Annicchiarico G - Search Results

1

Proinflammatory Cytokines and Antiskin Autoantibodies in Patients With Inherited Epidermolysis Bullosa.

Annicchiarico G, Morgese MG, Esposito S, Lopalco G, Lattarulo M, Tampoia M, Bonamonte D, Brunetti L, Vitale A, Lapadula G, Cantarini L, Iannone F. Annicchiarico G, et al. Medicine (Baltimore). 2015 Oct;94(42):e1528. doi: 10.1097/MD.0000000000001528. Medicine (Baltimore). 2015. PMID: 26496255 Free PMC article.

2

Prevalence of specific anti-skin autoantibodies in a cohort of patients with inherited epidermolysis bullosa.

Tampoia M, Bonamonte D, Filoni A, Garofalo L, Morgese MG, Brunetti L, Di Giorgio C, Annicchiarico G. Tampoia M, et al. Among authors: annicchiarico g. Orphanet J Rare Dis. 2013 Sep 4;8:132. doi: 10.1186/1750-1172-8-132. Orphanet J Rare Dis. 2013. PMID: 24007552 Free PMC article.

3

Canakinumab in recessive dystrophic epidermolysis bullosa: a novel unexpected weapon for non-healing wounds?

Annicchiarico G, Lopalco G, Morgese MG, Cantarini L, Iannone F. Annicchiarico G, et al. Clin Exp Rheumatol. 2016 Sep-Oct;34(5):961-962. Epub 2016 Feb 9. Clin Exp Rheumatol. 2016. PMID: 26885873 No abstract available.

4

Improvement of renal function in epidermolysis bullosa patients after gluten free diet: two cases.

Annicchiarico G, Morgese MG, Brunetti L, Tampoia M, Garofalo L, Aceto G, Fiore T, Mauro S, Minelli M. Annicchiarico G, et al. Eur Rev Med Pharmacol Sci. 2012 Oct;16 Suppl 4:138-41. Eur Rev Med Pharmacol Sci. 2012. PMID: 23090831

5

Psychiatric symptoms and quality of life in patients affected by epidermolysis bullosa.

Margari F, Lecce PA, Santamato W, Ventura P, Sportelli N, Annicchiarico G, Bonifazi E. Margari F, et al. Among authors: annicchiarico g. J Clin Psychol Med Settings. 2010 Dec;17(4):333-9. doi: 10.1007/s10880-010-9205-4. J Clin Psychol Med Settings. 2010. PMID: 21120591

6

Procedural analgesia with nitrous oxide at home for epidermolysis bullosa: A case report.

Murciano M, Laterza C, Attolini E, Storelli S, Dipietro G, Rubino A, Annicchiarico G. Murciano M, et al. Among authors: annicchiarico g. Medicine (Baltimore). 2022 Jan 7;101(1):e28474. doi: 10.1097/MD.0000000000028474. Medicine (Baltimore). 2022. PMID: 35029895 Free PMC article.

7

The Italian National Rare Diseases Registry.

Taruscio D, Kodra Y, Ferrari G, Vittozzi L; National Rare Diseases Registry Collaborating Group. Taruscio D, et al. Blood Transfus. 2014 Apr;12 Suppl 3(Suppl 3):s606-13. doi: 10.2450/2014.0064-14s. Blood Transfus. 2014. PMID: 24922301 Free PMC article.

8

ClC-1 mutations in myotonia congenita patients: insights into molecular gating mechanisms and genotype-phenotype correlation.

Imbrici P, Maggi L, Mangiatordi GF, Dinardo MM, Altamura C, Brugnoni R, Alberga D, Pinter GL, Ricci G, Siciliano G, Micheli R, Annicchiarico G, Lattanzi G, Nicolotti O, Morandi L, Bernasconi P, Desaphy JF, Mantegazza R, Camerino DC. Imbrici P, et al. Among authors: annicchiarico g. J Physiol. 2015 Sep 15;593(18):4181-99. doi: 10.1113/JP270358. Epub 2015 Jul 14. J Physiol. 2015. PMID: 26096614 Free PMC article.

9

Pro-Fibrotic Phenotype in a Patient with Segmental Stiff Skin Syndrome via TGF-β Signaling Overactivation.

Fusco C, Nardella G, Augello B, Boccafoschi F, Palumbo O, Fusaro L, Notarangelo A, Barbano R, Parrella P, Annicchiarico G, De Meco C, Micale L, Graziano P, Castori M. Fusco C, et al. Among authors: annicchiarico g. Int J Mol Sci. 2020 Jul 20;21(14):5141. doi: 10.3390/ijms21145141. Int J Mol Sci. 2020. PMID: 32698527 Free PMC article.

10

Mid-Aortic Syndrome: A Rare Cause of Renovascular Hypertension in Childhood Treated Percutaneously with an Unusual Vascular Access.

Stea ED, Meliota G, Carbone V, Torres D, Santangelo L, Piscopo G, Giordano P, Annicchiarico G, Vairo U, Giordano M. Stea ED, et al. Among authors: annicchiarico g. Curr Pediatr Rev. 2020;16(4):320-324. doi: 10.2174/1573396316666200609170003. Curr Pediatr Rev. 2020. PMID: 32516103

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