Search Results - "Sharifinejad, N."

Comprehensive comparison between 222 CTLA‐4 haploinsufficiency and 212 LRBA deficiency patients: a systematic review by Jamee, M., Hosseinzadeh, S., Sharifinejad, N., Zaki‐Dizaji, M., Matloubi, M., Hasani, M., Baris, S., Alsabbagh, M., Lo, B., Azizi, G.

“…Summary Cytotoxic T lymphocyte antigen 4 (CTLA‐4) haploinsufficiency (CHAI) and lipopolysaccharide‐responsive beige‐like anchor (LRBA) deficiency (LATAIE) are…”
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The clinical, molecular, and therapeutic features of patients with IL10/IL10R deficiency: a systematic review by Sharifinejad, Niusha, Zaki-Dizaji, Majid, Sepahvandi, Roya, Fayyaz, Farimah, Dos Santos Vilela, Maria Marluce, ElGhazali, Gehad, Abolhassani, Hassan, Ochs, Hans D, Azizi, Gholamreza

“…Interleukin10 (IL10) and IL10 receptor (IL10R) deficiencies are monogenic inborn errors of immunity (IEI) causing early-onset inflammatory bowel diseases…”
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Clinical, immunological, and genetic features in 780 patients with autoimmune lymphoproliferative syndrome (ALPS) and ALPS‐like diseases: A systematic review by 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

“…Background Autoimmune lymphoproliferative syndrome (ALPS) is a group of genetic disorders characterized by early‐onset lymphoproliferation, autoimmune…”
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Clinical, Immunological, and Genetic Features in 49 Patients With ZAP-70 Deficiency: A Systematic Review by Sharifinejad, Niusha, Jamee, Mahnaz, Zaki-Dizaji, Majid, Lo, Bernice, Shaghaghi, Mohammadreza, Mohammadi, Hamed, Jadidi-Niaragh, Farhad, Shaghaghi, Shiva, Yazdani, Reza, Abolhassani, Hassan, Aghamohammadi, Asghar, Azizi, Gholamreza

“…Zeta-Chain Associated Protein Kinase 70 kDa (ZAP-70) deficiency is a rare combined immunodeficiency (CID) caused by recessive homozygous/compound heterozygous…”
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The Autoimmune Manifestations in Patients with Genetic Defects in the B Cell Development and Differentiation Stages by 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

“…Purpose Primary B cell defects manifesting as predominantly antibody deficiencies result from variable inborn errors of the B cell lineage and their…”
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Clinical, immunological, and genetic features in 938 patients with autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED): a systematic review by Sharifinejad, Niusha, Zaki-Dizaji, Majid, Tebyanian, Shafi, Zainaldain, Hamed, Jamee, Mahnaz, Rizvi, Fatema Sadaat, Hosseinzadeh, Soheila, Fayyaz, Farimah, Hamedifar, Haleh, Sabzevari, Araz, Matloubi, Mojdeh, Heropolitańska-Pliszka, Edyta, Aghamahdi, Fatemeh, Abolhassani, Hassan, Azizi, Gholamreza

“…: Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED) is a rare inborn immune error characterized by a triad of chronic mucocutaneous…”
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Protein Kinase C-Delta Defect in Autoimmune Lymphoproliferative Syndrome-Like Disease: First Case from the National Iranian Registry and Review of the Literature by Sharifinejad, Niusha, Azizi, Gholamreza, Behniafard, Nasrin, Zaki-Dizaji, Majid, Jamee, Mahnaz, Yazdani, Reza, Abolhassani, Hassan, Aghamohammadi, Asghar

“…Protein kinase C is a family of serine/threonine kinases that play a key role in the adaptive immune cell signaling, as well as regulation of growth,…”
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Autoimmunity in monogenic combined immune deficiencies with associated or syndromic features by 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

“…Combined immune deficiencies (CIDs) with associated or syndromic features are a highly heterogeneous subgroup of inherited immune disorders. These patients…”
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Autoimmune versus Non-autoimmune Cutaneous Features in Monogenic Patients with Inborn Errors of Immunity by 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

“…Cutaneous manifestations are one of the most common presentations among patients with inborn errors of immunity (IEI). These skin manifestations are often…”
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