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Florian Stögbauer

Research Profile

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Germany

Genes & Molecular Sequences

Single Nucleotide Polymorphism

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TOP 3
Christoph Kellinghaus; Florian Stögbauer
Treatment of status epilepticus in a large community hospital.
Silke Appenzeller; Anja Schirmacher; Hartmut Halfter; Sebastian Bäumer; Manuela Pendziwiat; Vincent Timmerman; Peter De Jonghe; Klára Fekete; Florian Stögbauer; Peter Lüdemann; Margret Hund; Elgar Susanne Quabius; E Bernd Ringelstein; Gregor Kuhlenbäumer
Autosomal-dominant striatal degeneration is caused by a mutation in the phosphodiesterase 8B gene.
Klaus Berger; Florian Stögbauer; Monika Stoll; Jürgen Wellmann; Andreas Huge; Suzanne Cheng; Christof Kessler; Ulrich John; Gerd Assmann; E Bernd Ringelstein; Harald Funke
The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case-control studies.

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All Publications

2012: Christoph Kellinghaus; Florian Stögbauer
Treatment of status epilepticus in a large community hospital.
Epilepsy & behavior : E&B 2012;23(3):235-40.
2010: Silke Appenzeller; Anja Schirmacher; Hartmut Halfter; Sebastian Bäumer; Manuela Pendziwiat; Vincent Timmerman; Peter De Jonghe; Klára Fekete; Florian Stögbauer; Peter Lüdemann; Margret Hund; Elgar Susanne Quabius; E Bernd Ringelstein; Gregor Kuhlenbäumer
Autosomal-dominant striatal degeneration is caused by a mutation in the phosphodiesterase 8B gene.
American journal of human genetics 2010;86(1):83-7.
2007: Klaus Berger; Florian Stögbauer; Monika Stoll; Jürgen Wellmann; Andreas Huge; Suzanne Cheng; Christof Kessler; Ulrich John; Gerd Assmann; E Bernd Ringelstein; Harald Funke
The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case-control studies.
Human genetics 2007;121(2):169-78.
2006: Hartmut Halfter; Matthias Friedrich; Ansgar Resch; Michael Kullmann; Florian Stögbauer; E Bernd Ringelstein; Ludger Hengst
Oncostatin M induces growth arrest by inhibition of Skp2, Cks1, and cyclin A expression and induced p21 expression.
Cancer research 2006;66(13):6530-9.
2006: Gregor Kuhlenbäumer; K Berger; A Huge; E Lange; Christof Kessler; U John; Harald Funke; Darius Günther Nabavi; Florian Stögbauer; E Bernd Ringelstein; M Stoll
Evaluation of single nucleotide polymorphisms in the phosphodiesterase 4D gene (PDE4D) and their association with ischaemic stroke in a large German cohort.
Journal of neurology, neurosurgery, and psychiatry 2006;77(4):521-4.
2006: Sonja Schwaag; Stefan Evers; Anja Schirmacher; Florian Stögbauer; E Bernd Ringelstein; Gregor Kuhlenbäumer
Genetic variants of the NOTCH3 gene in migraine--a mutation analysis and association study.
Cephalalgia : an international journal of headache 2006;26(2):158-61.
2005: Gregor Kuhlenbäumer; Mark C Hannibal; Eva Nelis; Anja Schirmacher; Nathalie Verpoorten; Jan Meuleman; Giles D J Watts; Els De Vriendt; Peter Young; Florian Stögbauer; Hartmut Halfter; Joy Irobi; Dirk Goossens; Jurgen Del-Favero; Benjamin G Betz; Hyun Hor; Gerhard Kurlemann; Thomas D Bird; Eila Airaksinen; Tarja Mononen; Adolfo Pou Serradell; José M Prats; Christine Van Broeckhoven; Peter De Jonghe; Vincent Timmerman; E Bernd Ringelstein; Phillip F Chance
Mutations in SEPT9 cause hereditary neuralgic amyotrophy.
