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La ricerca find articoli where authors phrase all words ' Stogbauer, F' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 48 riferimenti
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    1. Droste, DW; Junker, K; Stogbauer, F; Lowens, S; Besselmann, M; Braun, B; Ringelstein, EB
      Clinically silent circulating microemboli in 20 patients with carotid or vertebral artery dissection

      CEREBROVASCULAR DISEASES
    2. Riemann, B; Kopka, K; Stogbauer, F; Halfter, H; Ketteler, S; Phan, TQV; Franzius, C; Weckesser, M; Ringelstein, EB; Schober, O
      Kinetic parameters of 3-[I-123]iodo-L-alpha-methyl tyrosine ([I-123]IMT) transport in human GOS3 glioma cells

      NUCLEAR MEDICINE AND BIOLOGY
    3. Meuleman, J; Kuhlenbaumer, G; Audenaert, D; Hunermund, G; Hor, H; Young, P; Stogbauer, F; Ringelstein, EB; Van Broeckhoven, C; De Jonghe, P; Timmerman, V
      Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy(HNA)

      HUMAN GENETICS
    4. Dziewas, R; Stogbauer, F; Oelerich, M; Ritter, M; Husstedt, IW
      A case of adrenomyeloneuropathy with unusual lesion pattern in magnetic resonance imaging

      JOURNAL OF NEUROLOGY
    5. Kuhlenbaumer, G; Meuleman, J; De Jonghe, P; Falck, B; Young, P; Hunermund, G; Van Broeckhoven, C; Timmerman, V; Stogbauer, F
      Hereditary neuralgic amyotrophy (HNA) is genetically heterogeneous

      JOURNAL OF NEUROLOGY
    6. Kuhlenbaumer, G; Kress, W; Ringelstein, EB; Stogbauer, F
      Thirty-seven CAG repeats in the androgen receptor gene in two healthy individuals

      JOURNAL OF NEUROLOGY
    7. Orstavik, K; Heier, MS; Young, P; Stogbauer, F
      Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies

      MUSCLE & NERVE
    8. Dziewas, R; Ludemann, P; Konrad, C; Stogbauer, F
      Simple method for placing nasogastric tubes in patients with dysphagiap

      LANCET
    9. Friedrich, M; Hoss, N; Stogbauer, F; Senner, V; Paulus, W; Ringelstein, EB; Halfter, H
      Complete inhibition of in vivo glioma growth by oncostatin M

      JOURNAL OF NEUROCHEMISTRY
    10. Kopka, K; Riemann, B; Friedrich, M; Winters, S; Halfter, H; Weckesser, M; Stogbauer, F; Ringelstein, EB; Schober, O
      Characterization of 3-[I-123]iodo-L-alpha-methyl tyrosine transport in astrocytes of neonatal rats

      JOURNAL OF NEUROCHEMISTRY
    11. Kuhlenbaumer, G; Stogbauer, F; Timmerman, V; De Jonghe, P
      Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection

      NEUROMUSCULAR DISORDERS
    12. Riemann, B; Stogbauer, F; Kopka, K; Halfter, H; Lasic, M; Schirmacher, A; Kuwert, T; Weckesser, M; Ringelstein, EB; Schober, O
      Kinetics of 3-[I-123]iodo-L-alpha-methyltyrosine transport in rat C6 glioma cells (vol 27, pg 1870, 2000)

      EUROPEAN JOURNAL OF NUCLEAR MEDICINE
    13. Riemann, B; Stogbauer, F; Kopka, K; Halfter, H; Lasic, M; Schirmacher, A; Kuwert, T; Weckesser, M; Ringelstein, EB; Schober, O
      Kinetics of 3-[I-123]iodo-L-alpha-methyltyrosine transport in rat C6 glioma cells (vol 27, pg 1274, 2000)

      EUROPEAN JOURNAL OF NUCLEAR MEDICINE
    14. Young, P; Stogbauer, F; Eller, B; de Jonghe, P; Lofgren, A; Timmerman, V; Rautenstrauss, B; Oexle, K; Grehl, H; Kuhlenbaumer, G; Van Broeckhoven, C; Ringelstein, EB; Funke, H
      PMP22 Thr118Met is not a clinically relevant CMT1 marker

      JOURNAL OF NEUROLOGY
    15. Frese, A; Bethke, F; Ludemann, P; Stogbauer, F
      Development of myasthenia gravis in a patient with multiple sclerosis during treatment with glatiramer acetate

      JOURNAL OF NEUROLOGY
    16. Schirmacher, A; Winters, S; Fischer, S; Goeke, J; Galla, HJ; Kullnick, U; Ringelstein, EB; Stogbauer, F
      Electromagnetic fields (1.8 GHz) increase the permeability to sucrose of the blood-brain barrier in vitro

      BIOELECTROMAGNETICS
    17. Halfter, H; Postert, C; Friedrich, M; Ringelstein, EB; Stogbauer, F
      Activation of the Jak-Stat- and MAPK-pathways by oncostatin M is not sufficient to cause growth inhibition of human glioma cells

