de Sanctis L - Search Results

1

de Sanctis L, Delmastro L, Russo MC, Matarazzo P, Lala R, de Sanctis C. de Sanctis L, et al. Among authors: de sanctis c. J Pediatr Endocrinol Metab. 2006 May;19 Suppl 2:577-82. doi: 10.1515/jpem.2006.19.s2.577. J Pediatr Endocrinol Metab. 2006. PMID: 16789620 Review.

2

[Diagnosis of ambiguous genitalia].

de Sanctis C, Einaudi S, De Sanctis L. de Sanctis C, et al. Among authors: de sanctis l. Arch Ital Urol Nefrol Androl. 1990 Mar;62(1):165-9. Arch Ital Urol Nefrol Androl. 1990. PMID: 2141711 Review. Italian.

3

Growth impairment, IGF I hyposecretion and thyroid dysfunction in children with perinatal HIV-1 infection.

Matarazzo P, Palomba E, Lala R, Ciuti E, Altare F, de Sanctis L, Tovo PA. Matarazzo P, et al. Among authors: de sanctis l. Acta Paediatr. 1994 Oct;83(10):1029-34. doi: 10.1111/j.1651-2227.1994.tb12977.x. Acta Paediatr. 1994. PMID: 7841697

4

Growth hormone treatment in irradiated children with brain tumors.

Corrias A, Picco P, Einaudi S, de Sanctis L, Besenzon L, Garrè ML, Brach del Prever A, de Sanctis C. Corrias A, et al. Among authors: de sanctis c, de sanctis l. J Pediatr Endocrinol Metab. 1997 Jan-Feb;10(1):41-9. doi: 10.1515/jpem.1997.10.1.41. J Pediatr Endocrinol Metab. 1997. PMID: 9364341

5

Searching for Arg201 mutations in the GNAS1 gene in Italian patients with McCune-Albright syndrome.

de Sanctis L, Romagnolo D, Greggio N, Genitori L, Lala R, de Sanctis C. de Sanctis L, et al. Among authors: de sanctis c. J Pediatr Endocrinol Metab. 2002;15 Suppl 3:883-9. J Pediatr Endocrinol Metab. 2002. PMID: 12199346

6

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: de sanctis c. 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

7

Pubertal development in patients with McCune-Albright syndrome or pseudohypoparathyroidism.

de Sanctis C, Lala R, Matarazzo P, Andreo M, de Sanctis L. de Sanctis C, et al. Among authors: de sanctis l. J Pediatr Endocrinol Metab. 2003 Mar;16 Suppl 2:293-6. J Pediatr Endocrinol Metab. 2003. PMID: 12729407 Review.

8

Brachydactyly in 14 genetically characterized pseudohypoparathyroidism type Ia patients.

de Sanctis L, Vai S, Andreo MR, Romagnolo D, Silvestro L, de Sanctis C. de Sanctis L, et al. Among authors: de sanctis c. J Clin Endocrinol Metab. 2004 Apr;89(4):1650-5. doi: 10.1210/jc.2003-030850. J Clin Endocrinol Metab. 2004. PMID: 15070926

9

Parental origin of Gsalpha mutations in the McCune-Albright syndrome and in isolated endocrine tumors.

Mantovani G, Bondioni S, Lania AG, Corbetta S, de Sanctis L, Cappa M, Di Battista E, Chanson P, Beck-Peccoz P, Spada A. Mantovani G, et al. Among authors: de sanctis l. J Clin Endocrinol Metab. 2004 Jun;89(6):3007-9. doi: 10.1210/jc.2004-0194. J Clin Endocrinol Metab. 2004. PMID: 15181091

10

McCune-Albright syndrome in a boy may present with a monolateral macroorchidism as an early and isolated clinical manifestation.

Arrigo T, Pirazzoli P, De Sanctis L, Leone O, Wasniewska M, Messina MF, De Luca F. Arrigo T, et al. Among authors: de sanctis l, de luca f. Horm Res. 2006;65(3):114-9. doi: 10.1159/000091279. Epub 2006 Feb 2. Horm Res. 2006. PMID: 16462147

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

214 results

Search Page