Nature genetics 2005;37(10):1044-6.
2005: Helmut Franke; Joachim Streckert; Andreas K Bitz; Johannes Goeke; Volkert W Hansen; E Bernd Ringelstein; Heiner Nattkämper; Hans-Joachim Galla; Florian Stögbauer
Effects of Universal Mobile Telecommunications System (UMTS) electromagnetic fields on the blood-brain barrier in vitro.
Radiation research 2005;164(3):258-69.
2005: Wolfgang Völker; Michael Besselmann; Ralf Dittrich; Darius Günther Nabavi; Carsten Konrad; Rainer Dziewas; Stefan Evers; S Grewe; Stefan C Krämer; Rainald Bachmann; Florian Stögbauer; E Bernd Ringelstein; Gregor Kuhlenbäumer
Generalized arteriopathy in patients with cervical artery dissection.
Neurology 2005;64(9):1508-13.
2005: Yoo J Lee; Carsten Hohoff; Katharina Domschke; Philipp Sand; Gregor Kuhlenbäumer; Anja Schirmacher; Christine M Freitag; Jobst Meyer; Gerald Stöber; Petra Franke; Markus M Nöthen; Jürgen Fritze; Rolf Fimmers; Henk Garritsen; Florian Stögbauer; Jürgen Deckert
Norepinephrine transporter (NET) promoter and 5'-UTR polymorphisms: association analysis in panic disorder.
Neuroscience letters 2005;377(1):40-3.
2005: Carsten Konrad; Claus Langer; G A Müller; Klaus Berger; Rainer Dziewas; Florian Stögbauer; Darius Günther Nabavi; Ralf Junker; E Bernd Ringelstein; Gregor Kuhlenbäumer
Protease inhibitors in spontaneous cervical artery dissections.
Stroke; a journal of cerebral circulation 2005;36(1):9-13.
2004: Carsten Konrad; Georg A Müller; Claus Langer; Gregor Kuhlenbäumer; Klaus Berger; Darius Günther Nabavi; Rainer Dziewas; Florian Stögbauer; E Bernd Ringelstein; Ralf Junker
Plasma homocysteine, MTHFR C677T, CBS 844ins68bp, and MTHFD1 G1958A polymorphisms in spontaneous cervical artery dissections.
Journal of neurology 2004;251(10):1242-8.
2004: Gregor Kuhlenbäumer; Peter Lüdemann; Anja Schirmacher; Els De Vriendt; Gert Hünermund; Peter Young; M Hund-Georgiadis; Gerhard Schuierer; H Möller; E Bernd Ringelstein; Christine Van Broeckhoven; Vincent Timmerman; Florian Stögbauer
Autosomal dominant striatal degeneration (ADSD): clinical description and mapping to 5q13-5q14.
Neurology 2004;62(12):2203-8.
2004: Rainer Dziewas; M Ritter; Matthias Schilling; Carsten Konrad; S Oelenberg; Darius Günther Nabavi; Florian Stögbauer; E Bernd Ringelstein; Peter Lüdemann
Pneumonia in acute stroke patients fed by nasogastric tube.
Journal of neurology, neurosurgery, and psychiatry 2004;75(6):852-6.
2004: Katharina Domschke; Christine M Freitag; Gregor Kuhlenbäumer; Anja Schirmacher; Philipp Sand; Peter Nyhuis; Christian Jacob; Jürgen Fritze; Petra Franke; Marcella Rietschel; Henk Garritsen; Rolf Fimmers; Markus M Nöthen; Klaus-Peter Lesch; Florian Stögbauer; Jürgen Deckert
Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2004;7(2):183-8.
2004: Gregor Kuhlenbäumer; E Bernd Ringelstein; Florian Stögbauer
[Spontaneous dissection of brain providing neck artery].
Fortschritte der Neurologie-Psychiatrie 2004;72(5):282-91; quiz 292-3.
