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Results: 1-20 |
Results: 20
LUMBAR SPINAL NEURINOMA PRESENTING WITH NOCTURNAL PAIN - A CASE-REPORT
Authors: OELERICH M STOGBAUER F SCHUL C
Citation: M. Oelerich et al., LUMBAR SPINAL NEURINOMA PRESENTING WITH NOCTURNAL PAIN - A CASE-REPORT, Clinical imaging, 22(1), 1998, pp. 60-64
HEREDITARY NEURALGIC AMYOTROPHY (HNA) - C LINICAL FINDINGS AND MOLECULAR-GENETICS
Authors: STOGBAUER F YOUNG P KUHLENBAUMER G MEULEMAN J TIMMERMAN V VANBROECKHOVEN C KURLEMANN G RINGELSTEIN EB
Citation: F. Stogbauer et al., HEREDITARY NEURALGIC AMYOTROPHY (HNA) - C LINICAL FINDINGS AND MOLECULAR-GENETICS, Fortschritte der Neurologie, Psychiatrie, 66(1), 1998, pp. 10-14
ABSENCE OF MUTATIONS IN PERIPHERAL MYELIN PROTEIN-22, MYELIN PROTEIN ZERO, AND CONNEXIN-32 IN AUTOSOMAL RECESSIVE DEJERINE-SOTTAS-SYNDROME
Authors: STOGBAUER F YOUNG P WIEBUSCH H TIMMERMAN V KUHLENBAUMER G NELIS E RINGELSTEIN EB KURLEMANN G ASSMANN G VANBROECKHOVEN C FUNKE H
Citation: F. Stogbauer et al., ABSENCE OF MUTATIONS IN PERIPHERAL MYELIN PROTEIN-22, MYELIN PROTEIN ZERO, AND CONNEXIN-32 IN AUTOSOMAL RECESSIVE DEJERINE-SOTTAS-SYNDROME, Neuroscience letters, 240(1), 1998, pp. 1-4
GROWTH-INHIBITION OF NEWLY ESTABLISHED HUMAN GLIOMA CELL-LINES BY LEUKEMIA INHIBITORY FACTOR
Authors: HALFTER H KREMERSKOTHEN J WEBER J HACKERKLOM U BARNEKOW A RINGELSTEIN EB STOGBAUER F
Citation: H. Halfter et al., GROWTH-INHIBITION OF NEWLY ESTABLISHED HUMAN GLIOMA CELL-LINES BY LEUKEMIA INHIBITORY FACTOR, Journal of neuro-oncology, 39(1), 1998, pp. 1-18
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
Authors: STOGBAUER F YOUNG P KERSCHENSTEINER M RINGELSTEIN EB ASSMANN G FUNKE H
Citation: F. Stogbauer et al., 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, 21(9), 1998, pp. 1199-1201
FAMILIAL AUTOSOMAL-DOMINANT CARPAL-TUNNEL SYNDROME PRESENTING IN A 5-YEAR-OLD CASE
Authors: STOGBAUER F YOUNG P FUNKE H
Citation: F. Stogbauer et al., FAMILIAL AUTOSOMAL-DOMINANT CARPAL-TUNNEL SYNDROME PRESENTING IN A 5-YEAR-OLD CASE, Muscle & nerve, 21(4), 1998, pp. 551-551
INCIDENCE AND RISK-FACTORS FOR STROKE IN AN OCCUPATIONAL COHORT - THEPROCAM STUDY
Authors: BERGER K SCHULTE H STOGBAUER F ASSMANN G
Citation: K. Berger et al., INCIDENCE AND RISK-FACTORS FOR STROKE IN AN OCCUPATIONAL COHORT - THEPROCAM STUDY, Stroke, 29(8), 1998, pp. 1562-1566
PCR-BASED STRATEGY FOR THE DIAGNOSIS OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES AND CHARCOT-MARIE-TOOTH-DISEASE TYPE 1A
Authors: YOUNG P STOGBAUER F WIEBUSCH H LOFGREN A TIMMERMAN V VANBROECKHOVEN C RINGELSTEIN EB ASSMANN G FUNKE H
Citation: P. Young et al., PCR-BASED STRATEGY FOR THE DIAGNOSIS OF HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES AND CHARCOT-MARIE-TOOTH-DISEASE TYPE 1A, Neurology, 50(3), 1998, pp. 760-763
THE X-CHROMOSOMAL RECESSIVE SPINOBULBAR MUSCULAR-ATROPHY (TYPE KENNEDY) - DESCRIPTION OF A FAMILY, CLINICAL-FEATURES, MOLECULAR-GENETICS, DIFFERENTIAL-DIAGNOSIS AND THERAPY
Authors: KUHLENBAUMER G BOCCHICCHIO M KRESS W YOUNG P OBERWITTLER C STOGBAUER F
Citation: G. Kuhlenbaumer et al., THE X-CHROMOSOMAL RECESSIVE SPINOBULBAR MUSCULAR-ATROPHY (TYPE KENNEDY) - DESCRIPTION OF A FAMILY, CLINICAL-FEATURES, MOLECULAR-GENETICS, DIFFERENTIAL-DIAGNOSIS AND THERAPY, Nervenarzt, 69(8), 1998, pp. 660-665
REFINEMENT OF THE HEREDITARY NEURALGIC AMYOTROPHY (HNA) LOCUS TO CHROMOSOME 17Q24-Q25
Authors: STOGBAUER F YOUNG P TIMMERMAN V SPOELDERS P RINGELSTEIN EB VANBROECKHOVEN C KURLEMANN G
