NUCARO, ANNA LISA
NUCARO, ANNA LISA
Istituto di Ricerca Genetica e Biomedica - IRGB
X-Linked Mental Retardation and Conjuntival Teleangectasias: Correction of the Previously Reported Karyotype.
2014 Cianchetti, Carlo; Nucaro, ANNA LISA
Microbial changes in subgigival plaque and polymicrobial intracellular flora in buccal cells after fixed orthodontic appliance therapy: a preliminary study
2013 C Montaldo; M Erriu; FMG Pili; C Peluffo; A Nucaro; G Orrù G; Denotti
Cryptic chromosome rearrangements in five patients, with normal and/or abnormal karyotype...
2012 Cabras, V; Milia, A; Montaldo, C; Nucaro, A
Detection of cryptic chromosome rearrangements by Bac Genome Array- CGH in five patients with normal and/or abnormal karyotype...
2012 Cabras, V; Milia, A; Montaldo, C; Nucaro, A
Individuazione di riarrangiamenti cromosomici criptici in 5 pazienti con RM associato ad autismo e/o epilessia mediante Array-CGH....
2012 Nucaro, A; Cabras, V; Zorco, S; Milia, A; Montaldo, C
Ring 20 syndrome mosaicism and epilepsy: a case with duplication of two Bac clones in 2oq11.21-q11.22 defined by genome array- CGH.
2012 Cabras V; Erriu M; Loi M; Milia A; Montaldo C; Nucaro A.
The down-up bone bridge approach for cochlear and middle ear implants: our experience in 34 patients.
2012 Achena, F; Montaldo, C; Nucaro, A
A new variant of Potocky- Lupsky syndrome in two unrelated patients affected by severe epileptic encephalopathy, detected by Genome Array-CGH.
2011 Nucaro, ANNA LISA; Montaldo, Caterina; Zorco, Stefania; Santini, Noemi; Dettori, Tinuccia; Caria, Paola; Milia, Angela; Cianchetti, Carlo; Pruna, Dario
Chromosome 8p23.2-pter: a critical region for mental retardation, autism and epilepsy?
2011 A. Nucaro; T. Pisano; I. Chillotti; C. Montaldo; D. Pruna
Detection of a BAC clone duplication in 17p11.2 in two unrelated patients, affected by severe epileptic encephalopathy, by Genome Array-CGH: a new variant of Potocky- Lupsky syndrome?
2011 Nucaro, ANNA LISA; Montaldo, Caterina; Dettori, Tinuccia; Caria, Paola; Zorco Noemi Santini, Stefania; Milia, Angela; Vanni, Roberta; Cianchetti, Carlo; Pruna, Dario
DUPLICAZIONE 17p11.2 IN DUE PAZIENTI CON ENCEFALOPATIA EPILETTICA: VARIANTE DELLA SINDROME DI POTOCKI-LUPSKI O NUOVA ENTITA SINDROMICA?
2011 Nucaro, A; Asunis, M; Montaldo, C; Virdis, M; Madeddu, F; Serci, Mc; Cianchetti, C; Pruna, D
Encefalopatia epilettica da duplicazione 17p11.2: due pazienti con variante della sindrome di Potocki-Lupski o una nuova entità sindromica?
2011 Asunis, M; Nucaro, A; Madeddu, F; Serci, Mc; Cianchetti, C; Pruna, D
HLA-DQB1 HAPLOTYPES AND THEIR RELATION TO ORAL SIGNS LINKED TO CELIAC DISEASE DIAGNOSIS.
2011 Erriu, M; Sanna, S; Nucaro, A; Orru, G; Garau, V; Montaldo, C
A new case of dup/del 8p associated with autism and epilepsy detected by genome array- CGH.
2010 A. Nucaro; T. Pisano; I. Chillotti; S. Zorco; N. Santini; C. Montaldo; C. Cianchetti; D. Pruna.
A rapid method for HLA haplotype typization. A preliminary study on celiac disease
2010 Erriu M; Boscarelli F; Peluffo C; Orrù G; Nucaro A; Zorco S; Santini N; Montaldo C
METHYLENTETRAHYDROFOLATE REDUCTASE (MTHFR) C677T POLYMORPHISMS IN SARDINIAN AND SICILIAN CROHN S DISEASE PATIENTS: EVIDENCE FOR GENETIC HETEROGENEITY WITHIN MEDITERRANEAN AREAS?
2010 R. ROSSINO; L. LOY; L. RIGOLI; S. COMUNALE; A. GILLI; C. SARDU; F. DANJOU; A. NUCARO; F. BOY; M. CONGIA; W. FRIES; P. USAI.
Paraplegia spastica progressiva come segno associato di tetrasomia 18p.
2010 A. Nucaro; I. Chillotti; T. Pisano; D. Pruna; C. Cianchetti.
POLIMORFISMI DEL GENE MTHFR SU PAZIENTI SARDI CON IDB: STUDIO PRELIMINARE.
2010 Rossino, R; Diana, D; Erriu, M; Montaldo, C; Milia, A; Nucaro, A; Usai, P; Congia, M
PREVALENZA E SCOMPARSA A LIVELLO ORALE DEL PAPILLOMA VIRUS UMANO AD ALTO RISCHIO (HR-HPV) IN UNA POPOLAZIONE SANA PRESSO LA COMUNITA DI RECUPERO DI SAN PATRIGNANO
2010 Peluffo, C; Zorco, S; Santini, N; Erriu, M; Orru, G; Nucaro, A; Montaldo, C
Progressive spastic paraplegia as a feature of tetrasomy 18p
2010 Nucaro, A; Chillotti, I; Pisano, T; Pruna, D; Cianchetti, C