Weber G - Search Results

1

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. Among authors: weber g. J Clin Endocrinol Metab. 2000 Nov;85(11):4243-8. doi: 10.1210/jcem.85.11.6986. J Clin Endocrinol Metab. 2000. PMID: 11095461

2

Study of the effects of bromocriptine on sexual impotence.

Ambrosi B, Bara R, Travaglini P, Weber G, Beck Peccoz P, Rondena M, Elli R, Faglia G. Ambrosi B, et al. Among authors: weber g. Clin Endocrinol (Oxf). 1977 Nov;7(5):417-21. doi: 10.1111/j.1365-2265.1977.tb03351.x. Clin Endocrinol (Oxf). 1977. PMID: 338206 Clinical Trial.

3

Bone density and bone metabolism are normal after long-term gluten-free diet in young celiac patients.

Mora S, Barera G, Beccio S, Proverbio MC, Weber G, Bianchi C, Chiumello G. Mora S, et al. Among authors: weber g. Am J Gastroenterol. 1999 Feb;94(2):398-403. doi: 10.1111/j.1572-0241.1999.867_r.x. Am J Gastroenterol. 1999. PMID: 10022636

4

Molecular analysis of the Pendred's syndrome gene and magnetic resonance imaging studies of the inner ear are essential for the diagnosis of true Pendred's syndrome.

Fugazzola L, Mannavola D, Cerutti N, Maghnie M, Pagella F, Bianchi P, Weber G, Persani L, Beck-Peccoz P. Fugazzola L, et al. Among authors: weber g. J Clin Endocrinol Metab. 2000 Jul;85(7):2469-75. doi: 10.1210/jcem.85.7.6694. J Clin Endocrinol Metab. 2000. PMID: 10902795 Clinical Trial.

5

Post-surgical metabolic imbalance in adolescents with renal hypophosphatemic rickets.

Prinster C, Weber G, Beccio S, Meneghel M, Mora S, Chiumello G. Prinster C, et al. Among authors: weber g. J Pediatr Endocrinol Metab. 2000 Jun;13(6):657-8. doi: 10.1515/jpem.2000.13.6.657. J Pediatr Endocrinol Metab. 2000. PMID: 10905391 No abstract available.

6

Hyperplastic pituitary gland, high serum glycoprotein hormone alpha-subunit, and variable circulating thyrotropin (TSH) levels as hallmark of central hypothyroidism due to mutations of the TSH beta gene.

Bonomi M, Proverbio MC, Weber G, Chiumello G, Beck-Peccoz P, Persani L. Bonomi M, et al. Among authors: weber g. J Clin Endocrinol Metab. 2001 Apr;86(4):1600-4. doi: 10.1210/jcem.86.4.7411. J Clin Endocrinol Metab. 2001. PMID: 11297590

7

A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism.

Alberti L, Proverbio MC, Costagliola S, Weber G, Beck-Peccoz P, Chiumello G, Persani L. Alberti L, et al. Among authors: weber g. Eur J Endocrinol. 2001 Sep;145(3):249-54. doi: 10.1530/eje.0.1450249. Eur J Endocrinol. 2001. PMID: 11517004

8

Germline mutations of TSH receptor gene as cause of nonautoimmune subclinical hypothyroidism.

Alberti L, Proverbio MC, Costagliola S, Romoli R, Boldrighini B, Vigone MC, Weber G, Chiumello G, Beck-Peccoz P, Persani L. Alberti L, et al. Among authors: weber g. J Clin Endocrinol Metab. 2002 Jun;87(6):2549-55. doi: 10.1210/jcem.87.6.8536. J Clin Endocrinol Metab. 2002. PMID: 12050212

9

Recombinant human TSH testing is a valuable tool for differential diagnosis of congenital hypothyroidism during L-thyroxine replacement.

Fugazzola L, Persani L, Mannavola D, Reschini E, Vannucchi G, Weber G, Beck-Peccoz P. Fugazzola L, et al. Among authors: weber g. Clin Endocrinol (Oxf). 2003 Aug;59(2):230-6. doi: 10.1046/j.1365-2265.2003.01830.x. Clin Endocrinol (Oxf). 2003. PMID: 12864801

10

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. Among authors: weber g. 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.

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