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 *

156 related articles for article (PubMed ID: 36397171)

  • 21. Bacillus Calmette-Guérin (BCG)-associated hemophagocytic lymphohistiocytosis in the setting of IFN-γR1 deficiency: A diagnostic dilemma.
    Razaghian A; Parvaneh L; Delkhah M; Abbasi A; Sadeghirad P; Shahrooei M; Parvaneh N
    EJHaem; 2020 Jul; 1(1):334-337. PubMed ID: 35847695
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Disseminated Bacillus Calmette-Guérin and Susceptibility to Mycobacterial Infections-Implications on Bacillus Calmette-Guérin Vaccinations.
    Lee PP
    Ann Acad Med Singap; 2015 Aug; 44(8):297-301. PubMed ID: 26477962
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature.
    Azarsiz E; Karaca N; Karaca E; Aksu G; Genel F; Gulez N; Ozen S; Kutukculer N
    Asian Pac J Allergy Immunol; 2023 Dec; 41(4):372-378. PubMed ID: 33638623
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Three novel compound heterozygous IL12RB1 mutations in Chinese patients with Mendelian susceptibility to mycobacterial disease.
    Zhou X; Jia W; Ni Z; Wang A; Liu Z; Hou M; Zhou M; Tang Z; Zhang D; Li L; Han T; Tan Y; Luo G; Wang J; Wu Y; Zhang X
    PLoS One; 2019; 14(4):e0215648. PubMed ID: 30998751
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Evaluation of interleukin-12 receptor β1 and interferon gamma receptor 1 deficiency in patients with disseminated BCG infection.
    Pourakbari B; Hosseinpour Sadeghi R; Mahmoudi S; Parvaneh N; Keshavarz Valian S; Mamishi S
    Allergol Immunopathol (Madr); 2019; 47(1):38-42. PubMed ID: 30268380
    [TBL] [Abstract][Full Text] [Related]  

  • 26. IL-12Rβ1 deficiency corresponding to concurrency of two diseases, mendelian susceptibility to mycobacterial disease and Crohn's disease.
    Khoshnevisan R; Nekooei-Marnany N; Klein C; Kotlarz D; Behnam M; Ostadi V; Yaran M; Rezaei A; Sherkat R
    J Clin Tuberc Other Mycobact Dis; 2019 Dec; 17():100123. PubMed ID: 31788565
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Pulmonary Hypertension Caused by Fibrosing Mediastinitis.
    Wang A; Su H; Duan Y; Jiang K; Li Y; Deng M; Long X; Wang H; Zhang M; Zhang Y; Cao Y
    JACC Asia; 2022 Jun; 2(3):218-234. PubMed ID: 36338410
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Mendelian susceptibility to mycobacterial disease: a case report of disseminated infection due to Mycobacterium avium].
    Darleguy A; Bost-Bru C; Pagnier A; Plantaz D; Piolat C; Nugues F; Picard C
    Arch Pediatr; 2013 Jul; 20(7):758-61. PubMed ID: 23726680
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Bacille Calmette-Guérin lymphadenitis and recurrent oral candidiasis in an infant with a new mutation leading to interleukin-12 receptor beta-1 deficiency.
    Aytekin C; Dogu F; Tuygun N; Tanir G; Guloglu D; Boisson-Dupuis S; Bustamante J; Feinberg J; Casanova JL; Ikinciogullari A
    J Investig Allergol Clin Immunol; 2011; 21(5):401-4. PubMed ID: 21905505
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi Arabia.
    Alodayani AN; Al-Otaibi AM; Deswarte C; Frayha HH; Bouaziz M; AlHelale M; Le Voyer T; Nieto-Patlan A; Rattina V; AlZahrani M; Halwani R; Al Sohime F; Al-Mousa H; Al-Muhsen S; Alhajjar SH; Dhayhi NS; Abel L; Casanova JL; Bin-Hussain I; AlBarrak MS; Al-Jumaah SA; Bustamante J
    J Clin Immunol; 2018 Apr; 38(3):278-282. PubMed ID: 29589181
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The Child with Recurrent Mycobacterial Disease.
    Reed B; Dolen WK
    Curr Allergy Asthma Rep; 2018 Jun; 18(8):44. PubMed ID: 29936646
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Bacille Calmette-Guérin infection and disease with fatal outcome associated with a point mutation in the interleukin-12/interleukin-23 receptor beta-1 chain in two Mexican families.
    Pedraza-Sánchez S; Herrera-Barrios MT; Aldana-Vergara R; Neumann-Ordoñez M; González-Hernández Y; Sada-Díaz E; de Beaucoudrey L; Casanova JL; Torres-Rojas M
    Int J Infect Dis; 2010 Sep; 14 Suppl 3():e256-60. PubMed ID: 20171917
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Case Report: BCG-Triggered Hemophagocytic Lymphohistiocytosis in an Infant With X-Linked Recessive Mendelian Susceptibility to Mycobacterial Disease Due to a Variant of Chronic Granulomatous Disease.
    Al-Hammadi S; Yahya AM; Al-Amri A; Shibli A; Balhaj GB; Tawil MI; Vijayan R; Souid AK
    Front Pediatr; 2021; 9():687538. PubMed ID: 34268280
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular analysis for patients with IL-12 receptor β1 deficiency.
    Ramirez-Alejo N; Blancas-Galicia L; Yamazaki-Nakashimada M; García-Rodríguez SE; Rivas-Larrauri F; Paolo-Cienfuegos DP; Alcantara-Salinas A; Espinosa-Rosales F; Santos-Argumedo L
    Clin Genet; 2014 Aug; 86(2):161-6. PubMed ID: 23952477
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Fibrosing mediastinitis mimicking sarcoidosis.
    Ferrer Galván M; Rodríguez Portal JA; Serrano Gorarredona MP; Gómez Izquierdo L
    Clin Respir J; 2015 Jan; 9(1):125-8. PubMed ID: 24405501
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mendelian susceptibility to mycobacterial disease: genetic, immunological, and clinical features of inborn errors of IFN-γ immunity.
    Bustamante J; Boisson-Dupuis S; Abel L; Casanova JL
    Semin Immunol; 2014 Dec; 26(6):454-70. PubMed ID: 25453225
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Immune defects in active mycobacterial diseases in patients with primary immunodeficiency diseases (PIDs).
    Lee WI; Huang JL; Yeh KW; Jaing TH; Lin TY; Huang YC; Chiu CH
    J Formos Med Assoc; 2011 Dec; 110(12):750-8. PubMed ID: 22248828
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A rare mutation causing autosomal dominant STAT1 deficiency in a South African multiplex kindred with disseminated BCG infection.
    Greybe L; Leung D; Wieselthaler N; le Roux DM; Chan KW; Lau YL; Eley B
    BMC Pediatr; 2023 Jul; 23(1):378. PubMed ID: 37516851
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Two novel STAT1 mutations cause Mendelian susceptibility to mycobacterial disease.
    Liu Z; Zhou M; Yuan C; Ni Z; Liu W; Tan Y; Zhang D; Zhou X; Zou T; Wang J; Hou M; Peng X; Zhang X
    Biochem Biophys Res Commun; 2022 Feb; 591():124-129. PubMed ID: 34815077
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Phenotypic and immune functional profiling of patients with suspected Mendelian Susceptibility to Mycobacterial Disease in South Africa.
    van Coller A; Glanzmann B; Cornelissen H; Möller M; Kinnear C; Esser M; Glashoff R
    BMC Immunol; 2021 Sep; 22(1):62. PubMed ID: 34517836
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.