Hasil Pencarian - Ingo Kennerknecht

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  1. 1
    The early time course of compensatory face processing in congenital prosopagnosia.

    The early time course of compensatory face processing in congenital prosopagnosia. oleh Rainer Stollhoff, Jürgen Jost, Tobias Elze, Ingo Kennerknecht

    Diterbitkan 2010-01-01
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  2. 2
    Deficits in long-term recognition memory reveal dissociated subtypes in congenital prosopagnosia.

    Deficits in long-term recognition memory reveal dissociated subtypes in congenital prosopagnosia. oleh Rainer Stollhoff, Jürgen Jost, Tobias Elze, Ingo Kennerknecht

    Diterbitkan 2011-01-01
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  3. 3
    Extreme founder effect associated with hyperglycemia and hyperlipidemia on the island of NIAS/Indonesia

    Extreme founder effect associated with hyperglycemia and hyperlipidemia on the island of NIAS/Indonesia oleh Ingo Kennerknecht, Johannes M. Hämmerle, Manfred Fobker, Jerzy-Roch Nofer

    Diterbitkan 2024-09-01
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  4. 4
    Neoplasia in Cri du Chat Syndrome from Italian and German Databases

    Neoplasia in Cri du Chat Syndrome from Italian and German Databases oleh Andrea Guala, Marianna Spunton, Silvia Kalantari, Ingo Kennerknecht, Cesare Danesino

    Diterbitkan 2017-01-01
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  5. 5
    Face Perception and Test Reliabilities in Congenital Prosopagnosia in Seven Tests

    Face Perception and Test Reliabilities in Congenital Prosopagnosia in Seven Tests oleh Janina Esins, Johannes Schultz, Claudia Stemper, Ingo Kennerknecht, Isabelle Bülthoff

    Diterbitkan 2016-01-01
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  6. 6
    Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face Area

    Face Processing in Developmental Prosopagnosia: Altered Neural Representations in the Fusiform Face Area oleh Alexa Haeger, Alexa Haeger, Alexa Haeger, Christophe Pouzat, Volker Luecken, Karim N’Diaye, Christian Elger, Ingo Kennerknecht, Nikolai Axmacher, Vera Dinkelacker, Vera Dinkelacker

    Diterbitkan 2021-11-01
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  7. 7
    MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta

    MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta oleh Uschi Lindert, Wayne A. Cabral, Surasawadee Ausavarat, Siraprapa Tongkobpetch, Katja Ludin, Aileen M. Barnes, Patra Yeetong, Maryann Weis, Birgit Krabichler, Chalurmpon Srichomthong, Elena N. Makareeva, Andreas R. Janecke, Sergey Leikin, Benno Röthlisberger, Marianne Rohrbach, Ingo Kennerknecht, David R. Eyre, Kanya Suphapeetiporn, Cecilia Giunta, Joan C. Marini, Vorasuk Shotelersuk

    Diterbitkan 2016-07-01
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