2004: Gert Hünermund; Anja Schirmacher; Bernd Ringelstein; Peter Young; Giles D J Watts; Jan Meuleman; Eva Nelis; Phillip F Chance; Vincent Timmerman; Florian Stögbauer; Gregor Kuhlenbäumer
Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy.
Muscle & nerve 2004;29(4):601-4.
2004: Gregor Kuhlenbäumer; Uta S Müller; Michael Besselmann; Jürgen Rauterberg; Horst Robenek; Gert Hünermund; Tobias Brandt; E Bernd Ringelstein; Florian Stögbauer; Ingrid Hausser
Neither collagen 8A1 nor 8A2 mutations play a major role in cervical artery dissection. A mutation analysis and linkage study.
Journal of neurology 2004;251(3):357-9.
2004: V G Hösing; Anja Schirmacher; Gregor Kuhlenbäumer; Christine M Freitag; Philipp Sand; C Schlesiger; Christian Jacob; Jürgen Fritze; Petra Franke; Marcella Rietschel; Henk Garritsen; Markus M Nöthen; Rolf Fimmers; Florian Stögbauer; Jürgen Deckert
Cholecystokinin- and cholecystokinin-B-receptor gene polymorphisms in panic disorder.
Journal of neural transmission. Supplementum 2004;(68):147-56.
2003: Marc Cruts; Bart Dermaut; Rosa Rademakers; Marleen Van den Broeck; Florian Stögbauer; Christine Van Broeckhoven
Novel APP mutation V715A associated with presenile Alzheimer's disease in a German family.
Journal of neurology 2003;250(11):1374-5.
2003: Rainer Dziewas; Carsten Konrad; Bianca Dräger; Stefan Evers; Michael Besselmann; Peter Lüdemann; Gregor Kuhlenbäumer; Florian Stögbauer; E Bernd Ringelstein
Cervical artery dissection--clinical features, risk factors, therapy and outcome in 126 patients.
Journal of neurology 2003;250(10):1179-84.
2003: Rainer Dziewas; Matthias Schilling; Carsten Konrad; Florian Stögbauer; Peter Lüdemann
Placing nasogastric tubes in stroke patients with dysphagia: efficiency and tolerability of the reflex placement.
Journal of neurology, neurosurgery, and psychiatry 2003;74(10):1429-31.
2003: Rainer Dziewas; Florian Stögbauer; Peter Lüdemann
Risk factors for pneumonia in patients with acute stroke.
Stroke; a journal of cerebral circulation 2003;34(8):e105; author reply e105.
2003: Anne Hofer; Marcella Hermans; Nina Kubassek; Matthias Sitzer; Harald Funke; Florian Stögbauer; Vytautas Ivaskevicius; Johannes Oldenburg; Johannes Burtscher; Ulrich Knopp; Beate Schoch; Isabel Wanke; Frank Hübner; Wolfgang Deinsberger; Bernhard Meyer; Hans Boecher-Schwarz; Werner Poewe; Andreas Raabe; Helmuth Steinmetz; Georg Auburger
Elastin polymorphism haplotype and intracranial aneurysms are not associated in Central Europe.
Stroke; a journal of cerebral circulation 2003;34(5):1207-11.
2003: Carsten Konrad; Darius Günther Nabavi; Ralf Junker; Rainer Dziewas; Henning Henningsen; Florian Stögbauer
Spontaneous internal carotid artery dissection and alpha-1-antitrypsin deficiency.
Acta neurologica Scandinavica 2003;107(3):233-6.
2003: Katharina Domschke; Gregor Kuhlenbäumer; Anja Schirmacher; Cristina Lorenzi; Lluis Armengol; D DiBella; M Gratacos; Henk Garritsen; Markus M Nöthen; Petra Franke; Philipp Sand; Jürgen Fritze; G Perez; Wolfgang Maier; Walter Sibrowski; Xavier Estivill; laura bellodi; E Bernd Ringelstein; Volker Arolt; R Martin-Santos; Marco Catalano; Florian Stögbauer; Jürgen Deckert
Human nuclear transcription factor gene CREM: genomic organization, mutation screening, and association analysis in panic disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;117B(1):70-8.
