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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 9, 2023. (Total: 217811Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Agammaglobulinemia and BTK[original query]
A genotype-phenotype correlation study in a group of 54 patients with X-linked agammaglobulinemia.
The Journal of allergy and clinical immunology 2005 Sep 116 (3): 690-7.
López-Granados Eduardo, Pérez de Diego Rebeca, Ferreira Cerdán Antonio, Fontán Casariego Gumersindo, García Rodríguez Maria Cr
Genetic analysis of patients with defects in early B-cell development.
Immunological reviews 2005 1 203 216-34.
Conley Mary Ellen, Broides Arnon, Hernandez-Trujillo Vivian, Howard Vanessa, Kanegane Hirokazu, Miyawaki Toshio, Shurtleff Sheila
Genotype-phenotype correlation in Bruton's tyrosine kinase deficiency.
Journal of pediatric hematology/oncology 2008 Sep 30 (9): 679-83.
Teimourian Shahram, Nasseri Saeed, Pouladi Nima, Yeganeh Mehdi, Aghamohammadi Asgh
Prevalence of BTK mutations in male Algerian patterns with agammaglobulinemia and severe B cell lymphopenia.
Clinical immunology (Orlando, Fla.) 2015 Sep .
Boushaki Soraya, Tahiat Azzedine, Meddour Yanis, Chan Koon Wing, Chaib Samia, Benhalla Nafissa, Smati Leila, Bensnouci Abdellatif, Lau Yu-Lung, Magdinier Frédérique, Djidjik Ré
A novel BTK gene mutation, c.82delC (p.Arg28 Alafs5), in a Korean family with X-linked agammaglobulinemia.
Korean journal of pediatrics 2016 12 59 (Suppl 1): S49-S52.
Lee Jeongeun, Rhee Minhee, Min Taek Ki, Bang Hae In, Jang Mi-Ae, Kang Eun-Suk, Kim Hee-Jin, Yang Hyeon-Jong, Pyun Bok Ya
Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort.
The journal of allergy and clinical immunology. In practice 2018 9 7 (3): 864-878.e9.
Yazdani Reza, Abolhassani Hassan, Kiaee Fatemeh, Habibi Sima, Azizi Gholamreza, Tavakol Marzieh, Chavoshzadeh Zahra, Mahdaviani Seyed Alireza, Momen Tooba, Gharagozlou Mohammad, Movahedi Masoud, Hamidieh Amir Ali, Behniafard Nasrin, Nabavi Mohammamd, Bemanian Mohammad Hassan, Arshi Saba, Molatefi Rasol, Sherkat Roya, Shirkani Afshin, Amin Reza, Aleyasin Soheila, Faridhosseini Reza, Jabbari-Azad Farahzad, Mohammadzadeh Iraj, Ghaffari Javad, Shafiei Alireza, Kalantari Arash, Mansouri Mahboubeh, Mesdaghi Mehrnaz, Babaie Delara, Ahanchian Hamid, Khoshkhui Maryam, Soheili Habib, Eslamian Mohammad Hossein, Cheraghi Taher, Dabbaghzadeh Abbas, Tavassoli Mahmoud, Kalmarzi Rasoul Nasiri, Mortazavi Seyed Hamidreza, Kashef Sara, Esmaeilzadeh Hossein, Tafaroji Javad, Khalili Abbas, Zandieh Fariborz, Sadeghi-Shabestari Mahnaz, Darougar Sepideh, Behmanesh Fatemeh, Akbari Hedayat, Zandkarimi Mohammadreza, Abolnezhadian Farhad, Fayezi Abbas, Moghtaderi Mojgan, Ahmadiafshar Akefeh, Shakerian Behzad, Sajedi Vahid, Taghvaei Behrang, Safari Mojgan, Heidarzadeh Marzieh, Ghalebaghi Babak, Fathi Seyed Mohammad, Darabi Behzad, Bazregari Saeed, Bazargan Nasrin, Fallahpour Morteza, Khayatzadeh Alireza, Javahertrash Naser, Bashardoust Bahram, Zamani Mohammadali, Mohsenzadeh Azam, Ebrahimi Sarehsadat, Sharafian Samin, Vosughimotlagh Ahmad, Tafakoridelbari Mitra, Rahim Maziar, Ashournia Parisa, Razaghian Anahita, Rezaei Arezou, Samavat Ashraf, Mamishi Setareh, Khazaei Hossein Ali, Mohammadi Javad, Negahdari Babak, Parvaneh Nima, Rezaei Nima, Lougaris Vassilios, Giliani Silvia, Plebani Alessandro, Ochs Hans D, Hammarström Lennart, Aghamohammadi Asgh
[Genetic study of an X-linked agammaglobulinemia pedigree caused by an BTK mutation].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2021 11 38 (11): 1081-1086.
Wei Chenxi, Yang Rujing, Yuan Xiaogeng, Yu Shihui, Qin Jianping, Tian Xinxian, Zhang M
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