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A hypomorphic recombination-activating gene 1 ( RAG1 ) mutation resulting in a phenotype resembling common variable immunodeficiency
A hypomorphic recombination-activating gene 1 ( RAG1 ) mutation resulting in a phenotype resembling common variable immunodeficiency
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A hypomorphic recombination-activating gene 1 ( RAG1 ) mutation resulting in a phenotype resembling common variable immunodeficiency

Abolhassani, Hassan, MD ; Wang, Ning, PhD ; Aghamohammadi, Asghar, MD, PhD ; Rezaei, Nima, MD, PhD ; Lee, Yu Nee, PhD ; Frugoni, Francesco, PhD ; Notarangelo, Luigi D., MD ; Pan-Hammarström, Qiang, MD, PhD ; Hammarström, Lennart, MD, PhD

Journal of allergy and clinical immunology, 2014-12, Vol.134 (6), p.1375-1380 [Periódico revisado por pares]

New York, NY: Elsevier Inc

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2
Family study of pediatric patients with primary antibody deficiencies
Family study of pediatric patients with primary antibody deficiencies
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Family study of pediatric patients with primary antibody deficiencies

Rezaei, Nima ; Abolhassani, Hassan ; Kasraian, Amir ; Mohammadinejad, Payam ; Sadeghi, Bamdad ; Aghamohammadi, Asghar

Iranian journal of allergy, asthma, and immunology, 2013-12, Vol.12 (4), p.377-382 [Periódico revisado por pares]

Iran: Tehran University of Medical Sciences

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3
Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome
Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome
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Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome

Abolhassani, Hassan ; Landegren, Nils ; Bastard, Paul ; Materna, Marie ; Modaresi, Mohammadreza ; Du, Likun ; Aranda-Guillén, Maribel ; Sardh, Fabian ; Zuo, Fanglei ; Zhang, Peng ; Marcotte, Harold ; Marr, Nico ; Khan, Taushif ; Ata, Manar ; Al-Ali, Fatima ; Pescarmona, Remi ; Belot, Alexandre ; Béziat, Vivien ; Zhang, Qian ; Casanova, Jean-Laurent ; Kämpe, Olle ; Zhang, Shen-Ying ; Hammarström, Lennart ; Pan-Hammarström, Qiang

Journal of clinical immunology, 2022-04, Vol.42 (3), p.471-483 [Periódico revisado por pares]

New York: Springer US

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4
From variant of uncertain significance to likely pathogenic in two siblings with atypical RAG2 Deficiency: a case report and review of the literature
From variant of uncertain significance to likely pathogenic in two siblings with atypical RAG2 Deficiency: a case report and review of the literature
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From variant of uncertain significance to likely pathogenic in two siblings with atypical RAG2 Deficiency: a case report and review of the literature

Taghizadeh, Nima ; Mohammadi, Soha ; Abolhassani, Hassan ; Shokri, Sima ; Nabavi, Mohammad ; Fallahpour, Morteza ; Bemanian, Mohammad Hassan

BMC pediatrics, 2024-02, Vol.24 (1), p.116-116, Article 116 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
X-Linked TLR7 Deficiency Underlies Critical COVID-19 Pneumonia in a Male Patient with Ataxia-Telangiectasia
X-Linked TLR7 Deficiency Underlies Critical COVID-19 Pneumonia in a Male Patient with Ataxia-Telangiectasia
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X-Linked TLR7 Deficiency Underlies Critical COVID-19 Pneumonia in a Male Patient with Ataxia-Telangiectasia

Abolhassani, Hassan ; Vosughimotlagh, Ahmad ; Asano, Takaki ; Landegren, Nils ; Boisson, Bertrand ; Delavari, Samaneh ; Bastard, Paul ; Aranda-Guillén, Maribel ; Wang, Yating ; Zuo, Fanglei ; Sardh, Fabian ; Marcotte, Harold ; Du, Likun ; Zhang, Shen-Ying ; Zhang, Qian ; Rezaei, Nima ; Kämpe, Olle ; Casanova, Jean-Laurent ; Hammarström, Lennart ; Pan-Hammarström, Qiang

