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A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotype.
Palumbo S, Cirillo G, Sanchez G, Aiello F, Fachin A, Baldo F, Pellegrin MC, Cassio A, Salerno M, Maghnie M, Faienza MF, Wasniewska M, Fintini D, Giacomozzi C, Ciccone S, Miraglia Del Giudice E, Tornese G, Grandone A. Palumbo S, et al. Among authors: baldo f. J Endocrinol Invest. 2023 Jun;46(6):1233-1240. doi: 10.1007/s40618-022-01997-y. Epub 2022 Dec 28. J Endocrinol Invest. 2023. PMID: 36577869
Delayed pubarche.
Baldo F, Barbi E, Tornese G. Baldo F, et al. Ital J Pediatr. 2021 Sep 6;47(1):180. doi: 10.1186/s13052-021-01134-0. Ital J Pediatr. 2021. PMID: 34488834 Free PMC article. Review.
A new family with a case of severe early-onset muscle fatigue and a peculiar maternally inherited painful swelling in chewing muscles associated with homoplasmic m.15992A>T mutation in mitochondrial tRNAPro.
Ghirigato E, Terenzi F, Baglivo M, Zanetti N, Baldo F, Murru FM, Bobbo M, Barbi E, Zeviani M, Bruno I, Lamantea E. Ghirigato E, et al. Among authors: baldo f. Neuromuscul Disord. 2023 Dec;33(12):972-977. doi: 10.1016/j.nmd.2023.11.001. Epub 2023 Nov 4. Neuromuscul Disord. 2023. PMID: 38030461
Infant with a big head and 'crossed' polysyndactyly.
Tamaro G, Baldo F, Spedicati B, Taddio A, Faletra F, Barbi E. Tamaro G, et al. Among authors: baldo f. J Paediatr Child Health. 2023 May;59(5):770-771. doi: 10.1111/jpc.16063. Epub 2022 Jun 18. J Paediatr Child Health. 2023. PMID: 35716028 No abstract available.
A child without kneecaps.
Baldo F, Magnolato A, Bruno I, Faletra F, Carbone M, Barbi E. Baldo F, et al. J Paediatr Child Health. 2022 Mar;58(3):550. doi: 10.1111/jpc.1_15519. J Paediatr Child Health. 2022. PMID: 35244310 No abstract available.
73 results