Berit Jordan

Summary

Affiliation: Martin Luther University
Country: Germany

Publications

  1. ncbi request reprint Successful treatment of MuSK antibody-positive myasthenia gravis with rituximab
    Berit Hain
    Department of Neurology, Martin Luther University of Halle Wittenberg, Ernst Grube Strasse 40, 06120 Halle Saale, Germany
    Muscle Nerve 33:575-80. 2006
  2. doi request reprint [Neuromyelitis optica: a separate disease entity associated with aquaporin-4-antibodies]
    B Jordan
    Klinik und Poliklinik fur Neurologie, Martin Luther Universitat Halle Wittenberg, Halle Saale
    Fortschr Neurol Psychiatr 76:21-7. 2008
  3. doi request reprint [Polymyositis associated with thymoma]
    B Jordan
    Klinik und Poliklinik fur Neurologie, Martin Luther Universitat Halle Wittenberg, Ernst Grube Strasse 40, 06097, Halle Saale, Deutschland
    Nervenarzt 80:708-11. 2009
  4. doi request reprint Camptocormia phenotype of FSHD: a clinical and MRI study on six patients
    Berit Jordan
    Department of Neurology, Martin Luther University Halle Wittenberg, Halle Saale, Germany
    J Neurol 258:866-73. 2011
  5. doi request reprint [Facioscapulohumeral muscular dystrophy. Clinical picture, atypical forms, diagnostics, genetics]
    B Jordan
    Klinik fur Neurologie, Martin Luther Universitat Halle Wittenberg, Halle Saale
    Nervenarzt 82:712-22. 2011
  6. doi request reprint Beevor's sign in facioscapulohumeral muscular dystrophy: an old sign with new implications
    Katharina Eger
    Neurologische Klinik und Poliklinik, Universitätsklinikum Halle, Martin Luther University of Halle Wittenberg, Ernst Grube Strasse 40, 06097, Halle Saale, Germany
    J Neurol 257:436-8. 2010
  7. ncbi request reprint Hybrid genes between HLA-A2 and HLA-A3 constructed by in vivo recombination allow mapping of HLA-A2 and HLA-A3 polymorphic antigenic determinants
    J Sire
    Centre d Immunologie, Institut National de la Sante et de la Recherche Medicale, Marseille, France
    J Immunol 140:2422-30. 1988
  8. ncbi request reprint [Klüver-Bucy syndrome in humans]
    C Gaul
    Klinik fur Psychiatrie und Psychotherapie, Martin Luther Universitat, Halle Wittenberg
    Nervenarzt 78:821-3. 2007

Collaborators

Detail Information

Publications8

  1. ncbi request reprint Successful treatment of MuSK antibody-positive myasthenia gravis with rituximab
    Berit Hain
    Department of Neurology, Martin Luther University of Halle Wittenberg, Ernst Grube Strasse 40, 06120 Halle Saale, Germany
    Muscle Nerve 33:575-80. 2006
    ..The patient continued to remain stable 12 months after initiation of therapy. This case report demonstrates that rituximab may be an effective and tolerable treatment in MuSK antibody-positive myasthenia gravis...
  2. doi request reprint [Neuromyelitis optica: a separate disease entity associated with aquaporin-4-antibodies]
    B Jordan
    Klinik und Poliklinik fur Neurologie, Martin Luther Universitat Halle Wittenberg, Halle Saale
    Fortschr Neurol Psychiatr 76:21-7. 2008
    ..In addition, the identification of AQP-4 antibodies supports peripheral humoral autoimmune pathogenesis in NMO and permits early initiation of effective therapy for prevention of attack-related disability...
  3. doi request reprint [Polymyositis associated with thymoma]
    B Jordan
    Klinik und Poliklinik fur Neurologie, Martin Luther Universitat Halle Wittenberg, Ernst Grube Strasse 40, 06097, Halle Saale, Deutschland
    Nervenarzt 80:708-11. 2009
    ..Due to the simultaneous occurrence of these paraneoplastic diseases, the criteria for exact diagnosis (serum creatine kinase, EMG, ocular involvement) overlap. This diagnostic dilemma can appreciably complicate the therapeutic approach...
  4. doi request reprint Camptocormia phenotype of FSHD: a clinical and MRI study on six patients
    Berit Jordan
    Department of Neurology, Martin Luther University Halle Wittenberg, Halle Saale, Germany
    J Neurol 258:866-73. 2011
    ..The involvement of hip extensor muscles in FSHD might considerably contribute to the clinical phenotype of camptocormia due to axial muscle involvement...
  5. doi request reprint [Facioscapulohumeral muscular dystrophy. Clinical picture, atypical forms, diagnostics, genetics]
    B Jordan
    Klinik fur Neurologie, Martin Luther Universitat Halle Wittenberg, Halle Saale
    Nervenarzt 82:712-22. 2011
    ..Penetrance of this dominantly inherited disorder is high, exhibiting a great phenotypic variability in clinical pattern and disease progression even among affected members of the same family...
  6. doi request reprint Beevor's sign in facioscapulohumeral muscular dystrophy: an old sign with new implications
    Katharina Eger
    Neurologische Klinik und Poliklinik, Universitätsklinikum Halle, Martin Luther University of Halle Wittenberg, Ernst Grube Strasse 40, 06097, Halle Saale, Germany
    J Neurol 257:436-8. 2010
    ..However, especially in atypical cases, Beevor's sign might help in the diagnosis of FSHD...
  7. ncbi request reprint Hybrid genes between HLA-A2 and HLA-A3 constructed by in vivo recombination allow mapping of HLA-A2 and HLA-A3 polymorphic antigenic determinants
    J Sire
    Centre d Immunologie, Institut National de la Sante et de la Recherche Medicale, Marseille, France
    J Immunol 140:2422-30. 1988
    ..But aspartic residue 161 contributes with glutamic acid residue 152 in the formation of the A3 epitope recognized by the anti-A3 mAb X1.23.2...
  8. ncbi request reprint [Klüver-Bucy syndrome in humans]
    C Gaul
    Klinik fur Psychiatrie und Psychotherapie, Martin Luther Universitat, Halle Wittenberg
    Nervenarzt 78:821-3. 2007
    ..Seizures are another frequent symptom. Here we describe KBS in a female inpatient aged 30 in whom KBS and psychotic symptoms occurred together...