      MOLECULAR BRAIN RESEARCH
    18. Stogbauer, F; Young, P; Kuhlenbaumer, G; De Jonghe, P; Timmerman, V
      Hereditary recurrent focal neuropathies - Clinical and molecular features

      NEUROLOGY
    19. Besselmann, M; Vennemann, B; Lowens, S; Ringelstein, EB; Stogbauer, F
      Internal carotid artery dissection

      NEUROLOGY
    20. Gasser, T; Dichgans, M; Jurkat-Rott, K; Klockgether, T; Klopstock, T; Kretzschmar, H; Lehmann-Horn, F; Reichmann, H; Rolfs, A; Sander, T; Stogbauer, F
      Molecular diagnosis of hereditary neurological diseases. A position paper

      NERVENARZT
    21. Halfter, H; Stogbauer, F; Friedrich, M; Serve, S; Serve, H; Ringelstein, EB
      Oncostatin M-mediated growth inhibition of human glioblastoma cells does not depend on Stat3 or on mitogen-activated protein kinase activation

      JOURNAL OF NEUROCHEMISTRY
    22. Meuleman, J; Kuhlenbaumer, G; Schirmacher, A; Wehnert, M; De Jonghe, P; De Vriendt, E; Young, P; Airaksinen, E; Pou-Serradell, A; Prats, JM; Ringelstein, B; Stogbauer, F; Van Broeckhoven, C; Timmerman, V
      Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25

      EUROPEAN JOURNAL OF HUMAN GENETICS
    23. Oelerich, M; Stogbauer, F; Kurlemann, G; Schul, C; Schuierer, G
      Craniocervical artery dissection: MR imaging and MR angiographic findings

      EUROPEAN RADIOLOGY
    24. Kuhlenbaumer, G; Schirmacher, A; Meuleman, J; Tissir, F; Del-Favero, J; Stogbauer, F; Young, P; Ringelstein, B; Van Broeckhoven, C; Timmerman, V
      A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes

      GENOMICS
    25. Riemann, B; Stogbauer, F; Kopka, K; Halfter, H; Lasic, M; Schirmacher, A; Kuwert, T; Weckesser, M; Ringelstein, EB; Schober, O
      Kinetics of 3-[I-123]iodo-L-alpha-methyltyrosine transport in rat C6 glioma cells

      EUROPEAN JOURNAL OF NUCLEAR MEDICINE
    26. Weis, J; Schonrock, LM; Zuchner, SL; Lie, DC; Sure, U; Schul, C; Stogbauer, F; Ringelstein, EB; Halfter, H
      CNTF and its receptor subunits in human gliomas

      JOURNAL OF NEURO-ONCOLOGY
    27. Frese, A; Bethke, F; Ludemann, P; Stogbauer, F
      Enhanced spasticity in primary progressive MS patients treated with interferon beta-1b

      NEUROLOGY
    28. Stogbauer, F; Young, P; Kuhlenbaumer, G; Kiefer, R; Timmerman, V; Ringelstein, EB; Wang, JF; Schroder, JM; Van Broeckhoven, C; Weis, J
      Autosomal dominant burning feet syndrome

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    29. OELERICH M; STOGBAUER F; SCHUL C
      LUMBAR SPINAL NEURINOMA PRESENTING WITH NOCTURNAL PAIN - A CASE-REPORT

      Clinical imaging
    30. STOGBAUER F; YOUNG P; KUHLENBAUMER G; MEULEMAN J; TIMMERMAN V; VANBROECKHOVEN C; KURLEMANN G; RINGELSTEIN EB
      HEREDITARY NEURALGIC AMYOTROPHY (HNA) - C LINICAL FINDINGS AND MOLECULAR-GENETICS

      Fortschritte der Neurologie, Psychiatrie
    31. STOGBAUER F; YOUNG P; WIEBUSCH H; TIMMERMAN V; KUHLENBAUMER G; NELIS E; RINGELSTEIN EB; KURLEMANN G; ASSMANN G; VANBROECKHOVEN C; FUNKE H
      ABSENCE OF MUTATIONS IN PERIPHERAL MYELIN PROTEIN-22, MYELIN PROTEIN ZERO, AND CONNEXIN-32 IN AUTOSOMAL RECESSIVE DEJERINE-SOTTAS-SYNDROME

      Neuroscience letters
    32. HALFTER H; KREMERSKOTHEN J; WEBER J; HACKERKLOM U; BARNEKOW A; RINGELSTEIN EB; STOGBAUER F
      GROWTH-INHIBITION OF NEWLY ESTABLISHED HUMAN GLIOMA CELL-LINES BY LEUKEMIA INHIBITORY FACTOR

