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Year | Number of Results |
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2005 | 2 |
2006 | 1 |
2009 | 1 |
2020 | 1 |
2022 | 1 |
2024 | 1 |
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Page 1
Tungiasis: Case Report of a Traveller to Kenya.
Case Rep Dermatol. 2009 Sep 5;1(1):29-34. doi: 10.1159/000235654.
Case Rep Dermatol. 2009.
PMID: 20652110
Free PMC article.
Multi-Gene Next-Generation Sequencing for Molecular Diagnosis of Autosomal Recessive Congenital Ichthyosis: A Genotype-Phenotype Study of Four Italian Patients.
Fioretti T, Auricchio L, Piccirillo A, Vitiello G, Ambrosio A, Cattaneo F, Ammendola R, Esposito G.
Fioretti T, et al. Among authors: auricchio l.
Diagnostics (Basel). 2020 Nov 24;10(12):995. doi: 10.3390/diagnostics10120995.
Diagnostics (Basel). 2020.
PMID: 33255364
Free PMC article.
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Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry.
Limongelli G, Iucolano S, Monda E, Elefante P, De Stasio C, Lubrano I, Caiazza M, Mazzella M, Fimiani F, Galdo M, De Marchi G, Esposito M, Rubino M, Cirillo A, Fusco A, Esposito A, Trama U, Esposito S, Scarano G, Sepe J, Andria G, Orlando V, Menditto E, Chiodini P; Campania Rare Disease Network.
Limongelli G, et al.
J Public Health (Oxf). 2022 Aug 25;44(3):586-594. doi: 10.1093/pubmed/fdab137.
J Public Health (Oxf). 2022.
PMID: 33982102
Free PMC article.
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Comprehensive Molecular Analysis of Disease-Related Genes as First-Tier Test for Early Diagnosis, Classification, and Management of Patients Affected by Nonsyndromic Ichthyosis.
Fioretti T, Martora F, De Maggio I, Ambrosio A, Piscopo C, Vallone S, Amato F, Passaro D, Acquaviva F, Gaudiello F, Di Girolamo D, Maiolo V, Zarrilli F, Esposito S, Vitiello G, Auricchio L, Sammarco E, Brasi D, Petillo R, Gambale A, Cattaneo F, Ammendola R, Nappa P, Esposito G.
Fioretti T, et al. Among authors: auricchio l.
Biomedicines. 2024 May 17;12(5):1112. doi: 10.3390/biomedicines12051112.
Biomedicines. 2024.
PMID: 38791074
Free PMC article.
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Cutaneous manifestations as presenting sign of autoimmune lymphoproliferative syndrome in childhood.
Auricchio L, Vitiello L, Adriani M, Ferri P, Chiocchetti A, Pettinato G, Racioppi L, Maiuri L, Dianzani U, Pignata C.
Auricchio L, et al.
Dermatology. 2005;210(4):336-40. doi: 10.1159/000084762.
Dermatology. 2005.
PMID: 15942224
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Nail dystrophy associated with a heterozygous mutation of the nude/SCID human FOXN1 (WHN) gene.
Auricchio L, Adriani M, Frank J, Busiello R, Christiano A, Pignata C.
Auricchio L, et al.
Arch Dermatol. 2005 May;141(5):647-8. doi: 10.1001/archderm.141.5.647.
Arch Dermatol. 2005.
PMID: 15897400
No abstract available.
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Epidermolysis bullosa simplex with mottled pigmentation due to de novo P25L mutation in keratin 5 in an Italian patient.
Pascucci M, Posteraro P, Pedicelli C, Provini A, Auricchio L, Paradisi M, Castiglia D.
Pascucci M, et al. Among authors: auricchio l.
Eur J Dermatol. 2006 Nov-Dec;16(6):620-2.
Eur J Dermatol. 2006.
PMID: 17229601
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