147 results on '"Goldberg-Stern, H."'
Search Results
2. Neuropsychological aspects of benign childhood epilepsy with centrotemporal spikes
3. AN UNUSUALLY SEVERE PHENOTYPE IN A FAMILY WITH A NOVEL SCN1A MUTATION: FROM GEFS+ TO DRAVET SYNDROME: p846
4. Multicenter long-term follow-up of children with idiopathic West syndrome: ACTH versus vigabatrin - CME questions
5. Parry-Romberg syndrome: follow-up imaging during suppressive therapy
6. Progressive spinocerebellar degeneration "plus" associated with Langerhans cell histiocytosis: a new paraneoplastic syndrome?
7. Endocrine Effects of Valproate versus Carbamazepine in Males with Epilepsy: A Prospective Study
8. OP14 – 2647: RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasia
9. P757: Hyperventilation during routine EEG recording: are “3 minutes” really necessary?
10. PP2.1 – 1874 Ohtahara syndrome in two half siblings due to a novel SCN2A mutation
11. PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures
12. Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study
13. 3FC1.3 Long term follow up in children with infantile thiamine deficiency
14. A 9-year-old boy with acute psychosis and non-convulsive status epilepticus
15. Erratum to: “Neuropsychological aspects of benign childhood epilepsy with centrotemporal spikes” [Seizure: European Journal of Epilepsy 19 (2010) 12–16]
16. Epilepsy in children with infantile thiamine deficiency
17. ESP012 Normal MRI West syndrome cases: therapy type and diagnostic delay as prognostic factors
18. GnRH agonist treatment in girls with precocious puberty does not compromise post-pubertal uterine size
19. Antibodies to glutamate receptor subtype 3 (GluR3) are found in some patients suffering from epilepsy as the main disease, but not in patients whose epilepsy accompanies antiphospholipid syndrome or Sneddon's syndrome
20. Machado‐Joseph (Azorean) disease in a Yemenite Jewish family in Israel
21. Abnormal evoked potentials in Miller-Fisher syndrome: further evidence of combined peripheral and central demyelination.
22. Detection and measurement of an endogenous clonidine-displacing substance in human cerebrospinal fluid
23. Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes.
24. P03-546 - A 9-year-old boy with acute psychosis and non-convulsive status epilepticus
25. The prognostic significance of glial fibrillary acidic protein staining in medulloblastoma.
26. Seizure frequency and characteristics in children with Down syndrome
27. MachadoJoseph Azorean disease in a Yemenite Jewish family in Israel
28. Multiplex families with epilepsy: Success of clinical and molecular genetic characterization
29. Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: A European collaborative study
30. Language dysfunction after frontal lobe partial seizures.
31. Detection and measurement of an endogenous clonidine-displacing substance (CDS) in human cerebrospinal fluid (CSF)
32. Ondansetron for hallucinosis in advanced Parkinson's disease.
33. Baseline characteristics and predictors for early implantation of vagus nerve stimulation therapy in people with drug-resistant epilepsy: Observations from an international prospective outcomes registry (CORE-VNS).
34. Whole exome sequencing and co-expression analysis identify an SCN1A variant that modifies pathogenicity in a family with genetic epilepsy and febrile seizures plus.
35. Focal Epilepsy in Individuals with Laron Syndrome.
36. Pathogenic MAST3 Variants in the STK Domain Are Associated with Epilepsy.
37. Epilepsy and electroencephalogram evolution in YWHAG gene mutation: A new phenotype and review of the literature.
38. Widespread cortical dyslamination in epilepsy patients with malformations of cortical development.
39. Corrigendum to "Absence seizure provocation during routine EEG: Does position of the child during hyperventilation affect diagnostic yield?" [Seizure 79 (2020) 86-89].
40. Evolution of EEG Findings in Pontocerebellar Hypoplasia Type 2A: Normal EEG in the First Few Months followed by Abnormal Tracing over the Years.
41. Absence seizure provocation during routine EEG: Does position of the child during hyperventilation affect the diagnostic yield?
42. Lysine acetyltransferase 8 is involved in cerebral development and syndromic intellectual disability.
43. A de novo GABRA2 missense mutation in severe early-onset epileptic encephalopathy with a choreiform movement disorder.
44. Genetic epilepsy with febrile seizures plus: Refining the spectrum.
45. Dual array EEG-fMRI: An approach for motion artifact suppression in EEG recorded simultaneously with fMRI.
46. Polymicrogyria and myoclonic epilepsy in autosomal recessive cutis laxa type 2A.
47. RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasia.
48. Multiplex families with epilepsy: Success of clinical and molecular genetic characterization.
49. De novo KCNB1 mutations in infantile epilepsy inhibit repetitive neuronal firing.
50. Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome.
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