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Results: 1-25 | 26-50 | 51-75 | 76-87
Results: 1-25/87
REDUCED INTRANEURONAL LIPOFUSCIN CONTENT IN DEMENTIA WITH LEWY BODIESCOMPARED WITH ALZHEIMERS-DISEASE AND CONTROLS
Authors: DRACH LM BOHL J WACH S SCHLOTE W GOEBEL HH
Citation: Lm. Drach et al., REDUCED INTRANEURONAL LIPOFUSCIN CONTENT IN DEMENTIA WITH LEWY BODIESCOMPARED WITH ALZHEIMERS-DISEASE AND CONTROLS, Dementia and geriatric cognitive disorders, 9(1), 1998, pp. 1-5
LYSOSOMAL AND PEROXISOMAL DISORDERS - RECENT ADVANCES - INTRODUCTION
Authors: GOEBEL HH LAKE BD
Citation: Hh. Goebel et Bd. Lake, LYSOSOMAL AND PEROXISOMAL DISORDERS - RECENT ADVANCES - INTRODUCTION, Brain pathology, 8(1), 1998, pp. 73-78
THE NEURONAL CEROID-LIPOFUSCINOSES - RECENT ADVANCES
Authors: GOEBEL HH SHARP JD
Citation: Hh. Goebel et Jd. Sharp, THE NEURONAL CEROID-LIPOFUSCINOSES - RECENT ADVANCES, Brain pathology, 8(1), 1998, pp. 151-162
CONGENITAL MYOPATHIES WITH INCLUSION-BODIES - A BRIEF REVIEW
Authors: GOEBEL HH
Citation: Hh. Goebel, CONGENITAL MYOPATHIES WITH INCLUSION-BODIES - A BRIEF REVIEW, Neuromuscular disorders, 8(3-4), 1998, pp. 162-168
LOCALIZATION OF THE GIANT AXONAL NEUROPATHY GENE TO CHROMOSOME 16Q24
Authors: FLANIGAN KM CRAWFORD TO GRIFFIN JW GOEBEL HH KOHLSCHUTTER A RANELLS J CAMFIELD PR PTACEK LJ
Citation: Km. Flanigan et al., LOCALIZATION OF THE GIANT AXONAL NEUROPATHY GENE TO CHROMOSOME 16Q24, Annals of neurology, 43(1), 1998, pp. 143-148
PROGRESSIVE CEREBELLAR-ATAXIA IN JUVENILE GM(2)-GANGLIOSIDOSIS TYPE SANDHOFF
Authors: BECK M SIEBER N GOEBEL HH
Citation: M. Beck et al., PROGRESSIVE CEREBELLAR-ATAXIA IN JUVENILE GM(2)-GANGLIOSIDOSIS TYPE SANDHOFF, European journal of pediatrics, 157(10), 1998, pp. 866-867
MEGALENCEPHALY, MEGA CORPUS-CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT - A PREVIOUSLY UNDESCRIBED SYNDROME
Authors: GOHLICHRATMANN G BAETHMANN M LORENZ P GARTNER J GOEBEL HH ENGELBRECHT V CHRISTEN HJ LENARD HG VOIT T
Citation: G. Gohlichratmann et al., MEGALENCEPHALY, MEGA CORPUS-CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT - A PREVIOUSLY UNDESCRIBED SYNDROME, American journal of medical genetics, 79(3), 1998, pp. 161-167
CELL-DEATH AND OXIDATIVE DAMAGE IN INFLAMMATORY MYOPATHIES
Authors: TEWS DS GOEBEL HH
Citation: Ds. Tews et Hh. Goebel, CELL-DEATH AND OXIDATIVE DAMAGE IN INFLAMMATORY MYOPATHIES, Clinical immunology and immunopathology (Print), 87(3), 1998, pp. 240-247
SPECT STUDY OF A GERMAN CADASIL FAMILY - A PHENOTYPE WITH MIGRAINE AND PROGRESSIVE DEMENTIA ONLY
Authors: MELLIES JK BAUMER T MULLER JA TOURNIERLASSERVE E CHABRIAT H KNOBLOCH O HACKELOER HJ GOEBEL HH WETZIG L HALLER P
Citation: Jk. Mellies et al., SPECT STUDY OF A GERMAN CADASIL FAMILY - A PHENOTYPE WITH MIGRAINE AND PROGRESSIVE DEMENTIA ONLY, Neurology, 50(6), 1998, pp. 1715-1721
CONGENITAL NEUROMUSCULAR DISORDER WITH ELECTRON-DENSE SPHEROIDS
