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List of works by Claudia Vianna Maurer-Morelli

A Locus Identified on Chromosome18P11.31 is Associated with Hippocampal Abnormalities in a Family with Mesial Temporal Lobe Epilepsy ⬇️

scientific article published on August 10, 2012

A Prediction Algorithm for Drug Response in Patients with Mesial Temporal Lobe Epilepsy Based on Clinical and Genetic Information

scientific article

A comparison between different reference genes for expression studies in human hippocampal tissue

scientific article published on 3 May 2012

Cyclooxygenase-1 as a Potential Therapeutic Target for Seizure Suppression: Evidences from Zebrafish Pentylenetetrazole-Seizure Model.

scientific article published on 15 November 2016

Downregulation of 14q32 microRNAs in Primary Human Desmoplastic Medulloblastoma

scientific article published on 25 September 2013

Expression and activity of thimet oligopeptidase (TOP) are modified in the hippocampus of subjects with temporal lobe epilepsy (TLE).

scientific article

Family-Based Genetic Association for Molar-Incisor Hypomineralization

scientific article published on 14 May 2016

Indomethacin treatment prior to pentylenetetrazole-induced seizures downregulates the expression of il1b and cox2 and decreases seizure-like behavior in zebrafish larvae

scientific article

Insertional translocation of 15q25-q26 into 11p13 and duplication at 8p23.1 characterized by high resolution arrays in a boy with congenital malformations and aniridia

scientific article published on 18 September 2012

Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation.

scientific article published on 13 November 2014

LINKGEN: a new algorithm to process data in genetic linkage studies.

scientific article

Linkage study of voltage-gated potassium channels in familial mesial temporal lobe epilepsy.

scientific article

MRI and EEG as long-term seizure outcome predictors in familial mesial temporal lobe epilepsy

scientific article published on 28 November 2012

Mutations in PYCR1 gene in three families with autosomal recessive cutis laxa, type 2 ⬇️

scientific article published on March 24, 2013

Normal ATXN3 Allele but Not CHIP Polymorphisms Modulates Age at Onset in Machado-Joseph Disease.

scientific article published on 19 November 2012

Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum.

scientific article

Segregation analysis in mesial temporal lobe epilepsy with hippocampal atrophy

scientific article published in February 2010

THE SCN2A gene is not a likely candidate for familial mesial temporal lobe epilepsy

scientific article published on 17 August 2006

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