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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Primary immunodeficiency disorders [original query]
Study of alpha1-antitrypsin phenotypes frequencies in patients with primary antibody deficiency.
Iranian journal of allergy, asthma, and immunology 2006 Jun 5 (2): 69-74.
Fazlollahi Mohammad Reza, Aghamohammadi Asghar, Hosseini Reza Farid, Lotfi Abbas Sahebghadam, Khoshdel Alireza, Farhoudi Abolhassan, Movahedi Masoud, Gharagozlou Mohammad, Mozaffari Habibeh, Zandieh Fariborz, Mansouri Mahboubeh, Ghaffari Javad, Rezaei Ni
Diagnostic approach to the hyper-IgE syndromes: immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitis.
The Journal of allergy and clinical immunology 2010 Sep 126 (3): 611-7.e1.
Schimke Lena F, Sawalle-Belohradsky Julie, Roesler Joachim, Wollenberg Andreas, Rack Anita, Borte Michael, Rieber Nikolaus, Cremer Reinhold, Maass Eberhart, Dopfer Roland, Reichenbach Janine, Wahn Volker, Hoenig Manfred, Jansson Annette F, Roesen-Wolff Angela, Schaub Bianca, Seger Reinhard, Hill Harry R, Ochs Hans D, Torgerson Troy R, Belohradsky Bernd H, Renner Ellen
The loss of the CD16 B73.1/Leu11c epitope occurring in some primary immunodeficiency diseases is not associated with the FcgammaRIIIa-48L/R/H polymorphism.
International journal of molecular medicine 2010 Sep 26 (3): 435-42.
Lenart Marzena, Trzyna Elzbieta, Rutkowska Magdalena, Bukowska-Strakova Karolina, Szaflarska Anna, Pituch-Noworolska Anna, Szczepanik Antoni, Zembala Marek, Siedlar Maci
A New IL-2RG Gene Mutation in an X-linked SCID Identified through TREC/KREC Screening: a Case Report.
Iranian journal of allergy, asthma, and immunology 2015 Aug 14 (4): 457-61.
Nourizadeh Maryam, Borte Stephan, Fazlollahi MohammadReza, Hammarström Lennart, Pourpak Zah
Targeted next-generation sequencing for genetic diagnosis of 160 patients with primary immunodeficiency in south China.
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2018 8 29 (8): 863-872.
Xia Yu, He Tingyan, Luo Yin, Li Chengrong, Lim Che Kang, Abolhassani Hassan, Yang Jun, Hammarström Lenna
Severe Facial Herpes Vegetans and Viremia in NFKB2-Deficient Common Variable Immunodeficiency.
Frontiers in pediatrics 2019 4 7 61.
Parsons Karyn, Cipriano Sarah D, Rosen Lindsey B, Browne Sarah K, Walter Jolan E, Stone Bryan L, Keeshin Susana, Chen Kar
Genetic mutations and immunological features of severe combined immunodeficiency patients in Iran.
Immunology letters 2019 Oct .
Shahbazi Zahra, Yazdani Reza, Shahkarami Sepideh, Shahbazi Shirin, Hamid Mohammad, Sadeghi-Shabestari Mahnaz, Momen Tooba, Aleyasin Soheila, Esmaeilzadeh Hossein, Darougar Sepideh, Delavari Sama, Mahdaviani Seyed Alireza, Ahanchian Hamid, Behmanesh Fatemeh, Kiaee Fatemeh, Chavoshzade Zahra, Shariat Mansoureh, Keramatipour Mohammad, Rezaei Nima, Abolhassani Hassan, Parvaneh Nima, Mahdian Reza, Aghamohammadi Asgh
Contribution of genetic variants associated with primary immunodeficiencies to childhood-onset systemic lupus erythematous.
The Journal of allergy and clinical immunology 2022 12 .
Wu Chao-Yi, Fan Wen-Lang, Yang Huang-Yu, Chu Pi-Shuang, Liao Pei-Chun, Chen Li-Chen, Yao Tsung-Chieh, Yeh Kuo-Wei, Ou Liang-Shiou, Lin Syh-Jae, Lee Wen-I, Huang Jing-Lo
An exploratory analysis of associations of genetic variation with the efficacy of tocilizumab in severe COVID-19 patients. A pharmacogenetic study based on next-generation sequencing.
Frontiers in pharmacology 2024 9 15 1426826.
Alejandro Durán-Sotuela, Jorge Vázquez-García, Sara Relaño-Fernández, Vanesa Balboa-Barreiro, Juan Fernández-Tajes, Francisco J Blanco, Ignacio Rego-Pér
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