ROMEO, NELIDE
ROMEO, NELIDE
Istituto per i Sistemi Agricoli e Forestali del Mediterraneo - ISAFOM
HOMOZYGOUS R596G VARIANT IN TRIM32 GENE RELATED TO LGMD IN A NON-HUTTERITE PATIENT
2023 Patrizia Spadafora; Luigi Citrigno; Selene De Benedittis; Antonio Qualtieri; Francesca Cavalcanti; Gemma Di Palma; Olivier Gallo; Nelide Romeo
I villaggi della Riforma agraria in Sila: uno studio di caso
2022 ANTONELLA VELTRI; MASSIMO VELTRI; NELIDE ROMEO; ENZO VALENTE; SONIA VIVONA
Genomic analysis identifies a new EIF2B3 gene variant detected in an uncertain case of CADASIL disease
2021 A Cerantonio; S De Benedittis; PL Lanza; M Muglia; F Cavalcanti; P Spadafora; N Romeo; O Gallo; G Di Palma; R Mazzei; A Qualtieri; L Citrigno;
La ricerca del benessere attraverso la permanenza in ambienti naturali: uno studio di caso in epoca Covid-19
2021 Sonia Vivona; Nelide Romeo; Paola Sdao; Antonella Veltri
LC-MALDI-TOF ISD MS analysis is an effective, simple and rapid method of investigation for histones characterization: Application to EBV lymphoblastoid cell lines
2021 DE BENEDITTIS, Selene; Gaspari, Marco; Magariello, Angela; Spadafora, Patrizia; Citrigno, Luigi; Romeo, Nelide; Qualtieri, Antonio
IDENTITA' FEMMINILE E SCLEROSI MULTIPLA
2018 ROMEO NELIDE; QUALTIERI ANTONIO; MAGARIELLO ANGELA; DE BENEDITTIS SELENE; SPADAFORA PATRIZIA
Tay Sachs in South Italy
2017 Spadafora, Patrizia; Tagarelli, Giuseppe; Romeo, Nelide; Liguori, Maria
G56S and ARG143SER mutations in CAV3 and FKRP gene respectively contribute to the expression of phenotypic characteristics of an LGMD patient of southern Italy
2016 Patrizia Spadafora; Antonio Qualtieri; Nelide Romeo; Angelo Bagalà; Matteo De Bartolo
Identification of a patient affected by "Juvenile-chronic" Tay Sachs disease in South Italy.
2016 Maria Liguori; Giuseppe Tagarelli; Nelide Romeo; Angelo Bagalà; Patrizia Spadafora
From Disease to Holiness: Religious-based health remedies of Italian folk medicine (XIX-XX century)
2015 Nelide Romeo; Olivier Gallo; Giuseppe Tagarelli
An Italian child with myophosphorylase deficiency but with no detectable mutation in the exons of the PYGM gene
2014 Spadafora, Patrizia; Romeo, Nelide; Qualtieri, Antonio
Color vision inpatients with Parkinson disease. Usefulness of three pseudoisochromatic tests
2011 Tagarelli A.; Piro A.; Tagarelli G.; Lagonia P.; Romeo N.; Nicoletti G.; Gambardella A.; Fletcher R.; Quattrone A.
Colour vision in patients with Parkinson disease. Usefulness of three pseudoisochromatic tests
2011 Tagarelli, A; Piro, A; Tagarelli, G; Lagonia, P; Romeo, N; Nicoletti, G; Gambardella, A; Fletcher, R; Quattrone, A
Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease.
2008 DE MARCO, ELVIRA VALERIA; Tarantino, P; Rocca, Fe; Provenzano, G; Civitelli, D; De Luca, V; Annesi, F; Carrideo, S; Cirò Candiano, Ic; Romeo, N; Nicoletti, G; Marconi, R; Novellino, F; Morelli, M; Quattrone, A; Annesi, G
Dopaminergic modulation of cognitive interference after pharmacological washout in Parkinson's disease
2007 Fera, F; Nicoletti, G; Cerasa, A; Romeo, N; Gallo, O; Gioia, Mc; Arabia, G; Pugliese, P; Zappia, M; Quattrone, A
Dopaminergic modulation of cognitive interference after pharmacological washout in parkinson's disease
2007 Fera, F; Nicoletti, G; Cerasa, A; Romeo, N; Gallo, O; Arabia, G; Pugliese, P; Zappia, M; Quattrone, A
Fas antigen and sporadic Alzheimer's disease in Southern Italy:evaluation of two polymorphisms in the TNFRSF6 gene.
2007 Andreoli, Virginia; Nicoletti, Giuseppe; Romeo, Nelide; Condino, Francesca; La Russa, Antonella; Liguori, Maria; Manna, Ida; Spadafora, Patrizia; Quattrone, Aldo; Cittadella, Rita
Alzheimer s Disease and the Cystatin C gene polymorphism: an association study.
2006 Cittadella, R; Condino, F; Romeo, N; Nicoletti, G; Andreoli, V
Alzheimer's Disease and the Cystatin C gene polymorphism: an association study
2006 Cittadella R.;Condino F.;Romeo N.;Nicoletti G.;Andreoli V.
Genetic association of a cystatin C gene polymorphism with late-onset Alzheimer disease.
