous Features in Monogenic Patients with Inborn Errors of Immunity von Sharifinejad, Niusha, Azizi, Gholamreza, Rasouli, Seyed Erfan, Chavoshzadeh, Zahra, Mahdaviani, Seyed Alireza, Tavakol, Marzieh, Sadri, Homa, Nabavi, Mohammad, Ebrahimi, Sareh Sadat, Shirkani, Afshin, Vosughi Motlagh, Ahmad, Momen, Tooba, Sharafian, Samin, Mesdaghi, Mehrnaz, Eslami, Narges, Delavari, Samaneh, Bahrami, Sasan, Yazdani, Reza, Rezaei, Nima, Abolhassani, Hassan

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