Journal of clinical immunology, 2022-01, Vol.42 (1), p.1-9 [Periódico revisado por pares]

New York: Springer US

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6
JAGN1 mutation with distinct clinical features; two case reports and literature review
JAGN1 mutation with distinct clinical features; two case reports and literature review
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JAGN1 mutation with distinct clinical features; two case reports and literature review

Hojabri, Mahsa ; Farsi, Yeganeh ; Jamee, Mahnaz ; Abolhassani, Hassan ; Khani, Hedieh Haji Khodaverdi ; Karimi, Abdollah ; Mesdaghi, Mehrnaz ; Chavoshzadeh, Zahra ; Sharafian, Samin

BMC pediatrics, 2023-04, Vol.23 (1), p.206-206, Article 206 [Periódico revisado por pares]

England: BioMed Central Ltd

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7
Genetic Risk Variants for Class Switching Recombination Defects in Ataxia-Telangiectasia Patients
Genetic Risk Variants for Class Switching Recombination Defects in Ataxia-Telangiectasia Patients
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Genetic Risk Variants for Class Switching Recombination Defects in Ataxia-Telangiectasia Patients

Amirifar, Parisa ; Mehrmohamadi, Mahya ; Ranjouri, Mohammad Reza ; Akrami, Seyed Mohammad ; Rezaei, Nima ; Saberi, Ali ; Yazdani, Reza ; Abolhassani, Hassan ; Aghamohammadi, Asghar

Journal of clinical immunology, 2022-01, Vol.42 (1), p.72-84 [Periódico revisado por pares]

New York: Springer US

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8
Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS Deficiency
Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS Deficiency
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Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS Deficiency

Abolhassani, Hassan ; El-Sherbiny, Yasser M. ; Arumugakani, Gururaj ; Carter, Clive ; Richards, Stephen ; Lawless, Dylan ; Wood, Philip ; Buckland, Matthew ; Heydarzadeh, Marzieh ; Aghamohammadi, Asghar ; Hambleton, Sophie ; Hammarström, Lennart ; Burns, Siobhan O ; Doffinger, Rainer ; Savic, Sinisa

Journal of clinical immunology, 2020-02, Vol.40 (2), p.277-288 [Periódico revisado por pares]

New York: Springer US

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9
Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency
Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency
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Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency

Sefer, Asena Pinar ; Abolhassani, Hassan ; Ober, Franziska ; Kayaoglu, Basak ; Bilgic Eltan, Sevgi ; Kara, Altan ; Erman, Baran ; Surucu Yilmaz, Naz ; Aydogmus, Cigdem ; Aydemir, Sezin ; Charbonnier, Louis-Marie ; Kolukisa, Burcu ; Azizi, Gholamreza ; Delavari, Samaneh ; Momen, Tooba ; Aliyeva, Simuzar ; Kendir Demirkol, Yasemin ; Tekin, Saban ; Kiykim, Ayca ; Baser, Omer Faruk ; Cokugras, Haluk ; Gursel, Mayda ; Karakoc-Aydiner, Elif ; Ozen, Ahmet ; Krappmann, Daniel ; Chatila, Talal A. ; Rezaei, Nima ; Baris, Safa

Journal of clinical immunology, 2022-04, Vol.42 (3), p.634-652 [Periódico revisado por pares]

New York: Springer US

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10
Clinical and Immunologic Characteristics of Non-Hematologic Cancers in Patients with Inborn Errors of Immunity
Clinical and Immunologic Characteristics of Non-Hematologic Cancers in Patients with Inborn Errors of Immunity
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Clinical and Immunologic Characteristics of Non-Hematologic Cancers in Patients with Inborn Errors of Immunity

Delavari, Samaneh ; Wang, Yating ; Moeini Shad, Tannaz ; Pashangzadeh, Salar ; Nazari, Farzad ; Salami, Fereshte ; Abolhassani, Hassan

Cancers, 2023, Vol.15 (3), p.764 [Periódico revisado por pares]

Switzerland: MDPI AG

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