H H Jung

Summary

Affiliation: University Hospital
Country: Switzerland

Publications

  1. doi request reprint [Wilson's Disease]
    S P Ramseier
    Neurologische Klinik und Poliklinik, Universitatsspital, 8091 Zurich
    Praxis (Bern 1994) 99:175-82. 2010
  2. doi request reprint [Amyotrophic lateral sclerosis--diagnosis and treatment]
    H H Jung
    Klinik für Neurologie und Neuromuskuläres Zentrum, Universitatsspital Zurich
    Praxis (Bern 1994) 101:907-14. 2012
  3. pmc Phenotypic variation of autosomal-dominant corticobasal degeneration
    Hans H Jung
    Department of Neurology, University Hospital Zurich, Zurich, Switzerland
    Eur Neurol 67:142-50. 2012
  4. pmc Neuroacanthocytosis syndromes
    Hans H Jung
    Department of Neurology, University Hospital Zurich, Zurich, Switzerland
    Orphanet J Rare Dis 6:68. 2011
  5. ncbi request reprint McLeod syndrome: a neurohaematological disorder
    H H Jung
    Department of Neurology, University Hospital Zurich, Frauenklinikstrasse 26, 8091 Zurich, Switzerland
    Vox Sang 93:112-21. 2007
  6. ncbi request reprint Phenotypes of female adrenoleukodystrophy
    H H Jung
    Department of Neurology, University Hospital Zurich, Frauenklinikstrasse 26, 8091 Zurich, Switzerland
    Neurology 68:960-1. 2007
  7. doi request reprint Evolution of striatal degeneration in McLeod syndrome
    P O Valko
    Department of Neurology, University Hospital Zurich, Zurich, Switzerland
    Eur J Neurol 17:612-8. 2010
  8. ncbi request reprint Long-term course of L-dopa-responsive dystonia caused by tyrosine hydroxylase deficiency
    A Schiller
    Department of Neurology, University Hospital Zurich, Zurich, Switzerland
    Neurology 63:1524-6. 2004
  9. ncbi request reprint Kell and XK immunohistochemistry in McLeod myopathy
    H H Jung
    Department of Neurology, University Hospital Zurich, 8091 Zurich, Switzerland
    Muscle Nerve 24:1346-51. 2001
  10. ncbi request reprint McLeod syndrome: a novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings
    H H Jung
    Department of Neurology, University Hospital Zurich, Switzerland
    Ann Neurol 49:384-92. 2001

Collaborators

Detail Information

Publications14

  1. doi request reprint [Wilson's Disease]
    S P Ramseier
    Neurologische Klinik und Poliklinik, Universitatsspital, 8091 Zurich
    Praxis (Bern 1994) 99:175-82. 2010
    ..Lifelong decoppering treatment must be maintained. For the detection of deterioration of the disease or adverse effects of the medication as well as for the assessment of therapeutic compliance, regular clinical controls are necessary...
  2. doi request reprint [Amyotrophic lateral sclerosis--diagnosis and treatment]
    H H Jung
    Klinik für Neurologie und Neuromuskuläres Zentrum, Universitatsspital Zurich
    Praxis (Bern 1994) 101:907-14. 2012
    ..However, symptomatic treatments to ameliorate spasticity, drooling, speech and swallowing problems, and assisted ventilation to treat respiratory failure are essential...
  3. pmc Phenotypic variation of autosomal-dominant corticobasal degeneration
    Hans H Jung
    Department of Neurology, University Hospital Zurich, Zurich, Switzerland
    Eur Neurol 67:142-50. 2012
    ..Clinical presentation and course might be determined by additional, yet unknown, genetic modifying factors...
  4. pmc Neuroacanthocytosis syndromes
    Hans H Jung
    Department of Neurology, University Hospital Zurich, Zurich, Switzerland
    Orphanet J Rare Dis 6:68. 2011
    ..Other symptoms including psychiatric manifestations should be managed in a symptom-oriented manner. NA syndromes have a relentlessly progressive course usually over two to three decades...
  5. ncbi request reprint McLeod syndrome: a neurohaematological disorder
    H H Jung
    Department of Neurology, University Hospital Zurich, Frauenklinikstrasse 26, 8091 Zurich, Switzerland
    Vox Sang 93:112-21. 2007
    ..Therefore, asymptomatic carriers of the McLeod blood group phenotype should have a careful genetic counseling, neurological examination and a cardiologic evaluation for the presence of a treatable cardiomyopathy...
  6. ncbi request reprint Phenotypes of female adrenoleukodystrophy
    H H Jung
    Department of Neurology, University Hospital Zurich, Frauenklinikstrasse 26, 8091 Zurich, Switzerland
    Neurology 68:960-1. 2007
  7. doi request reprint Evolution of striatal degeneration in McLeod syndrome
    P O Valko
    Department of Neurology, University Hospital Zurich, Zurich, Switzerland
    Eur J Neurol 17:612-8. 2010
    ..Neuroimaging studies revealed striatal atrophy with predominance of the caudate nucleus. Our previous cross-sectional MRI study showed an association of volume loss in the caudate nucleus and putamen with the disease duration...
  8. ncbi request reprint Long-term course of L-dopa-responsive dystonia caused by tyrosine hydroxylase deficiency
    A Schiller
    Department of Neurology, University Hospital Zurich, Zurich, Switzerland
    Neurology 63:1524-6. 2004
    ..Although the l-dopa therapy was delayed up to 20 years after disease onset, there were no cognitive or neurologic sequelae of the long-term catecholamine deficit...
  9. ncbi request reprint Kell and XK immunohistochemistry in McLeod myopathy
    H H Jung
    Department of Neurology, University Hospital Zurich, 8091 Zurich, Switzerland
    Muscle Nerve 24:1346-51. 2001
    ....
  10. ncbi request reprint McLeod syndrome: a novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings
    H H Jung
    Department of Neurology, University Hospital Zurich, Switzerland
    Ann Neurol 49:384-92. 2001
    ..Therefore, patients with psychiatric signs or symptoms segregating in an X-linked trait should be examined for acanthocytosis and Kell/Kx blood group serology...
  11. ncbi request reprint Severe hypothermia in a patient with cerebral relapse of Whipple's disease
    B Himmelmann
    Department of Internal Medicine, University Hospital of Zurich, CH 8091, Zurich, Switzerland
    Infection 32:119-21. 2004
    ..Hypothermia is a rare hypothalamic manifestation of cerebral Whipple's disease...
  12. ncbi request reprint Neurologic phenotypes associated with acanthocytosis
    R H Walker
    Department of Neurology, James J Peters Veterans Affairs Medical Center, Bronx, NY 10468, USA
    Neurology 68:92-8. 2007
    ..As in other neurodegenerative conditions, animal models are a promising strategy for the development of such therapies...
  13. ncbi request reprint Spinal phenotype of cerebrotendinous xanthomatosis--a pitfall in the diagnosis of multiple sclerosis
    D Bartholdi
    J Neurol 251:105-7. 2004
  14. ncbi request reprint Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas
    S Laberge-le Couteulx
    INSERM U25, Faculte de Medecine Necker, 156 rue de Vaugirard, 75730 Paris Cedex 15, France
    Nat Genet 23:189-93. 1999
    ..9), a member of the RAS family of GTPases, is mutated in CCM1 families. Our data suggest the involvement of the RAP1A signal transduction pathway in vasculogenesis or angiogenesis...