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Results: 1-25 | 26-31
Results: 1-25/31
NEW GENETIC CONCEPTS AND STROKE PREVENTION
Authors: AUBURGER G
Citation: G. Auburger, NEW GENETIC CONCEPTS AND STROKE PREVENTION, Cerebrovascular diseases, 8, 1998, pp. 28-32
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
ESTABLISHMENT OF AN ANDALUSIAN FAMILY COLLECTION FOR BIPOLAR AFFECTIVE-DISORDER
Authors: OROZCO G RIVAS F GOMEZ MI BORDALLO A ORTEGA MV REQUENA J KLIMKE A GAEBEL W LARISCH R MULLERGARTNER HW AUBURGER G PROPPING P RIETSCHEL M NOTHEN MM
Citation: G. Orozco et al., ESTABLISHMENT OF AN ANDALUSIAN FAMILY COLLECTION FOR BIPOLAR AFFECTIVE-DISORDER, American journal of medical genetics, 81(6), 1998, pp. 544-545
THE UBIQUITIN PATHWAY IN PARKINSONS-DISEASE
Authors: LEROY E BOYER R AUBURGER G LEUBE B ULM G MEZEY E HARTA G BROWNSTEIN MJ JONNALAGADA S CHERNOVA T DEHEJIA A LAVEDAN C GASSER T STEINBACH PJ WILKINSON KD POLYMEROPOULOS MH
Citation: E. Leroy et al., THE UBIQUITIN PATHWAY IN PARKINSONS-DISEASE, Nature, 395(6701), 1998, pp. 451-452
FINE-SCALE MAPPING PLACES DLG1, THE GENE ENCODING HDLG, TELOMERIC TO THE OPA1 CANDIDATE REGION
Authors: ALEXANDER C STATHAKIS DG LIN LH RAHMAN S BRYANT PJ AUBURGER G CHISHTI AH
Citation: C. Alexander et al., FINE-SCALE MAPPING PLACES DLG1, THE GENE ENCODING HDLG, TELOMERIC TO THE OPA1 CANDIDATE REGION, Mammalian genome, 8(10), 1997, pp. 795-796
FREQUENCY OF FAMILIAL INHERITANCE AMONG 488 INDEX PATIENTS WITH IDIOPATHIC FOCAL DYSTONIA AND CLINICAL VARIABILITY IN A LARGE FAMILY
Authors: LEUBE B KESSLER KR GOECKE T AUBURGER G BENECKE R
Citation: B. Leube et al., FREQUENCY OF FAMILIAL INHERITANCE AMONG 488 INDEX PATIENTS WITH IDIOPATHIC FOCAL DYSTONIA AND CLINICAL VARIABILITY IN A LARGE FAMILY, Movement disorders, 12(6), 1997, pp. 1000-1006
SPORADIC FOCAL DYSTONIA IN NORTHWEST GERMANY - MOLECULAR-BASIS ON CHROMOSOME 18P
Authors: LEUBE B HENDGEN T KESSLER KR KNAPP M BENECKE R AUBURGER G
Citation: B. Leube et al., SPORADIC FOCAL DYSTONIA IN NORTHWEST GERMANY - MOLECULAR-BASIS ON CHROMOSOME 18P, Annals of neurology, 42(1), 1997, pp. 111-114
EVIDENCE FOR DYT7 BEING A COMMON-CAUSE OF CERVICAL DYSTONIA (TORTICOLLIS) IN CENTRAL-EUROPE
Authors: LEUBE B HENDGEN T KESSLER KR KNAPP M BENECKE R AUBURGER G
Citation: B. Leube et al., EVIDENCE FOR DYT7 BEING A COMMON-CAUSE OF CERVICAL DYSTONIA (TORTICOLLIS) IN CENTRAL-EUROPE, American journal of medical genetics, 74(5), 1997, pp. 529-532
GENE LOCUS FPD1 OF THE DYSTONIC MOUNT-REBACK TYPE OF AUTOSOMAL-DOMINANT PAROXYSMAL CHOREOATHETOSIS
Authors: HOFELE K BENECKE R AUBURGER G
Citation: K. Hofele et al., GENE LOCUS FPD1 OF THE DYSTONIC MOUNT-REBACK TYPE OF AUTOSOMAL-DOMINANT PAROXYSMAL CHOREOATHETOSIS, Neurology, 49(5), 1997, pp. 1252-1257
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
MUTATION DETECTION IN MACHADO-JOSEPH DISEASE USING REPEAT EXPANSION DETECTION
Authors: LINDBLAD K LUNKES A MACIEL P STEVANIN G ZANDER C KLOCKGETHER T RATZLAFF T BRICE A ROULEAU GA HUDSON T AUBURGER G SCHALLING M
Citation: K. Lindblad et al., MUTATION DETECTION IN MACHADO-JOSEPH DISEASE USING REPEAT EXPANSION DETECTION, Molecular medicine, 2(1), 1996, pp. 77-85
