Post-traumatic lipoma of the parotid gland: case report

Por Dispenza, F, De Stefano, A, Romano, G, Mazzoni, A
Publicado em 2008

Otosclerosis associated with type B-1 inner ear malformation

Por De Stefano, A, Dispenza, F, Aggarwal, N, Russo, A
Publicado em 2010

The discovery of stapes

Por DISPENZA, F., CAPPELLO, F, KULAMARVA, G., DE STEFANO, A.
Publicado em 2013

Canal switch and re-entry phenomenon in benign paroxysmal positional vertigo: difference between immediate and delayed occurrence

Por DISPENZA, F., DE STEFANO, A., COSTANTINO, C., RANDO, D., GIGLIONE, M., STAGNO, R., BENNICI, E.
Publicado no Acta Otorhinolaryngol Ital (2015)

Treatment of central and sensorineural tinnitus with orally administered Melatonin and Sulodexide: personal experience from a randomized controlled study

Por Neri, G, De Stefano, A, Baffa, C, Kulamarva, G, Di Giovanni, P, Petrucci, G, Poliandri, A, Dispenza, F, Citraro, L, Croce, A
Publicado em 2009

Systematic review with meta‐analysis: rifaximin is effective and safe for the treatment of small intestine bacterial overgrowth

Por Gatta, L., Scarpignato, C., McCallum, R.W., Lombardo, L., Pimentel, M., D'Incà, R., Gasbarrini, A., De Stefano, A., Cerda, E.
Publicado no Aliment Pharmacol Ther (2017)

Common Variants in the 5′ Region of the Leptin Gene Are Associated with Body Mass Index in Men from the National Heart, Lung, and Blood Institute Family Heart Study

Por Jiang, Y., Wilk, J. B., Borecki, I., Williamson, S., DeStefano, A. L., Xu, G., Liu, J., Ellison, R. C., Province, M., Myers, R. H.
Publicado em 2004

Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.

Por Bonné-Tamir, B., DeStefano, A. L., Briggs, C. E., Adair, R., Franklyn, B., Weiss, S., Korostishevsky, M., Frydman, M., Baldwin, C. T., Farrer, L. A.
Publicado em 1996

KRAS mutation detection by high-resolution melting analysis significantly predicts clinical benefit of cetuximab in metastatic colorectal cancer

Por Malapelle, U, Carlomagno, C, Salatiello, M, De Stefano, A, De Luca, C, Bianco, R, Marciano, R, Cimminiello, C, Bellevicine, C, De Placido, S, Troncone, G
Publicado em 2012

Autosomal dominant orthostatic hypotensive disorder maps to chromosome 18q.

Por DeStefano, A L, Baldwin, C T, Burzstyn, M, Gavras, I, Handy, D E, Joost, O, Martel, T, Nicolaou, M, Schwartz, F, Streeten, D H, Farrer, L A, Gavras, H
Publicado em 1998

The Alzheimer's Disease Sequencing Project: Study design and sample selection

Por Beecham, Gary W., Bis, J.C., Martin, E.R., Choi, S.-H., DeStefano, A. L., van Duijn, C.M., Fornage, M., Gabriel, S.B., Koboldt, D.C., Larson, D.E., Naj, A.C., Psaty, B.M., Salerno, W., Bush, W.S., Foroud, T.M., Wijsman, E., Farrer, L.A., Goate, A., Haines, J.L., Pericak-Vance, Margaret A., Boerwinkle, E., Mayeux, R., Seshadri, S., Schellenberg, G.
Publicado no Neurol Genet (2017)

ATP5H/KCTD2 locus is associated with Alzheimer's disease risk

Por Boada, M, Antúnez, C, Ramírez-Lorca, R, DeStefano, A L, González-Pérez, A, Gayán, J, López-Arrieta, J, Ikram, M A, Hernández, I, Marín, J, Galán, J J, Bis, J C, Mauleón, A, Rosende-Roca, M, Moreno-Rey, C, Gudnasson, V, Morón, F J, Velasco, J, Carrasco, J M, Alegret, M, Espinosa, A, Vinyes, G, Lafuente, A, Vargas, L, Fitzpatrick, A L, Launer, L J, Sáez, M E, Vázquez, E, Becker, J T, López, O L, Serrano-Ríos, M, Tárraga, L, van Duijn, C M, Real, L M, Seshadri, S, Ruiz, A
Publicado em 2014

Haplotypes and gene expression implicate the MAPT region for Parkinson disease: The GenePD Study

Por Tobin, J.E., Latourelle, J.C., Lew, M.F., Klein, C., Suchowersky, O., Shill, H.A., Golbe, L.I., Mark, M.H., Growdon, J.H., Wooten, G.F., Racette, B.A., Perlmutter, J.S., Watts, R., Guttman, M., Baker, K.B., Goldwurm, S., Pezzoli, G., Singer, C., Saint-Hilaire, M.H., Hendricks, A.E., Williamson, S., Nagle, M.W., Wilk, J.B., Massood, T., Laramie, J.M., DeStefano, A.L., Litvan, I., Nicholson, G., Corbett, A., Isaacson, S., Burn, D.J., Chinnery, P.F., Pramstaller, P.P., Sherman, S., Al-hinti, J., Drasby, E., Nance, M., Moller, A.T., Ostergaard, K., Roxburgh, R., Snow, B., Slevin, J.T., Cambi, F., Gusella, J.F., Myers, R.H.
Publicado em 2008