• 3157 Citations
  • 26 h-Index
20002019
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Fingerprint Dive into the research topics where Emiliano Giardina is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 1 Similar Profiles
Psoriasis Medicine & Life Sciences
Genes Medicine & Life Sciences
Psoriatic Arthritis Medicine & Life Sciences
Mutation Medicine & Life Sciences
Macular Degeneration Medicine & Life Sciences
Single Nucleotide Polymorphism Medicine & Life Sciences
Population Medicine & Life Sciences
DNA Medicine & Life Sciences

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Research Output 2000 2019

  • 3157 Citations
  • 26 h-Index
  • 110 Article
  • 3 Review article
  • 1 Letter

Atopic eczema: Genetic analysis of COL6A5, COL8A1, and COL10A1 in mediterranean populations

Strafella, C., Caputo, V., Minozzi, G., Milano, F., Arcangeli, M., Sobhy, N., Abdelmaksood, R., Hashad, D., Vakirlis, E., Novelli, G., Cascella, R. & Giardina, E., Jan 1 2019, In : BioMed Research International. 2019, 3457898.

Research output: Contribution to journalArticle

Open Access
Atopic Dermatitis
Gene encoding
Genes
Population
Biomarkers
1 Citation (Scopus)

Doyne honeycomb retinal dystrophy - Functional improvement following subthreshold nanopulse laser treatment: A case report

Cusumano, A., Falsini, B., Giardina, E., Cascella, R., Sebastiani, J. & Marshall, J., Jan 10 2019, In : Journal of Medical Case Reports. 13, 1, 5.

Research output: Contribution to journalArticle

Open Access
Lasers
Electroretinography
Visual Acuity
Therapeutics
Light Signal Transduction

Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era

Zampatti, S., Colantoni, L., Strafella, C., Galota, R. M., Caputo, V., Campoli, G., Pagliaroli, G., Carboni, S., Mela, J., Peconi, C., Gambardella, S., Cascella, R. & Giardina, E., Jan 1 2019, In : Neurogenetics.

Research output: Contribution to journalReview article

Facioscapulohumeral Muscular Dystrophy
Technology
Muscles
Professional Education
Inborn Genetic Diseases

Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis

Musumeci, M. L., Fiorentini, F., Bianchi, L., Cascella, R., Giardina, E., Caputo, V. & Micali, G., Oct 1 2019, In : Journal of the European Academy of Dermatology and Venereology : JEADV. 33, p. 36-39 4 p.

Research output: Contribution to journalArticle

Pachyonychia Congenita
Hidradenitis Suppurativa
Pilonidal Sinus
Cysts
Exons

Limb-Girdle Muscular Dystrophies (LGMDs): The clinical application of NGS analysis, a family case report

Strafella, C., Campoli, G., Galota, R. M., Caputo, V., Pagliaroli, G., Carboni, S., Zampatti, S., Peconi, C., Mela, J., Sancricca, C., Primiano, G., Minozzi, G., Servidei, S., Cascella, R. & Giardina, E., Jan 1 2019, In : Frontiers in Neurology. 10, JUN, 619.

Research output: Contribution to journalArticle

Open Access
Limb-Girdle Muscular Dystrophies
Cardiomyopathies
Mothers
Inheritance Patterns
Mutation