2003: Stefan Evers; Florian Stögbauer
Genetic association of Huntington's disease and restless legs syndrome? A family report.
Movement disorders : official journal of the Movement Disorder Society 2003;18(2):225-7.
2003: Rainer Dziewasa; Michael Freund; Peter Lüdemann; Markus Müller; Martin Ritter; Dirk W Droste; Florian Stögbauer
Treatment options in vertebrobasilar dolichoectasia--case report and review of the literature.
European neurology 2003;49(4):245-7.
2003: Rainer Dziewas; Peter Soros; Carsten Konrad; Florian Stögbauer; Peter Lüdemann
Placing nasogastric tubes and intracranial pressure.
Journal of neurosurgical anesthesiology 2003;15(1):55-6.
2002: Gregor Kuhlenbäumer; Peter Young; Gert Hünermund; Bernd Ringelstein; Florian Stögbauer
Clinical features and molecular genetics of hereditary peripheral neuropathies.
Journal of neurology 2002;249(12):1629-50.
2002: Rainer Dziewas; Florian Stögbauer; Michael Freund; Peter Lüdemann; Tanya Imai; Christian Holzapfel; P Bernd Ringelstein
Late onset postpartum eclampsia: a rare and difficult diagnosis.
Journal of neurology 2002;249(9):1287-91.
2002: Tobias Loddenkemper; Kerstin Grote; Stefan Evers; Michael Oelerich; Florian Stögbauer
Neurological manifestations of the oculodentodigital dysplasia syndrome.
Journal of neurology 2002;249(5):584-95.
2002: Gregor Kuhlenbäumer; Peter Young; Christoph Oberwittler; Gert Hünermund; Anja Schirmacher; Katharina Domschke; Bernd Ringelstein; Florian Stögbauer
Giant axonal neuropathy (GAN): case report and two novel mutations in the gigaxonin gene.
Neurology 2002;58(8):1273-6.
2001: Gregor Kuhlenbäumer; Jan Meuleman; Peter De Jonghe; B Falck; Peter Young; Gert Hünermund; Christine Van Broeckhoven; Vincent Timmerman; Florian Stögbauer
Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous.
Journal of neurology 2001;248(10):861-5.
2001: Peter Young; K Grote; Gregor Kuhlenbäumer; O Debus; H Kurlemann; Hartmut Halfter; Harald Funke; E Bernd Ringelstein; Florian Stögbauer
Mutation analysis in Chariot-Marie Tooth disease type 1: point mutations in the MPZ gene and the GJB1 gene cause comparable phenotypic heterogeneity.
Journal of neurology 2001;248(5):410-5.
2001: Jan Meuleman; Gregor Kuhlenbäumer; Dominique Audenaert; Gert Hünermund; H Hor; Peter Young; Florian Stögbauer; E Bernd Ringelstein; Christine Van Broeckhoven; Peter De Jonghe; Vincent Timmerman
Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA).
Human genetics 2001;108(5):390-3.
2001: Rainer Dziewas; Florian Stögbauer; Michael Oelerich; M Ritter; Ingo-W Husstedt
A case of adrenomyeloneuropathy with unusual lesion pattern in magnetic resonance imaging.
Journal of neurology 2001;248(4):341-2.
2001: Burkhard Riemann; Klaus Kopka; Florian Stögbauer; Hartmut Halfter; S Ketteler; T Q Phan; Christiane Franzius; Matthias Weckesser; E Bernd Ringelstein; Otmar Schober
Kinetic parameters of 3-[(123)I]iodo-L-alpha-methyl tyrosine ([(123)I]IMT) transport in human GOS3 glioma cells.
Nuclear medicine and biology 2001;28(3):293-7.
2001: Matthias Friedrich; N Höss; Florian Stögbauer; Volker Senner; W Paulus; E Bernd Ringelstein; Hartmut Halfter
Complete inhibition of in vivo glioma growth by oncostatin M.
Journal of neurochemistry 2001;76(5):1589-92.
2001: Florian Stögbauer
[Molecular genetics of hereditary neuropathies].
Revista de neurologia 2001;32(2):156-64.
2001: Dirk W Droste; K Junker; Florian Stögbauer; S Lowens; Michael Besselmann; B Braun; E Bernd Ringelstein
Clinically silent circulating microemboli in 20 patients with carotid or vertebral artery dissection.
Cerebrovascular diseases (Basel, Switzerland) 2001;12(3):181-5.
2001: Gregor Kuhlenbäumer; W Kress; E Bernd Ringelstein; Florian Stögbauer
Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals.
Journal of neurology 2001;248(1):23-6.
2001: Klaus Kopka; Burkhard Riemann; Matthias Friedrich; S Winters; Hartmut Halfter; Matthias Weckesser; Florian Stögbauer; E Bernd Ringelstein; Otmar Schober
Characterization of 3-[(123)I]iodo-L-alpha-methyl tyrosine transport in astrocytes of neonatal rats.
Journal of neurochemistry 2001;76(1):97-104.
2000: Florian Stögbauer; Vincent Timmerman; Christine Van Broeckhoven
71st ENMC International Workshop, 6th workshop of the European Charcot-Marie-Tooth disease consortium: hereditary recurrent focal neuropathies, 24-25 September 1999, Soestduinen, the Netherlands.
Neuromuscular disorders : NMD 2000;10(7):518-24.
2000: Gregor Kuhlenbäumer; Florian Stögbauer; Vincent Timmerman; Peter De Jonghe
Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection. On behalf of the European CMT Consortium.
Neuromuscular disorders : NMD 2000;10(7):515-7.
2000: Hartmut Halfter; C Postert; Matthias Friedrich; E Bernd Ringelstein; Florian Stögbauer
Activation of the Jak-Stat- and MAPK-pathways by oncostatin M is not sufficient to cause growth inhibition of human glioma cells.
Brain research. Molecular brain research 2000;80(2):198-206.
2000: Hartmut Halfter; Florian Stögbauer; Matthias Friedrich; S Serve; Hubert Serve; E Bernd Ringelstein
Oncostatin M-mediated growth inhibition of human glioblastoma cells does not depend on stat3 or on mitogen-activated protein kinase activation.
Journal of neurochemistry 2000;75(3):973-81.
2000: Anja Schirmacher; S Winters; S Fischer; J Goeke; H J Galla; U Kullnick; E Bernd Ringelstein; Florian Stögbauer
Electromagnetic fields (1.8 GHz) increase the permeability to sucrose of the blood-brain barrier in vitro.
Bioelectromagnetics 2000;21(5):338-45.
2000: Florian Stögbauer; Peter Young; Gregor Kuhlenbäumer; Peter De Jonghe; Vincent Timmerman
Hereditary recurrent focal neuropathies: clinical and molecular features.
Neurology 2000;54(3):546-51.
2000: Michael Besselmann; B Vennemann; S Lowens; E Bernd Ringelstein; Florian Stögbauer
Internal carotid artery dissection.
Neurology 2000;54(2):442.
1999: Gregor Kuhlenbäumer; Anja Schirmacher; Jan Meuleman; F Tissir; Jurgen Del-Favero; Florian Stögbauer; Peter Young; Bernd Ringelstein; Christine Van Broeckhoven; Vincent Timmerman
A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes.
Genomics 1999;62(2):242-50.
1999: J Meulemann; Gregor Kuhlenbäumer; Anja Schirmacher; Manfred Wehnert; Peter De Jonghe; Els De Vriendt; Peter Young; E Airaksinen; A Pou-Serradell; J M Prats; Bernd Ringelstein; Florian Stögbauer; Christine Van Broeckhoven; Vincent Timmerman
Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25.
European journal of human genetics : EJHG 1999;7(8):920-7.
