Boonyawat B - Search Results

1

Combined de-novo mutation and non-random X-chromosome inactivation causing Wiskott-Aldrich syndrome in a female with thrombocytopenia.

Boonyawat B, Dhanraj S, Al Abbas F, Zlateska B, Grunenbaum E, Roifman CM, Steele L, Meyn S, Blanchette V, Scherer SW, Swierczek S, Prchal J, Zhu Q, Torgerson TR, Ochs HD, Dror Y. Boonyawat B, et al. J Clin Immunol. 2013 Oct;33(7):1150-5. doi: 10.1007/s10875-013-9927-9. Epub 2013 Aug 14. J Clin Immunol. 2013. PMID: 23943155

2

Bone marrow failure and developmental delay caused by mutations in poly(A)-specific ribonuclease (PARN).

Dhanraj S, Gunja SM, Deveau AP, Nissbeck M, Boonyawat B, Coombs AJ, Renieri A, Mucciolo M, Marozza A, Buoni S, Turner L, Li H, Jarrar A, Sabanayagam M, Kirby M, Shago M, Pinto D, Berman JN, Scherer SW, Virtanen A, Dror Y. Dhanraj S, et al. Among authors: boonyawat b. J Med Genet. 2015 Nov;52(11):738-48. doi: 10.1136/jmedgenet-2015-103292. Epub 2015 Sep 4. J Med Genet. 2015. PMID: 26342108

3

A novel mutation of WAS gene in a boy with Mycobacterium bovis infection in spleen.

Pacharn P, Boonyawat B, Tantemsapya N, Visitsunthorn N, Jirapongsananuruk O. Pacharn P, et al. Among authors: boonyawat b. Asian Pac J Allergy Immunol. 2017 Sep;35(3):166-170. doi: 10.12932/AP0792. Asian Pac J Allergy Immunol. 2017. PMID: 27996282 Free article.

4

X-Linked Chronic Granulomatous Disease: Initial Presentation with Intracranial Hemorrhage from Vitamin K Deficiency in Infant.

Boonyawat B, Suksawat Y, Pacharn P, Suwanpakdee P, Traivaree C. Boonyawat B, et al. Case Rep Pediatr. 2018 Jun 24;2018:7041204. doi: 10.1155/2018/7041204. eCollection 2018. Case Rep Pediatr. 2018. PMID: 30034904 Free PMC article.

5

Three novel homozygous ITGB2 mutations among two patients with leukocyte adhesion defect type-1: Two case reports.

Suksawat Y, Pacharn P, Siripipattanamongkol N, Boonyawat B. Suksawat Y, et al. Among authors: boonyawat b. World J Clin Pediatr. 2022 Sep 9;11(5):429-436. doi: 10.5409/wjcp.v11.i5.429. eCollection 2022 Sep 9. World J Clin Pediatr. 2022. PMID: 36185095 Free PMC article.

6

A First Case Report of Subependymoma in PTPN11 Mutation-Associated Noonan Syndrome.

Boonyawat B, Charoenpitakchai M, Suwanpakdee P. Boonyawat B, et al. Case Rep Neurol Med. 2019 Sep 16;2019:6091059. doi: 10.1155/2019/6091059. eCollection 2019. Case Rep Neurol Med. 2019. PMID: 31637070 Free PMC article.

7

Molecular analysis of beta-globin gene mutations among Thai beta-thalassemia children: results from a single center study.

Boonyawat B, Monsereenusorn C, Traivaree C. Boonyawat B, et al. Appl Clin Genet. 2014 Dec 10;7:253-8. doi: 10.2147/TACG.S73058. eCollection 2014. Appl Clin Genet. 2014. PMID: 25525381 Free PMC article.

8

Genotype-phenotype correlation among beta-thalassemia and beta-thalassemia/HbE disease in Thai children: predictable clinical spectrum using genotypic analysis.

Traivaree C, Monsereenusorn C, Rujkijyanont P, Prasertsin W, Boonyawat B. Traivaree C, et al. Among authors: boonyawat b. J Blood Med. 2018 Apr 10;9:35-41. doi: 10.2147/JBM.S159295. eCollection 2018. J Blood Med. 2018. PMID: 29695942 Free PMC article.

9

Disseminated cryptococcosis in two boys with novel mutation of CD40 Ligand-Associated X-linked hyper-IgM syndrome.

Pacharn P, Phongsamart W, Boonyawat B, Jirapongsananuruk O, Visitsunthorn N, Chokephaibulkit K. Pacharn P, et al. Among authors: boonyawat b. Asian Pac J Allergy Immunol. 2021 Mar;39(1):31-34. doi: 10.12932/AP-140218-0265. Asian Pac J Allergy Immunol. 2021. PMID: 30447657 Free article.

10

Clinical and molecular genetic features of Hb H and AE Bart's diseases in central Thai children.

Traivaree C, Boonyawat B, Monsereenusorn C, Rujkijyanont P, Photia A. Traivaree C, et al. Among authors: boonyawat b. Appl Clin Genet. 2018 Apr 3;11:23-30. doi: 10.2147/TACG.S161152. eCollection 2018. Appl Clin Genet. 2018. PMID: 29662324 Free PMC article.

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