نتائج البحث - Boot, Erik
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AMPT-induced monoamine depletion in humans: evaluation of two alternative [(123)I]IBZM SPECT procedures حسب Boot, Erik, Booij, Jan, Hasler, Gregor, Zinkstok, Janneke R., de Haan, Lieuwe, Linszen, Don H., van Amelsvoort, Thérèse A.
منشور في 2008نص -
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Neuropsychiatric expression and catatonia in 22q11.2 deletion syndrome: An overview and case series حسب Butcher, Nancy J., Boot, Erik, Lang, Anthony E., Andrade, Danielle, Vorstman, Jacob, McDonald-McGinn, Donna, Bassett, Anne S.
منشور في 2018نص -
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F72. NEUROCOGNITION AND ADAPTIVE FUNCTIONING IN THE 22Q11.2 DELETION SYNDROME MODEL OF SCHIZOPHRENIA حسب Ania, Fiksinski, Breetvelt, Elemi, Vorstman, Jacob, Chow, Eva, Lee, Erin, Palmer, Lisa, Boot, Erik, Butcher, Nancy, Kahn, Rene, Bassett, Anne
منشور في 2018نص -
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A mouse model of 22q11.2 deletions: Molecular and behavioral signatures of Parkinson’s disease and schizophrenia حسب Sumitomo, Akiko, Horike, Kouta, Hirai, Kazuko, Butcher, Nancy, Boot, Erik, Sakurai, Takeshi, Nucifora, Frederick C., Bassett, Anne S., Sawa, Akira, Tomoda, Toshifumi
منشور في 2018نص -
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Proton Magnetic Resonance Spectroscopy in 22q11 Deletion Syndrome حسب da Silva Alves, Fabiana, Boot, Erik, Schmitz, Nicole, Nederveen, Aart, Vorstman, Jacob, Lavini, Christina, Pouwels, Petra, de Haan, Lieuwe, Linszen, Don, van Amelsvoort, Therese
منشور في 2011نص -
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Correction: Proton Magnetic Resonance Spectroscopy in 22q11 Deletion Syndrome حسب da Silva Alves, Fabiana, Boot, Erik, Schmitz, Nicole, Nederveen, Aart, Vorstman, Jacob, Lavini, Christina, Pouwels, Petra, de Haan, Lieuwe, Linszen, Don, van Amelsvoort, Therese
منشور في 2011نص -
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Movement Disorders and Other Motor Abnormalities in Adults With 22q11.2 Deletion Syndrome حسب Boot, Erik, Butcher, Nancy J, van Amelsvoort, Thérèse AMJ, Lang, Anthony E, Marras, Connie, Pondal, Margarita, Andrade, Danielle M, Fung, Wai Lun Alan, Bassett, Anne S
منشور في 2015نص -
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Functional Gene-Expression Analysis Shows Involvement of Schizophrenia-Relevant Pathways in Patients with 22q11 Deletion Syndrome حسب van Beveren, Nico J. M., Krab, Lianne C., Swagemakers, Sigrid, Buitendijk, Gabriella, Boot, Erik, van der Spek, Peter, Elgersma, Ype, van Amelsvoort, Therese A. M. J.
منشور في 2012نص -
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Correction: Functional Gene-Expression Analysis Shows Involvement of Schizophrenia-Relevant Pathways in Patients with 22q11 Deletion Syndrome حسب van Beveren, Nico J. M., Krab, Lianne C., Swagemakers, Sigrid, Buitendijk, Gabriëe H.S., Boot, Erik, van der Spek, Peter, Elgersma, Ype, van Amelsvoort, Therese A. M. J.
منشور في 2012نص -
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All-cause mortality and survival in adults with 22q11.2 deletion syndrome حسب Van, Lily, Heung, Tracy, Graffi, Justin, Ng, Enoch, Malecki, Sarah, Van Mil, Spencer, Boot, Erik, Corral, Maria, Chow, Eva W. C., Hodgkinson, Kathleen A., Silversides, Candice, Bassett, Anne S.
منشور في 2019نص -
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22q11.2 microdeletion and increased risk for type 2 diabetes حسب Van, Lily, Heung, Tracy, Malecki, Sarah L., Fenn, Christian, Tyrer, Andrea, Sanches, Marcos, Chow, Eva W.C., Boot, Erik, Corral, Maria, Dash, Satya, George, Susan R., Bassett, Anne S.
منشور في 2020نص