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Year | Number of Results |
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2017 | 2 |
2019 | 1 |
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Page 1
A Zebra at the Rodeo: Dyspnea, Hematuria, and a Family History of Arthritis.
Arthritis Care Res (Hoboken). 2022 Feb;74(2):165-170. doi: 10.1002/acr.24368. Epub 2022 Jan 5.
Arthritis Care Res (Hoboken). 2022.
PMID: 32598558
No abstract available.
A Novel STAT3 Mutation in a Qatari Patient With Hyper-IgE Syndrome.
Chaimowitz NS, Branch J, Reyes A, Vargas-Hernández A, Orange JS, Forbes LR, Ehlayel M, Purayil SC, Al-Nesf MA, Vogel TP.
Chaimowitz NS, et al. Among authors: branch j.
Front Pediatr. 2019 Apr 24;7:130. doi: 10.3389/fped.2019.00130. eCollection 2019.
Front Pediatr. 2019.
PMID: 31069200
Free PMC article.
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Th17/1 and ex-Th17 cells are detected in patients with polyarticular juvenile arthritis and increase following treatment.
Wood S, Branch J, Vasquez P, DeGuzman MM, Brown A, Sagcal-Gironella AC, Singla S, Ramirez A, Vogel TP.
Wood S, et al. Among authors: branch j.
Pediatr Rheumatol Online J. 2024 Mar 2;22(1):32. doi: 10.1186/s12969-024-00965-5.
Pediatr Rheumatol Online J. 2024.
PMID: 38431635
Free PMC article.
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Molecular Screening of 43 Brazilian Families Diagnosed with Leber Congenital Amaurosis or Early-Onset Severe Retinal Dystrophy.
Porto FBO, Jones EM, Branch J, Soens ZT, Maia IM, Sena IFG, Sampaio SAM, Simões RT, Chen R.
Porto FBO, et al. Among authors: branch j.
Genes (Basel). 2017 Nov 29;8(12):355. doi: 10.3390/genes8120355.
Genes (Basel). 2017.
PMID: 29186038
Free PMC article.
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Leveraging splice-affecting variant predictors and a minigene validation system to identify Mendelian disease-causing variants among exon-captured variants of uncertain significance.
Soens ZT, Branch J, Wu S, Yuan Z, Li Y, Li H, Wang K, Xu M, Rajan L, Motta FL, Simões RT, Lopez-Solache I, Ajlan R, Birch DG, Zhao P, Porto FB, Sallum J, Koenekoop RK, Sui R, Chen R.
Soens ZT, et al. Among authors: branch j.
Hum Mutat. 2017 Nov;38(11):1521-1533. doi: 10.1002/humu.23294. Epub 2017 Aug 18.
Hum Mutat. 2017.
PMID: 28714225
Free PMC article.
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