نتائج البحث - Christiane Kehrer

  • يعرض 1 - 10 نتائج من 10
تنقيح النتائج
  1. 1
    The natural course of gross motor deterioration in metachromatic leukodystrophy

    The natural course of gross motor deterioration in metachromatic leukodystrophy حسب Christiane Kehrer, Gunnar Blumenstock, Volkmar Gieselmann, Ingeborg Krägeloh‐Mann

    منشور في 2011
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  2. 2
    Development and reliability of a classification system for gross motor function in children with metachromatic leucodystrophy

    Development and reliability of a classification system for gross motor function in children with metachromatic leucodystrophy حسب Christiane Kehrer, Gunnar Blumenstock, Christa Raabe, Ingeborg Krägeloh‐Mann

    منشور في 2010
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  3. 3
    The impact of severe rare chronic neurological disease in childhood on the quality of life of families—a study on MLD and PCH2

    The impact of severe rare chronic neurological disease in childhood on the quality of life of families—a study on MLD and PCH2 حسب Louisa Ammann-Schnell, Samuel Groeschel, Christiane Kehrer, Saskia Frölich, Ingeborg Krägeloh‐Mann

    منشور في 2021
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  4. 4
    Metachromatic leukodystrophy: natural course of cerebral MRI changes in relation to clinical course

    Metachromatic leukodystrophy: natural course of cerebral MRI changes in relation to clinical course حسب Samuel Groeschel, Christiane Kehrer, Corinna Engel, Christine í Dali, Annette Bley, Robert Steinfeld, Wolfgang Grodd, Ingeborg Krägeloh‐Mann

    منشور في 2011
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  5. 5
    Cerebral gray and white matter changes and clinical course in metachromatic leukodystrophy

    Cerebral gray and white matter changes and clinical course in metachromatic leukodystrophy حسب Samuel Groeschel, Christine í Dali, Philipp Clas, Judith Böhringer, Morten Dunø, Christian Krarup, Christiane Kehrer, Marko Wilke, Ingeborg Krägeloh‐Mann

    منشور في 2012
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  6. 6
    Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohort

    Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohort حسب Christiane Kehrer, Samuel Groeschel, B. Kustermann‐Kuhn, Friederike Bürger, Wolfgang Köhler, Alfried Kohlschütter, Annette Bley, Robert Steinfeld, Volkmar Gieselmann, Ingeborg Krägeloh‐Mann

    منشور في 2014
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  7. 7
    Predicting clinical phenotypes of metachromatic leukodystrophy based on the arylsulfatase A activity and the ARSA genotype? – Chances and challenges

    Predicting clinical phenotypes of metachromatic leukodystrophy based on the arylsulfatase A activity and the ARSA genotype? – Chances and challenges حسب Vidiyaah Santhanakumaran, Samuel Groeschel, K. Harzer, Christiane Kehrer, Saskia Elgün, Stefanie Beck‐Wödl, Holger Hengel, Lüdger Schöls, Tobias B. Haack, Ingeborg Krägeloh‐Mann, Lucia Laugwitz

    منشور في 2022
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  8. 8
    Long-term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Juvenile Metachromatic Leukodystrophy Compared With Nontransplanted Control Patients

    Long-term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Juvenile Metachromatic Leukodystrophy Compared With Nontransplanted Control Patients حسب Samuel Groeschel, Jörn‐Sven Kühl, Annette Bley, Christiane Kehrer, Bernhard Weschke, Michaela Döring, Judith Böhringer, Johanna Schrum, René Santer, Alfried Kohlschütter, Ingeborg Krägeloh‐Mann, Ingo Müller

    منشور في 2016
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  9. 9
    Phenotypic variation between siblings with Metachromatic Leukodystrophy

    Phenotypic variation between siblings with Metachromatic Leukodystrophy حسب Saskia Elgün, Jakob Waibel, Christiane Kehrer, Diane van Rappard, Judith Böhringer, Stefanie Beck‐Wödl, Jennifer Just, Lüdger Schöls, Nicole I. Wolf, Ingeborg Krägeloh‐Mann, Samuel Groeschel

    منشور في 2019
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  10. 10
    Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra‐rare disease

    Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra‐rare disease حسب Laura Adang, Lars Schlotawa, Samuel Groeschel, Christiane Kehrer, K. Harzer, Orna Staretz‐Chacham, Thiago Oliveira Silva, Ida Vanessa Döederlein Schwartz, Jutta Gärtner, Mauricio De Castro, Carrie Costin, Esperanza Font–Montgomery, Thomas Dierks, Karthikeyan Radhakrishnan, Rebecca C. Ahrens‐Nicklas

    منشور في 2020
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:

أدوات البحث: