HAX1 mutations causing severe congenital neuropenia and neurological disease lead to cerebral microstructural abnormalities documented by quantitative MRI
Boztug, Kaan, Ding, Xiao‐Qi, Hartmann, Hans, Ziesenitz, Lena, Schäffer, Alejandro A., Diestelhorst, Jana, Pfeifer, Dietmar, Appaswamy, Giridharan, Kehbel, Sonja, Simon, Thorsten, Al Jefri, Abdullah, Lanfermann, Heinrich, Klein, Christoph
Published in American journal of medical genetics. Part A (01.12.2010)
Published in American journal of medical genetics. Part A (01.12.2010)
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Journal Article
HAX1 Mutations causing SCN and Neurological Disease Lead to Microstructural Abnormalities Revealed by Quantitative MRI
Boztug, Kaan, Ding, Xiao-Qi, Hartmann, Hans, Ziesenitz, Lena, Schäffer, Alejandro A., Diestelhorst, Jana, Pfeifer, Dietmar, Appaswamy, Giridharan, Kehbel, Sonja, Simon, Thorsten, Jefri, Abdullah Al, Lanfermann, Heinrich, Klein, Christoph
Published in American journal of medical genetics. Part A (01.12.2010)
Published in American journal of medical genetics. Part A (01.12.2010)
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Journal Article
Value of quantitative analysis of routine clinical MRI sequences in ALS
Ding, Xiao-Qi, Kollewe, Katja, Blum, Katrin, Körner, Sonja, Kehbel, Sonja, Dengler, Reinhard, Lanfermann, Heinrich, Petri, Susanne
Published in Amyotrophic lateral sclerosis (01.11.2011)
Published in Amyotrophic lateral sclerosis (01.11.2011)
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Journal Article
HAX1 mutations causing severe congenital neuropenia and neurological disease lead to cerebral microstructural abnormalities documented by quantitative MRI
Boztug, Kaan, Ding, Xiao-Qi, Hartmann, Hans, Ziesenitz, Lena, Schäffer, Alejandro A., Diestelhorst, Jana, Pfeifer, Dietmar, Appaswamy, Giridharan, Kehbel, Sonja, Simon, Thorsten, Al Jefri, Abdullah, Lanfermann, Heinrich, Klein, Christoph
Published in American Journal of Medical Genetics Part A (01.12.2010)
Published in American Journal of Medical Genetics Part A (01.12.2010)
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