1999: Burkhard Riemann; Florian Stögbauer; Klaus Kopka; Hartmut Halfter; M Lasic; Anja Schirmacher; Torsten Kuwert; Matthias Weckesser; E Bernd Ringelstein; Otmar Schober
Kinetics of 3-[(123)I]iodo-l-alpha-methyltyrosine transport in rat C6 glioma cells.
European journal of nuclear medicine 1999;26(10):1274-8.
1999: Jan Meuleman; Gregor Kuhlenbäumer; Anja Schirmacher; Manfred Wehnert; Peter Young; Florian Stögbauer; E Bernd Ringelstein; Christine Van Broeckhoven; Vincent Timmerman
Hereditary neuralgic amyotrophy: mutation analysis of candidate genes.
Annals of the New York Academy of Sciences 1999;883():443-4.
1999: Florian Stögbauer; Peter Young; Gregor Kuhlenbäumer; Reinhard Kiefer; Vincent Timmerman; E Bernd Ringelstein; J F Wang; J M Schröder; Christine Van Broeckhoven; J Weis
Autosomal dominant burning feet syndrome.
Journal of neurology, neurosurgery, and psychiatry 1999;67(1):78-81.
1999: Hartmut Halfter; Matthias Friedrich; C Postert; E Bernd Ringelstein; Florian Stögbauer
Activation of Jak-Stat and MAPK2 pathways by oncostatin M leads to growth inhibition of human glioma cells.
Molecular cell biology research communications : MCBRC 1999;1(2):109-16.
1999: Joachim Weis; L M Schönrock; Stephan Zuchner; DC Lie; U Sure; Christoph Schul; Florian Stögbauer; E Bernd Ringelstein; Hartmut Halfter
CNTF and its receptor subunits in human gliomas.
Journal of neuro-oncology 1999;44(3):243-53.
1999: Michael Oelerich; Florian Stögbauer; Gerhard Kurlemann; Christoph Schul; Gerhard Schuierer
Craniocervical artery dissection: MR imaging and MR angiographic findings.
European radiology 1999;9(7):1385-91.
1998: Florian Stögbauer; Peter Young; M Kerschensteiner; E Bernd Ringelstein; Gerd Assmann; Harald Funke
Recurrent brachial plexus palsies as the only clinical expression of hereditary neuropathy with liability to pressure palsies associated with a de novo deletion of the peripheral myelin protein-22 gene.
Muscle & nerve 1998;21(9):1199-201.
1998: Hartmut Halfter; Joachim Kremerskothen; J Weber; Ursula Hacker-Klom; Angelika Barnekow; E Bernd Ringelstein; Florian Stögbauer
Growth inhibition of newly established human glioma cell lines by leukemia inhibitory factor.
Journal of neuro-oncology 1998;39(1):1-18.
1998: Gregor Kuhlenbäumer; M Bocchicchio; W Kress; Peter Young; Christoph Oberwittler; Florian Stögbauer
[X-chromosomal recessive spinobulbar muscular atrophy (Kennedy type). Description of a family, clinical aspects, molecular genetics, differential diagnosis and therapy].
Der Nervenarzt 1998;69(8):660-5.
1998: Klaus Berger; H Schulte; Florian Stögbauer; Gerd Assmann
Incidence and risk factors for stroke in an occupational cohort: the PROCAM Study. Prospective Cardiovascular Muenster Study.
Stroke; a journal of cerebral circulation 1998;29(8):1562-6.
1998: Peter Young; Florian Stögbauer; Heiko Wiebusch; Ann Löfgren; Vincent Timmerman; Christine Van Broeckhoven; E Bernd Ringelstein; Gerd Assmann; Harald Funke
PCR-based strategy for the diagnosis of hereditary neuropathy with liability to pressure palsies and Charcot-Marie-Tooth disease type 1A.
Neurology 1998;50(3):760-3.
