مُحمَّد ميقاتي
Mikati, Mohamad
ميقاتي، محمد
VIAF ID: 305025384 (Personal)
Permalink: http://viaf.org/viaf/305025384
Preferred Forms
- 100 1 _ ‡a Mikati, Mohamad
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- 100 1 _ ‡a Mikati, Mohamad
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- 100 0 _ ‡a مُحمَّد ميقاتي
4xx's: Alternate Name Forms (3)
Works
Title | Sources |
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Effects of a single dose of erythropoietin on subsequent seizure susceptibility in rats exposed to acute hypoxia at P10. | |
Effects of creatine and cyclocreatine supplementation on kainate induced injury in pre-pubescent rats | |
Effects of nimodipine on the behavioral sequalae of experimental status epilepticus in prepubescent rats | |
Effects of quisqualic acid and glutamate on subsequent learning, emotionality, and seizure susceptibility in the immature and mature animal. | |
Efficacy of gabapentin therapy in children with refractory partial seizures | |
Electroencephalographic and seizure manifestations in two patients with folate receptor autoimmune antibody-mediated primary cerebral folate deficiency. | |
Electroencephalographic discharges of temporal lobe seizures in children and young adults. | |
Enhancing early child development, c2013: | |
Epilepsy surgery in a developing country (Lebanon): ten years experience and predictors of outcome. | |
The epileptology of alternating hemiplegia of childhood | |
Equal antipyretic effectiveness of oral and rectal acetaminophen: a randomized controlled trial [ISRCTN11886401]. | |
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy | |
The Expanding Clinical Spectrum of Genetic Pediatric Epileptic Encephalopathies. | |
Expanding spectrum of paroxysmal events in children: potential mimickers of epilepsy. | |
Experience with hyperphenylalaninemia in a developing country: unusual clinical manifestations and a novel gene mutation | |
Focal features in West syndrome indicating candidacy for surgery. | |
Functional recovery following resection of an epileptogenic focus in the motor hand area | |
Gap junctional intercellular communication in hypoxia-ischemia-induced neuronal injury. | |
Genetic diagnosis in Lafora disease: Genotype-phenotype correlations and diagnostic pitfalls | |
Goldenhar syndrome associated with prenatal maternal Fluoxetine ingestion: Cause or coincidence? | |
High-performance liquid chromatography method for quantifying sphingomyelin in rat brain | |
Importance of voltage-dependent inactivation in N-type calcium channel regulation by G-proteins | |
Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant | |
Intracarotid propofol testing: a comparative study with amobarbital | |
Intraoperative electrocorticography and cortical stimulation in children | |
Introduction | |
Iron deficiency in young Lebanese children: association with elevated blood lead levels | |
Isolated adipic aciduria. | |
Lack of apoptosis in the hypoxic brain of a rat model mimicking cyanotic heart disease. | |
Landau-Kleffner syndrome: consistent response to repeated intravenous gamma-globulin doses: a case report. | |
Letter: Antiepileptogenic and neuroprotective effects of erythropoietin: recent data. | |
Long-term behavioral deficits following pilocarpine seizures in immature rats. | |
Long-term effects of acute and of chronic hypoxia on behavior and on hippocampal histology in the developing brain. | |
Long-term patterns of weight changes during topiramate therapy: an observational study | |
Long-term tolerability and efficacy of lamotrigine in infants 1 to 24 months old. | |
Managing Lafora body disease with vagal nerve stimulation. | |
Marked benefits in physical activity and well-being, but not in functioning domains, 2 years after successful epilepsy surgery in children | |
Mechanisms of increased hippocampal excitability in the Mashl+/- mouse model of Na+ /K+ -ATPase dysfunction | |
Medical treatment of patients with infantile spasms. | |
Microcephaly, hypergonadotropic hypogonadism, short stature, and minor anomalies: a new syndrome. | |
Motor variant of chronic inflammatory demyelinating polyneuropathy in a child | |
Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H. | |
Neuroprotective effect of chronic infusion of basic fibroblast growth factor on seizure-associated hippocampal damage | |
Neuroprotective effect of felbamate after kainic acid-induced status epilepticus. | |
Normalization of quality of life three years after temporal lobectomy: a controlled study. | |
Novel mutation causing partial biotinidase deficiency in a Syrian boy with infantile spasms and retardation | |
Oculogyric crises secondary to lamotrigine overdosage | |
A patient with duplication (7)(p22.1pter) characterized by array-CGH | |
Pattern-induced partial seizures with repetitive affectionate kissing: an unusual manifestation of right temporal lobe epilepsy. | |
Pediatric Sudden Unexpected Death in Epilepsy: What Have we Learned from Animal and Human Studies, and Can we Prevent it? | |
Phenobarbital does not alter phenytoin steady-state serum concentration or pharmacokinetics | |
Pilocarpine seizures cause age-dependent impairment in auditory location discrimination. | |
Possible induction of West syndrome by oxcarbazepine therapy in a patient with complex partial seizures. | |
Potential neuroprotective effects of continuous topiramate therapy in the developing brain. | |
Predictors of bone density in ambulatory patients on antiepileptic drugs. | |
Principles of drug treatment in children. | |
Programmed cell death in the lithium pilocarpine model: evidence for NMDA receptor and ceramide-mediated mechanisms | |
Protracted epileptiform encephalopathy: an unusual form of partial complex status epilepticus. | |
Pseudoseizure manifestations in two preschool age children | |
Psychogenic seizures: video telemetry observations in 27 patients. | |
Pyridoxine-dependent epilepsy: EEG investigations and long-term follow-up | |
Quality of life after surgery for intractable partial epilepsy in children: a cohort study with controls. | |
Quality of life after vagal nerve stimulator insertion. | |
Quinidine in the treatment of KCNT1-positive epilepsies | |
Quisqualic acid-induced seizures during development: a behavioral and EEG study. | |
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes | |
Refractory status epilepticus in children with and without prior epilepsy or status epilepticus | |
Relationship of carbamazepine reduction rate to seizure frequency during inpatient telemetry | |
Response of infantile spasms to levetiracetam | |
Response to immunotherapy in a patient with Landau-Kleffner syndrome and GRIN2A mutation. | |
Risk factors for development of subclinical hypothyroidism during valproic acid therapy | |
Seizure predisposition after perinatal hypoxia: effects of subsequent age and of an epilepsy predisposing gene mutation | |
Significance of Epilepsy & behavior: my personal experience and views | |
Stiripentol in Dravet syndrome: results of a retrospective U.S. study. | |
Structural connectivity of the frontal lobe in children with drug-resistant partial epilepsy | |
The syndrome of hyperostosis and hyperphosphatemia | |
Technetium-99m HmPAO brain SPECT and outcome of hemispherectomy for intractable seizures | |
Time from convulsive status epilepticus onset to anticonvulsant administration in children | |
Unusual presentation of Kearns-Sayre syndrome in early childhood | |
Use of subdural grids and strip electrodes to identify a seizure focus in children | |
Venous sinus thrombosis in a renal transplant patient | |
Visual aids to medical data and computational diagnostics: new frontiers in pediatric neurology | |
What is their fate after magnesium sulfate? | |
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