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Results: 1-25 | 26-27
Results: 1-25/27
ALA30PRO MUTATION IN THE GENE ENCODING ALPHA-SYNUCLEIN IN PARKINSONS-DISEASE
Authors: KRUGER R KUHN W MULLER T WOITALLA D GRAEBER M KOSEL S PRZUNTEK H EPPLEN JT SCHOLS L RIESS O
Citation: R. Kruger et al., ALA30PRO MUTATION IN THE GENE ENCODING ALPHA-SYNUCLEIN IN PARKINSONS-DISEASE, Nature genetics, 18(2), 1998, pp. 106-108
AN ISOFORM OF ATAXIN-3 ACCUMULATES IN THE NUCLEUS OF NEURONAL CELLS IN AFFECTED BRAIN-REGIONS OF SCA3 PATIENTS
Authors: SCHMIDT T LANDWEHRMEYER GB SCHMITT I TROTTIER Y AUBURGER G LACCONE F KLOCKGETHER T VOLPEL M EPPLEN JT SCHOLS L RIESS O
Citation: T. Schmidt et al., AN ISOFORM OF ATAXIN-3 ACCUMULATES IN THE NUCLEUS OF NEURONAL CELLS IN AFFECTED BRAIN-REGIONS OF SCA3 PATIENTS, Brain pathology, 8(4), 1998, pp. 669-679
COLLISION TECHNIQUE IN MARTIN-GRUBER ANASTOMOSIS
Authors: AMOIRIDIS G SCHOLS L PRZUNTEK H WOHRLE J
Citation: G. Amoiridis et al., COLLISION TECHNIQUE IN MARTIN-GRUBER ANASTOMOSIS, Muscle & nerve, 21(10), 1998, pp. 1354-1355
SPINOCEREBELLAR ATAXIA TYPE-6 - GENOTYPE AND PHENOTYPE IN GERMAN KINDREDS
Authors: SCHOLS L KRUGER R AMOIRIDIS G PRZUNTEK H EPPLEN JT RIESS O
Citation: L. Schols et al., SPINOCEREBELLAR ATAXIA TYPE-6 - GENOTYPE AND PHENOTYPE IN GERMAN KINDREDS, Journal of Neurology, Neurosurgery and Psychiatry, 64(1), 1998, pp. 67-73
THE NATURAL-HISTORY OF DEGENERATIVE ATAXIA - A RETROSPECTIVE STUDY IN466 PATIENTS
Authors: KLOCKGETHER T LUDTKE R KRAMER B BURK K SCHOLS L RIESS O LACCONE F BOESCH S LOPESCENDES I BRICE A INZELBERG R ZILBER N DICHGANS J
Citation: T. Klockgether et al., THE NATURAL-HISTORY OF DEGENERATIVE ATAXIA - A RETROSPECTIVE STUDY IN466 PATIENTS, Brain, 121, 1998, pp. 589-600
SCA6 IS CAUSED BY MODERATE CAG EXPANSION IN THE ALPHA(1A)-VOLTAGE-DEPENDENT CALCIUM-CHANNEL GENE
Authors: RIESS O SCHOLS L BOTTGER H NOLTE D VIEIRASAECKER AMM SCHIMMING C KREUZ F MACEK M KREBSOVA A MACEK M KLOCKGETHER T ZUHLKE C LACCONE FA
Citation: O. Riess et al., SCA6 IS CAUSED BY MODERATE CAG EXPANSION IN THE ALPHA(1A)-VOLTAGE-DEPENDENT CALCIUM-CHANNEL GENE, Human molecular genetics, 6(8), 1997, pp. 1289-1293
MOLECULAR-GENETICS, CLASSIFICATION AND PH ENOTYPES IN HEREDITARY ATAXIAS
Authors: SCHOLS L RIESS O AMOIRIDIS G RIESS A PRZUNTEK H EPPLEN JT
Citation: L. Schols et al., MOLECULAR-GENETICS, CLASSIFICATION AND PH ENOTYPES IN HEREDITARY ATAXIAS, Fortschritte der Neurologie, Psychiatrie, 65(2), 1997, pp. 79-89
AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA - PHENOTYPIC DIFFERENCES IN GENETICALLY DEFINED SUBTYPES
Authors: SCHOLS L AMOIRIDIS G BUTTNER T PRZUNTEK H EPPLEN JT RIESS O
Citation: L. Schols et al., AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA - PHENOTYPIC DIFFERENCES IN GENETICALLY DEFINED SUBTYPES, Annals of neurology, 42(6), 1997, pp. 924-932
