نتائج البحث - Jean‐Jacques Martin

تنقيح النتائج
  1. 1
    The monoaminergic footprint of depression and psychosis in dementia with Lewy bodies compared to Alzheimer’s disease

    The monoaminergic footprint of depression and psychosis in dementia with Lewy bodies compared to Alzheimer’s disease حسب Yannick Vermeiren, Debby Van Dam, Tony Aerts, Sebastiaan Engelborghs, Jean‐Jacques Martin, Peter Paul De Deyn

    منشور في 2015
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    Artigo
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  2. 2
    Cerebrospinal Fluid P-Tau181P: Biomarker for Improved Differential Dementia Diagnosis

    Cerebrospinal Fluid P-Tau181P: Biomarker for Improved Differential Dementia Diagnosis حسب Hanne Struyfs, Ellis Niemantsverdriet, Joery Goossens, Erik Fransén, Jean‐Jacques Martin, Peter Paul De Deyn, Sebastiaan Engelborghs

    منشور في 2015
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    Artigo
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  3. 3
    Overdiagnosing Vascular Dementia using Structural Brain Imaging for Dementia Work-Up

    Overdiagnosing Vascular Dementia using Structural Brain Imaging for Dementia Work-Up حسب Ellis Niemantsverdriet, Bart Feyen, Nathalie Le Bastard, Jean‐Jacques Martin, Johan Goeman, Peter Paul De Deyn, Sebastiaan Engelborghs

    منشور في 2015
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  4. 4
    Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group.

    Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group. حسب Peter Raeymaekers, Vincent Timmerman, Eva Nelis, Wim Van Hul, Peter De Jonghe, Jean‐Jacques Martin, Christine Van Broeckhoven

    منشور في 1992
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  5. 5
    Brain Serotonergic and Noradrenergic Deficiencies in Behavioral Variant Frontotemporal Dementia Compared to Early-Onset Alzheimer’s Disease

    Brain Serotonergic and Noradrenergic Deficiencies in Behavioral Variant Frontotemporal Dementia Compared to Early-Onset Alzheimer’s Disease حسب Yannick Vermeiren, Jana Janssens, Tony Aerts, Jean‐Jacques Martin, Anne Sieben, Debby Van Dam, Peter Paul De Deyn

    منشور في 2016
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  6. 6
    Cerebrospinal Fluid Aβ1-40 Improves Differential Dementia Diagnosis in Patients with Intermediate P-tau181P Levels

    Cerebrospinal Fluid Aβ1-40 Improves Differential Dementia Diagnosis in Patients with Intermediate P-tau181P Levels حسب Sylvie Slaets, Nathalie Le Bastard, Jean‐Jacques Martin, Kristel Sleegers, Christine Van Broeckhoven, Peter Paul De Deyn, Sebastiaan Engelborghs

    منشور في 2013
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  7. 7
    The genetics and neuropathology of frontotemporal lobar degeneration

    The genetics and neuropathology of frontotemporal lobar degeneration حسب Anne Sieben, Tim Van Langenhove, Sebastiaan Engelborghs, Jean‐Jacques Martin, Paul Boon, Patrick Cras, P. De Deyn, Patrick Santens, Christine Van Broeckhoven, Marc Cruts

    منشور في 2012
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    Revisão
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  8. 8
    Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala→Gly mutation

    Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala→Gly mutation حسب Patrick Cras, F. van Harskamp, Lydia Hendriks, C. Ceuterick, Cornelia M. van Duijn, S Stefanko, Albert Hofman, J. M. Kros, Christine Van Broeckhoven, Jean‐Jacques Martin, F. van Harskamp

    منشور في 1998
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  9. 9
    Genetic risk and transcriptional variability of amyloid precursor protein in Alzheimer's disease

    Genetic risk and transcriptional variability of amyloid precursor protein in Alzheimer's disease حسب Nathalie Brouwers, Kristel Sleegers, Sebastiaan Engelborghs, Veerle Bogaerts, Sally Serneels, Koorosh Kamali, Ellen Corsmit, Evelyn De Leenheir, Jean‐Jacques Martin, Peter Paul De Deyn, Christine Van Broeckhoven, Jessie Theuns

    منشور في 2006
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  10. 10
    Linezolid-Induced Inhibition of Mitochondrial Protein Synthesis

    Linezolid-Induced Inhibition of Mitochondrial Protein Synthesis حسب An S. De Vriese, Rudy Van Coster, Joél Smet, Sara Seneca, A. M. Lovering, Lindsey Van Haute, Ludo Vanopdenbosch, Jean‐Jacques Martin, Chantal Ceuterick‐de Groote, Stefaan J. Vandecasteele, Johan R. Boelaert

    منشور في 2006
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  11. 11
    A Decade of Cerebrospinal Fluid Biomarkers for Alzheimer’s Disease in Belgium

    A Decade of Cerebrospinal Fluid Biomarkers for Alzheimer’s Disease in Belgium حسب Charisse Somers, Hanne Struyfs, Joery Goossens, Ellis Niemantsverdriet, Jill Luyckx, Naomi De Roeck, Ellen De Roeck, Bart De Vil, Patrick Cras, Jean‐Jacques Martin, Peter-Paul De Deyn, Maria Bjerke, Sebastiaan Engelborghs

