Showing 1 - 3 results of 3 for search 'Bogna Brockhuis', query time: 0.02s Refine Results
  1. 1
    Two Rare Variants in <i>PLAU</i> and <i>BACE1</i> Genes—Do They Contribute to Semantic Dementia Clinical Phenotype?

    Two Rare Variants in <i>PLAU</i> and <i>BACE1</i> Genes—Do They Contribute to Semantic Dementia Clinical Phenotype? by Katarzyna Gaweda-Walerych, Emilia J. Sitek, Małgorzata Borczyk, Mariusz Berdyński, Ewa Narożańska, Bogna Brockhuis, Michał Korostyński, Jarosław Sławek, Cezary Zekanowski

    Published 2021-11-01
    Get full text
    Article
  2. 2
    A Patient with Corticobasal Syndrome and Progressive Non-Fluent Aphasia (CBS-PNFA), with Variants in <i>ATP7B</i>, <i>SETX</i>, <i>SORL1</i>, and <i>FOXP1</i> Genes

    A Patient with Corticobasal Syndrome and Progressive Non-Fluent Aphasia (CBS-PNFA), with Variants in <i>ATP7B</i>, <i>SETX</i>, <i>SORL1</i>, and <i>FOXP1</i> Genes by Katarzyna Gaweda-Walerych, Emilia J. Sitek, Małgorzata Borczyk, Ewa Narożańska, Bogna Brockhuis, Michał Korostyński, Michał Schinwelski, Mariusz Siemiński, Jarosław Sławek, Cezary Zekanowski

    Published 2022-12-01
    Get full text
    Article
  3. 3
    A patient with posterior cortical atrophy possesses a novel mutation in the presenilin 1 gene.

    A patient with posterior cortical atrophy possesses a novel mutation in the presenilin 1 gene. by Emilia J Sitek, Ewa Narożańska, Beata Pepłońska, Sławomir Filipek, Anna Barczak, Maria Styczyńska, Krzysztof Mlynarczyk, Bogna Brockhuis, Erik Portelius, Dorota Religa, Maria Barcikowska, Jarosław Sławek, Cezary Żekanowski

    Published 2013-01-01
    Get full text
    Article

Search Tools: