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Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism.
De Sanctis L, Romagnolo D, Olivero M, Buzi F, Maghnie M, Scirè G, Crino A, Baroncelli GI, Salerno M, Di Maio S, Cappa M, Grosso S, Rigon F, Lala R, De Sanctis C, Dianzani I. De Sanctis L, et al. Among authors: salerno m. Pediatr Res. 2003 May;53(5):749-55. doi: 10.1203/01.PDR.0000059752.07086.A2. Epub 2003 Mar 5. Pediatr Res. 2003. PMID: 12621129
Liver abnormalities in Turner syndrome.
Salerno M, Di Maio S, Gasparini N, Rizzo M, Ferri P, Vajro P. Salerno M, et al. Eur J Pediatr. 1999 Aug;158(8):618-23. doi: 10.1007/s004310051163. Eur J Pediatr. 1999. PMID: 10445338
Liver abnormalities during growth hormone treatment.
Salerno M, Di Maio S, Ferri P, Lettiero T, Di Maria F, Vajro P. Salerno M, et al. J Pediatr Gastroenterol Nutr. 2000 Aug;31(2):149-51. doi: 10.1097/00005176-200008000-00011. J Pediatr Gastroenterol Nutr. 2000. PMID: 10941966
[Hirsutism and hypertrichosis].
Di Maio S, Salerno M, Tenore A. Di Maio S, et al. Among authors: salerno m. Minerva Pediatr. 2000 Sep;52(9):469-73. Minerva Pediatr. 2000. PMID: 11126652 Review. Italian. No abstract available.
[Adolescents with chronic pathology: body image].
Officioso A, Salerno M, Bruzzese E, Alessio M, Di Maio S. Officioso A, et al. Among authors: salerno m. Minerva Pediatr. 2000 Oct;52(10):539-40. Minerva Pediatr. 2000. PMID: 11144736 Italian. No abstract available.
Monitoring therapy for central precocious puberty.
Salerno M, Di Maio S, Tenore A. Salerno M, et al. Pediatrics. 2002 Dec;110(6):1255; author reply 1255. doi: 10.1542/peds.110.6.1255. Pediatrics. 2002. PMID: 12456929 No abstract available.
1,014 results