Citation: F. Stogbauer et al., REFINEMENT OF THE HEREDITARY NEURALGIC AMYOTROPHY (HNA) LOCUS TO CHROMOSOME 17Q24-Q25, Human genetics, 99(5), 1997, pp. 685-687
PMP22 FRAMESHIFT MUTATION AND HEREDITARY NEUROPATHY WITH LIABILITY TOPRESSURE PALSIES - REPLY
Authors: YOUNG P WIEBUSCH H STOGBAUER F RINGELSTEIN B ASSMANN G FUNKE H
Citation: P. Young et al., PMP22 FRAMESHIFT MUTATION AND HEREDITARY NEUROPATHY WITH LIABILITY TOPRESSURE PALSIES - REPLY, Neurology, 49(5), 1997, pp. 1478-1479
A NOVEL FRAMESHIFT MUTATION IN PMP22 ACCOUNTS FOR HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES
Authors: YOUNG P WIEBUSCH H STOGBAUER F RINGELSTEIN B ASSMANN G FUNKE H
Citation: P. Young et al., A NOVEL FRAMESHIFT MUTATION IN PMP22 ACCOUNTS FOR HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES, Neurology, 48(2), 1997, pp. 450-452
MERALGIA PARAESTHETICA, A RARE CAUSE OF C IRCUMSCRIBED ALOPECIA
Authors: NABAVI DG GEORGIADIS D STOGBAUER F MICHAEL N HUSSTEDT IW
Citation: Dg. Nabavi et al., MERALGIA PARAESTHETICA, A RARE CAUSE OF C IRCUMSCRIBED ALOPECIA, Deutsche Medizinische Wochenschrift, 121(25-26), 1996, pp. 834-838
A NOVEL TECHNIQUE FOR IDENTIFICATION OF DOPPLER MICROEMBOLIC SIGNALS BASED ON THE COINCIDENCE METHOD - IN-VITRO AND IN-VIVO EVALUATION
Authors: GEORGIADIS D GOEKE J HILL M KONIG M NABAVI DG STOGBAUER F ZUNKER P RINGELSTEIN EB
Citation: D. Georgiadis et al., A NOVEL TECHNIQUE FOR IDENTIFICATION OF DOPPLER MICROEMBOLIC SIGNALS BASED ON THE COINCIDENCE METHOD - IN-VITRO AND IN-VIVO EVALUATION, Stroke, 27(4), 1996, pp. 683-686
DETECTION OF DOPPLER MICROEMBOLIC SIGNALS IN PATIENTS WITH POTENTIAL CARDIAC EMBOLIC SOURCES
Authors: NABAVI DG KONIG M GEORGIADIS D MUMME T LEHMANN S HILL M ZUNKER P STOGBAUER F FECHTRUP C BORGGREFE M RINGELSTEIN EB
Citation: Dg. Nabavi et al., DETECTION OF DOPPLER MICROEMBOLIC SIGNALS IN PATIENTS WITH POTENTIAL CARDIAC EMBOLIC SOURCES, Stroke, 27(4), 1996, pp. 798-798
MOLECULAR-BIOLOGY AND GENETICS OF HEREDIT ARY MOTOR AND SENSORY NEUROPATHIES
Authors: STOGBAUER F HALFTER H YOUNG P RINGELSTEIN EB
Citation: F. Stogbauer et al., MOLECULAR-BIOLOGY AND GENETICS OF HEREDIT ARY MOTOR AND SENSORY NEUROPATHIES, Nervenarzt, 67(12), 1996, pp. 987-997
4 FREQUENTLY OBSERVED POLYMORPHISMS IN THE 3'-UTR OF HUMAN PERIPHERALMYELIN PROTEIN-22 (PMP22) - IDENTIFICATION OF DIFFERENT HAPLOTYPES
Authors: YOUNG P WIEBUSCH H STOGBAUER F RINGELSTEIN B ASSMANN G FUNKE H
Citation: P. Young et al., 4 FREQUENTLY OBSERVED POLYMORPHISMS IN THE 3'-UTR OF HUMAN PERIPHERALMYELIN PROTEIN-22 (PMP22) - IDENTIFICATION OF DIFFERENT HAPLOTYPES, Clinical genetics, 49(6), 1996, pp. 321-322
ANTICOAGULANT MONITORING WITH TRANSCRANIAL DOPPLER - REPLY
Authors: GEORGIADIS D KONIG M ZUNKER P STOGBAUER F RINGELSTEIN EB
Citation: D. Georgiadis et al., ANTICOAGULANT MONITORING WITH TRANSCRANIAL DOPPLER - REPLY, Lancet, 345(8941), 1995, pp. 58-58
MICROEMBOLIC SIGNALS IN PATIENTS REFERRED FOR ECHOCARDIOGRAPHY
Authors: GEORGIADIS D KONIG M ZUNKER P NABAVI D STOGBAUER F RINGELSTEIN EB
Citation: D. Georgiadis et al., MICROEMBOLIC SIGNALS IN PATIENTS REFERRED FOR ECHOCARDIOGRAPHY, Stroke, 26(3), 1995, pp. 525-525
ANTICOAGULATION MONITORING WITH TRANSCRANIAL DOPPLER
Authors: GEORGIADIS D HILL M ZUNKER P STOGBAUER F RINGELSTEIN EB
Citation: D. Georgiadis et al., ANTICOAGULATION MONITORING WITH TRANSCRANIAL DOPPLER, Lancet, 344(8933), 1994, pp. 1373-1374
Risultati: 1-20 |