F Stogbauer

Summary

Country: Germany

Publications

  1. ncbi request reprint Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndrome
    F Stogbauer
    Klinik und Poliklinik fur Neurologie, Westfalische Wilhelms Universitat Munster, Germany
    Neurosci Lett 240:1-4. 1998
  2. ncbi request reprint [Molecular genetics of hereditary neuropathies]
    F Stogbauer
    Westfälische Wilhelms Universität Münster Klinik und Poliklinik für Neurologie, Munster, 48129, Alemania
    Rev Neurol 32:156-64. 2001
  3. pmc Autosomal dominant burning feet syndrome
    F Stogbauer
    Department of Neurology, University of Munster, Germany
    J Neurol Neurosurg Psychiatry 67:78-81. 1999
  4. ncbi request reprint Hereditary recurrent focal neuropathies: clinical and molecular features
    F Stogbauer
    Klinik and Poliklinik für Neurologie, Westfalische Wilhelms Universitat, Munster, Germany
    Neurology 54:546-51. 2000
  5. ncbi request reprint Oncostatin M-mediated growth inhibition of human glioblastoma cells does not depend on stat3 or on mitogen-activated protein kinase activation
    H Halfter
    Department of Neurology, Westfalische Wilhelms Universitat Munster, Germany
    J Neurochem 75:973-81. 2000
  6. pmc Evaluation of single nucleotide polymorphisms in the phosphodiesterase 4D gene (PDE4D) and their association with ischaemic stroke in a large German cohort
    G Kuhlenbaumer
    Department of Neurology and Leibniz Institute for Atherosclerosis Research, University of Munster, Albert Schweitzer Str 33, 48129, Munster, Germany
    J Neurol Neurosurg Psychiatry 77:521-4. 2006
  7. ncbi request reprint Characterization of 3-[(123)I]iodo-L-alpha-methyl tyrosine transport in astrocytes of neonatal rats
    K Kopka
    Department of Nuclear Medicine, Westfalische Wilhelms Universitat Munster, Germany
    J Neurochem 76:97-104. 2001
  8. ncbi request reprint Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous
    G Kuhlenbaumer
    Department of Neurology, Westfalische Wilhelms University, Munster, Germany
    J Neurol 248:861-5. 2001
  9. ncbi request reprint Autosomal dominant striatal degeneration (ADSD): clinical description and mapping to 5q13-5q14
    G Kuhlenbaumer
    Department of Neurology, University of Munster, Germany
    Neurology 62:2203-8. 2004
  10. ncbi request reprint [Spontaneous dissection of brain providing neck artery]
    G Kuhlenbaumer
    Klinik und Poliklinik fur Neurologie, Westfalische Wilhelms Universitat Munster
    Fortschr Neurol Psychiatr 72:282-91; quiz 292-3. 2004

