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Dr. Gottlieb et al reply.
Gottlieb C, Berard RA, Levy DM, Fortin E. Gottlieb C, et al. J Rheumatol. 2023 Jul 1:jrheum.2023-0509. doi: 10.3899/jrheum.2023-0509. Online ahead of print. J Rheumatol. 2023. PMID: 37399460
Canadian Rheumatology Association Recommendations for the Screening, Monitoring, and Treatment of Juvenile Idiopathic Arthritis-Associated Uveitis.
Berard R, Ng HY, Human A, Piskin D, Dhalla M, Gottlieb C, Batthish M, Chédeville G, Forest C, Fortin E, Gardiner J, Gerhold K, Jastrzebski A, Lang B, Miettunen PMH, Morgenstern S, Morin MP, Rosenberg A, Rumsey DG, Solarte CE, Tehrani N, Duffy KW, Pardo JP, Hazlewood GS, Levy DM. Berard R, et al. Among authors: gottlieb c. J Rheumatol. 2023 Mar;50(3):390-399. doi: 10.3899/jrheum.220261. Epub 2022 Oct 15. J Rheumatol. 2023. PMID: 36243417 Free article.
Specific combination of compound heterozygous mutations in 17β-hydroxysteroid dehydrogenase type 4 (HSD17B4) defines a new subtype of D-bifunctional protein deficiency.
McMillan HJ, Worthylake T, Schwartzentruber J, Gottlieb CC, Lawrence SE, Mackenzie A, Beaulieu CL, Mooyer PA; FORGE Canada Consortium; Wanders RJ, Majewski J, Bulman DE, Geraghty MT, Ferdinandusse S, Boycott KM. McMillan HJ, et al. Among authors: gottlieb cc. Orphanet J Rare Dis. 2012 Nov 22;7:90. doi: 10.1186/1750-1172-7-90. Orphanet J Rare Dis. 2012. PMID: 23181892 Free PMC article.
297 results