MODERATE EXPANSION OF A NORMALLY BIALLELIC TRINUCLEOTIDE REPEAT IN SPINOCEREBELLAR ATAXIA TYPE-2
Authors: PULST SM NECHIPORUK A NECHIPORUK T GISPERT S CHEN XN LOPESCENDES I PEARLMAN S STARKMAN S OROZCODIAZ G LUNKES A DEJONG P ROULEAU GA AUBURGER G KORENBERG JR FIGUEROA C SAHBA S
Citation: Sm. Pulst et al., MODERATE EXPANSION OF A NORMALLY BIALLELIC TRINUCLEOTIDE REPEAT IN SPINOCEREBELLAR ATAXIA TYPE-2, Nature genetics, 14(3), 1996, pp. 269-276
IDIOPATHIC TORSION DYSTONIA - ASSIGNMENT OF A GENE TO CHROMOSOME 18P IN A GERMAN FAMILY WITH ADULT-ONSET, AUTOSOMAL-DOMINANT INHERITANCE AND PURELY FOCAL DISTRIBUTION
Authors: LEUBE B RUDNICKI D RATZLAFF T KESSLER KR BENECKE R AUBURGER G
Citation: B. Leube et al., IDIOPATHIC TORSION DYSTONIA - ASSIGNMENT OF A GENE TO CHROMOSOME 18P IN A GERMAN FAMILY WITH ADULT-ONSET, AUTOSOMAL-DOMINANT INHERITANCE AND PURELY FOCAL DISTRIBUTION, Human molecular genetics, 5(10), 1996, pp. 1673-1677
A GENE FOR AUTOSOMAL-DOMINANT PAROXYSMAL CHOREOATHETOSIS SPASTICITY (CSE) MAPS TO THE VICINITY OF A POTASSIUM CHANNEL GENE-CLUSTER ON CHROMOSOME 1P, PROBABLY WITHIN 2 CM BETWEEN D1S443 AND D1S197
Authors: AUBURGER G RATZLAFF T LUNKES A NELLES HW LEUBE B BINKOFSKI F KUGEL H HEINDEL W SEITZ R BENECKE R WITTE OW VOIT T
Citation: G. Auburger et al., A GENE FOR AUTOSOMAL-DOMINANT PAROXYSMAL CHOREOATHETOSIS SPASTICITY (CSE) MAPS TO THE VICINITY OF A POTASSIUM CHANNEL GENE-CLUSTER ON CHROMOSOME 1P, PROBABLY WITHIN 2 CM BETWEEN D1S443 AND D1S197, Genomics, 31(1), 1996, pp. 90-94
ANALYSIS OF 2 PEDIGREES WITH AUTOSOMAL-DOMINANT PAROXYSMAL CHOREOATHETOSIS - ASSIGNMENT OF A GENE LOCUS TO PROBABLY 2 CM BETWEEN D1S443 ANDD1S197 ON CHROMOSOME 1P, IN PROXIMITY TO A POTASSIUM CHANNEL GENE-CLUSTER
Authors: HOFELE K RATZLAFF T LUNKES A NELLES HW RUDY B PRZUNTEK H AUBURGER G
Citation: K. Hofele et al., ANALYSIS OF 2 PEDIGREES WITH AUTOSOMAL-DOMINANT PAROXYSMAL CHOREOATHETOSIS - ASSIGNMENT OF A GENE LOCUS TO PROBABLY 2 CM BETWEEN D1S443 ANDD1S197 ON CHROMOSOME 1P, IN PROXIMITY TO A POTASSIUM CHANNEL GENE-CLUSTER, Cytogenetics and cell genetics, 72(2-3), 1996, pp. 148-149
ACTIVATION AND DEGRADATION OF BENZOATE, 3-PHENYLPROPIANATE AND CROTONATE BY SYNTROPHUS-BUSWELLII STRAIN GA - EVIDENCE FOR ELECTRON-TRANSPORT PHOSPHORYLATION DURING CROTONATE RESPIRATION
Authors: AUBURGER G WINTER J
Citation: G. Auburger et J. Winter, ACTIVATION AND DEGRADATION OF BENZOATE, 3-PHENYLPROPIANATE AND CROTONATE BY SYNTROPHUS-BUSWELLII STRAIN GA - EVIDENCE FOR ELECTRON-TRANSPORT PHOSPHORYLATION DURING CROTONATE RESPIRATION, Applied microbiology and biotechnology, 44(6), 1996, pp. 807-815
GENETIC-MAPPING OF THE SPINOCEREBELLAR ATAXIA-2 (SCA2) LOCUS ON CHROMOSOME-12Q23-Q24.1
Authors: HERNANDEZ A MAGARINO C GISPERT S SANTOS N LUNKES A OROZCO G HEREDERO L BECKMANN J AUBURGER G
Citation: A. Hernandez et al., GENETIC-MAPPING OF THE SPINOCEREBELLAR ATAXIA-2 (SCA2) LOCUS ON CHROMOSOME-12Q23-Q24.1, Genomics, 25(2), 1995, pp. 433-435
AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA LINKED TO SCA3 IN GERMAN FAMILIES
Authors: KLOCKGETHER T BURK K BRICE A AUBURGER G
