Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Seizures and MTHFR[original query] |
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Homocysteine, pharmacogenetics, and neurotoxicity in children with leukemia. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2003 Aug 21 (16): 3084-91. Kishi Shinji, Griener James, Cheng Cheng, Das Soma, Cook Edwin H, Pei Deqing, Hudson Melissa, Rubnitz Jeffrey, Sandlund John T, Pui Ching-Hon, Relling Mary |
Cerebral venous sinus thrombosis in childhood: clinical aspects and neurological and cognitive long-term outcome in three cases. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2004 12 25 (5): 296-300. Buccino G, Cossu G, De Fanti A, Manotti C, Izzi G C, Mancia |
Methylenetetrahydrofolate reductase C677T-polymorphism and its association with alcohol withdrawal seizure. Alcoholism, clinical and experimental research 2006 Dec 30 (12): 1966-71. Lutz Ulrich C, Batra Anil, Kolb Werner, Machicao Fausto, Maurer Sandra, Köhnke Michael |
Inherited thrombophilia in childhood arterial stroke: data from Lebanon. Pediatric neurology 2011 Sep 45 (3): 155-8. Muwakkit Samar A, Majdalani Marianne, Hourani Roula, Mahfouz Rami A, Otrock Zaher K, Bilalian Christina, Chan Anthony K, Abboud Miguel, Mikati Mohamad |
MTHFR C677T genotype as a risk factor for epilepsy including post-traumatic epilepsy in a representative military cohort. Journal of neurotrauma 2011 Sep 28 (9): 1739-45. Scher Ann I, Wu Holly, Tsao Jack W, Blom Henk J, Feit Preethy, Nevin Remington L, Schwab Karen |
Epilepsy control with carbamazepine monotherapy from a genetic perspective. BMC pharmacology & toxicology 2018 Nov 19 (1): 73. Ullah Shakir, Ali Niaz, Khan Adnan, Ali Saad, Nazish Haleema Rehna, Uddin Z |
The Role of Factor V Leiden, Prothrombin G20210A, and MTHFR C677T Mutations in Neonatal Cerebral Sinovenous Thrombosis. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2019 4 25 1076029619834352. Garrido-Barbero Maria, Arnaez Juan, Loureiro Begoña, Arca Gemma, Agut Thais, Garcia-Alix Alfre |
MTHFR Gene Polymorphisms and Cardiovascular Risk Factors, Clinical-Imagistic Features and Outcome in Cerebral Venous Sinus Thrombosis. Brain sciences 2020 12 11 (1): . Gogu Anca Elena, Jianu Dragos Catalin, Dumitrascu Victor, Ples Horia, Stroe Alina Zorina, Docu Axelerad Daniel, Docu Axelerad A |
[Genotype and phenotype analysis of neonates with neonatal encephalopathy complicated with perinatal hypoxic event]. Zhonghua er ke za zhi = Chinese journal of pediatrics 2021 3 59 (4): 280-285. Xiao T T, Yang L, Wu B B, Peng X M, Wang H J, Cheng G Q, Wang L S, Cao Y, Hu L Y, Zhou W |
AS3MT Polymorphism: A Risk Factor for Epilepsy Susceptibility and Adverse Drug Reactions to Valproic Acid and Oxcarbazepine Treatment in Children From South China. Frontiers in neuroscience 2021 12 15 705297. Fan Xiaomei, Chen Yuna, Lu Jieluan, Li Wenzhou, Li Xi, Guo Huijuan, Chen Qing, Yang Yanxia, Xia Hanbi |
Susceptibility to preoperative seizures in glioma patients with elevated homocysteine levels. Epilepsia open 2023 7 . Xiaohan Chi, Jingjing Lu, Zhengguang Guo, Junmei Wang, Gaifen Liu, Zeping Jin, Yi Wang, Qianhe Zhang, Tai Sun, Nan Ji, Yang Zha |
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