List of works - Michele C Landemberger

Asymmetric cortical high signal on diffusion weighted-MRI in a case of Creutzfeldt-Jakob disease

scientific article published in June 2005

Codon 129 polymorphism of prion protein gene in is not a risk factor for Alzheimer's disease

scientific article published in July 2013

Cognitive performance of patients with mesial temporal lobe epilepsy is not associated with human prion protein gene variant allele at codons 129 and 171.

scientific article published on 3 April 2006

Complex movement disorders in fatal familial insomnia: a clinical and genetic discussion.

scientific article

Cortical malformations are associated with a rare polymorphism of cellular prion protein

scientific article published on 01 August 2004

Creutzfeldt-Jakob disease associated with a missense mutation at codon 200 of the prion protein gene in Brazil.

scientific article published in April 2007

Disease-associated mutations in the prion protein impair laminin-induced process outgrowth and survival

scientific article

First case of V180I rare mutation in a Brazilian patient with Creutzfeldt-Jakob disease.

scientific article published on 2 November 2017

High capacity and low cost detection of prion protein gene variant alleles by denaturing HPLC.

scientific article published in October 2004

High phenotypic variability in Gerstmann-Sträussler-Scheinker disease.

scientific article

Impaired exercise capacity, but unaltered mitochondrial respiration in skeletal or cardiac muscle of mice lacking cellular prion protein.

scientific article

Loss of STI1-mediated neuronal survival and differentiation in disease-associated mutations of prion protein

scientific article published on 16 January 2018

PrPC displays an essential protective role from oxidative stress in an astrocyte cell line derived from PrPC knockout mice

scientific article published on 26 December 2011

Prion diseases are undercompulsory notification in Brazil: Surveillance of cases evaluated by biochemicaland/or genetic markers from 2005 to 2007.

scientific article published in October 2007

Prnp gene and cerebellum volume in patients with refractory mesial temporal lobe epilepsy

scientific article published on 5 October 2013

Sexual disinhibition and agrypnia excitata in fatal familial insomnia.

scientific article published on 25 May 2016

List of works by Michele C Landemberger

Asymmetric cortical high signal on diffusion weighted-MRI in a case of Creutzfeldt-Jakob disease

Codon 129 polymorphism of prion protein gene in is not a risk factor for Alzheimer's disease

Cognitive performance of patients with mesial temporal lobe epilepsy is not associated with human prion protein gene variant allele at codons 129 and 171.

Complex movement disorders in fatal familial insomnia: a clinical and genetic discussion.

Cortical malformations are associated with a rare polymorphism of cellular prion protein

Creutzfeldt-Jakob disease associated with a missense mutation at codon 200 of the prion protein gene in Brazil.

Disease-associated mutations in the prion protein impair laminin-induced process outgrowth and survival

First case of V180I rare mutation in a Brazilian patient with Creutzfeldt-Jakob disease.

High capacity and low cost detection of prion protein gene variant alleles by denaturing HPLC.

High phenotypic variability in Gerstmann-Sträussler-Scheinker disease.

Impaired exercise capacity, but unaltered mitochondrial respiration in skeletal or cardiac muscle of mice lacking cellular prion protein.

Loss of STI1-mediated neuronal survival and differentiation in disease-associated mutations of prion protein

PrPC displays an essential protective role from oxidative stress in an astrocyte cell line derived from PrPC knockout mice

Prion diseases are undercompulsory notification in Brazil: Surveillance of cases evaluated by biochemicaland/or genetic markers from 2005 to 2007.

Prnp gene and cerebellum volume in patients with refractory mesial temporal lobe epilepsy

Sexual disinhibition and agrypnia excitata in fatal familial insomnia.