BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

268 related articles for article (PubMed ID: 33377626)

  • 1. Novel mutations in hyper-IgM syndrome type 2 and X-linked agammaglobulinemia detected in three patients with primary immunodeficiency disease.
    Chen X; Liu F; Yuan L; Zhang M; Chen K; Wu Y
    Mol Genet Genomic Med; 2021 Jan; 9(1):e1552. PubMed ID: 33377626
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical characteristics and prenatal diagnosis for 22 families in Henan Province of China with X-linked agammaglobulinemia (XLA) related to Bruton's tyrosine kinase (BTK) gene mutations.
    Gao S; Hu S; Duan H; Wang L; Kong X
    BMC Med Genet; 2020 Jun; 21(1):131. PubMed ID: 32552675
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort.
    Yazdani R; Abolhassani H; Kiaee F; Habibi S; Azizi G; Tavakol M; Chavoshzadeh Z; Mahdaviani SA; Momen T; Gharagozlou M; Movahedi M; Hamidieh AA; Behniafard N; Nabavi M; Bemanian MH; Arshi S; Molatefi R; Sherkat R; Shirkani A; Amin R; Aleyasin S; Faridhosseini R; Jabbari-Azad F; Mohammadzadeh I; Ghaffari J; Shafiei A; Kalantari A; Mansouri M; Mesdaghi M; Babaie D; Ahanchian H; Khoshkhui M; Soheili H; Eslamian MH; Cheraghi T; Dabbaghzadeh A; Tavassoli M; Kalmarzi RN; Mortazavi SH; Kashef S; Esmaeilzadeh H; Tafaroji J; Khalili A; Zandieh F; Sadeghi-Shabestari M; Darougar S; Behmanesh F; Akbari H; Zandkarimi M; Abolnezhadian F; Fayezi A; Moghtaderi M; Ahmadiafshar A; Shakerian B; Sajedi V; Taghvaei B; Safari M; Heidarzadeh M; Ghalebaghi B; Fathi SM; Darabi B; Bazregari S; Bazargan N; Fallahpour M; Khayatzadeh A; Javahertrash N; Bashardoust B; Zamani M; Mohsenzadeh A; Ebrahimi S; Sharafian S; Vosughimotlagh A; Tafakoridelbari M; Rahim M; Ashournia P; Razaghian A; Rezaei A; Samavat A; Mamishi S; Khazaei HA; Mohammadi J; Negahdari B; Parvaneh N; Rezaei N; Lougaris V; Giliani S; Plebani A; Ochs HD; Hammarström L; Aghamohammadi A
    J Allergy Clin Immunol Pract; 2019 Mar; 7(3):864-878.e9. PubMed ID: 30240888
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A Novel
    Han SP; Lin YF; Weng HY; Tsai SF; Fu LS
    Front Immunol; 2019; 10():1953. PubMed ID: 31481959
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Distinct Clinical Features and Novel Mutations in Taiwanese Patients With X-Linked Agammaglobulinemia.
    Yeh YH; Hsieh MY; Lee WI; Huang JL; Chen LC; Yeh KW; Ou LS; Yao TC; Wu CY; Lin SJ
    Front Immunol; 2020; 11():2001. PubMed ID: 33013854
    [No Abstract]   [Full Text] [Related]  

