These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 28900865)

  • 1. Genetic Counseling in Primary Immunodeficiency Disorders: An Emerging Experience in Egypt.
    El Hawary RE; Meshaal SS; Abd Elaziz DS; Elsharkawy MA; Alkady RS; Lotfy S; El-Sheikhah A; Hassan A; Galal NM; Boutros JA; Elmarsafy AM
    Mol Diagn Ther; 2017 Dec; 21(6):677-684. PubMed ID: 28900865
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The effects of prenatal genetic analysis on fetuses born to carrier mothers with primary immunodeficiency diseases.
    Lee WI; Huang JL; Yeh KW; Cheng PJ; Jaing TH; Lin SJ; Chen LC; Ou LS; Yao TC
    Ann Med; 2016; 48(1-2):103-10. PubMed ID: 26856578
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Customised molecular diagnosis of primary immune deficiency disorders in New Zealand: an efficient strategy for a small developed country.
    Ameratunga R; Woon ST
    N Z Med J; 2009 Oct; 122(1304):46-53. PubMed ID: 19859091
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rapid Flow cytometric prenatal diagnosis of primary immunodeficiency (PID) disorders.
    Mishra A; Gupta M; Dalvi A; Ghosh K; Madkaikar M
    J Clin Immunol; 2014 Apr; 34(3):316-22. PubMed ID: 24535004
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis and genetic analysis of X-linked immunodeficiency disorders.
    Puck JM
    Pediatr Res; 1993 Jan; 33(1 Suppl):S29-33; discussion S33-4. PubMed ID: 8433872
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular diagnosis of primary immunodeficiency diseases in a developing country: Iran as an example.
    Latif AH; Tabassomi F; Abolhassani H; Hammarström L
    Expert Rev Clin Immunol; 2014 Mar; 10(3):385-96. PubMed ID: 24450304
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detection of RAG mutations and prenatal diagnosis in families presenting with either T-B- severe combined immunodeficiency or Omenn's syndrome.
    Tabori U; Mark Z; Amariglio N; Etzioni A; Golan H; Biloray B; Toren A; Rechavi G; Dalal I
    Clin Genet; 2004 Apr; 65(4):322-6. PubMed ID: 15025726
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal test for X-linked severe combined immunodeficiency by analysis of maternal X-chromosome inactivation and linkage analysis.
    Puck JM; Krauss CM; Puck SM; Buckley RH; Conley ME
    N Engl J Med; 1990 Apr; 322(15):1063-6. PubMed ID: 2320067
    [No Abstract]   [Full Text] [Related]  

  • 9. Mutations in Recombination Activating Gene 1 and 2 in patients with severe combined immunodeficiency disorders in Egypt.
    Meshaal S; El Hawary R; Elsharkawy M; Mousa RK; Farid RJ; Abd Elaziz D; Alkady R; Galal N; Massaad MJ; Boutros J; Elmarsafy A
    Clin Immunol; 2015 Jun; 158(2):167-73. PubMed ID: 25869295
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Critical Role of Prenatal Genetic Study in Prevention of Primary Immunodeficiency in High-risk Families: The Largest Report of 107 Cases.
    Modarresi SZ; Sabetkish N; Badalzadeh M; Tajik S; Esmaeili B; Fazlollahi MR; Houshmand M; Gharehdaghi J; Niroomanesh S; Rahimi Sherbaf F; Alizadeh Z; Khodayari Namini N; Maddah M; Pourpak Z; Moin M
    Iran J Allergy Asthma Immunol; 2020 Oct; 19(5):478-483. PubMed ID: 33463115
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Patterns of Primary Immunodeficiency Disorders Among a Highly Consanguineous Population: Cairo University Pediatric Hospital's 5-Year Experience.
    Galal N; Meshaal S; Elhawary R; ElAziz DA; Alkady R; Lotfy S; Eldash A; Boutros J; Elmarsafy A
    J Clin Immunol; 2016 Oct; 36(7):649-55. PubMed ID: 27484503
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Targeted next-generation sequencing: a novel diagnostic tool for primary immunodeficiencies.
    Nijman IJ; van Montfrans JM; Hoogstraat M; Boes ML; van de Corput L; Renner ED; van Zon P; van Lieshout S; Elferink MG; van der Burg M; Vermont CL; van der Zwaag B; Janson E; Cuppen E; Ploos van Amstel JK; van Gijn ME
    J Allergy Clin Immunol; 2014 Feb; 133(2):529-34. PubMed ID: 24139496
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Consanguinity and primary immunodeficiencies.
    Al-Herz W; Aldhekri H; Barbouche MR; Rezaei N
    Hum Hered; 2014; 77(1-4):138-43. PubMed ID: 25060276
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Next Generation Sequencing Data Analysis in Primary Immunodeficiency Disorders - Future Directions.
    Fang M; Abolhassani H; Lim CK; Zhang J; Hammarström L
    J Clin Immunol; 2016 May; 36 Suppl 1():68-75. PubMed ID: 26993986
    [TBL] [Abstract][Full Text] [Related]  

  • 15. X-linked severe combined immunodeficiency syndrome: the first Korean case with gamma c chain gene mutation and subsequent genetic counseling.
    Jo EK; Kumaki S; Wei D; Tsuchiya S; Kanegane H; Song CH; Noh HY; Kim YO; Kim SY; Chung HY; Kim YH; Kook H
    J Korean Med Sci; 2004 Feb; 19(1):123-6. PubMed ID: 14966353
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Primary immune deficiency disorders in the South Pacific: the clinical utility of a customized genetic testing program in New Zealand.
    Ameratunga R; Woon ST; Brewerton M; Koopmans W; Jordan A; Brothers S; Singh R
    Ann N Y Acad Sci; 2011 Nov; 1238():53-64. PubMed ID: 22129053
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases.
    Al-Mousa H; Abouelhoda M; Monies DM; Al-Tassan N; Al-Ghonaium A; Al-Saud B; Al-Dhekri H; Arnaout R; Al-Muhsen S; Ades N; Elshorbagi S; Al Gazlan S; Sheikh F; Dasouki M; El-Baik L; Elamin T; Jaber A; Kheir O; El-Kalioby M; Subhani S; Al Idrissi E; Al-Zahrani M; Alhelale M; Alnader N; Al-Otaibi A; Kattan R; Al Abdelrahman K; Al Breacan MM; Bin Humaid FS; Wakil SM; Alzayer F; Al-Dusery H; Faquih T; Al-Hissi S; Meyer BF; Hawwari A
    J Allergy Clin Immunol; 2016 Jun; 137(6):1780-1787. PubMed ID: 26915675
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Comprehensive Genetic Results for Primary Immunodeficiency Disorders in a Highly Consanguineous Population.
    Al-Herz W; Chou J; Delmonte OM; Massaad MJ; Bainter W; Castagnoli R; Klein C; Bryceson YT; Geha RS; Notarangelo LD
    Front Immunol; 2018; 9():3146. PubMed ID: 30697212
    [No Abstract]   [Full Text] [Related]  

  • 19. [Primary immunodeficiency 1991: new uses and prospects of genetic counseling].
    Notarangelo LD; Parolini O; Lusardi M; Mazzolari E; Ugazio AG
    Pediatr Med Chir; 1991; 13(2):129-33. PubMed ID: 1896377
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic counseling and prenatal diagnosis for hereditary hearing loss in high-risk families.
    Yin A; Liu C; Zhang Y; Wu J; Mai M; Ding H; Yang J; Zhang X
    Int J Pediatr Otorhinolaryngol; 2014 Aug; 78(8):1356-9. PubMed ID: 24913939
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.