Collaborators

Detail Information

Publications26

  1. ncbi request reprint Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndrome
    F Stogbauer
    Klinik und Poliklinik fur Neurologie, Westfalische Wilhelms Universitat Munster, Germany
    Neurosci Lett 240:1-4. 1998
    ..We conclude that DSS also exists as a distinct genetic entity with autosomal recessive inheritance as originally defined by Dejerine and Sottas in 1893...
  2. ncbi request reprint [Molecular genetics of hereditary neuropathies]
    F Stogbauer
    Westfälische Wilhelms Universität Münster Klinik und Poliklinik für Neurologie, Munster, 48129, Alemania
    Rev Neurol 32:156-64. 2001
    ..Significant progress in the understanding of the molecular genetics and pathophysiology of inherited neuropathies has been achieved during the last years...
  3. pmc Autosomal dominant burning feet syndrome
    F Stogbauer
    Department of Neurology, University of Munster, Germany
    J Neurol Neurosurg Psychiatry 67:78-81. 1999
    ..The autosomal dominant burning feet syndrome is neither allelic to HSAN I nor to CMT 2B and thus represents a distinct genetic entity...
  4. ncbi request reprint Hereditary recurrent focal neuropathies: clinical and molecular features
    F Stogbauer
    Klinik and Poliklinik für Neurologie, Westfalische Wilhelms Universitat, Munster, Germany
    Neurology 54:546-51. 2000
    ....
  5. ncbi request reprint Oncostatin M-mediated growth inhibition of human glioblastoma cells does not depend on stat3 or on mitogen-activated protein kinase activation
    H Halfter
    Department of Neurology, Westfalische Wilhelms Universitat Munster, Germany
    J Neurochem 75:973-81. 2000
    ....
  6. pmc Evaluation of single nucleotide polymorphisms in the phosphodiesterase 4D gene (PDE4D) and their association with ischaemic stroke in a large German cohort
    G Kuhlenbaumer
    Department of Neurology and Leibniz Institute for Atherosclerosis Research, University of Munster, Albert Schweitzer Str 33, 48129, Munster, Germany
    J Neurol Neurosurg Psychiatry 77:521-4. 2006
    ..In conclusion, this study was unable to demonstrate an association between the six SNPs which had showed significant single marker association with stroke in the Icelandic stroke cohort and ischaemic stroke in a large German cohort...
  7. ncbi request reprint Characterization of 3-[(123)I]iodo-L-alpha-methyl tyrosine transport in astrocytes of neonatal rats
    K Kopka
    Department of Nuclear Medicine, Westfalische Wilhelms Universitat Munster, Germany
    J Neurochem 76:97-104. 2001
    ..However, sodium-independent maximum transport velocities (V(max)) differed significantly between neonatal astrocytes and C6 glioma cells (11.1 +/- 0.3 and 39.9 +/- 3.3 nmol/mg protein/10 min, respectively)...
  8. ncbi request reprint Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous
    G Kuhlenbaumer
    Department of Neurology, Westfalische Wilhelms University, Munster, Germany
    J Neurol 248:861-5. 2001
    ..These results demonstrate that clinically homogeneous classical HNA is genetically heterogeneous...
  9. ncbi request reprint Autosomal dominant striatal degeneration (ADSD): clinical description and mapping to 5q13-5q14
    G Kuhlenbaumer
    Department of Neurology, University of Munster, Germany
    Neurology 62:2203-8. 2004
    ..To describe the clinical and neuroradiologic features and chromosomal mapping of a novel autosomal dominant disease affecting the basal ganglia...
  10. ncbi request reprint [Spontaneous dissection of brain providing neck artery]
    G Kuhlenbaumer
    Klinik und Poliklinik fur Neurologie, Westfalische Wilhelms Universitat Munster
    Fortschr Neurol Psychiatr 72:282-91; quiz 292-3. 2004
  11. ncbi request reprint Genetic variants of the NOTCH3 gene in migraine--a mutation analysis and association study
    S Schwaag
    Department of Neurology, University of Munster, Munster, Germany
    Cephalalgia 26:158-61. 2006
    ..No mutations in exons 3 and 4 of the NOTCH3 gene were found in 97 patients with migraine. However, association analysis revealed significant association of the single nucleotide polymorphism (SNP) rs1043994 with migraine...
  12. ncbi request reprint Protease inhibitors in spontaneous cervical artery dissections
    Carsten Konrad
    Department of Neurology, University of Munster, Munster, Germany
    Stroke 36:9-13. 2005
    ..Here we present the first large investigation of the protease inhibitor hypothesis in patients with sCAD...
  13. ncbi request reprint Giant axonal neuropathy (GAN): case report and two novel mutations in the gigaxonin gene
    G Kuhlenbaumer
    Department of Neurology, University of Munster, Germany
    Neurology 58:1273-6. 2002
    ..The authors report two novel mutations confirming that GAN is caused by mutations in the gigaxonin gene and raise the question whether some mutations may cause a mild subclinical neuropathy...
  14. ncbi request reprint Generalized arteriopathy in patients with cervical artery dissection
    W Volker
    Institute of Atherosclerosis Research, University of Munster, Munster, Germany
    Neurology 64:1508-13. 2005
    ..To make an ultrastructural comparison of superficial temporal artery (STA) biopsy specimens from patients with spontaneous cervical artery dissection (sCAD) and controls...
