A. Gargiulo

Lamin A/C sustains PcG protein architecture, maintaining transcriptional repression at target genes

E. Cesarini, F. Marullo, B. Bodega, 2015, The Journal of cell biology.

Immunohistochemical and immunochemical characterization of the distribution of leptin‐like proteins in the gastroenteric tract of two teleosts (Dicentrarchus labrax and Carassius auratus L.) with different feeding habits

P. De Girolamo, E. Varricchio, A. Gargiulo, 2011, Microscopy research and technique.

Ultrastructural Modifications of Cells in the Intestine of Dugesia Lugubris

A. Gargiulo, R. Pascolini, 1975 .

Efficacy of a combined intracerebral and systemic gene delivery approach for the treatment of a severe lysosomal storage disorder.

A. Ballabio, A. Fraldi, E. Surace, 2011, Molecular therapy : the journal of the American Society of Gene Therapy.

AAV-mediated tyrosinase gene transfer restores melanogenesis and retinal function in a model of oculo-cutaneous albinism type I (OCA1).

E. Surace, L. Domenici, A. Auricchio, 2009, Molecular therapy : the journal of the American Society of Gene Therapy.

Molecular and clinical characterization of albinism in a large cohort of Italian patients.

A. Ciccodicola, E. Surace, E. Fazzi, 2011, Investigative ophthalmology & visual science.

MicroRNA-Restricted Transgene Expression in the Retina

E. Surace, S. Banfi, M. Bacci, 2011, PloS one.

Evaluation of Italian patients with leber congenital amaurosis due to AIPL1 mutations highlights the potential applicability of gene therapy.

E. Surace, S. Banfi, M. Bacci, 2011, Investigative ophthalmology & visual science.

Filamin A is mutated in X-linked chronic idiopathic intestinal pseudo-obstruction with central nervous system involvement.

A. Ciccodicola, A. Ballabio, W. Reardon, 2007, American journal of human genetics.

The Role of Optical Coherence Tomography in an Atypical Case of Oculocutaneous Albinism: A Case Report

E. Surace, F. Testa, S. Rossi, 2012, Case Reports in Ophthalmology.