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Teplizumab and β-Cell Function in Newly Diagnosed Type 1 Diabetes.
Ramos EL, Dayan CM, Chatenoud L, Sumnik Z, Simmons KM, Szypowska A, Gitelman SE, Knecht LA, Niemoeller E, Tian W, Herold KC; PROTECT Study Investigators. Ramos EL, et al. N Engl J Med. 2023 Dec 7;389(23):2151-2161. doi: 10.1056/NEJMoa2308743. Epub 2023 Oct 18. N Engl J Med. 2023. PMID: 37861217 Clinical Trial.
[Primary peritonitis in an adolescent boy].
Farkas L, Lazáry G, Köves I, Csákváry V, Rónaky R, Nagy T. Farkas L, et al. Among authors: csakvary v. Orv Hetil. 2020 Jun;161(23):977-979. doi: 10.1556/650.2020.31757. Orv Hetil. 2020. PMID: 32453696 Hungarian.
Mutational spectrum of smith-lemli-opitz syndrome patients in hungary.
Balogh I, Koczok K, Szabó GP, Török O, Hadzsiev K, Csábi G, Balogh L, Dzsudzsák E, Ajzner E, Szabó L, Csákváry V, Oláh AV. Balogh I, et al. Among authors: csakvary v. Mol Syndromol. 2012 Nov;3(5):215-22. doi: 10.1159/000343923. Epub 2012 Nov 9. Mol Syndromol. 2012. PMID: 23293579 Free PMC article.
Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Macimorelin in Children with Suspected Growth Hormone Deficiency: An Open-Label, Group Comparison, Dose-Escalation Trial.
Csákváry V, Ammer N, Bagci EB, Bolshova OV, Damholt BB, Katanic D, Mikhailova E, Muzsnai Á, Raduk D, Senatorova G, Szalecki M, Teifel M, Vajda Z, Zelinska N, Chaychenko T. Csákváry V, et al. Horm Res Paediatr. 2021;94(7-8):239-250. doi: 10.1159/000519232. Epub 2021 Aug 26. Horm Res Paediatr. 2021. PMID: 34438400 Free article.
Neonatal severe hyperparathyroidism associated with a novel de novo heterozygous R551K inactivating mutation and a heterozygous A986S polymorphism of the calcium-sensing receptor gene.
Tõke J, Czirják G, Patócs A, Enyedi B, Gergics P, Csákváry V, Enyedi P, Tóth M. Tõke J, et al. Among authors: csakvary v. Clin Endocrinol (Oxf). 2007 Sep;67(3):385-92. doi: 10.1111/j.1365-2265.2007.02896.x. Epub 2007 Jun 7. Clin Endocrinol (Oxf). 2007. PMID: 17555508
12 results