2006 Andreoli, V; Trecroci, F; Condino, F; Romeo, N; Nicoletti, G; Valentino, P; Cittadella, R
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| HOMOZYGOUS R596G VARIANT IN TRIM32 GENE RELATED TO LGMD IN A NON-HUTTERITE PATIENT | 1-gen-2023 | Patrizia Spadafora; Luigi Citrigno; Selene De Benedittis; Antonio Qualtieri; Francesca Cavalcanti; Gemma Di Palma; Olivier Gallo; Nelide Romeo | |
| I villaggi della Riforma agraria in Sila: uno studio di caso | 1-gen-2022 | ANTONELLA VELTRI; MASSIMO VELTRI; NELIDE ROMEO; ENZO VALENTE; SONIA VIVONA | |
| Genomic analysis identifies a new EIF2B3 gene variant detected in an uncertain case of CADASIL disease | 1-gen-2021 | A Cerantonio; S De Benedittis; PL Lanza; M Muglia; F Cavalcanti; P Spadafora; N Romeo; O Gallo; G Di Palma; R Mazzei; A Qualtieri; L Citrigno; | |
| La ricerca del benessere attraverso la permanenza in ambienti naturali: uno studio di caso in epoca Covid-19 | 1-gen-2021 | Sonia Vivona; Nelide Romeo; Paola Sdao; Antonella Veltri | |
| LC-MALDI-TOF ISD MS analysis is an effective, simple and rapid method of investigation for histones characterization: Application to EBV lymphoblastoid cell lines | 1-gen-2021 | DE BENEDITTIS, Selene; Gaspari, Marco; Magariello, Angela; Spadafora, Patrizia; Citrigno, Luigi; Romeo, Nelide; Qualtieri, Antonio | |
| IDENTITA' FEMMINILE E SCLEROSI MULTIPLA | 1-gen-2018 | ROMEO NELIDE; QUALTIERI ANTONIO; MAGARIELLO ANGELA; DE BENEDITTIS SELENE; SPADAFORA PATRIZIA | |
| Tay Sachs in South Italy | 1-gen-2017 | Spadafora, Patrizia; Tagarelli, Giuseppe; Romeo, Nelide; Liguori, Maria | |
| G56S and ARG143SER mutations in CAV3 and FKRP gene respectively contribute to the expression of phenotypic characteristics of an LGMD patient of southern Italy | 1-gen-2016 | Patrizia Spadafora; Antonio Qualtieri; Nelide Romeo; Angelo Bagalà; Matteo De Bartolo | |
| Identification of a patient affected by "Juvenile-chronic" Tay Sachs disease in South Italy. | 1-gen-2016 | Maria Liguori; Giuseppe Tagarelli; Nelide Romeo; Angelo Bagalà; Patrizia Spadafora | |
| From Disease to Holiness: Religious-based health remedies of Italian folk medicine (XIX-XX century) | 1-gen-2015 | Nelide Romeo; Olivier Gallo; Giuseppe Tagarelli | |
| An Italian child with myophosphorylase deficiency but with no detectable mutation in the exons of the PYGM gene | 1-gen-2014 | Spadafora, Patrizia; Romeo, Nelide; Qualtieri, Antonio | |
| Color vision inpatients with Parkinson disease. Usefulness of three pseudoisochromatic tests | 1-gen-2011 | Tagarelli A.; Piro A.; Tagarelli G.; Lagonia P.; Romeo N.; Nicoletti G.; Gambardella A.; Fletcher R.; Quattrone A. | |
| Colour vision in patients with Parkinson disease. Usefulness of three pseudoisochromatic tests | 1-gen-2011 | Tagarelli, A; Piro, A; Tagarelli, G; Lagonia, P; Romeo, N; Nicoletti, G; Gambardella, A; Fletcher, R; Quattrone, A | |
| Alpha-synuclein promoter haplotypes and dementia in Parkinson's disease. | 1-gen-2008 | DE MARCO, ELVIRA VALERIA; Tarantino, P; Rocca, Fe; Provenzano, G; Civitelli, D; De Luca, V; Annesi, F; Carrideo, S; Cirò Candiano, Ic; Romeo, N; Nicoletti, G; Marconi, R; Novellino, F; Morelli, M; Quattrone, A; Annesi, G | |
| Dopaminergic modulation of cognitive interference after pharmacological washout in Parkinson's disease | 1-gen-2007 | Fera, F; Nicoletti, G; Cerasa, A; Romeo, N; Gallo, O; Gioia, Mc; Arabia, G; Pugliese, P; Zappia, M; Quattrone, A | |
| Dopaminergic modulation of cognitive interference after pharmacological washout in parkinson's disease | 1-gen-2007 | Fera, F; Nicoletti, G; Cerasa, A; Romeo, N; Gallo, O; Arabia, G; Pugliese, P; Zappia, M; Quattrone, A | |
| Fas antigen and sporadic Alzheimer's disease in Southern Italy:evaluation of two polymorphisms in the TNFRSF6 gene. | 1-gen-2007 | Andreoli, Virginia; Nicoletti, Giuseppe; Romeo, Nelide; Condino, Francesca; La Russa, Antonella; Liguori, Maria; Manna, Ida; Spadafora, Patrizia; Quattrone, Aldo; Cittadella, Rita | |
| Alzheimer s Disease and the Cystatin C gene polymorphism: an association study. | 1-gen-2006 | Cittadella, R; Condino, F; Romeo, N; Nicoletti, G; Andreoli, V | |
| Alzheimer's Disease and the Cystatin C gene polymorphism: an association study | 1-gen-2006 | Cittadella R.;Condino F.;Romeo N.;Nicoletti G.;Andreoli V. | |
| Genetic association of a cystatin C gene polymorphism with late-onset Alzheimer disease. | 1-gen-2006 | Andreoli, V; Trecroci, F; Condino, F; Romeo, N; Nicoletti, G; Valentino, P; Cittadella, R |