Authors: GOEBEL HH HOCHFELD M SCHULTZE C
Citation: Hh. Goebel et al., CONGENITAL NEUROMUSCULAR DISORDER WITH ELECTRON-DENSE SPHEROIDS, Journal of neuropathology and experimental neurology, 57(5), 1998, pp. 40-40
NO EVIDENCE FOR HETEROGENEITY IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY
Authors: KRESS W HALLIGERKELLER B GRIMM T PORSCHKE H ENGELHARDT A GOEBEL HH MULLERMYSOK B
Citation: W. Kress et al., NO EVIDENCE FOR HETEROGENEITY IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY, Journal of Medical Genetics, 35(7), 1998, pp. 613-614
ALCOHOL-RELATED ACUTE AXONAL POLYNEUROPATHY - A DIFFERENTIAL-DIAGNOSIS OF GUILLAIN-BARRE-SYNDROME
Authors: WOHRLE JC SPENGOS K STEINKE W GOEBEL HH HENNERICI M
Citation: Jc. Wohrle et al., ALCOHOL-RELATED ACUTE AXONAL POLYNEUROPATHY - A DIFFERENTIAL-DIAGNOSIS OF GUILLAIN-BARRE-SYNDROME, Archives of neurology, 55(10), 1998, pp. 1329-1334
DESMIN-RELATED MYOPATHIES
Authors: GOEBEL HH
Citation: Hh. Goebel, DESMIN-RELATED MYOPATHIES, Current opinion in neurology, 10(5), 1997, pp. 426-429
METABOLIC DISEASES
Authors: GOEBEL HH
Citation: Hh. Goebel, METABOLIC DISEASES, Brain pathology, 7(4), 1997, pp. 1057-1059
MORPHOLOGICAL DIAGNOSIS OF NEURODEGENERATIVE CNS DISORDERS BY EXTRACEREBRAL BIOPSY
Authors: GOEBEL HH
Citation: Hh. Goebel, MORPHOLOGICAL DIAGNOSIS OF NEURODEGENERATIVE CNS DISORDERS BY EXTRACEREBRAL BIOPSY, Brain pathology, 7(4), 1997, pp. 1059-1061
A EUROPEAN FAMILY WITH HISTIDINE-58 TRANSTHYRETIN MUTATION IN FAMILIAL AMYLOID POLYNEUROPATHY
Authors: GOEBEL HH SEDDIGH S HOPF HC UEMICHI T BENSON MD MCKUSICK VA
Citation: Hh. Goebel et al., A EUROPEAN FAMILY WITH HISTIDINE-58 TRANSTHYRETIN MUTATION IN FAMILIAL AMYLOID POLYNEUROPATHY, Neuromuscular disorders, 7(4), 1997, pp. 229-230
CONGENITAL MYOPATHY WITH EXCESS OF THIN MYOFILAMENTS
Authors: GOEBEL HH ANDERSON JR HUBNER C OEXLE K WARLO I
Citation: Hh. Goebel et al., CONGENITAL MYOPATHY WITH EXCESS OF THIN MYOFILAMENTS, Neuromuscular disorders, 7(3), 1997, pp. 160-168
NEMALINE MYOPATHY WITH INTRANUCLEAR RODS - INTRANUCLEAR ROD MYOPATHY
Authors: GOEBEL HH WARLO I
Citation: Hh. Goebel et I. Warlo, NEMALINE MYOPATHY WITH INTRANUCLEAR RODS - INTRANUCLEAR ROD MYOPATHY, Neuromuscular disorders, 7(1), 1997, pp. 13-19
OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN A NORTHERN GERMAN FAMILY LINKEDTO CHROMOSOME 14Q, AND PRESENTING CARNITINE DEFICIENCY
Authors: PORSCHKE H KRESS W REICHMANN H GOEBEL HH GRIMM T
Citation: H. Porschke et al., OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN A NORTHERN GERMAN FAMILY LINKEDTO CHROMOSOME 14Q, AND PRESENTING CARNITINE DEFICIENCY, Neuromuscular disorders, 7, 1997, pp. 57-62
CONGENITAL CYTOPLASMIC BODY MYOPATHY - CASE-REPORT
Authors: REED L YOUNG J GOEBEL HH SCHOCHET SS
Citation: L. Reed et al., CONGENITAL CYTOPLASMIC BODY MYOPATHY - CASE-REPORT, Journal of child neurology, 12(2), 1997, pp. 149-152
