Search Results - "Grieco, Gaetano S"

Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2 by Antonaci, Fabio, Ravaglia, Sabrina, Grieco, Gaetano S., Gagliardi, Stella, Cereda, Cristina, Costa, Alfredo

“…Background The mechanisms of genotype-phenotype interaction in Familiar Hemiplegic migraine type 2 (FHM2) are still far from clear. Different ATP1A2 mutations…”
Get full text

Possible Involvement of the CACNA1E Gene in Migraine: A Search for Single Nucleotide Polymorphism in Different Clinical Phenotypes by Ambrosini, Anna, D'Onofrio, Mara, Buzzi, Maria Gabriella, Arisi, Ivan, Grieco, Gaetano S., Pierelli, Francesco, Santorelli, Filippo M., Schoenen, Jean

“…Objective To search for differences in prevalence of a CACNA1E variant between migraine without aura, various phenotypes of migraine with aura, and healthy…”
Get full text

Genetics Influences Drug Consumption in Medication Overuse Headache, Not in Migraine: Evidence From Wolframin His611Arg Polymorphism Analysis by Di Lorenzo, Cherubino, Di Lorenzo, Giorgio, Coppola, Gianluca, Parisi, Vincenzo, Grieco, Gaetano S, Santorelli, Filippo Maria, Pascale, Esterina, Pierelli, Francesco

“…The Wolframin His611Arg polymorphism can influence drug consumption in psychiatric patients with impulsive addictive behavior. This cross-sectional study aims…”
Get full text

The Revolution in Migraine Genetics: From Aching Channels Disorders to a Next-Generation Medicine by Pellacani, Simona, Sicca, Federico, Di Lorenzo, Cherubino, Grieco, Gaetano S, Valvo, Giulia, Cereda, Cristina, Rubegni, Anna, Santorelli, Filippo M

“…Channelopathies are a heterogeneous group of neurological disorders resulting from dysfunction of ion channels located in cell membranes and organelles. The…”
Get full text

Migraine headache: a review of the molecular genetics of a common disorder by Di Lorenzo, Cherubino, Grieco, Gaetano S., Santorelli, Filippo M.

“…This tutorial summarises the state-of-the-art on migraine genetics and looks at the possible future direction of this field of research. The view of migraine…”
Get full text

Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy by BELLO, Luca, PIVA, Luisa, CHIARA MOTTA, Maria, GRIECO, Gaetano S, NAPOLITANO, Sara, MAGRI, Francesca, D'AMICO, Adele, ASTREA, Guja, MESSINA, Sonia, SFRAMELI, Maria, LUCA VITA, Gian, BOFFI, Patrizia, BARP, Andrea, MONGINI, Tiziana, FERLINI, Alessandra, GUALANDI, Francesca, SORARU, Gianni, ERMANI, Mario, VITA, Giuseppe, BATTINI, Roberta, BERTINI, Enrico, COMI, Giacomo P, BERARDINELLI, Angela, TAGLIA, Antonella, MINETTI, Carlo, BRUNO, Claudio, MERCURI, Eugenio, POLITANO, Luisa, ANGELINI, Corrado, HOFFMAN, Eric P, PEGORARO, Elena, PICILLO, Esther, VASCO, Gessica, PANE, Marika, PREVITALI, Stefano C, TORRENTE, Yvan, GAZZERRO, Elisabetta

“…To test the effect of the single nucleotide polymorphism -66 T>G (rs28357094) in the osteopontin gene (SPP1) on functional measures over 12 months in Duchenne…”
Get full text

The upstream Variable Number Tandem Repeat polymorphism of the monoamine oxidase type A gene influences trigeminal pain-related evoked responses by Di Lorenzo, Cherubino, Daverio, Andrea, Pasqualetti, Patrizio, Coppola, Gianluca, Giannoudas, Ioannis, Barone, Ylenia, Grieco, Gaetano S., Niolu, Cinzia, Pascale, Esterina, Santorelli, Filippo M., Nicoletti, Ferdinando, Pierelli, Francesco, Siracusano, Alberto, Seri, Stefano, Di Lorenzo, Giorgio

“…Monoamines have an important role in neural plasticity, a key factor in cortical pain processing that promotes changes in neuronal network connectivity…”
Get full text

Molecular genotype in migraine by Di Lorenzo, Cherubino, Grieco, Gaetano S, Rubegni, Anna, Santorelli, Filippo M

Get full text

The Val66Met polymorphism of the BDNF gene influences trigeminal pain-related evoked responses by Di Lorenzo, Cherubino, Di Lorenzo, Giorgio, Daverio, Andrea, Pasqualetti, Patrizio, Coppola, Gianluca, Giannoudas, Ioannis, Barone, Ylenia, Grieco, Gaetano S, Niolu, Cinzia, Pascale, Esterina, Santorelli, Filippo M, Nicoletti, Ferdinando, Pierelli, Francesco, Siracusano, Alberto, Seri, Stefano

“…Cortical pain processing is associated with large-scale changes in neuronal connectivity, resulting from neural plasticity phenomena of which brain-derived…”
Get more information

Pharmacogenomics of episodic migraine: time has come for a step forward by Viana, Michele, Terrazzino, Salvatore, Genazzani, Armando A, Grieco, Gaetano S, Cargnin, Sarah, Santorelli, Filippo M, Pierelli, Francesco, Tassorelli, Cristina, Nappi, Giuseppe, Di Lorenzo, Cherubino

“…Migraine is characterized by heterogeneous behavior in response to drugs. Many resources have been invested in attempting to unravel the genetic basis of…”
Get more information

