Ciana G - Search Results

1

Chronic pain in Gaucher disease: skeletal or neuropathic origin?

Devigili G, De Filippo M, Ciana G, Dardis A, Lettieri C, Rinaldo S, Macor D, Moro A, Eleopra R, Bembi B. Devigili G, et al. Among authors: ciana g. Orphanet J Rare Dis. 2017 Aug 31;12(1):148. doi: 10.1186/s13023-017-0700-7. Orphanet J Rare Dis. 2017. PMID: 28859662 Free PMC article.

2

Long-term bone mineral density response to enzyme replacement therapy in a retrospective pediatric cohort of Gaucher patients.

Ciana G, Deroma L, Franzil AM, Dardis A, Bembi B. Ciana G, et al. J Inherit Metab Dis. 2012 Nov;35(6):1101-6. doi: 10.1007/s10545-012-9476-z. Epub 2012 Mar 23. J Inherit Metab Dis. 2012. PMID: 22441841

3

Did the temporary shortage in supply of imiglucerase have clinical consequences? Retrospective observational study on 34 italian Gaucher type I patients.

Deroma L, Sechi A, Dardis A, Macor D, Liva G, Ciana G, Bembi B. Deroma L, et al. Among authors: ciana g. JIMD Rep. 2013;7:117-22. doi: 10.1007/8904_2012_158. Epub 2012 Jul 1. JIMD Rep. 2013. PMID: 23430505 Free PMC article.

4

Long term effects of enzyme replacement therapy in an Italian cohort of type 3 Gaucher patients.

Sechi A, Deroma L, Dardis A, Ciana G, Bertin N, Concolino D, Linari S, Perria C, Bembi B. Sechi A, et al. Among authors: ciana g. Mol Genet Metab. 2014 Nov;113(3):213-8. doi: 10.1016/j.ymgme.2014.07.022. Epub 2014 Aug 4. Mol Genet Metab. 2014. PMID: 25127542

5

Bone complications in children with Gaucher disease.

Bembi B, Ciana G, Mengel E, Terk MR, Martini C, Wenstrup RJ. Bembi B, et al. Among authors: ciana g. Br J Radiol. 2002;75 Suppl 1:A37-44. doi: 10.1259/bjr.75.suppl_1.750037. Br J Radiol. 2002. PMID: 12036831 Review.

6

Long-term observational, non-randomized study of enzyme replacement therapy in late-onset glycogenosis type II.

Bembi B, Pisa FE, Confalonieri M, Ciana G, Fiumara A, Parini R, Rigoldi M, Moglia A, Costa A, Carlucci A, Danesino C, Pittis MG, Dardis A, Ravaglia S. Bembi B, et al. Among authors: ciana g. J Inherit Metab Dis. 2010 Dec;33(6):727-35. doi: 10.1007/s10545-010-9201-8. Epub 2010 Sep 14. J Inherit Metab Dis. 2010. PMID: 20838899 Clinical Trial.

7

Enzyme replacement therapy in juvenile glycogenosis type II: a longitudinal study.

Deroma L, Guerra M, Sechi A, Ciana G, Cisilino G, Dardis A, Bembi B. Deroma L, et al. Among authors: ciana g. Eur J Pediatr. 2014 Jun;173(6):805-13. doi: 10.1007/s00431-013-2258-2. Epub 2014 Jan 7. Eur J Pediatr. 2014. PMID: 24395639

8

Accurate Molecular Diagnosis of Gaucher Disease Using Clinical Exome Sequencing as a First-Tier Test.

Zampieri S, Cattarossi S, Pavan E, Barbato A, Fiumara A, Peruzzo P, Scarpa M, Ciana G, Dardis A. Zampieri S, et al. Among authors: ciana g. Int J Mol Sci. 2021 May 24;22(11):5538. doi: 10.3390/ijms22115538. Int J Mol Sci. 2021. PMID: 34073924 Free PMC article.

9

Value of the Rare Disease Registry of the Italian Region Friuli Venezia Giulia.

Valent F, Deroma L, Moro A, Ciana G, Martina P, De Martin F, Michelesio E, Da Riol MR, Macor D, Bembi B; Rare Disease Network of the Friuli Venezia Giulia Region. Valent F, et al. Among authors: ciana g. Value Health. 2019 Sep;22(9):1003-1011. doi: 10.1016/j.jval.2019.04.1917. Epub 2019 May 24. Value Health. 2019. PMID: 31511176 Free article.

10

In vitro and in vivo effects of Ambroxol chaperone therapy in two Italian patients affected by neuronopathic Gaucher disease and epilepsy.

Ciana G, Dardis A, Pavan E, Da Riol RM, Biasizzo J, Ferino D, Zanatta M, Boni A, Antonini L, Crichiutti G, Bembi B. Ciana G, et al. Mol Genet Metab Rep. 2020 Nov 21;25:100678. doi: 10.1016/j.ymgmr.2020.100678. eCollection 2020 Dec. Mol Genet Metab Rep. 2020. PMID: 33294373 Free PMC article.

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