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Results: 1-25 | 26-44
Results: 1-25/44
MISSENSE MUTATIONS IN DESMIN ASSOCIATED WITH FAMILIAL CARDIAC AND SKELETAL MYOPATHY
Authors: GOLDFARB LG PARK KY CERVENAKOVA L GOROKHOVA S LEE HS VASCONCELOS O NAGLE JW SEMINOMORA C SIVAKUMAR K DALAKAS MC
Citation: Lg. Goldfarb et al., MISSENSE MUTATIONS IN DESMIN ASSOCIATED WITH FAMILIAL CARDIAC AND SKELETAL MYOPATHY, Nature genetics, 19(4), 1998, pp. 402-403
COMPARATIVE NEUROPATHOLOGY OF KURU WITH THE NEW VARIANT OF CREUTZFELDT-JAKOB-DISEASE - EVIDENCE FOR STRAIN OF AGENT PREDOMINATING OVER GENOTYPE OF HOST
Authors: MCLEAN CA IRONSIDE JW ALPERS MP BROWN PW CERVENAKOVA L ANDERSON R MASTERS CL
Citation: Ca. Mclean et al., COMPARATIVE NEUROPATHOLOGY OF KURU WITH THE NEW VARIANT OF CREUTZFELDT-JAKOB-DISEASE - EVIDENCE FOR STRAIN OF AGENT PREDOMINATING OVER GENOTYPE OF HOST, Brain pathology, 8(3), 1998, pp. 429-437
GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE WITH A117V MUTATION IN A 2ND FRENCH-ALSATIAN FAMILY
Authors: HELDT N BOELLAARD JW BROWN P CERVENAKOVA L DOERRSCHOTT J THOMAS C SCHERER C ROHMER F
Citation: N. Heldt et al., GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE WITH A117V MUTATION IN A 2ND FRENCH-ALSATIAN FAMILY, Clinical neuropathology, 17(4), 1998, pp. 229-234
ROUSSY-LEVY-SYNDROME IS ASSOCIATED WITH A DNA DUPLICATION ON CHROMOSOME 17P11.2
Authors: SAMBUUGHIN N KOFFMAN B DALAKAS MC SMITH ACM CERVENAKOVA L MECK J GARVEY M SYED N HALLETT M GOLDFARB LG
Citation: N. Sambuughin et al., ROUSSY-LEVY-SYNDROME IS ASSOCIATED WITH A DNA DUPLICATION ON CHROMOSOME 17P11.2, Annals of neurology, 44(3), 1998, pp. 116-116
VILIUISK ENCEPHALOMYELITIS - AN EMERGING CONTAGIOUS-DISEASE
Authors: GOLDFARB LG PLATONOV FA CERVENAKOVA L MCLEAN CL MASTERS C GAJDUSEK DC ALEXEEV VP KRIVOSHAPKIN VG
Citation: Lg. Goldfarb et al., VILIUISK ENCEPHALOMYELITIS - AN EMERGING CONTAGIOUS-DISEASE, Annals of neurology, 44(3), 1998, pp. 120-120
APOE IN NON-ALZHEIMER AMYLOIDOSES - TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES
Authors: CHAPMAN J CERVENAKOVA L LEE HS ESTUPINAN J RICHARDSON S VNENCAKJONES CL GAJDUSEK DC KORCZYN AD BROWN P GOLDFARB LG
Citation: J. Chapman et al., APOE IN NON-ALZHEIMER AMYLOIDOSES - TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES, Neurology, 51(2), 1998, pp. 548-553
THE ALA53THR POINT MUTATION IN THE ALPHA-SYNUCLEIN GENE IS ABSENT IN ASHKENAZI JEWISH PATIENTS WITH FAMILIAL OR SPORADIC PARKINSONS-DISEASE
Authors: GOLDFARB LG LEE HS ISAACSON S CHAPMAN J GOROKHOVA S CERVENAKOVA L
Citation: Lg. Goldfarb et al., THE ALA53THR POINT MUTATION IN THE ALPHA-SYNUCLEIN GENE IS ABSENT IN ASHKENAZI JEWISH PATIENTS WITH FAMILIAL OR SPORADIC PARKINSONS-DISEASE, Neurology, 50(4), 1998, pp. 2105-2105
ANCESTRAL ORIGINS OF THE PRNP E200K MUTATION CAUSING FAMILIAL CREUTZFELDT-JAKOB-DISEASE
Authors: LEE HS SAMBUUGHIN N CERVENAKOVA L CHAPMAN J AVIV R POCCHIARI M KORCZYN A AVIV R GAJDUSEK C BROWN P LITVAK S GOLDFARB LG