DIFFERENTIAL STABILITY OF THE (GAA)(N) TRACT IN THE FRIEDREICH-ATAXIA(STM7) GENE
Authors: EPPLEN C EPPLEN JT FRANK G MITERSKI B SANTOS EJM SCHOLS L
Citation: C. Epplen et al., DIFFERENTIAL STABILITY OF THE (GAA)(N) TRACT IN THE FRIEDREICH-ATAXIA(STM7) GENE, Human genetics, 99(6), 1997, pp. 834-836
POLYMORPHISMS IN THE PMP-22 GENE REGION (17P11.2-12) ARE CRUCIAL FOR SIMPLIFIED DIAGNOSIS OF DUPLICATIONS DELETIONS
Authors: HAUPT A SCHOLS L PRZUNTEK H EPPLEN JT
Citation: A. Haupt et al., POLYMORPHISMS IN THE PMP-22 GENE REGION (17P11.2-12) ARE CRUCIAL FOR SIMPLIFIED DIAGNOSIS OF DUPLICATIONS DELETIONS, Human genetics, 99(5), 1997, pp. 688-691
TRANSMISSION DISTORTION OF THE MUTANT ALLELES IN SPINOCEREBELLAR ATAXIA
Authors: RIESS O EPPLEN JT AMOIRIDIS G PRZUNTEK H SCHOLS L
Citation: O. Riess et al., TRANSMISSION DISTORTION OF THE MUTANT ALLELES IN SPINOCEREBELLAR ATAXIA, Human genetics, 99(2), 1997, pp. 282-284
EXTENSOR DIGITORUM BREVIS INNERVATED BY THE TIBIAL NERVE (ALL TIBIAL FOOT) - ANOMALOUS INNERVATION OR TECHNICAL PITFALL - REPLY
Authors: AMOIRIDIS G SCHOLS L
Citation: G. Amoiridis et L. Schols, EXTENSOR DIGITORUM BREVIS INNERVATED BY THE TIBIAL NERVE (ALL TIBIAL FOOT) - ANOMALOUS INNERVATION OR TECHNICAL PITFALL - REPLY, Muscle & nerve, 20(7), 1997, pp. 907-908
MOTOR EVOKED-POTENTIALS IN THE SPINOCEREBELLAR ATAXIAS TYPE-1 AND TYPE-3
Authors: SCHOLS L AMOIRIDIS G LANGKAFEL M SCHOLS S PRZUNTEK H
Citation: L. Schols et al., MOTOR EVOKED-POTENTIALS IN THE SPINOCEREBELLAR ATAXIAS TYPE-1 AND TYPE-3, Muscle & nerve, 20(2), 1997, pp. 226-228
MOTOR FIBERS IN THE SURAL NERVE OF HUMANS
Authors: AMOIRIDIS G SCHOLS L AMERIDIS N PRZUNTEK H
Citation: G. Amoiridis et al., MOTOR FIBERS IN THE SURAL NERVE OF HUMANS, Neurology, 49(6), 1997, pp. 1725-1728
FRIEDREICHS ATAXIA - REVISION OF THE PHENOTYPE ACCORDING TO MOLECULAR-GENETICS
Authors: SCHOLS L AMOIRIDIS G PRZUNTEK H FRANK G EPPLEN JT EPPLEN C
Citation: L. Schols et al., FRIEDREICHS ATAXIA - REVISION OF THE PHENOTYPE ACCORDING TO MOLECULAR-GENETICS, Brain, 120, 1997, pp. 2131-2140
SPINOCEREBELLAR ATAXIA TYPE-2 - GENOTYPE AND PHENOTYPE IN GERMAN KINDREDS
Authors: SCHOLS L GISPERT S VORGERD M VIEIRASAECKER MM BLANKE P AUBURGER G AMOIRIDIS G MEVES S EPPLEN JT PRZUNTEK H PULST SM RIESS O
Citation: L. Schols et al., SPINOCEREBELLAR ATAXIA TYPE-2 - GENOTYPE AND PHENOTYPE IN GERMAN KINDREDS, Archives of neurology, 54(9), 1997, pp. 1073-1080
MITOCHONDRIAL DISORDERS IN DEGENERATIVE ATAXIAS
Authors: SCHOLS L REICHMANN H AMOIRIDIS G SEIBEL P WAGENER S SEUFERT S PRZUNTEK H
Citation: L. Schols et al., MITOCHONDRIAL DISORDERS IN DEGENERATIVE ATAXIAS, European journal of neurology, 3(1), 1996, pp. 55-60
FACT AND FALLACY IN CLINICAL AND ELECTROPHYSIOLOGICAL STUDIES OF ANOMALOUS INNERVATION OF THE INTRINSIC FOOT MUSCLES
