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Expanding the phenotype of Wiedemann-Steiner syndrome: Craniovertebral junction anomalies.
Giangiobbe S, Caraffi SG, Ivanovski I, Maini I, Pollazzon M, Rosato S, Trimarchi G, Lauriello A, Marinelli M, Nicoli D, Baldo C, Laurie S, Flores-Daboub J, Provenzano A, Andreucci E, Peluso F, Rizzo R, Stewart H, Lachlan K, Bayat A, Napoli M, Carboni G, Baker J, Mendel A, Piatelli G, Pantaleoni C, Mattina T, Prontera P, Mendelsohn NJ, Giglio S, Zuffardi O, Garavelli L. Giangiobbe S, et al. Among authors: rizzo r. Am J Med Genet A. 2020 Dec;182(12):2877-2886. doi: 10.1002/ajmg.a.61859. Epub 2020 Oct 11. Am J Med Genet A. 2020. PMID: 33043602
A New Patient with Potocki-Lupski Syndrome: A Literature Review.
Praticò AD, Falsaperla R, Rizzo R, Ruggieri M, Verrotti A, Pavone P. Praticò AD, et al. Among authors: rizzo r. J Pediatr Genet. 2018 Mar;7(1):29-34. doi: 10.1055/s-0037-1604479. Epub 2017 Jul 27. J Pediatr Genet. 2018. PMID: 29441219 Free PMC article.
Support of the histaminergic hypothesis in Tourette syndrome: association of the histamine decarboxylase gene in a large sample of families.
Karagiannidis I, Dehning S, Sandor P, Tarnok Z, Rizzo R, Wolanczyk T, Madruga-Garrido M, Hebebrand J, Nöthen MM, Lehmkuhl G, Farkas L, Nagy P, Szymanska U, Anastasiou Z, Stathias V, Androutsos C, Tsironi V, Koumoula A, Barta C, Zill P, Mir P, Müller N, Barr C, Paschou P. Karagiannidis I, et al. Among authors: rizzo r. J Med Genet. 2013 Nov;50(11):760-4. doi: 10.1136/jmedgenet-2013-101637. Epub 2013 Jul 3. J Med Genet. 2013. PMID: 23825391
Treatment options for tic disorders.
Rizzo R, Gulisano M. Rizzo R, et al. Expert Rev Neurother. 2020 Jan;20(1):55-63. doi: 10.1080/14737175.2020.1698950. Epub 2019 Dec 3. Expert Rev Neurother. 2020. PMID: 31795779 Review.
849 results