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Neuromuscular and Neuroendocrinological Features Associated With ZC4H2-Related Arthrogryposis Multiplex Congenita in a Sicilian Family: A Case Report.
Piccolo G, d'Annunzio G, Amadori E, Riva A, Borgia P, Tortora D, Maghnie M, Minetti C, Gitto E, Iacomino M, Baldassari S, Fiorillo C, Zara F, Striano P, Salpietro V. Piccolo G, et al. Front Neurol. 2021 Jul 12;12:704747. doi: 10.3389/fneur.2021.704747. eCollection 2021. Front Neurol. 2021. PMID: 34322088 Free PMC article.
Anterior chest wall deformities in children with neurofibromatosis type 1.
Chelleri C, Guerriero V, Torre M, Brolatti N, Piccolo G, Mattioli G, Boero S, Minetti C, Diana MC. Chelleri C, et al. Among authors: piccolo g. Acta Paediatr. 2021 Feb;110(2):594-595. doi: 10.1111/apa.15529. Epub 2020 Aug 29. Acta Paediatr. 2021. PMID: 32777120 No abstract available.
Caring for children and adolescents with type 1 diabetes mellitus: Italian Society for Pediatric Endocrinology and Diabetology (ISPED) statements during COVID-19 pandemia.
d'Annunzio G, Maffeis C, Cherubini V, Rabbone I, Scaramuzza A, Schiaffini R, Minuto N, Piccolo G, Maghnie M. d'Annunzio G, et al. Among authors: piccolo g. Diabetes Res Clin Pract. 2020 Oct;168:108372. doi: 10.1016/j.diabres.2020.108372. Epub 2020 Aug 20. Diabetes Res Clin Pract. 2020. PMID: 32827594 Free PMC article. Review.
Genotype-Phenotype Correlations in Neurofibromatosis Type 1: A Single-Center Cohort Study.
Scala M, Schiavetti I, Madia F, Chelleri C, Piccolo G, Accogli A, Riva A, Salpietro V, Bocciardi R, Morcaldi G, Di Duca M, Caroli F, Verrico A, Milanaccio C, Viglizzo G, Traverso M, Baldassari S, Scudieri P, Iacomino M, Piatelli G, Minetti C, Striano P, Garrè ML, De Marco P, Diana MC, Capra V, Pavanello M, Zara F. Scala M, et al. Among authors: piccolo g. Cancers (Basel). 2021 Apr 14;13(8):1879. doi: 10.3390/cancers13081879. Cancers (Basel). 2021. PMID: 33919865 Free PMC article.
RNF213 variant in a patient with Legius syndrome associated with moyamoya syndrome.
Romanisio G, Chelleri C, Scala M, Piccolo G, Carlini B, Gatti L, Capra V, Zara F, Bersano A, Pavanello M, De Marco P, Diana MC. Romanisio G, et al. Among authors: piccolo g. Mol Genet Genomic Med. 2021 Jun;9(6):e1669. doi: 10.1002/mgg3.1669. Epub 2021 May 3. Mol Genet Genomic Med. 2021. PMID: 33939317 Free PMC article. No abstract available.
Prominent and Regressive Brain Developmental Disorders Associated with Nance-Horan Syndrome.
Casto C, Dipasquale V, Ceravolo I, Gambadauro A, Aliberto E, Galletta K, Granata F, Ceravolo G, Falzia E, Riva A, Piccolo G, Cutrupi MC, Striano P, Accogli A, Zara F, Di Rosa G, Gitto E, Calì E, Efthymiou S, Salpietro V, Houlden H, Chimenz R. Casto C, et al. Among authors: piccolo g. Brain Sci. 2021 Aug 29;11(9):1150. doi: 10.3390/brainsci11091150. Brain Sci. 2021. PMID: 34573171 Free PMC article.
359 results