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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 - 6 (of 6 Records)

Query Trace: Syndrome and NOTCH3[original query]
Parkinsonism in a pair of monozygotic CADASIL twins sharing the R1006C mutation: a transcranial sonography study.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2016 Feb .
Ragno Michele, Sanguigni Sandro, Manca Antonio, Pianese Luigi, Paci Cristina, Berbellini Alfonso, Cozzolino Valeria, Gobbato Roberto, Peluso Silvio, De Michele Giusep
Identification of genetic variants for clinical management of familial colorectal tumors.
BMC medical genetics 2018 2 19 (1): 26.
Dominguez-Valentin Mev, Nakken Sigve, Tubeuf Hélène, Vodak Daniel, Ekstrøm Per Olaf, Nissen Anke M, Morak Monika, Holinski-Feder Elke, Martins Alexandra, Møller Pål, Hovig Eivi
Identification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates.
Respiratory research 2019 Aug 20 (1): 174.
Liu Xu, Mei Mei, Chen Xiang, Lu Yulan, Dong Xinran, Hu Liyuan, Hu Xiaojing, Cheng Guoqiang, Cao Yun, Yang Lin, Zhou Wenh
Genomic Characterization of Upper-Tract Urothelial Carcinoma in Patients With Lynch Syndrome.
JCO precision oncology 2019 3 2018 .
Donahu Timothy F, Bagrodia Aditya, Audenet François, Donoghue Mark T A, Cha Eugene K, Sfakianos John P, Sperling Dahlia, Al-Ahmadie Hikmat, Clendenning Mark, Rosty Christophe, Buchanan Daniel D, Jenkins Mark, Hopper John, Winship Ingrid, Templeton Allyson S, Walsh Michael F, Stadler Zsofia K, Iyer Gopa, Taylor Barry, Coleman Jonathan, Lindor Noralane M, Solit David B, Bochner Bernard
Possible association between a polymorphism of EPAS1 gene and persistent pulmonary hypertension of the newborn: a case-control study.
Jornal de pediatria 2021 Oct .
Nakwan Narongsak, Mahasirimongkol Surakameth, Satproedprai Nusara, Chaiyasung Tassamonwan, Kunhapan Punna, Charoenlap Cheep, Singkhamanan Kamonnut, Charalsawadi Chariyaw
Genetic Study of Cerebral Small Vessel Disease in Chinese Han Population.
Frontiers in neurology 2022 4 13 829438.
Wang Yunchao, Shi Changhe, Li Yusheng, Yu Wenkai, Wei Sen, Fan Yu, Mao Chengyuan, Yang Zhihua, Yu Lulu, Zhao Zichen, Li Shanshan, Gao Yuan, Xu Yumi
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