Drug consumption in medication overuse headache is influenced by brain-derived neurotrophic factor Val66Met polymorphism by Di Lorenzo, Cherubino, Di Lorenzo, Giorgio, Sances, Grazia, Ghiotto, Natascia, Guaschino, Elena, Grieco, Gaetano S., Santorelli, Filippo M., Casali, Carlo, Troisi, Alfonso, Siracusano, Alberto, Pierelli, Francesco

“…Medication overuse headache (MOH) can be considered a clinical condition at the boundaries between drug addiction and chronic pain disorder. The common…”
Get full text

A new GLUT-1 mutation in a family with glucose transporter 1 deficiency syndrome by Gagliardi, Stella, Davin, Annalisa, Ricca, Ivana, Grieco, Gaetano S., Zangaglia, Roberta, Pierelli, Francesco, Ghiroldi, Andrea, Pacchetti, Claudio, Casali, Carlo, Cereda, Cristina

Get full text

The interplay of two single nucleotide polymorphisms in the CACNA1A gene may contribute to migraine susceptibility by D’Onofrio, Mara, Ambrosini, Anna, Di Mambro, Alessandra, Arisi, Ivan, Santorelli, Filippo M., Grieco, Gaetano S., Nicoletti, Ferdinando, Nappi, Giuseppe, Pierelli, Francesco, Schoenen, Jean, Buzzi, Maria Gabriella

“…Migraine is a common disorder with a significant genetic component. Mutations in the CACNA1A gene are found in hemiplegic migraine (HM). Basilar-type (BM),…”
Get full text

An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing loss by Terracciano, Alessandra, Casali, Carlo, Grieco, Gaetano S., Orteschi, Daniela, Di Giandomenico, Silvia, Seminara, Laura, Di Fabio, Roberto, Carrozzo, Rosalba, Simonati, Alessandro, Stevanin, Giovanni, Zollino, Marcella, Santorelli, Filippo M.

“…Autosomal recessive spastic ataxia of Charlevoix–Saguenay is a neurodegenerative disorder characterized by early-onset, spastic ataxia and peripheral…”
Get full text

Six novel mutations of the RUNX2 gene in Italian patients with cleidocranial dysplasia by Tessa, Alessandra, Salvi, Sergio, Casali, Carlo, Garavelli, Livia, Digilio, M. Cristina, Dotti, M. Teresa, Giandomenico, Silvia Di, Valoppi, Manuela, Grieco, Gaetano S., Comanducci, Giovanna, Bianchini, Giacomo, Fortini, Daniela, Federico, Antonio, Giannotti, Aldo, Santorelli, Filippo M.

“…We report clinical and molecular findings in 14 patients with cleidocranial dysplasia (CCD), a well defined skeletal disorder with characteristic clinical…”
Get full text

Current insights into familial spastic paraparesis: new advances in an old disease by Fortini, Daniela, Cricchi, Federica, Di Fabio, Roberto, Damiano, Maria, Comanducci, Giovanna, Benedetti, Laura, Valoppi, Manuela, Grieco, Gaetano S, D'Eugenio, Ottavio, Celato, Andrea, Santorelli, Filippo, Casali, Carlo, Amabile, Giuseppe A, Pierelli, Francesco

“…Hereditary spastic paraparesis (HSP) comprises a clinically and genetically heterogeneous group of disorders characterized by progressive spasticity and…”
Get more information

The upstream V ariable N umber T andem R epeat polymorphism of the monoamine oxidase type A gene influences trigeminal pain‐related evoked responses by Di Lorenzo, Cherubino, Daverio, Andrea, Pasqualetti, Patrizio, Coppola, Gianluca, Giannoudas, Ioannis, Barone, Ylenia, Grieco, Gaetano S., Niolu, Cinzia, Pascale, Esterina, Santorelli, Filippo M., Nicoletti, Ferdinando, Pierelli, Francesco, Siracusano, Alberto, Seri, Stefano, Di Lorenzo, Giorgio

“…Abstract Monoamines have an important role in neural plasticity, a key factor in cortical pain processing that promotes changes in neuronal network…”
Get full text

The upstream Variable Number Tandem Repeat polymorphism of the monoamine oxidase type A gene influences trigeminal pain-related evoked responses : NEUROBIOLOGY OF PAIN by DI LORENZO, Cherubino, DAVERIO, Andrea, NICOLETTI, Ferdinando, PIERELLI, Francesco, SIRACUSANO, Alberto, SERI, Stefano, DI LORENZO, Giorgio, PASQUALETTI, Patrizio, COPPOLA, Gianluca, GIANNOUDAS, Ioannis, BARONE, Ylenia, GRIECO, Gaetano S, NIOLU, Cinzia, PASCALE, Esterina, SANTORELLI, Filippo M

Get full text

Six novel mutations of theRUNX2 gene in Italian patients with cleidocranial dysplasia by Tessa, Alessandra, Salvi, Sergio, Casali, Carlo, Garavelli, Livia, Digilio, M. Cristina, Dotti, M. Teresa, Giandomenico, Silvia Di, Valoppi, Manuela, Grieco, Gaetano S., Comanducci, Giovanna, Bianchini, Giacomo, Fortini, Daniela, Federico, Antonio, Giannotti, Aldo, Santorelli, Filippo M.

Get full text

Chronic diarrhea associated with the A3243G mtDNA mutation by SANTORELLI, F. M, VILLANOVA, M, MALANDRINI, A, GRIECO, G. S, PALMERI, S, MERLINI, L, CASALI, C

Get full text