1998: Florian Stögbauer; Peter Young; Heiko Wiebusch; Vincent Timmerman; Gregor Kuhlenbäumer; Eva Nelis; E Bernd Ringelstein; Gerhard Kurlemann; Gerd Assmann; Christine Van Broeckhoven; Harald Funke
Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndrome.
Neuroscience letters 1998;240(1):1-4.
1998: Florian Stögbauer; Peter Young; Gregor Kuhlenbäumer; Jan Meuleman; Vincent Timmerman; Christine Van Broeckhoven; Gerhard Kurlemann; E Bernd Ringelstein
[Hereditary neural amyotrophy (HNA): clinical and molecular genetic basis].
Fortschritte der Neurologie-Psychiatrie 1998;66(1):10-4.
1998: Hartmut Halfter; R Lotfi; R Westermann; Peter Young; E Bernd Ringelstein; Florian Stögbauer
Inhibition of growth and induction of differentiation of glioma cell lines by oncostatin M (OSM).
Growth factors (Chur, Switzerland) 1998;15(2):135-47.
1998: Michael Oelerich; Florian Stögbauer; Christoph Schul
Lumbar spinal neurinoma presenting with nocturnal pain. A case report.
Clinical imaging 1998;22(1):60-4.
1997: Florian Stögbauer; P Young; Vincent Timmerman; P Spoelders; E Bernd Ringelstein; Christine Van Broeckhoven; Gerhard Kurlemann
Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24-q25.
Human genetics 1997;99(5):685-7.
1997: Peter Young; Heiko Wiebusch; Florian Stögbauer; Bernd Ringelstein; Gerd Assmann; Harald Funke
A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies.
Neurology 1997;48(2):450-2.
1996: Florian Stögbauer; Hartmut Halfter; Peter Young; E Bernd Ringelstein
[Molecular biology and genetics of hereditary motor and sensory neuropathies].
Der Nervenarzt 1996;67(12):987-97.
1996: Darius Günther Nabavi; D Georgiadis; Florian Stögbauer; N Michael; Ingo-W Husstedt
[Meralgia paresthetica. A rare differential diagnosis of circumscribed alopecia].
Deutsche medizinische Wochenschrift (1946) 1996;121(25-26):834-8.
1996: Peter Young; Heiko Wiebusch; Florian Stögbauer; Bernd Ringelstein; Gerd Assmann; Harald Funke
Four frequently observed polymorphisms in the 3'-UTR of human peripheral myelin protein 22 (PMP22): identification of different haplotypes.
Clinical genetics 1996;49(6):321-2.
1996: D Georgiadis; J Goeke; M Hill; M König; Darius Günther Nabavi; Florian Stögbauer; Peter Zunker; E Bernd Ringelstein
A novel technique for identification of doppler microembolic signals based on the coincidence method: in vitro and in vivo evaluation.
Stroke; a journal of cerebral circulation 1996;27(4):683-6.
1995: D Georgiadis; M König; Peter Zunker; Darius Günther Nabavi; Florian Stögbauer; E Bernd Ringelstein
Microembolic signals inpatients referred for echocardiography.
Stroke; a journal of cerebral circulation 1995;26(3):525; author reply 526-7.
1994: D Georgiadis; M Hill; Peter Zunker; Florian Stögbauer; E Bernd Ringelstein
Anticoagulation monitoring with transcranial Doppler.
Lancet 1994;344(8933):1373-4.
1992: Klaus Unsicker; Florian Stögbauer
Screening of adrenal medullary neuropeptides for putative neurotrophic effects.
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 1992;10(2):171-9.
1990: Klaus Unsicker; Dieter Blottner; D Gehrke; Claudia Grothe; D Heymann; Florian Stögbauer; R Westermann
Characterization of trophic factors stored and secreted by neurons.
Advances in experimental medicine and biology 1990;265():63-73.
1988: R Westermann; Florian Stögbauer; Klaus Unsicker; R Lietzke
Calcium-dependence of chromogranin A-catecholamine interaction.
FEBS letters 1988;239(2):203-6.