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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 10 (of 10 Records)

Query Trace: Disease and KRIT1[original query]
CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: a case-control study.
International journal of molecular medicine 2012 Jun 29 (6): 1113-20.
D'Angelo Rosalia, Scimone Concetta, Rinaldi Carmela, Trimarchi Giuseppe, Italiano Domenico, Bramanti Placido, Amato Aldo, Sidoti Antoni
Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severity.
Cerebrovascular diseases (Basel, Switzerland) 2014 38 (6): 433-40.
Choquet Hélène, Pawlikowska Ludmila, Nelson Jeffrey, McCulloch Charles E, Akers Amy, Baca Beth, Khan Yasir, Hart Blaine, Morrison Leslie, Kim Helen,
GLYOXALASE I A111E, PARAOXONASE 1 Q192R AND L55M POLYMORPHISMS IN ITALIAN PATIENTS WITH SPORADIC CEREBRAL CAVERNOUS MALFORMATIONS: A PILOT STUDY.
Journal of biological regulators and homeostatic agents 0 29 (2): 493-500.
Rinaldi C, Bramanti P, Famà A, Scimone C, Donato L, Antognelli C, Alafaci C, Tomasello F, D'Angelo R, Sidoti
CCM3/SERPINI1 bidirectional promoter variants in patients with cerebral cavernous malformations: a molecular and functional study.
BMC medical genetics 2016 Oct 17 (1): 74.
Scimone Concetta, Bramanti Placido, Ruggeri Alessia, Donato Luigi, Alafaci Concetta, Crisafulli Concetta, Mucciardi Massimo, Rinaldi Carmela, Sidoti Antonina, D'Angelo Rosal
Cytochrome P450 and matrix metalloproteinase genetic modifiers of disease severity in Cerebral Cavernous Malformation type 1.
Free radical biology & medicine 2016 Jan .
Choquet Hélène, Trapani Eliana, Goitre Luca, Trabalzini Lorenza, Akers Amy, Fontanella Marco, Hart Blaine L, Morrison Leslie A, Pawlikowska Ludmila, Kim Helen, Retta Saverio Frances
Genome-wide Genotyping of Cerebral Cavernous Malformation Type 1 Individuals to Identify Genetic Modifiers of Disease Severity.
Methods in molecular biology (Clifton, N.J.) 2020 6 2152 77-84.
Choquet Hélène, Kim Hel
Global Assessment of Mendelian Stroke Genetic Prevalence in 101 635 Individuals From 7 Ethnic Groups.
Stroke 2020 Feb STROKEAHA119028840.
Grami Nickrooz, Chong Michael, Lali Ricky, Mohammadi-Shemirani Pedrum, Henshall David E, Rannikmäe Kristiina, Paré Guillau
Polymorphisms in genes related to oxidative stress and inflammation: Emerging links with the pathogenesis and severity of Cerebral Cavernous Malformation disease.
Free radical biology & medicine 2021 6 172 403-417.
Perrelli Andrea, Retta Saverio Frances
Clinicoradiologic data of familial cerebral cavernous malformation with age-related disease burden.
Annals of clinical and translational neurology 2023 1 10 (3): 373-383.
Kim Seondeuk, Moon Jangsup, Jung Keun-Hwa, Anh Seon-Jae, Lee Han Sang, Jang Yoonhyuk, Park Kyung-Il, Lee Sang Kun, Chu K
Comprehensive analysis of Novel mutations in CCM1/KRIT1 and CCM2/MGC4607 and their clinical implications in Cerebral Cavernous malformations.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2024 8 107947.
Gustavo da Fontoura Galvão, Luisa Menezes Trefilio, Andreza Lemos Salvio, Elielson Veloso da Silva, Soniza Vieira Alves-Leon, Fabrícia Lima Fontes-Dantas, Jorge Marcondes de Sou
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