Citation: Hs. Lee et al., ANCESTRAL ORIGINS OF THE PRNP E200K MUTATION CAUSING FAMILIAL CREUTZFELDT-JAKOB-DISEASE, Neurology, 50(4), 1998, pp. 3124-3124
GENERALIZED CHOREA AND SUBACUTE DEMENTIA ASSOCIATED WITH MUTATION IN CODON-178 OF THE PRION PROTEIN GENE
Authors: CONCHA M CERVENAKOVA L GIBBS CJ MEJIA H SINGER C
Citation: M. Concha et al., GENERALIZED CHOREA AND SUBACUTE DEMENTIA ASSOCIATED WITH MUTATION IN CODON-178 OF THE PRION PROTEIN GENE, Neurology, 50(4), 1998, pp. 65005-65005
CREUTZFELDT-JAKOB-DISEASE IN A HUSBAND-AND-WIFE
Authors: BROWN P CERVENAKOVA L MCSHANE L GOLDFARB LG BISHOP K BASTIAN F KIRKPATRICK J PICCARDO P GHETTI B GAJDUSEK DC
Citation: P. Brown et al., CREUTZFELDT-JAKOB-DISEASE IN A HUSBAND-AND-WIFE, Neurology, 50(3), 1998, pp. 684-688
PHENOTYPE-GENOTYPE STUDIES IN KURU - IMPLICATIONS FOR NEW VARIANT CREUTZFELDT-JAKOB-DISEASE
Authors: CERVENAKOVA L GOLDFARB LG GARRUTO R LEE HS GAJDUSEK DC BROWN P
Citation: L. Cervenakova et al., PHENOTYPE-GENOTYPE STUDIES IN KURU - IMPLICATIONS FOR NEW VARIANT CREUTZFELDT-JAKOB-DISEASE, Proceedings of the National Academy of Sciences of the United Statesof America, 95(22), 1998, pp. 13239-13241
SPORADIC FATAL DEMENTIA WITH THALAMIC GLIOSIS AND D178N PRP GENOTYPE BUT WITH ABSENCE OF SPONGIFORM CHANGE AND NEGATIVE PRP IMMUNOCYTOCHEMISTRY
Authors: BRETT FM CERVENAKOVA L COLLINGE J FARRELL MA GIBBS CJ TRAYNOR B STAUNTON H
Citation: Fm. Brett et al., SPORADIC FATAL DEMENTIA WITH THALAMIC GLIOSIS AND D178N PRP GENOTYPE BUT WITH ABSENCE OF SPONGIFORM CHANGE AND NEGATIVE PRP IMMUNOCYTOCHEMISTRY, Journal of neuropathology and experimental neurology, 57(5), 1998, pp. 93-93
A CASE OF SPORADIC CREUTZFELDT-JAKOB-DISEASE WITH A GERSTMANN-STAUSSLER-SCHEINKER PHENOTYPE BUT NO ALTERATIONS IN THE PRNP GENE
Authors: LIBERSKI PP BARCIKOWSKA M CERVENAKOVA L BRATOSIEWICZ J MARCZEWSKA M BROWN P GAJDUSEK DC
Citation: Pp. Liberski et al., A CASE OF SPORADIC CREUTZFELDT-JAKOB-DISEASE WITH A GERSTMANN-STAUSSLER-SCHEINKER PHENOTYPE BUT NO ALTERATIONS IN THE PRNP GENE, Acta Neuropathologica, 96(4), 1998, pp. 425-430
PATHOLOGY AND IMMUNOCYTOCHEMISTRY OF A KURU BRAIN
Authors: HAINFELLNER JA LIBERSKI PP GUIROY DC CERVENAKOVA L BROWN P GAJDUSEK DC BUDKA H
Citation: Ja. Hainfellner et al., PATHOLOGY AND IMMUNOCYTOCHEMISTRY OF A KURU BRAIN, Brain pathology, 7(1), 1997, pp. 547-553
PUTATIVE NEUROSURGICAL TRANSMISSION OF CREUTZFELDT-JAKOB-DISEASE WITHANALYSIS OF DONOR AND RECIPIENT - AGENT STRAINS
Authors: ELHACHIMI KH CHAUNU MP CERVENAKOVA L BROWN P FONCIN JF
Citation: Kh. Elhachimi et al., PUTATIVE NEUROSURGICAL TRANSMISSION OF CREUTZFELDT-JAKOB-DISEASE WITHANALYSIS OF DONOR AND RECIPIENT - AGENT STRAINS, Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie, 320(4), 1997, pp. 319-328
UNSTABLE 24-NUCLEOTIDE REPEAT EXPANSION IN TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES
Authors: CERVENAKOVA L BROWN P GAJDUSEK DC GOLDFARB LG
Citation: L. Cervenakova et al., UNSTABLE 24-NUCLEOTIDE REPEAT EXPANSION IN TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES, Annals of neurology, 42(3), 1997, pp. 3-3
