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Year | Number of Results |
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2019 | 1 |
2021 | 1 |
2023 | 1 |
2024 | 2 |
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Page 1
Thyroid Function Tests in Children and Adolescents With Trisomy 21: Definition of Syndrome-Specific Reference Ranges.
J Clin Endocrinol Metab. 2023 Oct 18;108(11):2779-2788. doi: 10.1210/clinem/dgad333.
J Clin Endocrinol Metab. 2023.
PMID: 37279507
Defining Kawasaki disease and pediatric inflammatory multisystem syndrome-temporally associated to SARS-CoV-2 infection during SARS-CoV-2 epidemic in Italy: results from a national, multicenter survey.
Cattalini M, Della Paolera S, Zunica F, Bracaglia C, Giangreco M, Verdoni L, Meini A, Sottile R, Caorsi R, Zuccotti G, Fabi M, Montin D, Meneghel A, Consolaro A, Dellepiane RM, Maggio MC, La Torre F, Marchesi A, Simonini G, Villani A, Cimaz R, Ravelli A, Taddio A; Rheumatology Study Group of the Italian Pediatric Society.
Cattalini M, et al.
Pediatr Rheumatol Online J. 2021 Mar 16;19(1):29. doi: 10.1186/s12969-021-00511-7.
Pediatr Rheumatol Online J. 2021.
PMID: 33726806
Free PMC article.
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Early anakinra treatment improves cardiac outcome of multisystem inflammatory syndrome in children, regardless of disease severity.
Taddio A, Della Paolera S, Abbagnato L, Agrusti A, Badolato R, Biscaro F, Caorsi R, Consolaro A, Dellepiane RM, Fabi M, Floretta I, Gattorno M, Giangreco M, La Torre F, Maggio MC, Mambelli L, Mauro A, Mastrolia MV, Meneghel A, Montin D, Ricci F, Simonini G, Smarrazzo A, Sottile R, Stucchi S, Tardi M, Verdoni L, Zuccotti G, Zunica F, Ravelli A, Cattalini M; Italian Society of Pediatric Rheumatology (ReumaPed).
Taddio A, et al.
Rheumatology (Oxford). 2024 Feb 1;63(2):366-375. doi: 10.1093/rheumatology/kead381.
Rheumatology (Oxford). 2024.
PMID: 37647645
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Endocrine, auxological and metabolic profile in children and adolescents with Down syndrome: from infancy to the first steps into adult life.
Molinari S, Fossati C, Nicolosi ML, Di Marco S, Faraguna MC, Limido F, Ocello L, Pellegrinelli C, Lattuada M, Gazzarri A, Lazzerotti A, Sala D, Vimercati C, Capitoli G, Daolio C, Biondi A, Balduzzi A, Cattoni A.
Molinari S, et al. Among authors: lazzerotti a.
Front Endocrinol (Lausanne). 2024 Apr 8;15:1348397. doi: 10.3389/fendo.2024.1348397. eCollection 2024.
Front Endocrinol (Lausanne). 2024.
PMID: 38654931
Free PMC article.
Review.
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Increasing evidence of hereditary lymphedema caused by CELSR1 loss-of-function variants.
Maltese PE, Michelini S, Ricci M, Maitz S, Fiorentino A, Serrani R, Lazzerotti A, Bruson A, Paolacci S, Benedetti S, Bertelli M.
Maltese PE, et al. Among authors: lazzerotti a.
Am J Med Genet A. 2019 Sep;179(9):1718-1724. doi: 10.1002/ajmg.a.61269. Epub 2019 Jun 18.
Am J Med Genet A. 2019.
PMID: 31215153
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