Alangari AA - Search Results

1

Case report: Durable response to ruxolitinib in a child with TREX1-related disorder.

Bin Khathlan Y, Almutairi S, Albadr FB, Alangari AA, Alsultan A. Bin Khathlan Y, et al. Among authors: alangari aa. Front Pediatr. 2023 Apr 28;11:1178919. doi: 10.3389/fped.2023.1178919. eCollection 2023. Front Pediatr. 2023. PMID: 37187582 Free PMC article.

2

LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency.

Alangari A, Alsultan A, Adly N, Massaad MJ, Kiani IS, Aljebreen A, Raddaoui E, Almomen AK, Al-Muhsen S, Geha RS, Alkuraya FS. Alangari A, et al. J Allergy Clin Immunol. 2012 Aug;130(2):481-8.e2. doi: 10.1016/j.jaci.2012.05.043. Epub 2012 Jun 19. J Allergy Clin Immunol. 2012. PMID: 22721650 Free PMC article.

3

A novel homozygous mutation in G6PC3 presenting as cyclic neutropenia and severe congenital neutropenia in the same family.

Alangari AA, Alsultan A, Osman ME, Anazi S, Alkuraya FS. Alangari AA, et al. J Clin Immunol. 2013 Nov;33(8):1403-6. doi: 10.1007/s10875-013-9945-7. Epub 2013 Oct 9. J Clin Immunol. 2013. PMID: 24105461

4

Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like disorder caused by loss-of-function mutations in LRBA.

Charbonnier LM, Janssen E, Chou J, Ohsumi TK, Keles S, Hsu JT, Massaad MJ, Garcia-Lloret M, Hanna-Wakim R, Dbaibo G, Alangari AA, Alsultan A, Al-Zahrani D, Geha RS, Chatila TA. Charbonnier LM, et al. Among authors: alangari aa. J Allergy Clin Immunol. 2015 Jan;135(1):217-27. doi: 10.1016/j.jaci.2014.10.019. Epub 2014 Nov 17. J Allergy Clin Immunol. 2015. PMID: 25468195 Free PMC article.

5

Multiple Family Members With Delayed Cord Separtion and Combined Immunodeficiency With Novel Mutation in IKBKB.

Alsum Z, AlZahrani MS, Al-Mousa H, Alkhamis N, Alsalemi AA, Shamseldin HE, Alkuraya FS, Alangari AA. Alsum Z, et al. Among authors: alangari aa. Front Pediatr. 2020 Feb 14;8:9. doi: 10.3389/fped.2020.00009. eCollection 2020. Front Pediatr. 2020. PMID: 32117824 Free PMC article.

6

X-linked lymphoproliferative disease associated with hypogammaglobulinemia and growth-hormone deficiency.

Alangari A, Abobaker A, Kanegane H, Miyawaki T. Alangari A, et al. Eur J Pediatr. 2006 Mar;165(3):165-7. doi: 10.1007/s00431-005-0023-x. Epub 2005 Nov 17. Eur J Pediatr. 2006. PMID: 16328363

7

JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency.

Alsohime F, Martin-Fernandez M, Temsah MH, Alabdulhafid M, Le Voyer T, Alghamdi M, Qiu X, Alotaibi N, Alkahtani A, Buta S, Jouanguy E, Al-Eyadhy A, Gruber C, Hasan GM, Bashiri FA, Halwani R, Hassan HH, Al-Muhsen S, Alkhamis N, Alsum Z, Casanova JL, Bustamante J, Bogunovic D, Alangari AA. Alsohime F, et al. Among authors: alangari aa. N Engl J Med. 2020 Jan 16;382(3):256-265. doi: 10.1056/NEJMoa1905633. N Engl J Med. 2020. PMID: 31940699 Free PMC article.

8

Treatment of disseminated mycobacterial infection with high-dose IFN-γ in a patient with IL-12Rβ1 deficiency.

Alangari AA, Al-Zamil F, Al-Mazrou A, Al-Muhsen S, Boisson-Dupuis S, Awadallah S, Kambal A, Casanova JL. Alangari AA, et al. Clin Dev Immunol. 2011;2011:691956. doi: 10.1155/2011/691956. Epub 2010 Dec 22. Clin Dev Immunol. 2011. PMID: 21234109 Free PMC article.

9

Menetrier`s disease in a Saudi child.

Alfares FA, Raddaoui EM, El-Mouzan MI, Alangari AA. Alfares FA, et al. Among authors: alangari aa. Saudi Med J. 2013 Nov;34(11):1192-4. Saudi Med J. 2013. PMID: 24252900

10

The effect of sand storms on acute asthma in Riyadh, Saudi Arabia.

Alangari AA, Riaz M, Mahjoub MO, Malhis N, Al-Tamimi S, Al-Modaihsh A. Alangari AA, et al. Ann Thorac Med. 2015 Jan-Mar;10(1):29-33. doi: 10.4103/1817-1737.146857. Ann Thorac Med. 2015. PMID: 25593604 Free PMC article.

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