about
Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24Shp2 negatively regulates growth in cardiomyocytes by controlling focal adhesion kinase/Src and mTOR pathwaysLINKGEN: a new algorithm to process data in genetic linkage studies.MEF2C silencing attenuates load-induced left ventricular hypertrophy by modulating mTOR/S6K pathway in miceGenetic testing in the epilepsies--report of the ILAE Genetics CommissionAncestral origins of the Machado-Joseph disease mutation: a worldwide haplotype studyMuscle excitability abnormalities in Machado-Joseph disease.Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families.Patterns of hippocampal abnormalities in malformations of cortical developmentFamily history of cancer in Brazil: is it being used?The genetics of epilepsies.Experimental animal model and RNA interference: a promising association for bladder cancer research.Caring for Machado-Joseph disease: current understanding and how to help patients.MicroRNAs: a new paradigm on molecular urological oncology.MRI-texture analysis of corpus callosum, thalamus, putamen, and caudate in Machado-Joseph disease.Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder.Normal ATXN3 Allele but Not CHIP Polymorphisms Modulates Age at Onset in Machado-Joseph Disease.Longitudinal MRI volumetric evaluation in patients with familial mesial temporal lobe epilepsy.Analysis of energetically biased transcripts of viruses and transposable elements.Epileptic features of patients with unilateral and bilateral schizencephaly.Repeated neural tube defects and valproate monotherapy suggest a pharmacogenetic abnormality.A comparison between different reference genes for expression studies in human hippocampal tissue.Dysautonomia is frequent in Machado-Joseph disease: clinical and neurophysiological evaluation.Brain glyceraldehyde-3-phosphate dehydrogenase activity in human trinucleotide repeat disorders.Molecular diagnosis of Huntington disease in Brazilian patients.Clinical presentation of juvenile Huntington disease.Clinical and genetic analysis of 29 Brazilian patients with Huntington's disease-like phenotype.Longitudinal analysis of regional grey matter loss in Huntington disease: effects of the length of the expanded CAG repeat.Evidence of thalamic dysfunction in Huntington disease by proton magnetic resonance spectroscopy.Spinal cord atrophy correlates with disability in Friedreich's ataxia.Neuroanatomical correlates of depression in Friedreich's ataxia: a voxel-based morphometry study.Infratentorial gray matter atrophy and excess in primary craniocervical dystonia.Axonal dysfunction in the deep white matter in Machado-Joseph disease.Expression profile and distribution of Efhc1 gene transcript during rodent brain development.A new missense mutation found in the FLNA gene in a family with bilateral periventricular nodular heterotopia (BPNH) alters the splicing process.Phosphoinositide-specific inositol polyphosphate 5-phosphatase IV inhibits inositide trisphosphate accumulation in hypothalamus and regulates food intake and body weight.Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum.Linkage study of voltage-gated potassium channels in familial mesial temporal lobe epilepsy.Outcome of surgical treatment in familial mesial temporal lobe epilepsy.Segregation analysis in mesial temporal lobe epilepsy with hippocampal atrophy.
P50
Q24539202-51C2D26D-01DA-4CD4-9F8F-71191E9CA4D1Q28854293-FA0762D7-41E8-4DEB-BD46-E926279AC60DQ31151101-7C75E55C-F0D7-4CA5-94C1-AE9F472F02CDQ33521236-64E07FC4-F388-4D15-A9D8-201A5416E894Q33794130-161922C8-113D-4F8E-B3BA-3C901CAD5A52Q33929425-7F70C1BB-B38D-449A-BBCB-3CA9EE9B011CQ34590492-0604694D-5160-4D34-83A4-0EA21ECE1F5CQ35956314-B9C4BE71-3562-4E43-A688-4BB6F38B1E0BQ36143012-41CA4F9E-5692-417E-8E53-CC6BDFE565B7Q37056314-FAB7C705-4F1A-4D47-9FE4-15FA69DC68EBQ37268832-FE7FE31E-7509-4375-BA15-5A36A485B876Q37392045-092CEAFD-B00C-4AC4-B124-5848E2FB6481Q37610601-251003A2-2F40-4494-86CF-6FCEAD2D0034Q37753387-3485F9F6-5C5C-4C80-B0EE-A3FBD97E05E6Q39960976-6D618B7C-78B8-4A06-AA56-402DA3146FB3Q40621263-FBA87007-47E0-481C-AB6D-F4F125BDB876Q41443029-05B7B7D0-75E7-4F8F-8833-405F63736EC5Q42117907-0424F5BD-8411-4EB7-84B6-4EBDA5D4C968Q42419111-6F964643-C167-4FCA-8166-3C6B1744409BQ42598148-D73643EE-3EA5-48FC-8945-A38BC97609A4Q43650811-7FD05A12-D030-4BDB-9B5E-32F0F4AE95BCQ43880639-BCC97611-0F3E-453D-9391-AE549C0547ADQ44898561-B2166BAF-FC47-411C-825B-0A5C3F5FADFDQ45296636-57DC99B4-DB5A-4F75-AE40-0ACBE118A475Q45300182-FE9D0B8F-A8CF-45FD-BC0C-3130663996D2Q45300768-043B4410-A2D6-43B5-B294-000437E969DEQ45303584-954CA213-4234-4543-82B0-1C2FFE65F248Q45305612-3ECF6917-5E31-4171-BCF3-58FECF097B0AQ45305917-0EB880FE-E994-4E32-89A4-5E561D7A43D9Q45717356-D1BC86A5-C8B7-4DB1-836B-EE7CB146CB4CQ45940295-45689329-C867-4F49-8114-86B71245258EQ46016674-99BF8CF9-6088-49E2-954C-D8F9D85C3EE3Q46594116-575F69D3-39EC-4FD4-878B-DD2DAB39E4C6Q46807760-C72F3B41-4CBF-450A-9C51-E02567750F9EQ46844981-9E74AEB3-A719-4525-BEF2-55C71F5DB79DQ47325116-9E7B2556-D771-4047-B9E5-8C9ADA28D8BEQ48160809-3529BFBB-6AEF-4CC6-BCE1-6493BA46BC1BQ48210021-9C44DBF8-4299-4409-8512-D9A0CAEB02B1Q48240881-B2252579-9CFE-405A-A8A8-32DD34B918A6Q48253184-0F8ED96B-AF29-49FF-81D6-02E76C84CEF3
P50
description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Iscia Lopes-Cendes
@ast
Iscia Lopes-Cendes
@en
Iscia Lopes-Cendes
@es
Iscia Lopes-Cendes
@nl
Iscia Lopes-Cendes
@sl
type
label
Iscia Lopes-Cendes
@ast
Iscia Lopes-Cendes
@en
Iscia Lopes-Cendes
@es
Iscia Lopes-Cendes
@nl
Iscia Lopes-Cendes
@sl
prefLabel
Iscia Lopes-Cendes
@ast
Iscia Lopes-Cendes
@en
Iscia Lopes-Cendes
@es
Iscia Lopes-Cendes
@nl
Iscia Lopes-Cendes
@sl
P106
P1153
7003572956
P21
P31
P496
0000-0002-6221-6822