      Journal of neuro-oncology
    33. STOGBAUER F; YOUNG P; KERSCHENSTEINER M; RINGELSTEIN EB; ASSMANN G; FUNKE H
      RECURRENT BRACHIAL-PLEXUS PALSIES 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
    34. STOGBAUER F; YOUNG P; FUNKE H
      FAMILIAL AUTOSOMAL-DOMINANT CARPAL-TUNNEL SYNDROME PRESENTING IN A 5-YEAR-OLD CASE

      Muscle & nerve
    35. BERGER K; SCHULTE H; STOGBAUER F; ASSMANN G
      INCIDENCE AND RISK-FACTORS FOR STROKE IN AN OCCUPATIONAL COHORT - THEPROCAM STUDY

      Stroke
    36. YOUNG P; STOGBAUER F; WIEBUSCH H; LOFGREN A; TIMMERMAN V; VANBROECKHOVEN C; RINGELSTEIN EB; ASSMANN G; FUNKE H
      PCR-BASED STRATEGY FOR THE DIAGNOSIS OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES AND CHARCOT-MARIE-TOOTH-DISEASE TYPE 1A

      Neurology
    37. KUHLENBAUMER G; BOCCHICCHIO M; KRESS W; YOUNG P; OBERWITTLER C; STOGBAUER F
      THE X-CHROMOSOMAL RECESSIVE SPINOBULBAR MUSCULAR-ATROPHY (TYPE KENNEDY) - DESCRIPTION OF A FAMILY, CLINICAL-FEATURES, MOLECULAR-GENETICS, DIFFERENTIAL-DIAGNOSIS AND THERAPY

      Nervenarzt
    38. STOGBAUER F; YOUNG P; TIMMERMAN V; SPOELDERS P; RINGELSTEIN EB; VANBROECKHOVEN C; KURLEMANN G
      REFINEMENT OF THE HEREDITARY NEURALGIC AMYOTROPHY (HNA) LOCUS TO CHROMOSOME 17Q24-Q25

      Human genetics
    39. YOUNG P; WIEBUSCH H; STOGBAUER F; RINGELSTEIN B; ASSMANN G; FUNKE H
      PMP22 FRAMESHIFT MUTATION AND HEREDITARY NEUROPATHY WITH LIABILITY TOPRESSURE PALSIES - REPLY

      Neurology
    40. YOUNG P; WIEBUSCH H; STOGBAUER F; RINGELSTEIN B; ASSMANN G; FUNKE H
      A NOVEL FRAMESHIFT MUTATION IN PMP22 ACCOUNTS FOR HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES

      Neurology
    41. GEORGIADIS D; GOEKE J; HILL M; KONIG M; NABAVI DG; STOGBAUER F; ZUNKER P; RINGELSTEIN EB
      A NOVEL TECHNIQUE FOR IDENTIFICATION OF DOPPLER MICROEMBOLIC SIGNALS BASED ON THE COINCIDENCE METHOD - IN-VITRO AND IN-VIVO EVALUATION

      Stroke
    42. NABAVI DG; KONIG M; GEORGIADIS D; MUMME T; LEHMANN S; HILL M; ZUNKER P; STOGBAUER F; FECHTRUP C; BORGGREFE M; RINGELSTEIN EB
      DETECTION OF DOPPLER MICROEMBOLIC SIGNALS IN PATIENTS WITH POTENTIAL CARDIAC EMBOLIC SOURCES

      Stroke
    43. STOGBAUER F; HALFTER H; YOUNG P; RINGELSTEIN EB
      MOLECULAR-BIOLOGY AND GENETICS OF HEREDIT ARY MOTOR AND SENSORY NEUROPATHIES

      Nervenarzt
    44. YOUNG P; WIEBUSCH H; STOGBAUER F; RINGELSTEIN B; ASSMANN G; FUNKE H
      4 FREQUENTLY OBSERVED POLYMORPHISMS IN THE 3'-UTR OF HUMAN PERIPHERALMYELIN PROTEIN-22 (PMP22) - IDENTIFICATION OF DIFFERENT HAPLOTYPES

      Clinical genetics
    45. NABAVI DG; GEORGIADIS D; STOGBAUER F; MICHAEL N; HUSSTEDT IW
      MERALGIA PARAESTHETICA, A RARE CAUSE OF C IRCUMSCRIBED ALOPECIA

      Deutsche Medizinische Wochenschrift
    46. GEORGIADIS D; KONIG M; ZUNKER P; STOGBAUER F; RINGELSTEIN EB
      ANTICOAGULANT MONITORING WITH TRANSCRANIAL DOPPLER - REPLY

      Lancet
    47. GEORGIADIS D; KONIG M; ZUNKER P; NABAVI D; STOGBAUER F; RINGELSTEIN EB
      MICROEMBOLIC SIGNALS IN PATIENTS REFERRED FOR ECHOCARDIOGRAPHY

      Stroke
    48. GEORGIADIS D; HILL M; ZUNKER P; STOGBAUER F; RINGELSTEIN EB
      ANTICOAGULATION MONITORING WITH TRANSCRANIAL DOPPLER

      Lancet


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 01/12/20 alle ore 20:01:26