Weber G - Search Results

1

Thyroid function in patients with Prader-Willi syndrome: an Italian multicenter study of 339 patients.

Iughetti L, Vivi G, Balsamo A, Corrias A, Crinò A, Delvecchio M, Gargantini L, Greggio NA, Grugni G, Hladnik U, Pilotta A, Ragusa L, Salvatoni A, Wasniewska M, Weber G, Predieri B. Iughetti L, et al. Among authors: weber g. J Pediatr Endocrinol Metab. 2019 Feb 25;32(2):159-165. doi: 10.1515/jpem-2018-0388. J Pediatr Endocrinol Metab. 2019. PMID: 30703060

2

Measurement of urinary iodine excretion to reveal iodine excess in neonatal transient hypothyroidism.

Bona G, Chiorboli E, Rapa A, Weber G, Vigone MC, Chiumello G. Bona G, et al. Among authors: weber g. J Pediatr Endocrinol Metab. 1998 Nov-Dec;11(6):739-43. doi: 10.1515/jpem.1998.11.6.739. J Pediatr Endocrinol Metab. 1998. PMID: 9829229

3

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.

4

Accuracy of fine needle aspiration biopsy of thyroid nodules in detecting malignancy in childhood: comparison with conventional clinical, laboratory, and imaging approaches.

Corrias A, Einaudi S, Chiorboli E, Weber G, Crinò A, Andreo M, Cesaretti G, de Sanctis L, Messina MF, Segni M, Cicchetti M, Vigone M, Pasquino AM, Spera S, de Luca F, Mussa GC, Bona G. Corrias A, et al. Among authors: weber g. J Clin Endocrinol Metab. 2001 Oct;86(10):4644-8. doi: 10.1210/jcem.86.10.7950. J Clin Endocrinol Metab. 2001. PMID: 11600519

5

Thyroid function and puberty.

Weber G, Vigone MC, Stroppa L, Chiumello G. Weber G, et al. J Pediatr Endocrinol Metab. 2003 Mar;16 Suppl 2:253-7. J Pediatr Endocrinol Metab. 2003. PMID: 12729400 Review.

6

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

7

Defective function of Fas in T cells from paediatric patients with autoimmune thyroid diseases.

Bona G, Defranco S, Chiocchetti A, Indelicato M, Biava A, Difranco D, Dianzani I, Ramenghi U, Corrias A, Weber G, De Sanctis V, Iughetti L, Radetti G, Dianzani U. Bona G, et al. Among authors: weber g. Clin Exp Immunol. 2003 Sep;133(3):430-7. doi: 10.1046/j.1365-2249.2003.02221.x. Clin Exp Immunol. 2003. PMID: 12930371 Free PMC article.

8

Testicular microlithiasis: an unreported feature of McCune-Albright syndrome in males.

Wasniewska M, De Luca F, Bertelloni S, Matarazzo P, Weber G, Crisafulli G, Valenzise M, Lala R. Wasniewska M, et al. Among authors: weber g. J Pediatr. 2004 Nov;145(5):670-2. doi: 10.1016/j.jpeds.2004.06.083. J Pediatr. 2004. PMID: 15520771

9

Influence of gender and pubertal stage at diagnosis on growth outcome in childhood thyrotoxicosis: results of a collaborative study.

Cassio A, Corrias A, Gualandi S, Tato' L, Cesaretti G, Volta C, Weber G, Bona G, Cappa M, Bal M, Bellone J, Cicognani A. Cassio A, et al. Among authors: weber g. Clin Endocrinol (Oxf). 2006 Jan;64(1):53-7. doi: 10.1111/j.1365-2265.2005.02415.x. Clin Endocrinol (Oxf). 2006. PMID: 16402928

10

Clinical presentation of McCune-Albright syndrome in males.

Wasniewska M, Matarazzo P, Weber G, Russo G, Zampolli M, Salzano G, Zirilli G, Bertelloni S; Italian Study Group for Alterations of Gs alpha Protein Function. Wasniewska M, et al. Among authors: weber g. J Pediatr Endocrinol Metab. 2006 May;19 Suppl 2:619-22. doi: 10.1515/jpem.2006.19.s2.619. J Pediatr Endocrinol Metab. 2006. PMID: 16789625

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