HIGH SEQUENCE HOMOLOGY OF THE PRP GENE IN MULE DEER AND ROCKY-MOUNTAIN ELK
Authors: CERVENAKOVA L ROHWER R WILLIAMS ES BROWN P GAJDUSEK DC
Citation: L. Cervenakova et al., HIGH SEQUENCE HOMOLOGY OF THE PRP GENE IN MULE DEER AND ROCKY-MOUNTAIN ELK, Lancet, 350(9072), 1997, pp. 219-220
THE D178N (CIS-129M) FATAL FAMILIAL INSOMNIA MUTATION ASSOCIATED WITHDIVERSE CLINICOPATHOLOGICAL PHENOTYPES IN AN AUSTRALIAN KINDRED
Authors: MCLEAN CA STOREY E GARDNER RJM TANNENBERG AEG CERVENAKOVA L BROWN P
Citation: Ca. Mclean et al., THE D178N (CIS-129M) FATAL FAMILIAL INSOMNIA MUTATION ASSOCIATED WITHDIVERSE CLINICOPATHOLOGICAL PHENOTYPES IN AN AUSTRALIAN KINDRED, Neurology, 49(2), 1997, pp. 552-558
GENETIC-REGULATION OF E-SELECTIN EXPRESSION IN RAT CNS ENDOTHELIAL-CELLS (EC)
Authors: WAGNEROVA J CERVENAKOVA L BALABANOV R DOREDUFFY P
Citation: J. Wagnerova et al., GENETIC-REGULATION OF E-SELECTIN EXPRESSION IN RAT CNS ENDOTHELIAL-CELLS (EC), Journal of neurochemistry, 69, 1997, pp. 152-152
GENETIC-REGULATION OF E-SELECTIN EXPRESSION IN RAT CNS ENDOTHELIAL-CELLS (EC)
Authors: WAGNEROVA J CERVENAKOVA L BALABANOV R DOREDUFFY P
Citation: J. Wagnerova et al., GENETIC-REGULATION OF E-SELECTIN EXPRESSION IN RAT CNS ENDOTHELIAL-CELLS (EC), Journal of neurochemistry, 69, 1997, pp. 152-152
INTERACTIONS BETWEEN ASTROCYTES AND OLIGODENDROGLIA IN HUMAN AND EXPERIMENTAL CREUTZFELDT-JAKOB-DISEASE AND SCRAPIE
Authors: LIBERSKI PP BROWN P CERVENAKOVA L GAJDUSEK DC
Citation: Pp. Liberski et al., INTERACTIONS BETWEEN ASTROCYTES AND OLIGODENDROGLIA IN HUMAN AND EXPERIMENTAL CREUTZFELDT-JAKOB-DISEASE AND SCRAPIE, Experimental neurology, 144(1), 1997, pp. 227-234
MIXED FEATURES OF ALZHEIMER-DISEASE AND CREUTZFELDT-JAKOB-DISEASE IN A FAMILY WITH A PRESENILIN-1 MUTATION IN CHROMOSOME-14
Authors: ELHACHIMI KH CERVENAKOVA L BROWN P GOLDFARB LG RUBENSTEIN R GAJDUSEK DC FONCIN JF
Citation: Kh. Elhachimi et al., MIXED FEATURES OF ALZHEIMER-DISEASE AND CREUTZFELDT-JAKOB-DISEASE IN A FAMILY WITH A PRESENILIN-1 MUTATION IN CHROMOSOME-14, AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION, 3(4), 1996, pp. 223-233
IS HEREDITARY INCLUSION-BODY MYOPATHY A FAMILIAL PRION DISEASE
Authors: CERVENAKOVA L SIVAKUMAR K NAGLE J DALAKAS MC GOLDFARB LG
Citation: L. Cervenakova et al., IS HEREDITARY INCLUSION-BODY MYOPATHY A FAMILIAL PRION DISEASE, Annals of neurology, 40(1), 1996, pp. 128-128
FATAL FAMILIAL INSOMNIA - A 7TH FAMILY
Authors: SILBURN P CERVENAKOVA L VARGHESE P TANNENBERG A BROWN P BOYLE R
Citation: P. Silburn et al., FATAL FAMILIAL INSOMNIA - A 7TH FAMILY, Neurology, 47(5), 1996, pp. 1326-1328
FAMILIAL CREUTZFELDT-JAKOB-DISEASE WITH A 5-REPEAT OCTAPEPTIDE INSERTMUTATION
Authors: COCHRAN EJ BENNETT DA CERVENAKOVA L KENNEY K BERNARD B FOSTER NL BENSON DF GOLDFARB LG BROWN P
Citation: Ej. Cochran et al., FAMILIAL CREUTZFELDT-JAKOB-DISEASE WITH A 5-REPEAT OCTAPEPTIDE INSERTMUTATION, Neurology, 47(3), 1996, pp. 727-733
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