Search Results - "Grieco, S"

Insulin growth factor 2 (IGF2) as an emergent target in psychiatric and neurological disorders. Review by Pardo, M., Cheng, Y., Sitbon, Y.H., Lowell, J.A., Grieco, S.F., Worthen, R.J., Desse, S., Barreda-Diaz, A.

“…[Display omitted] •The insulin growth factor 2 (IGF2) is abundantly expressed in the brain.•Inappropriate IGF2 expression is implicated in a growing number of…”
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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…”
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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…”
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New CACNA1A deletions are associated to migraine phenotypes by Grieco, G. S., Gagliardi, S., Ricca, I., Pansarasa, O., Neri, M., Gualandi, F., Nappi, G., Ferlini, A., Cereda, C.

“…Background Familial hemiplegic migraine type 1 (FHM1) is a form of migraine with aura caused by heterozygous mutations in 4 genes: CACNA1A, ATP1A2, SNC1A and…”
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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…”
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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…”
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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…”
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Effect of interferon free antiviral therapy on glomerular and tubular kidney involvement in hepatitis C virus child-A cirrhosis by Palazzo, D, Biliotti, E, Tinti, F, Bachetoni, A, Cappoli, A, Subic, M, D’Alessandro, M.D, Labriola, R, Grieco, S, Perinelli, P, Umbro, I, Volpicelli, L, Rucci, P, Mitterhofer, A.P, Taliani, G

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Ataxia with oculomotor apraxia type 2 : A clinical, pathologic, and genetic study by CRISCUOLO, C, CHESSA, L, PIERELLI, F, RIZZUTO, N, SANTORELLI, F. M, GALLOSTI, L, FILLA, A, CASALI, C, DI GIANDOMENICO, S, MANCINI, P, SACCA, F, GRIECO, G. S, PIANE, M, BARBIERI, F, DE MICHELE, G, BANFI, S

“…Ataxia with oculomotor apraxia type 2 (AOA2) is characterized by onset between age 10 and 22 years, cerebellar atrophy, peripheral neuropathy, oculomotor…”
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Glomerular and Tubular Kidney Involvement in HCV Child-A Cirrhosis by Palazzo, D, Biliotti, E, Tinti, F, Bachetoni, A, Perinelli, P, Cappoli, A, D’Alessandro, M.D, Grieco, S, Labriola, R, Subic, M, Umbro, I, Rucci, P, Mitterhofer, A.P, Taliani, G

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Familial basilar migraine associated with a new mutation in the ATP1A2 gene by AMBROSINI, A, D'ONOFRIO, M, BUZZI, M. G, SANTORELLI, F. M, PIERELLI, F, GRIECO, G. S, DI MAMBRO, A, MONTAGNA, G, FORTINI, D, NICOLETTI, F, NAPPI, G, SANCES, G, SCHOENEN, J

“…Basilar migraine (BM), familial hemiplegic migraine (FHM), and sporadic hemiplegic migraine (SHM) are phenotypically similar subtypes of migraine with aura,…”
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Effect of interferon free antiviral therapy on glomerular and tubular kidney involvement in HCV child-A cirrhosis by Palazzo, D, Biliotti, E, Tinti, F, Bachetoni, A, Volpicelli, L, Cappoli, A, D’Alessandro, M.D, Labriola, R, Perinelli, P, Grieco, S, Subic, M, Umbro, I, Rucci, P, Mitterhofer, A.P, Taliani, G

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Palmoplantar keratoderma and Charcot–Marie–Tooth disease: combination of two independent genetic diseases? Identification of two point mutations in the MPZ and KRT1 genes by whole‐exome sequencing by Gagliardi, S., Ricca, I., Ferrarini, A., Valente, M., Grieco, G.S., Piccolo, G., Alfonsi, E., Delledonne, M., Cereda, C.

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A cluster of fulminant Clostridium difficile colitis in an intensive care unit in Italy by Guastalegname, M., Grieco, S., Giuliano, S., Falcone, M., Caccese, R., Carfagna, P., D’ambrosio, M., Taliani, G., Venditti, M.

“…We describe, for the first time, a cluster of lethal fulminant health-care associated Clostridium difficile (CD) colitis in Italy, observed in the intensive…”
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Phenotypic diversity of lactic acid bacteria isolated from fermented sausages produced in Basilicata (Southern Italy) by Parente, E, Grieco, S, Crudele, M.A

“…Aims: to evaluate the evolution of lactic acid bacteria (LAB) populations in traditional fermented sausages (salsiccia and soppressata) produced in artisanal…”
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Evolution of microbial populations and biogenic amine production in dry sausages produced in Southern Italy by Parente, E, Martuscelli, M, Gardini, F, Grieco, S, Crudele, M.A, Suzzi, G

“…Aims: To evaluate the occurrence and evolution of biogenic amines during ripening of fermented sausages and their relationship with physico-chemical and…”
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In the ERA of New Direct Acting Antiviral Agents HCV Sequencing Allows the Most Accurate Subtype and Genotype Assignment by Aragri, M, Di Maio, V.C, Di Paolo, D, Cento, V, De Leonardis, F, Gianserra, L, Tontodonati, M, Micheli, V, Landonio, S, Manunta, A, Bertoli, A, Ciotti, M, Antonucci, F.P, Lenci, I, Francioso, S, Nicolini, L.A, Marenco, S, Teti, E, Lambiase, L, Milana, M, Maida, I, Di Biagio, A, Pellicelli, A, Nosotti, L, Grieco, S, Cacciatore, P, Romagnoli, D, Siciliano, M, D’Ettorre, G, Babudieri, S, Lichtner, M, Gentilucci, U.V, Romano, M, Sarrecchia, C, Grieco, A, Morisco, F, Mastroianni, C, Vecchiet, J, Puoti, M, D’Amico, E, Gasbarrini, A, Bruno, S, Magni, C, Mura, M.S, Taliani, G, Picciotto, A, Rizzardini, G, Andreoni, M, Pasquazzi, C, Parruti, G, Angelico, M, Perno, C.F, Silberstein, F.C

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Effect of the 50 bp deletion polymorphism in the SOD1 promoter on SOD1 mRNA levels in Italian ALS patients by Milani, P, Gagliardi, S, Bongioanni, P, Grieco, G.S, Dezza, M, Bianchi, M, Cova, E, Ceroni, M, Cereda, C

“…Abstract The genetic association between homozygosity for a 50 bp deletion polymorphism in the SOD1 promoter, 1684 bp upstream of the ATG, and an increased age…”
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Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type by GRIECO, G. S, MALANDRINI, A, FEDERICO, A, PIERELLI, F, BERTINI, E, CASALI, C, SANTORELLI, F. M, COMANDUCCI, G, LEUZZI, V, VALOPPI, M, TESSA, A, PALMERI, S, BENEDETTI, L, PIERALLINI, A, GAMBELLI, S

“…Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is an early-onset familial disease with prominent myelinated fibers in the optic fundus…”
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Mitochondrial DNA haplogroups influence the therapeutic response to riboflavin in migraineurs by DI LORENZO, C, PIERELLI, F, SCHOENEN, J, COPPOLA, G, GRIECO, G. S, RENGO, C, CICCOLELLA, M, MAGIS, D, BOLLA, M, CASALI, C, SANTORELLI, F. M

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