Citation: T. Klockgether et al., AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA LINKED TO SCA3 IN GERMAN FAMILIES, Annals of neurology, 38(2), 1995, pp. 299-299
ISOLATION AND PHYSIOLOGICAL CHARACTERIZATION OF SYNTROPHUS-BUSWELLII STRAIN GA FROM A SYNTROPHIC BENZOATE DEGRADING STRICTLY ANAEROBIC COCULTURE
Authors: AUBURGER G WINTER J
Citation: G. Auburger et J. Winter, ISOLATION AND PHYSIOLOGICAL CHARACTERIZATION OF SYNTROPHUS-BUSWELLII STRAIN GA FROM A SYNTROPHIC BENZOATE DEGRADING STRICTLY ANAEROBIC COCULTURE, Applied microbiology and biotechnology, 44(1-2), 1995, pp. 241-248
CLASSIFICATION AND DIAGNOSIS OF DEGENERAT IVE ATAXIAS
Authors: KLOCKGETHER T BURK K AUBURGER G DICHGANS J
Citation: T. Klockgether et al., CLASSIFICATION AND DIAGNOSIS OF DEGENERAT IVE ATAXIAS, Nervenarzt, 66(8), 1995, pp. 571-581
EXPANDED CAG REPEATS IN NEUROPSYCHIATRIC DISORDERS AND THE RED METHOD
Authors: SCHALLING M LINDBLAD K ZANDER C NYLANDER PO DEBRUYN A SOUREY D ENGSTRM C HOMGREN G HUDSON T CHOTAI J MENDLEWICZ J VANBROEKHOVEN C ADOLFSSON R CARREROVALEZUELA R PAYAMI H JOHNSON W STENROOS ES SHATTUC S NUTT J BRICELL A LITT M RATZLAFF T AUBURGER G
Citation: M. Schalling et al., EXPANDED CAG REPEATS IN NEUROPSYCHIATRIC DISORDERS AND THE RED METHOD, American journal of human genetics, 57(4), 1995, pp. 1312-1312
REFINEMENT OF THE OPA1 GENE LOCUS ON CHROMOSOME 3Q28-Q29 TO A REGION OF 2-8 CM, IN ONE CUBAN PEDIGREE WITH AUTOSOMAL-DOMINANT OPTIC ATROPHYTYPE KJER
Authors: LUNKES A HARTUNG U MAGARINO C RODRIGUEZ M PALMERO A RODRIGUEZ L HEREDERO L WEISSENBACH J WEBER J AUBURGER G
Citation: A. Lunkes et al., REFINEMENT OF THE OPA1 GENE LOCUS ON CHROMOSOME 3Q28-Q29 TO A REGION OF 2-8 CM, IN ONE CUBAN PEDIGREE WITH AUTOSOMAL-DOMINANT OPTIC ATROPHYTYPE KJER, American journal of human genetics, 57(4), 1995, pp. 968-970
LOCALIZATION OF THE CANDIDATE GENE D-AMINO-ACID OXIDASE OUTSIDE THE REFINED 1-CM REGION OF SPINOCEREBELLAR ATAXIA-2
Authors: CANCEL G STEVANIN G VERNANT JC DURR A LEPAGELEZIN A BELAL S BENHAMIDA M PULST S ROULEAU G WEISSENBACH J LEPASLIER D KUCHERLAPATI R MONTGOMERY K FUKUI K AUBURGER G
Citation: G. Cancel et al., LOCALIZATION OF THE CANDIDATE GENE D-AMINO-ACID OXIDASE OUTSIDE THE REFINED 1-CM REGION OF SPINOCEREBELLAR ATAXIA-2, American journal of human genetics, 57(4), 1995, pp. 972-975
AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA - REDUCTION OF THE FSPI CANDIDATE REGION ON CHROMOSOME 14Q TO 7-CM AND LOCUS HETEROGENEITY
Authors: GISPERT S SANTOS N DAMEN R VOIT T SCHULZ J KLOCKGETHER T OROZCO G KREUZ F WEISSENBACH J AUBURGER G
Citation: S. Gispert et al., AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPLEGIA - REDUCTION OF THE FSPI CANDIDATE REGION ON CHROMOSOME 14Q TO 7-CM AND LOCUS HETEROGENEITY, American journal of human genetics, 56(1), 1995, pp. 183-187
GENERATION OF A CHROMOSOME-12 IRRADIATION HYBRID PANEL CONTAINING FRAGMENTS OF THE SPINOCEREBELLAR ATAXIA-2 AND DARIERS-DISEASE CANDIDATE REGIONS
Authors: LUNKES A SCHROCK E AUBURGER G
Citation: A. Lunkes et al., GENERATION OF A CHROMOSOME-12 IRRADIATION HYBRID PANEL CONTAINING FRAGMENTS OF THE SPINOCEREBELLAR ATAXIA-2 AND DARIERS-DISEASE CANDIDATE REGIONS, Cytogenetics and cell genetics, 67(4), 1994, pp. 270-270
Risultati: 1-25 | 26-31