Weber G - Search Results

1

Clinical and molecular heterogeneity in a large series of patients with hypophosphatemic rickets.

Capelli S, Donghi V, Maruca K, Vezzoli G, Corbetta S, Brandi ML, Mora S, Weber G. Capelli S, et al. Among authors: weber g. Bone. 2015 Oct;79:143-9. doi: 10.1016/j.bone.2015.05.040. Epub 2015 Jun 5. Bone. 2015. PMID: 26051471

2

Pseudohypoparathyroidism, an often delayed diagnosis: a case series.

Donghi V, Mora S, Zamproni I, Chiumello G, Weber G. Donghi V, et al. Among authors: weber g. Cases J. 2009 May 28;2:6734. doi: 10.1186/1757-1626-2-6734. Cases J. 2009. PMID: 19829854 Free PMC article.

3

Vitamin D dependent rickets, diagnostic and therapeutic difficulties: two case reports.

Donghi V, Di Frenna M, di Lascio A, Chiumello G, Weber G. Donghi V, et al. Among authors: weber g. J Pediatr Endocrinol Metab. 2011;24(9-10):801-5. doi: 10.1515/jpem.2011.214. J Pediatr Endocrinol Metab. 2011. PMID: 22145480

4

X-linked hypophosphatemic rickets: an Italian experts' opinion survey.

Emma F, Cappa M, Antoniazzi F, Bianchi ML, Chiodini I, Eller Vainicher C, Di Iorgi N, Maghnie M, Cassio A, Balsamo A, Baronio F, de Sanctis L, Tessaris D, Baroncelli GI, Mora S, Brandi ML, Weber G, D'Ausilio A, Lanati EP. Emma F, et al. Among authors: weber g. Ital J Pediatr. 2019 May 31;45(1):67. doi: 10.1186/s13052-019-0654-6. Ital J Pediatr. 2019. PMID: 31151476 Free PMC article.

5

Bone density in young patients with congenital adrenal hyperplasia.

Mora S, Saggion F, Russo G, Weber G, Bellini A, Prinster C, Chiumello G. Mora S, et al. Among authors: weber g. Bone. 1996 Apr;18(4):337-40. doi: 10.1016/8756-3282(96)00003-8. Bone. 1996. PMID: 8726391

6

Bone turnover in neonates: changes of urinary excretion rate of collagen type I cross-linked peptides during the first days of life and influence of gestational age.

Mora S, Prinster C, Bellini A, Weber G, Proverbio MC, Puzzovio M, Bianchi C, Chiumello G. Mora S, et al. Among authors: weber g. Bone. 1997 Jun;20(6):563-6. doi: 10.1016/s8756-3282(97)00035-5. Bone. 1997. PMID: 9177872

7

Autosomal dominant hypocalcemia with mild type 5 Bartter syndrome.

Vezzoli G, Arcidiacono T, Paloschi V, Terranegra A, Biasion R, Weber G, Mora S, Syren ML, Coviello D, Cusi D, Bianchi G, Soldati L. Vezzoli G, et al. Among authors: weber g. J Nephrol. 2006 Jul-Aug;19(4):525-8. J Nephrol. 2006. PMID: 17048213

8

Mild TSH resistance: Clinical and hormonal features in childhood and adulthood.

Vigone MC, Di Frenna M, Guizzardi F, Gelmini G, de Filippis T, Mora S, Caiulo S, Sonnino M, Bonomi M, Persani L, Weber G. Vigone MC, et al. Among authors: weber g. Clin Endocrinol (Oxf). 2017 Nov;87(5):587-596. doi: 10.1111/cen.13387. Epub 2017 Jul 6. Clin Endocrinol (Oxf). 2017. PMID: 28561265

9

Comparison of clinical-radiological and molecular findings in hypochondroplasia.

Prinster C, Carrera P, Del Maschio M, Weber G, Maghnie M, Vigone MC, Mora S, Tonini G, Rigon F, Beluffi G, Severi F, Chiumello G, Ferrari M. Prinster C, et al. Among authors: weber g. Am J Med Genet. 1998 Jan 6;75(1):109-12. doi: 10.1002/(sici)1096-8628(19980106)75:1<109::aid-ajmg22>3.0.co;2-p. Am J Med Genet. 1998. PMID: 9450868

10

Longitudinal changes of bone density and bone resorption in hyperthyroid girls during treatment.

Mora S, Weber G, Marenzi K, Signorini E, Rovelli R, Proverbio MC, Chiumello G. Mora S, et al. Among authors: weber g. J Bone Miner Res. 1999 Nov;14(11):1971-7. doi: 10.1359/jbmr.1999.14.11.1971. J Bone Miner Res. 1999. PMID: 10571698 Free article. Clinical Trial.

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