  15. ncbi request reprint Activation of the Jak-Stat- and MAPK-pathways by oncostatin M is not sufficient to cause growth inhibition of human glioma cells
    H Halfter
    Clinic of Neurology, Westf Wilhelms Universität Münster, Albert Schweitzer Str 33, D 48129, Munster, Germany
    Brain Res Mol Brain Res 80:198-206. 2000
    ....
  16. ncbi request reprint A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies
    P Young
    Klinik und Poliklinik fur Neurologie, Westfähische Wilhelms Universität, Munster, Germany
    Neurology 48:450-2. 1997
    ..This mutation is predicted to alter the reading frame and to result in a delayed termination signal. We conclude that the functional consequences of the frameshift are equivalent to those of the PMP22 deletion allele...
  17. ncbi request reprint Human nuclear transcription factor gene CREM: genomic organization, mutation screening, and association analysis in panic disorder
    K Domschke
    Department of Psychiatry, University of Munster, Munster, Germany
    Am J Med Genet B Neuropsychiatr Genet 117:70-8. 2003
    ..Functional analysis of the observed CREM P 2 promoter polymorphism as well as studies in independent panic disorder samples are necessary...
  18. ncbi request reprint Spontaneous internal carotid artery dissection and alpha-1-antitrypsin deficiency
    C Konrad
    Department of Neurology, University of Muenster, Muenster, Germany
    Acta Neurol Scand 107:233-6. 2003
    ..The relevance of alpha-1-AT deficiency for spontaneous cervical arterial dissections is discussed...
  19. ncbi request reprint Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals
    G Kuhlenbaumer
    Klinik und Poliklinik für Neurologie Westfälische Wilhelms Universität Münster, Germany
    J Neurol 248:23-6. 2001
    ..Interestingly, his 85-year-old mother who has the genotype 37/51 CAG repeats is clinically unaffected as well. These results suggest an exactly defined border between normal and disease alleles...
  20. ncbi request reprint Activation of Jak-Stat and MAPK2 pathways by oncostatin M leads to growth inhibition of human glioma cells
    H Halfter
    Clinic of Neurology, Westf Wilhelms Universität Münster, Germany
    Mol Cell Biol Res Commun 1:109-16. 1999
    ..MAPK2 turns out to be a crucial mediator of the OSM effect in glioma cells since inhibition of MAPK activity by the Mek1 inhibitor PD98059 blocks the OSM-induced inhibition of DNA synthesis by about 70%...
  21. pmc Placing nasogastric tubes in stroke patients with dysphagia: efficiency and tolerability of the reflex placement
    R Dziewas
    Department of Neurology, University of Munster, Albert Schweitzer Str 33, D 48129 Munster, Germany
    J Neurol Neurosurg Psychiatry 74:1429-31. 2003
    ..We therefore suggest the use of reflex placement in patients who have suffered a stroke and need tube feeding due to dysphagia...
  22. ncbi request reprint Incidence and risk factors for stroke in an occupational cohort: the PROCAM Study. Prospective Cardiovascular Muenster Study
    K Berger
    Institute of Atherosclerosis Research, University of Muenster, Germany
    Stroke 29:1562-6. 1998
    ..The purpose of this study was to assess the incidence of stroke and the magnitude of classic stroke risk factors in an occupational cohort of white-collar and blue-collar workers...
  23. ncbi request reprint Clinically silent circulating microemboli in 20 patients with carotid or vertebral artery dissection
    D W Droste
    Department of Neurology, University of Munster, Germany
    Cerebrovasc Dis 12:181-5. 2001
    ..Detection of clinically silent circulating microemboli by transcranial Doppler sonography (TCD) is now widely investigated in patients with carotid artery disease in the hope to identify patients at increased risk for stroke...
  24. pmc Pneumonia in acute stroke patients fed by nasogastric tube
    R Dziewas
    Department of Neurology, University Hospital of Munster, Muenster, Germany
    J Neurol Neurosurg Psychiatry 75:852-6. 2004
    ..Aspiration pneumonia is the most important acute complication of stroke related dysphagia. Tube feeding is usually recommended as an effective and safe way to supply nutrition in dysphagic stroke patients...
  25. ncbi request reprint Electromagnetic fields (GSM 1800) do not alter blood-brain barrier permeability to sucrose in models in vitro with high barrier tightness
    Helmut Franke
    Klinik und Poliklinik fur Neurologie, Munster, Germany
    Bioelectromagnetics 26:529-35. 2005
    ..We thus could not confirm enhanced permeability of the BBB in vitro after EMF exposure as reported before since the in vitro barrier tightness in these experiments is now more like that of the in vivo situation...
  26. ncbi request reprint Kinetic parameters of 3-[(123)I]iodo-L-alpha-methyl tyrosine ([(123)I]IMT) transport in human GOS3 glioma cells
    B Riemann
    Department of Nuclear MedicineWestfälische Wilhelms Universität, Munster, Germany
    Nucl Med Biol 28:293-7. 2001
    ..1 +/- 1.5 microM). The maximum transport velocity (V(max)) amounted to 34.8 +/- 1.9 nmol/mg protein/10 min. Competitive inhibition experiments revealed that [(123)I]IMT transport is mediated principally by the sodium-independent system L...