Authors: AMOIRIDIS G SCHOLS L MEVES S PRZUNTEK H
Citation: G. Amoiridis et al., FACT AND FALLACY IN CLINICAL AND ELECTROPHYSIOLOGICAL STUDIES OF ANOMALOUS INNERVATION OF THE INTRINSIC FOOT MUSCLES, Muscle & nerve, 19(9), 1996, pp. 1227-1228
REPEAT LENGTH AND DISEASE PROGRESSION IN SPINOCEREBELLAR ATAXIA TYPE-3
Authors: KLOCKGETHER T KRAMER B LUDTKE R SCHOLS L LACCONE F
Citation: T. Klockgether et al., REPEAT LENGTH AND DISEASE PROGRESSION IN SPINOCEREBELLAR ATAXIA TYPE-3, Lancet, 348(9030), 1996, pp. 830-830
DRUG-INDUCED RHABDOMYOLYSIS AND PERIPHERA L-NERVE INJURY - RESULTS OFA TERRITORIAL ISCHEMIA IN THE COURSE OF SYSTEMIC HYPOTENSION
Authors: AMOIRIDIS G SCHOLS L POHLAU D BERGER K NIEMCZYK W PRZUNTEK H
Citation: G. Amoiridis et al., DRUG-INDUCED RHABDOMYOLYSIS AND PERIPHERA L-NERVE INJURY - RESULTS OFA TERRITORIAL ISCHEMIA IN THE COURSE OF SYSTEMIC HYPOTENSION, Nervenarzt, 67(12), 1996, pp. 1023-1026
RELATIONS BETWEEN GENOTYPE AND PHENOTYPE IN GERMAN PATIENTS WITH THE MACHADO-JOSEPH-DISEASE MUTATION
Authors: SCHOLS L AMOIRIDIS G EPPLEN JT LANGKAFEL M PRZUNTEK H RIESS O
Citation: L. Schols et al., RELATIONS BETWEEN GENOTYPE AND PHENOTYPE IN GERMAN PATIENTS WITH THE MACHADO-JOSEPH-DISEASE MUTATION, Journal of Neurology, Neurosurgery and Psychiatry, 61(5), 1996, pp. 466-470
REVERSIBLE URINARY RETENTION AS THE MAIN SYMPTOM IN THE FIRST MANIFESTATION OF A SYRINGOMYELIA
Authors: AMOIRIDIS G MEVES S SCHOLS L PRZUNTEK H
Citation: G. Amoiridis et al., REVERSIBLE URINARY RETENTION AS THE MAIN SYMPTOM IN THE FIRST MANIFESTATION OF A SYRINGOMYELIA, Journal of Neurology, Neurosurgery and Psychiatry, 61(4), 1996, pp. 407-408
TRINUCLEOTIDE EXPANSION WITHIN THE MJD1 GENE PRESENTS CLINICALLY AS SPINOCEREBELLAR ATAXIA AND OCCURS MOST FREQUENTLY IN GERMAN SCA PATIENTS
Authors: SCHOLS L VIEIRASAECKER AMM SCHOLS S PRZUNTEK H EPPLEN JT RIESS O
Citation: L. Schols et al., TRINUCLEOTIDE EXPANSION WITHIN THE MJD1 GENE PRESENTS CLINICALLY AS SPINOCEREBELLAR ATAXIA AND OCCURS MOST FREQUENTLY IN GERMAN SCA PATIENTS, Human molecular genetics, 4(6), 1995, pp. 1001-1005
HEAD TREMOR DUE TO BILATERAL THALAMIC AND MIDBRAIN INFARCTION
Authors: OTTO S BUTTNER T SCHOLS L WINDMEIER DT PRZUNTEK H
Citation: S. Otto et al., HEAD TREMOR DUE TO BILATERAL THALAMIC AND MIDBRAIN INFARCTION, Journal of neurology, 242(9), 1995, pp. 608-610
MATHADO-JOSEPH DISEASE MUTATIONS AS THE GENETIC-BASIS OF MOST SPINOCEREBELLAR ATAXIAS IN GERMANY
Authors: SCHOLS L AMOIRIDIS G LANGKAFEL M BUTTNER T PRZUNTEK H RIESS O VIEIRASAECKER AMM EPPLEN JT
Citation: L. Schols et al., MATHADO-JOSEPH DISEASE MUTATIONS AS THE GENETIC-BASIS OF MOST SPINOCEREBELLAR ATAXIAS IN GERMANY, Journal of Neurology, Neurosurgery and Psychiatry, 59(4), 1995, pp. 449-450
Risultati: 1-25 | 26-27