INFANTILE INTRANUCLEAR ROD MYOPATHY
Authors: GOEBEL HH PIIRSOO A WARLO I SCHOFER O KEHR S GAUDE M
Citation: Hh. Goebel et al., INFANTILE INTRANUCLEAR ROD MYOPATHY, Journal of child neurology, 12(1), 1997, pp. 22-30
LEUKOCYTES IN NEURONAL CEROID-LIPOFUSCINOSES - FUNCTION AND APOPTOSIS
Authors: KIESEIER BC WISNIEWSKI KE PARK E SCHULLERLEVIS G MEHTA PD GOEBEL HH
Citation: Bc. Kieseier et al., LEUKOCYTES IN NEURONAL CEROID-LIPOFUSCINOSES - FUNCTION AND APOPTOSIS, Brain & development, 19(5), 1997, pp. 317-322
THE HUMAN PRION DISEASES - FROM NEUROPATHOLOGY TO PATHOBIOLOGY AND MOLECULAR-GENETICS - FINAL REPORT OF AN EU CONCERTED ACTION
Authors: BUDKA H HAINFELLNER JA JELLINGER K KLEINERT R MAIER H PILZ P SCIOT R MARTIN JJ BOJSENMOLLER M LAURSEN H STTEGLBJAERG P HALTIA M KOVANEN J DELISLE MB DORMONT D LASMEZAS C GRAY F HAUW JJ SEILHEAN D HELDT N MIKOL J VITAL C FONCIN JF ELHACHIMI K KOPP N BERGMANN M BILZER T CERVOSNAVARRO J DIRINGER H FEIDEN W GOEBEL HH BOHL J GULLOTTA F JENDROSKA K KRETZSCHMAR HA LINKE RP MEYERMANN R BOELLAARD JW MEHRAEIN P SCHLOTE W SCHRODER JM SCHRODER R VOLK B WALTER GF HORI A WIESTLER OD BALLOYANNIS SJ DAVAKI P PATSOURIS E GEORGSSON G FARRELL M KEOHANE C BUGIANI O MACCHI G MASULLO C COSTANZI G POCCHIARI M RIZZUTTO N SCHIFFER D TRABATTONI GR GIANGASPERO F JANSEN GH GRINDE B MORK SJ SKULLERUD K LIMA C PIMENTEL J CRUZSANCHEZ FF BERCIANO JA MARTINEZLAGE J NAVARRO C CABELLO A BRUN A KRISTENSSON K LUNDBERG PO OLSSON Y COLLINGE J ESIRI MM GRAHAM D IRONSIDE JW LANTOS PL MACKENZIE JM SCARAVILLI F WELLER RO WILL RG ALLEN IV MIRAKHUR M MAJTENYI K LIBERSKI PP PETRESCU A MITROVA E POPOVIC M AGUZZI A JANZER RC PIZZOLATO G STAMM B VANDEVELDE M MASTERS CL TATEISHI J KITAMOTO T BROWN P
Citation: H. Budka et al., THE HUMAN PRION DISEASES - FROM NEUROPATHOLOGY TO PATHOBIOLOGY AND MOLECULAR-GENETICS - FINAL REPORT OF AN EU CONCERTED ACTION, Neuropathology and applied neurobiology, 23(5), 1997, pp. 416-422
DNA-FRAGMENTATION AND EXPRESSION OF APOPTOSIS-RELATED PROTEINS IN MUSCULAR-DYSTROPHIES
Authors: TEWS DS GOEBEL HH
Citation: Ds. Tews et Hh. Goebel, DNA-FRAGMENTATION AND EXPRESSION OF APOPTOSIS-RELATED PROTEINS IN MUSCULAR-DYSTROPHIES, Neuropathology and applied neurobiology, 23(4), 1997, pp. 331-338
WORKSHOP REPORT - DIAGNOSTIC (CLINICAL AND MORPHOLOGICAL) CRITERIA FOR ADULT NEURONAL CEROID-LIPOFUSCINOSIS (KUFS-DISEASE), HOPITAL-DE-LA-SALPETRIERE AFM-INSTITUT-DE-MYOLOGIE, PARIS, FRANCE, 5 DECEMBER 1996
Authors: RUCHOUX MM GOEBEL HH
Citation: Mm. Ruchoux et Hh. Goebel, WORKSHOP REPORT - DIAGNOSTIC (CLINICAL AND MORPHOLOGICAL) CRITERIA FOR ADULT NEURONAL CEROID-LIPOFUSCINOSIS (KUFS-DISEASE), HOPITAL-DE-LA-SALPETRIERE AFM-INSTITUT-DE-MYOLOGIE, PARIS, FRANCE, 5 DECEMBER 1996, Neuropathology and applied neurobiology, 23(3), 1997, pp. 262-263
Risultati: 1-25 | 26-50 | 51-75 | 76-87