492 results on '"Lopes-Cendes, I."'
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2. Identifying cellular markers of focal cortical dysplasia type II with cell-type deconvolution and single-cell signatures.
3. Cdc2-like kinase 2 in the hypothalamus is necessary to maintain energy homeostasis
4. Circulating nucleic acids in the plasma and serum as potential biomarkers in neurological disorders
5. Pioglitazone treatment increases food intake and decreases energy expenditure partially via hypothalamic adiponectin/adipoR1/AMPK pathway
6. The ILAE consensus classification of focal cortical dysplasia: An update proposed by an ad hoc task force of the ILAE diagnostic methods commission
7. New THAP1 mutation and role of putative modifier in TOR1A
8. Glucocerebrosidase gene variants in parkinsonian patients with Machado Joseph/spinocerebellar ataxia 3
9. Modulating Expression of Endogenous Interleukin 1 Beta in the Acute Phase of the Pilocarpine Model of Epilepsy May Change Animal Survival
10. Non-motor symptoms in patients with hereditary spastic paraplegia caused by SPG4 mutations
11. Abnormalities of hippocampal signal intensity in patients with familial mesial temporal lobe epilepsy
12. Role of non-coding RNAs in non-aging-related neurological disorders
13. Cerebral cortex involvement in Machado−Joseph disease
14. SPG4-related hereditary spastic paraplegia: frequency and mutation spectrum in Brazil
15. Dentate nuclei T2 relaxometry is a reliable neuroimaging marker in Friedreichʼs ataxia
16. Differential pattern of cerebellar atrophy in patients with tremor-predominant and bradikinesia-rigidity-predominat Parkinsonʼs disease: 1054
17. Longitudinal analysis of regional grey matter loss in Huntington disease: effects of the length of the expanded CAG repeat
18. The genetic architecture of the human cerebral cortex
19. The genetic architecture of the human cerebral cortex
20. Lithium carbonate and coenzyme Q10 reduce cell death in a cell model of Machado-Joseph disease
21. Patterns of hippocampal abnormalities in malformations of cortical development
22. IMAGING | Imaging Characterization of Familial Temporal Lobe Epilepsies
23. Polyglutamine-containing proteins in schizophrenia
24. Investigation of the 22q11.2 candidate region in patients with midline facial defects with hypertelorism
25. Clinical correlates of autonomic dysfunction in patients with Machado-Joseph disease
26. Sleep symptoms and their clinical correlates in Machado-Joseph disease
27. Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24
28. Chronic Pain in Machado-Joseph Disease: 3:15-3:30 PM
29. Clinical and Genetic Heterogeneity in Familial Temporal Lobe Epilepsy
30. Developmental and neurodegenerative damage in Friedreich's ataxia
31. Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
32. Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients
33. Cryptic anhydrobiotic potential in man: Implications in medicine
34. The relationship between blood serum BDNF and seizure frequency in temporal lobe epilepsy patients
35. A new phenotype associated with homozygousGRNmutations: complicated spastic paraplegia
36. Developmental and neurodegenerative damage in Friedreich's ataxia.
37. Molecular testing for late onset neurodegenerative disorders: a health care professionals' perspective
38. Positive family history for epilepsy anticipates age of first seizure in patients with focal cortical dysplasia
39. Mesial temporal lobe abnormalities in a family with 15q26qter trisomy
40. Ancestral Origins of the Machado-Joseph Disease Mutation: A Worldwide Haplotype Study
41. A New Locus for Generalized Epilepsy with Febrile Seizures Plus Maps to Chromosome 2
42. Cdc2-like kinase 2 in the hypothalamus is necessary to maintain energy homeostasis
43. NewTHAP1mutation and role of putative modifier inTOR1A
44. RNA sequencing reveals region-specific molecular mechanisms associated with epileptogenesis in a model of classical hippocampal sclerosis
45. Genotype-Phenotype correlation in Dravet Syndrome with SCN1A mutation increase efficiency of molecular diagnosis
46. The role of noncoding regions modifications in neurodegenerative disorders
47. Pioglitazone treatment increases food intake and decreases energy expenditure partially via hypothalamic adiponectin/adipoR1/AMPK pathway
48. Cerebral cortex involvement in Machado−Joseph disease
49. 045 — (MAR0116) Tumor necrosis factor-alpha gene expression in the brain of Wistar audiogenic rats
50. Dentate nuclei T2 relaxometry is a reliable neuroimaging marker in Friedreich's ataxia
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