Zobrazeno 1 - 10 of 163 pro vyhledávání: '"S. Grieco"'
1
Akademický článek
Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2
Autor: Fabio Antonaci, Sabrina Ravaglia, Gaetano S. Grieco, Stella Gagliardi, Cristina Cereda, Alfredo Costa
Publikováno v: The Journal of Headache and Pain, Vol 22, Iss 1, Pp 1-6 (2021)
Abstract Background The mechanisms of genotype-phenotype interaction in Familiar Hemiplegic migraine type 2 (FHM2) are still far from clear. Different ATP1A2 mutations have been described, with a spectrum of phenotypes ranging from mild to severe. No
Externí odkaz: https://doaj.org/article/de6b0ff12fad454db13927588837ed04
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2
Akademický článek
Hemorrhagic choroidal detachment as the presenting sign of uveal melanoma
Autor: Yewlin E. Chee, Raghu Mudumbai, Steven S. Saraf, Thellea Leveque, Verena S. Grieco, Monique A. Mogensen, Rebecca A. Yoda, Luis F. Gonzalez-Cuyar, Andrew W. Stacey
Publikováno v: American Journal of Ophthalmology Case Reports, Vol 23, Iss , Pp 101173- (2021)
Purpose: To describe two cases of medium-sized uveal melanoma presenting with hemorrhagic choroidal detachments. Observations: The first case is a 39-year-old man who presented with choroidal hemorrhage and angle closure glaucoma. The second case is
Externí odkaz: https://doaj.org/article/02ba6e9a720642a98766d3108ba4bfa4
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3
Akademický článek
Genetics Influences Drug Consumption in Medication Overuse Headache, Not in Migraine: Evidence From Wolframin His611Arg Polymorphism Analysis
Autor: Cherubino Di Lorenzo, Giorgio Di Lorenzo, Gianluca Coppola, Vincenzo Parisi, Gaetano S. Grieco, Filippo Maria Santorelli, Esterina Pascale, Francesco Pierelli
Publikováno v: Frontiers in Neurology, Vol 11 (2021)
Background: The Wolframin His611Arg polymorphism can influence drug consumption in psychiatric patients with impulsive addictive behavior. This cross-sectional study aims to assess the prevalence of the Wolframin His611Arg polymorphism in MOH, a seco
Externí odkaz: https://doaj.org/article/7e50587c23d740ea8ba35023f13f022e
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5
Akademický článek
New CACNA1A deletions are associated to migraine phenotypes
Autor: G. S. Grieco, S. Gagliardi, I. Ricca, O. Pansarasa, M. Neri, F. Gualandi, G. Nappi, A. Ferlini, C. Cereda
Publikováno v: The Journal of Headache and Pain, Vol 19, Iss 1, Pp 1-6 (2018)
Abstract 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 PRRT2, but further heterogeneity is expected. Here have been described clinical and
Externí odkaz: https://doaj.org/article/7e029d76e8b543f88c0e7badf79970e5
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6
Akademický článek
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7
Hemorrhagic choroidal detachment as the presenting sign of uveal melanoma
Autor: Monique A. Mogensen, Steven S. Saraf, Yewlin E. Chee, Rebecca A. Yoda, Raghu C. Mudumbai, Andrew W. Stacey, Luis F. Gonzalez-Cuyar, Verena S. Grieco, Thellea K Leveque
Publikováno v: American Journal of Ophthalmology Case Reports
American Journal of Ophthalmology Case Reports, Vol 23, Iss, Pp 101173-(2021)
Purpose To describe two cases of medium-sized uveal melanoma presenting with hemorrhagic choroidal detachments. Observations The first case is a 39-year-old man who presented with choroidal hemorrhage and angle closure glaucoma. The second case is a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61c2fba550249ced82874e8421258134
http://europepmc.org/articles/PMC8326186
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8
Characterization of HIV-1 Subtypes Among South Sudanese Patients
Autor: Brian T. Foley, Silvia Angeletti, Alessandra Borsetti, Stefania Farcomeni, S. Grieco, Gloria Taliani, Leonardo Sernicola, Michela Baesso, Massimo Ciccozzi, Lucia Fontanelli Sulekova, Maria Teresa Maggiorella, Alessandra Lo Presti
Publikováno v: AIDS Research and Human Retroviruses. 35:968-971
There is scarce data on circulation of genetic subtypes of HIV-1 in South Sudan due to decades of civil war. In this study, phylogenetic analysis of 10 strains collected from HIV-1-infected South Sudanese patients was performed. Partial
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::888e789f07d130133b85e00c3c5eb7f7
https://doi.org/10.1089/aid.2019.0133
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10
Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2
Autor: Stella Gagliardi, Sabrina Ravaglia, Cristina Cereda, Gaetano S. Grieco, Alfredo Costa, Fabio Antonaci
Publikováno v: The Journal of Headache and Pain
The Journal of Headache and Pain, Vol 22, Iss 1, Pp 1-6 (2021)
Background The mechanisms of genotype-phenotype interaction in Familiar Hemiplegic migraine type 2 (FHM2) are still far from clear. Different ATP1A2 mutations have been described, with a spectrum of phenotypes ranging from mild to severe. No genotype
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::738be101197d26e3f957842f5a4a56aa
https://pubmed.ncbi.nlm.nih.gov/33711927
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