  • 6. Delayed diagnosis of X-linked agammaglobulinaemia in a boy with recurrent meningitis.
    Zhang YN; Gao YY; Yang SD; Cao BB; Zheng KL; Wei P; Chen LF; Chen WX
    BMC Neurol; 2019 Dec; 19(1):320. PubMed ID: 31830942
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel
    Shaka Z; Mojtabavi H; Rayzan E; Zoghi S; Shahkarami S; Raul JH; Sedighi I; Boztug K; Rezaei N
    Allergol Immunopathol (Madr); 2021; 49(2):80-83. PubMed ID: 33641298
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of four novel mutations in BTK from six Chinese families with X-linked agammaglobulinemia.
    Zhou Q; Teng Y; Pan J; Shi Q; Liu Y; Zhang F; Liang D; Li Z; Wu L
    Clin Chim Acta; 2022 Jun; 531():48-55. PubMed ID: 35245483
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical and genetic profiles of patients with X-linked agammaglobulinemia from southeast Turkey: Novel mutations in BTK gene.
    Doğruel D; Serbes M; Şaşihüseyinoğlu AŞ; Yılmaz M; Altıntaş DU; Bişgin A
    Allergol Immunopathol (Madr); 2019; 47(1):24-31. PubMed ID: 30072168
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical features and mutational analysis of X-linked agammaglobulinemia patients in Malaysia.
    Chear CT; Ismail IH; Chan KC; Noh LM; Kassim A; Latiff AHA; Gill SS; Ramly NH; Tan KK; Sundaraj C; Choo CM; Mohamed SAS; Baharin MF; Zamri AS; Yahya SNHS; Mohamad SB; Ripen AM
    Front Immunol; 2023; 14():1252765. PubMed ID: 37809070
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Uncovering Low-Level Maternal Gonosomal Mosaicism in X-Linked Agammaglobulinemia: Implications for Genetic Counseling.
    Rivière JG; Franco-Jarava C; Martínez-Gallo M; Aguiló-Cucurull A; Blasco-Pérez L; Paramonov I; Antolín M; Martín-Nalda A; Soler-Palacín P; Colobran R
    Front Immunol; 2020; 11():46. PubMed ID: 32117230
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical characteristics and genetic profiles of 174 patients with X-linked agammaglobulinemia: Report from Shanghai, China (2000-2015).
    Chen XF; Wang WF; Zhang YD; Zhao W; Wu J; Chen TX
    Medicine (Baltimore); 2016 Aug; 95(32):e4544. PubMed ID: 27512878
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and Genetic Study of X-linked Agammaglobulinemia Patients (The Benefit of Early Diagnosis).
    Alizadeh Z; Dashti P; Mazinani M; Nourizadeh M; Shakerian L; Tajik S; Movahedi M; Mamishi S; Pourpak Z; Fazlollahi MR
    Iran J Allergy Asthma Immunol; 2020 Jun; 19(3):305-309. PubMed ID: 32615664
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations of Bruton's tyrosine kinase gene in Brazilian patients with X-linked agammaglobulinemia.
    Ramalho VD; Oliveira Júnior EB; Tani SM; Roxo Júnior P; Vilela MM
    Braz J Med Biol Res; 2010 Sep; 43(9):910-3. PubMed ID: 20721470
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel deletion mutation and structural abnormality in the Bruton's tyrosine kinase gene identified in a Chinese patient with X-linked agammaglobulinemia.
    Wang S; Lu Y; Li H; Wang Z; Mo X; Chai Z; Han J
    Clin Lab; 2014; 60(5):859-62. PubMed ID: 24839832
    [TBL] [Abstract][Full Text] [Related]  

  • 16. X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations.
    Aadam Z; Kechout N; Barakat A; Chan KW; Ben-Ali M; Ben-Mustapha I; Zidi F; Ailal F; Attal N; Doudou F; Abbadi MC; Kaddache C; Smati L; Touri N; Chemli J; Gargah T; Brini I; Bakhchane A; Charoute H; Jeddane L; El Atiqi S; El Hafidi N; Hida M; Saile R; Alj HS; Boukari R; Bejaoui M; Najib J; Barbouche MR; Lau YL; Mellouli F; Bousfiha AA
    J Clin Immunol; 2016 Apr; 36(3):187-94. PubMed ID: 26931785
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical features and mutation analysis of X-linked agammaglobulinemia in 20 Chinese patients.
    Qin X; Jiang LP; Tang XM; Wang M; Liu EM; Zhao XD
    World J Pediatr; 2013 Aug; 9(3):273-7. PubMed ID: 23335184
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel Bruton's tyrosine kinase gene (BTK) missense mutation in a Chinese family with X-linked agammaglobulinemia.
    Zheng B; Zhang Y; Jin Y; Yu H
    BMC Pediatr; 2014 Oct; 14():265. PubMed ID: 25316352
    [TBL] [Abstract][Full Text] [Related]  

  • 19. X-linked agammaglobulinemia - first case with Bruton tyrosine kinase mutation from Pakistan.
    Zaidi SK; Qureshi S; Qamar FN
    J Pak Med Assoc; 2017 Mar; 67(3):471-473. PubMed ID: 28304004
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of 22 novel BTK gene variants in B cell deficiency with hypogammaglobulinemia.
    Kraft MT; Pyle R; Dong X; Hagan JB; Varga E; van Hee M; Boyce TG; Pozos TC; Yilmaz-Demirdag Y; Bahna SL; Abraham RS
    Clin Immunol; 2021 Aug; 229():108788. PubMed ID: 34182127
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.