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Prolonged treatment for acute symptomatic refractory status epilepticus: outcome in children.
Neurology. 2003 Aug 12;61(3):398-401. doi: 10.1212/01.wnl.0000073139.53008.f2.
Neurology. 2003.
PMID: 12913208
Outcome of severe refractory status epilepticus in children.
Sahin M, Menache CC, Holmes GL, Riviello JJ.
Sahin M, et al. Among authors: menache cc.
Epilepsia. 2001 Nov;42(11):1461-7. doi: 10.1046/j.1528-1157.2001.21301.x.
Epilepsia. 2001.
PMID: 11879350
Free article.
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Prognostic value of neonatal discontinuous EEG.
Menache CC, Bourgeois BF, Volpe JJ.
Menache CC, et al.
Pediatr Neurol. 2002 Aug;27(2):93-101. doi: 10.1016/s0887-8994(02)00396-x.
Pediatr Neurol. 2002.
PMID: 12213608
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Enteral nutrition and corticosteroids in the treatment of acute Crohn's disease in children.
Heuschkel RB, Menache CC, Megerian JT, Baird AE.
Heuschkel RB, et al. Among authors: menache cc.
J Pediatr Gastroenterol Nutr. 2000 Jul;31(1):8-15. doi: 10.1097/00005176-200007000-00005.
J Pediatr Gastroenterol Nutr. 2000.
PMID: 10896064
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Current incidence of acute neurologic complications after open-heart operations in children.
Menache CC, du Plessis AJ, Wessel DL, Jonas RA, Newburger JW.
Menache CC, et al.
Ann Thorac Surg. 2002 Jun;73(6):1752-8. doi: 10.1016/s0003-4975(02)03534-8.
Ann Thorac Surg. 2002.
PMID: 12078765
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Neuroimaging in childhood arterial ischaemic stroke: evaluation of imaging modalities and aetiologies.
Buerki S, Roellin K, Remonda L, Mercati DG, Jeannet PY, Keller E, Luetschg J, Menache C, Ramelli GP, Schmitt-Mechelke T, Weissert M, Boltshauser E, Steinlin M.
Buerki S, et al.
Dev Med Child Neurol. 2010 Nov;52(11):1033-7. doi: 10.1111/j.1469-8749.2010.03685.x.
Dev Med Child Neurol. 2010.
PMID: 20477838
Free article.
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Early Brain Activity Relates to Subsequent Brain Growth in Premature Infants.
Benders MJ, Palmu K, Menache C, Borradori-Tolsa C, Lazeyras F, Sizonenko S, Dubois J, Vanhatalo S, Hüppi PS.
Benders MJ, et al.
Cereb Cortex. 2015 Sep;25(9):3014-24. doi: 10.1093/cercor/bhu097. Epub 2014 May 27.
Cereb Cortex. 2015.
PMID: 24867393
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Identification of a novel truncating mutation (S171X) in the Emerin gene in five members of a Caucasian American family with Emery-Dreifuss muscular dystrophy.
Menache CC, Brown CA, Donnelly JH, Shapiro F, Darras BT.
Menache CC, et al.
Hum Mutat. 2000 Jul;16(1):94. doi: 10.1002/1098-1004(200007)16:1<94::AID-HUMU27>3.0.CO;2-N.
Hum Mutat. 2000.
PMID: 10874323
No abstract available.
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