Machine Learning-Based Security Evaluation and Overhead Analysis of Logic Locking von Aghamohammadi, Yeganeh, Rezaei, Amin

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LIPSTICK: Corruptibility-Aware and Explainable Graph Neural Network-based Oracle-Less Attack on Logic Locking von Aghamohammadi, Yeganeh, Rezaei, Amin

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LIPSTICK: Corruptibility-Aware and Explainable Graph Neural Network-based Oracle-Less Attack on Logic Locking von Yeganeh Aghamohammadi, Rezaei, Amin

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IgA Deficiency: Correlation Between Clinical and Immunological Phenotypes von Aghamohammadi, Asghar, Cheraghi, Taher, Gharagozlou, Mohammad, Movahedi, Masoud, Rezaei, Nima, Yeganeh, Mehdi, Parvaneh, Nima, Abolhassani, Hassan, Pourpak, Zahra, Moin, Mostafa

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Severe primary antibody deficiency due to a novel mutation of mu heavy chain von Mohammadzadeh, I, Yeganeh, M, Aghamohammadi, A, Parvaneh, N, Behniafard, N, Abolhassani, H, Tabassomi, F, Hemmat, M, Kanegane, H, Miyawaki, T, Ohara, O, Rezaei, N

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Clinical, Immunological and Molecular Characteristics of 37 Iranian Patients with X-Linked Agammaglobulinemia von Aghamohammadi, Asghar, Fiorini, Maurilia, Moin, Mostafa, Parvaneh, Nima, Teimourian, Shahram, Yeganeh, Mehdi, Goffi, Francesca, Kanegane, Hirokazu, Amirzargar, Ali Akbar, Pourpak, Zahra, Rezaei, Nima, Salavati, Ali, Pouladi, Nima, Abdollahzade, Sina, Notarangelo, Luigi D., Miyawaki, Toshio, Plebani, Alessandro

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Severe combined immunodeficiency: A cohort of 40 patients von Yeganeh, Mehdi, Heidarzade, Marzieh, Pourpak, Zahra, Parvaneh, Nima, Rezaei, Nima, Gharagozlou, Mohammad, Movahedi, Masoud, Shabestari, Mahnaz Sadeghi, Mamishi, Setareh, Aghamohammadi, Asghar, Moin, Mostafa

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Genotype-phenotype correlation in Bruton's tyrosine kinase deficiency von Teimourian, Shahram, Nasseri, Saeed, Pouladi, Nima, Yeganeh, Mehdi, Aghamohammadi, Asghar

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Mortality and Morbidity in Common Variable Immunodeficiency von Aghamohammadi, Asghar, Pouladi, Nima, Parvaneh, Nima, Yeganeh, Mehdi, Movahedi, Masoud, Gharagolou, Mohamad, Pourpak, Zahra, Rezaei, Nima, Salavati, Ali, Abdollahzade, Sina, Moin, Mostafa

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Evaluation of humoral immune function in patients with bronchiectasis von Tabatabaie, Parviz, Aghamohammadi, Asghar, Mamishi, Setareh, Isaeian, Anna, Heidari, Golnaz, Abdollahzade, Sina, Pirouzi, Pirouz, Rezaei, Nima, Heidarnazhad, Hassan, Mirsaeid Ghazi, Bahram, Yeganeh, Mehdi, Cheraghi, Taher, Abolhasani, Hasan, Saghafi, Shiva, Alizadeh, Houman, Anaraki, Mohammad Reza

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Molecular characterization of Bruton's tyrosine kinase deficiency in 12 Iranian patients with presumed X-linked agammaglobulinemia von Nasseri, S, Sorouri, R, Pourpak, Z, Yeganeh, M, Aghamohammadi, A, Fiorini, M, Shahkarami, S, Mosallaei, M, Rezaei, N, Parvaneh, N

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The clinical, immunohematological, and molecular study of Iranian patients with severe congenital neutropenia von Rezaei, Nima, Moin, Mostafa, Pourpak, Zahra, Ramyar, Asghar, Izadyar, Mina, Chavoshzadeh, Zahra, Sherkat, Roya, Aghamohammadi, Asghar, Yeganeh, Mehdi, Mahmoudi, Maryam, Mahjoub, Fatemeh, Germeshausen, Manuela, Grudzien, Magda, Horwitz, Marshall S, Klein, Christoph, Farhoudi, Abolhassan

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Presence of Idiopathic Thrombocytopenic Purpura and autoimmune hemolytic anemia in the patients with common variable immunodeficiency von Ramyar, Asghar, Aghamohammadi, Asghar, Moazzami, Kasra, Rezaei, Nima, Yeganeh, Mehdi, Cheraghi, Taher, Pouladi, Nima, Heydari, Golnaz, Abolhassani, Hassan, Amirzargar, Ali Akbar, Parvaneh, Nima, Moin, Mostafa

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Cutaneous granulomas in common variable immunodeficiency: case report and review of literature von Aghamohammadi, Asghar, Abolhassani, Hassan, Rezaei, Nima, Kalantari, Najmoddin, Tamizifar, Banafshe, Cheraghi, Taher, Parvaneh, Nima, Yeganeh, Mehdi, Moazzami, Kasra, Ebrahimi-Daryani, Naser, Anaraki, Mohammad Reza

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Autoimmune lymphoproliferative syndrome: meticulous care for diagnosis von Parvaneh, Nima, Yeganeh, Mehdi, Aghamohammadi, Asghar

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Genotype-Phenotype Correlation in Bruton's Tyrosine Kinase Deficiency von Teimourian, Shahram, Nasseri, Saeed, Pouladi, Nima, Yeganeh, Mehdi, Aghamohammadi, Asghar

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Mortality and Morbidity in Common Variable Immunodeficiency von Aghamohammadi, A, Pouladi, N, Parvaneh, N, Yeganeh, M, Movahedi, M, Gharagolou, M, Pourpak, Z, Rezaei, N, Salavati, A, Abdollahzade, S, Moin, M

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Deficient Expression of Bruton's Tyrosine Kinase in Monocytes from X-Linked Agammaglobulinemia as Evaluated by a Flow Cytometric Analysis and its Clinical Application to Carrier De... von Aghamohammadi, A, Amirzargar, A A, Parvaneh, N, Marjousef, P, Moin, M, Farhoudi, A, Yeganeh, M, Miyawaki, T

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Other Well-Defined Immunodeficiencies von Yeganeh, Mehdi, Gambineri, Eleonora, Abolmaali, Kamran, Tamizifar, Banafshe, Español, Teresa

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The clinical and laboratory survey of Iranian patients with Hyper-IgE syndrome von Moin, Mostafa, Farhoudi, Abolhassan, Movahedi, Masoud, Rezaei, Nima, Pourpak, Zahra, Yeganeh, Mehdi, Gharagozlou, Mohammad, Mirsaeid Ghazi, Bahram, Arshi, Saba, Mansouri, Davoud, Sherkat, Roya, Kashef, Sara, Mahmoudi, Maryam, Nabavi, Mohammad, Aghamohammadi, Asghar

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