    منشور في 2016
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  12. 12
    Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene

    Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene حسب Lydia Hendriks, Cornelia M. van Duijn, Patrick Cras, Marc Cruts, Wim Van Hul, F. van Harskamp, Andrew Warren, Melvin G. McInnis, Stylianos E. Antonarakis, Jean‐Jacques Martin, Albert Hofman, Christine Van Broeckhoven

    منشور في 1992
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  13. 13
    Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degeneration

    Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degeneration حسب Joery Goossens, Maria Bjerke, Sara Van Mossevelde, Tobi Van den Bossche, Johan Goeman, Bart De Vil, Anne Sieben, Jean‐Jacques Martin, Patrick Cras, Peter Paul De Deyn, Christine Van Broeckhoven, Julie van der Zee, Sebastiaan Engelborghs

    منشور في 2018
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  14. 14
    Dense-Core Senile Plaques in the Flemish Variant of Alzheimer's Disease Are Vasocentric

    Dense-Core Senile Plaques in the Flemish Variant of Alzheimer's Disease Are Vasocentric حسب Samir Kumar‐Singh, Patrick Cras, Rong Wang, J. M. Kros, Johan van Swieten, Ursula Lübke, C. Ceuterick, Sally Serneels, Krist’l Vennekens, Jean‐Pierre Timmermans, Eric Van Marck, Jean‐Jacques Martin, Cornelia M. van Duijn, Christine Van Broeckhoven

    منشور في 2002
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  15. 15
    Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Early-Onset Myopathies

    Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Ea... حسب Ana Ferreiro, Susana Quijano-Roy, Claire Pichereau, Behzad Moghadaszadeh, Nathalie Goemans, Carsten G. Bönnemann, Heinz Jungbluth, Volker Straub, Marcello Villanova, Jean‐Paul Leroy, Norma B. Romero, Jean‐Jacques Martin, Francesco Muntoni, Thomas Voit, B. Estournet, Pascale Richard, Michel Fardeau, Pascale Guicheney

    منشور في 2002
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  16. 16
    Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS

    Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS حسب Ilse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, Wim Robberecht, Jean‐Jacques Martin, Rik Vandenberghe, Raf Sciot, Bart Dermaut, D. Goossens, Julie van der Zee, Tim De Pooter, Jurgen Del‐Favero, Patrick Santens, Peter De Jonghe, Peter P. De Deyn, Christine Van Broeckhoven, Marc Cruts

    منشور في 2008
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  17. 17
    A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD

    A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD حسب Julie van der Zee, Rosa Rademakers, Sebastiaan Engelborghs, Ilse Gijselinck, Veerle Bogaerts, Rik Vandenberghe, Patrick Santens, Jo Caekebeke, Tim De Pooter, Karin Peeters, Ursula Lübke, Marleen Van den Broeck, Jean‐Jacques Martin, Marc Cruts, Peter Paul De Deyn, Christine Van Broeckhoven, Bart Dermaut

    منشور في 2006
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  18. 18
    Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions

    Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions حسب Paola S. Denora, Katrien Smets, Federica Zolfanelli, Chantal Ceuterick-de Groote, Carlo Casali, Tine Deconinck, Anne Sieben, Michael Gonzales, Stephan Züchner, Frédéric Darios, D. Peeters, Alexis Brice, Alessandro Malandrini, Peter De Jonghe, Filippo M. Santorelli, Giovanni Stévanin, Jean‐Jacques Martin, Khalid Hamid El Hachimi

    منشور في 2016
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  19. 19
    Loss of Function of Glucocerebrosidase GBA2 Is Responsible for Motor Neuron Defects in Hereditary Spastic Paraplegia

    Loss of Function of Glucocerebrosidase GBA2 Is Responsible for Motor Neuron Defects in Hereditary Spastic Paraplegia حسب Elodie Martin, Rebecca Schüle, Katrien Smets, Agnès Rastetter, Amir Boukhris, José L. Loureiro, Michael Gonzalez, Emeline Mundwiller, Tine Deconinck, Marc Wessner, Ludmila Jornéa, Andrés Caballero-Oteyza, Alexandra Dürr, Jean‐Jacques Martin, Lüdger Schöls, Chokri Mhiri, Foudil Lamari, Stephan Züchner, Peter De Jonghe, Edor Kabashi, Alexis Brice, Giovanni Stévanin

    منشور في 2013
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  20. 20
    Mutated ATP10B increases Parkinson’s disease risk by compromising lysosomal glucosylceramide export

    Mutated ATP10B increases Parkinson’s disease risk by compromising lysosomal glucosylceramide export حسب Shaun Martin, Stefanie Smolders, Chris Van den Haute, Bavo Heeman, Sarah van Veen, David Crosiers, Igor Beletchi, Aline Verstraeten, Helena Gossye, Géraldine Gelders, Philippe Pals, Norin Nabil Hamouda, Sebastiaan Engelborghs, Jean‐Jacques Martin, Jan Eggermont, Peter Paul De Deyn, Patrick Cras, Veerle Baekelandt, Peter Vangheluwe, Christine Van Broeckhoven

    منشور في 2020
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