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benign infantile seizure (non-familial)相关文献:
Benign familial infantile seizures.
Vigevano F.
Brain Dev. 2005 Apr;27(3):172-7. doi: 10.1016/j.braindev.2003.12.012.
PMID:15737697
Benign familial and non-familial infantile seizures: a study of 64 patients.
Caraballo RH, Cersósimo RO, Espeche A, Fejerman N.
Epileptic Disord. 2003 Mar;5(1):45-9.
PMID:12773296
[Familial and non-familial benign infantile seizures: A homogeneous entity?].
Bourel-Ponchel E, Le Moing AG, Delignières A, De Broca A, Wallois F, Berquin P.
Rev Neurol (Paris). 2011 Aug-Sep;167(8-9):592-9. doi: 10.1016/j.neurol.2011.01.005. Epub 2011 May 17.
PMID:21592539
[The coincidence of benign non-familial infantile seizures type 2 with osteogenesis imperfecta type 1].
I DV, Aysina VA.
Zh Nevrol Psikhiatr Im S S Korsakova. 2022;122(5):128-131. doi: 10.17116/jnevro2022122051128.
PMID:35611912
Benign familial and non-familial infantile seizures (Fukuyama-Watanabe-Vigevano syndrome): a study of 14 cases from Saudi Arabia.
Saadeldin IY, Housawi Y, Al Nemri A, Al Hifzi I.
Brain Dev. 2010 May;32(5):378-84. doi: 10.1016/j.braindev.2009.04.014. Epub 2009 May 22.
PMID:19464832
PRRT2 is mutated in familial and non-familial benign infantile seizures.
Specchio N, Terracciano A, Trivisano M, Cappelletti S, Claps D, Travaglini L, Cusmai R, Marras CE, Zara F, Fusco L, Bertini E, Vigevano F.
Eur J Paediatr Neurol. 2013 Jan;17(1):77-81. doi: 10.1016/j.ejpn.2012.07.006. Epub 2012 Aug 17.
PMID:22902423
Benign infantile seizures and paroxysmal dyskinesia: a well-defined familial syndrome.
Espeche A, Cersosimo R, Caraballo RH.
Seizure. 2011 Nov;20(9):686-91. doi: 10.1016/j.seizure.2011.06.020. Epub 2011 Jul 20.
PMID:21764335
The spectrum of benign infantile seizures.
Specchio N, Vigevano F.
Epilepsy Res. 2006 Aug;70 Suppl 1:S156-67. doi: 10.1016/j.eplepsyres.2006.01.018. Epub 2006 Jul 11.
PMID:16837167
A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions.
Ishii A, Fukuma G, Uehara A, Miyajima T, Makita Y, Hamachi A, Yasukochi M, Inoue T, Yasumoto S, Okada M, Kaneko S, Mitsudome A, Hirose S.
Brain Dev. 2009 Jan;31(1):27-33. doi: 10.1016/j.braindev.2008.05.010. Epub 2008 Jul 21.
PMID:18640800
Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis.
Ishii A, Yasumoto S, Ihara Y, Inoue T, Fujita T, Nakamura N, Ohfu M, Yamashita Y, Takatsuka H, Taga T, Miyata R, Ito M, Tsuchiya H, Matsuoka T, Kitao T, Murakami K, Lee WT, Kaneko S, Hirose S.
Brain Dev. 2013 Jun;35(6):524-30. doi: 10.1016/j.braindev.2012.09.006. Epub 2012 Oct 13.
PMID:23073245
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