Mantovani G - Search Results

1

The Prevalence of GNAS Deficiency-Related Diseases in a Large Cohort of Patients Characterized by the EuroPHP Network.

Elli FM, Linglart A, Garin I, de Sanctis L, Bordogna P, Grybek V, Pereda A, Giachero F, Verrua E, Hanna P, Mantovani G, Perez de Nanclares G. Elli FM, et al. Among authors: mantovani g. J Clin Endocrinol Metab. 2016 Oct;101(10):3657-3668. doi: 10.1210/jc.2015-4310. Epub 2016 Jul 18. J Clin Endocrinol Metab. 2016. PMID: 27428667 Free article.

2

Mutational analysis of GNAS1 in patients with pseudohypoparathyroidism: identification of two novel mutations.

Mantovani G, Romoli R, Weber G, Brunelli V, De Menis E, Beccio S, Beck-Peccoz P, Spada A. Mantovani G, et al. J Clin Endocrinol Metab. 2000 Nov;85(11):4243-8. doi: 10.1210/jcem.85.11.6986. J Clin Endocrinol Metab. 2000. PMID: 11095461

3

Relevant cAMP-specific phosphodiesterase isoforms in human pituitary: effect of Gs(alpha) mutations.

Persani L, Borgato S, Lania A, Filopanti M, Mantovani G, Conti M, Spada A. Persani L, et al. Among authors: mantovani g. J Clin Endocrinol Metab. 2001 Aug;86(8):3795-800. doi: 10.1210/jcem.86.8.7779. J Clin Endocrinol Metab. 2001. PMID: 11502813

4

G protein mutations in endocrine diseases.

Lania A, Mantovani G, Spada A. Lania A, et al. Among authors: mantovani g. Eur J Endocrinol. 2001 Nov;145(5):543-59. doi: 10.1530/eje.0.1450543. Eur J Endocrinol. 2001. PMID: 11720871 Free article. Review.

5

The gsalpha gene: predominant maternal origin of transcription in human thyroid gland and gonads.

Mantovani G, Ballare E, Giammona E, Beck-Peccoz P, Spada A. Mantovani G, et al. J Clin Endocrinol Metab. 2002 Oct;87(10):4736-40. doi: 10.1210/jc.2002-020183. J Clin Endocrinol Metab. 2002. PMID: 12364467 Free article.

6

Growth hormone-releasing hormone resistance in pseudohypoparathyroidism type ia: new evidence for imprinting of the Gs alpha gene.

Mantovani G, Maghnie M, Weber G, De Menis E, Brunelli V, Cappa M, Loli P, Beck-Peccoz P, Spada A. Mantovani G, et al. J Clin Endocrinol Metab. 2003 Sep;88(9):4070-4. doi: 10.1210/jc.2002-022028. J Clin Endocrinol Metab. 2003. PMID: 12970263 Free article. Clinical Trial.

7

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. J Clin Endocrinol Metab. 2004 Jun;89(6):3007-9. doi: 10.1210/jc.2004-0194. J Clin Endocrinol Metab. 2004. PMID: 15181091

8

Biallelic expression of the Gsalpha gene in human bone and adipose tissue.

Mantovani G, Bondioni S, Locatelli M, Pedroni C, Lania AG, Ferrante E, Filopanti M, Beck-Peccoz P, Spada A. Mantovani G, et al. J Clin Endocrinol Metab. 2004 Dec;89(12):6316-9. doi: 10.1210/jc.2004-0558. J Clin Endocrinol Metab. 2004. PMID: 15579796

9

Resistance to growth hormone releasing hormone and gonadotropins in Albright's hereditary osteodystrophy.

Mantovani G, Spada A. Mantovani G, et al. J Pediatr Endocrinol Metab. 2006 May;19 Suppl 2:663-70. doi: 10.1515/jpem.2006.19.s2.663. J Pediatr Endocrinol Metab. 2006. PMID: 16789632 Review.

10

Mechanisms of disease: Mutations of G proteins and G-protein-coupled receptors in endocrine diseases.

Lania AG, Mantovani G, Spada A. Lania AG, et al. Among authors: mantovani g. Nat Clin Pract Endocrinol Metab. 2006 Dec;2(12):681-93. doi: 10.1038/ncpendmet0324. Nat Clin Pract Endocrinol Metab. 2006. PMID: 17143315 Review.

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