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Page 1
Mitchell-Riley Syndrome: Improving Clinical Outcomes and Searching for Functional Impact of RFX-6 Mutations.
Passone CGB, Vermillac G, Staels W, Besancon A, Kariyawasam D, Godot C, Lambe C, Talbotec C, Girard M, Chardot C, Berteloot L, Hachem T, Lapillonne A, Poidvin A, Storey C, Neve M, Stan C, Dugelay E, Fauret-Amsellem AL, Capri Y, Cavé H, Ybarra M, Chandra V, Scharfmann R, Bismuth E, Polak M, Carel JC, Pigneur B, Beltrand J. Passone CGB, et al. Front Endocrinol (Lausanne). 2022 Jun 22;13:802351. doi: 10.3389/fendo.2022.802351. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35813646 Free PMC article.
Growth Hormone Treatment for Adults With Prader-Willi Syndrome: A Meta-Analysis.
Rosenberg AGW, Passone CGB, Pellikaan K, Damiani D, van der Lely AJ, Polak M, Bernardo WM, de Graaff LCG. Rosenberg AGW, et al. Among authors: passone cgb. J Clin Endocrinol Metab. 2021 Sep 27;106(10):3068-3091. doi: 10.1210/clinem/dgab406. J Clin Endocrinol Metab. 2021. PMID: 34105729 Free PMC article.
COMPLEXITY OF PEDIATRIC CHRONIC DISEASE: CROSS-SECTIONAL STUDY WITH 16,237 PATIENTS FOLLOWED BY MULTIPLE MEDICAL SPECIALTIES.
Passone CGB, Grisi SJ, Farhat SC, Manna TD, Pastorino AC, Alveno RA, Miranda CVS, Waetge AR, Cordon MN, Odone-Filho V, Tannuri U, Carvalho WB, Carneiro-Sampaio M, Silva CA. Passone CGB, et al. Rev Paul Pediatr. 2019 Nov 25;38:e2018101. doi: 10.1590/1984-0462/2020/38/2018101. eCollection 2020. Rev Paul Pediatr. 2019. PMID: 31778404 Free PMC article.
Clinical application of ACMG-AMP guidelines in HNF1A and GCK variants in a cohort of MODY families.
Santana LS, Caetano LA, Costa-Riquetto AD, Quedas EPS, Nery M, Collett-Solberg P, Boguszewski MCS, Vendramini MF, Crisostomo LG, Floh FO, Zarabia ZI, Kohara SK, Guastapaglia L, Passone CGB, Sewaybricker LE, Jorge AAL, Teles MG. Santana LS, et al. Among authors: passone cgb. Clin Genet. 2017 Oct;92(4):388-396. doi: 10.1111/cge.12988. Epub 2017 Apr 12. Clin Genet. 2017. PMID: 28170077