967 results on '"Dulac O"'
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2. AKONIS—SIMS Excellence Brought To The Fab
3. Epileptic spasms with terror during sleep in CDKL5 encephalopathy
4. A prospective open-labeled trial with levetiracetam in pediatric epilepsy syndromes: Continuous spikes and waves during sleep is definitely a target
5. Vigabatrin bei Epilepsien des Kindesalters
6. Agenesis of the Corpus Callosum
7. Hemimegalencephaly
8. Long term response to steroid therapy in Rasmussen encephalitis
9. Séquelles neurologiques persistantes dues au paludisme cérébral dans une cohorte d’enfants au Mali
10. Functional imaging in the work-up of childhood epilepsy
11. Épilepsies néonatales et erreurs innées du métabolisme
12. Devastating epileptic encephalopathy in school-aged children (DESC): A pseudo encephalitis
13. EPILEPSY AND PCDH19 MUTATION CLINICAL AND ELECTROPHYSIOLOGICAL FEATURES IN 13 PATIENTS: p830
14. EARLY EPILEPTIC ENCEPHALOPATHIES ASSOCIATED WITH STXBP1 MUTATIONS: COULD WE BETTER DEFINE THE PHENOTYPE?: p814
15. IMPORTANCE OF SUBTLE CLINICAL FEATURES ASSOCIATED TO THE MOTOR PHENOMENON OF EPILEPTIC SPASMS FOR DIFFERENTIAL DIAGNOSIS: p752
16. TRANSITIONʼS GAP FROM PAEDIATRIC TO ADULT SYSTEM CARE OF PATIENTS WITH EPILEPTIC ENCEPHALOPATHY: A MYTH OR A REALITY?: p241
17. Stiripentol in severe myoclonic epilepsy in infancy: a randomised placebo-controlled syndrome-dedicated trial
18. PEDIATRIC AND ADULT EPILEPTOLOGY VANTAGE POINTS OF IGES: HOW DIFFERENT ARE THEY AND HOW CAN THEY MERGE?
19. Mutations in the mitochondrial glutamate carrier SLC25A22 in neonatal epileptic encephalopathy with suppression bursts
20. Presurgical language mapping in epileptic children: fMRI and depth electrode stimulation
21. Avancées actuelles sur les concepts pathogéniques et thérapeutiques de l’encéphalite de Rasmussen
22. Accelerated myelination in early Sturge-Weber syndrome: MRI-SPECT correlations
23. Effect of stiripentol on carbamazepine plasma concentration and metabolism in epileptic children
24. ‘Severe memory impairment in a child with bihippocampal injury after status epilepticus’
25. CRYPTOGENIC LATE ONSET EPILEPTIC SPASMS: AN OVERLOOKED SYNDROME OF EARLY CHILDHOOD?: 107
26. Molecular Genetic Dissection of Seizure-Type-Related Susceptibility Loci of Idiopathic Generalised Epilepsy: 040
27. Does the Gene Predict Prognosis?
28. Pathogenesis, diagnosis and treatment of Rasmussen encephalitis: A European consensus statement
29. Conduite du traitement par les antiépileptiques au long cours chez l’enfant avec épilepsie pharmaco-resistante
30. Ictal SPECT in children with epilepsy: comparison with intracranial EEG and relation to postsurgical outcome
31. ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies
32. Infantile Spasms in Down Syndrome: Good Response to a Short Course of Vigabatrin
33. Evaluations and Awards at the 4th European Congress of Epileptology, Florence, 7–12 October 2000
34. Recommendations on the clinical use of oxcarbazepine in the treatment of epilepsy: a consensus view
35. Genetic Predisposition to Severe Myoclonic Epilepsy in Infancy
36. Absence of mutations in major GEFS+ genes in myoclonic astatic epilepsy
37. Infantile spasms in Down syndrome—effects of delayed anticonvulsive treatment
38. Diagnosing idiopathic/cryptogenic epilepsy syndromes in infancy
39. Diffuse cortical dysplasia, or the 'double cortex' syndrome: the clinical and epileptic spectrum in 10 patients
40. Callosotomy for Epilepsy After West Syndrome
41. Stiripentol: Efficacy and Tolerability in Children with Epilepsy
42. Pyridoxine dependent epilepsy: a suggestive electroclinical pattern
43. Early diagnosis of subependymal giant cell astrocytoma in children with tuberous sclerosis
44. How to manage the impossible (HMI)? Anthropological research: understanding parents facing diagnosis of dravet syndrome in their child
45. Correlative Analysis in the Semiconductor Industry
46. Evidence of Late-Onset Infantile Spasms
47. Antiepileptic Drugs as a Cause of Worsening Seizures
48. Strategy of AED Treatment in Children.
49. Prophylactic antiepileptic treatment in Sturge–Weber disease
50. Efficacité et tolérance à long terme du stiripentol dans le traitement de l’épilepsie myoclonique sévère du nourrisson (syndrome de Dravet)
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