AAAAAA

   
Results: << | 101-125 | 126-150 | 151-175 | 176-200 | >>
Results: 101-125/227
HEREDITARY SPASTIC PARAPLEGIA - ADVANCES IN GENETIC RESEARCH
Authors: FINK JK HEIMANPATTERSON T BIRD T CAMBI F DUBE MP FIGLEWICZ DA FINK JK HAINES JL HEIMANPATTERSON T HENTATI A PERICAKVANCE MA RASKIND W ROULEAU GA SIDDIQUE T
Citation: Jk. Fink et al., HEREDITARY SPASTIC PARAPLEGIA - ADVANCES IN GENETIC RESEARCH, Neurology, 46(6), 1996, pp. 1507-1514
EXAMINATION OF THE PREVALENCE OF CHARCOT-MARIE-TOOTH-TYPE 2A AND REFINED MAPPING OF THE 1P36 LOCUS
Authors: VANCE JM DENTON PH MIDDLETON L LOEB D LENNON F STAJICH JM WOLPERT C PERICAKVANCE MA
Citation: Jm. Vance et al., EXAMINATION OF THE PREVALENCE OF CHARCOT-MARIE-TOOTH-TYPE 2A AND REFINED MAPPING OF THE 1P36 LOCUS, Neurology, 46(2), 1996, pp. 2011-2011
A COMPLETE GENOMIC SCREEN IN THE SEARCH FOR ADDITIONAL GENES IN LATE-ONSET (GREATER-THAN-60 YEARS) ALZHEIMER-DISEASE
Authors: PERICAKVANCE MA GASKELL PC SMALL GW SAUNDERS AM LOCKE PA TERMINASSIAN M PRITCHARD M ROBINSON C HAYNES CS GROWDON J GUSELLA J HAINES JL
Citation: Ma. Pericakvance et al., A COMPLETE GENOMIC SCREEN IN THE SEARCH FOR ADDITIONAL GENES IN LATE-ONSET (GREATER-THAN-60 YEARS) ALZHEIMER-DISEASE, Neurology, 46(2), 1996, pp. 23003-23003
GENETIC-ANALYSIS OF THE HLA REGION IN MULTIPLE-SCLEROSIS
Authors: HAUSER SL HAINES JL SEBOUN E OKSENBERG J GOODKIN DE LINCOLN R GUSELLA JF ROSES AD PERICAKVANCE MA
Citation: Sl. Hauser et al., GENETIC-ANALYSIS OF THE HLA REGION IN MULTIPLE-SCLEROSIS, Neurology, 46(2), 1996, pp. 34002-34002
A COMPLETE GENOMIC SCREEN FOR MULTIPLE-SCLEROSIS
Authors: HAINES JL SEBOUN E RIMMLER J GOODKIN DE LINCOLN R BAZYK A LEE A OKSENBERG J GUSELLA JF ROSES AD HAUSER SA PERICAKVANCE MA
Citation: Jl. Haines et al., A COMPLETE GENOMIC SCREEN FOR MULTIPLE-SCLEROSIS, Neurology, 46(2), 1996, pp. 34003-34003
GENETIC SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS - THE ROLE OF MAG, MBP, MOG, OMGP, AND PLP
Authors: SEBOUN E CARSIQUE R PAHMDINH D BOESPFLUGTANGUY O GOODKIN DE LATHROP M RIMMLER J HAINES JL OKSENBERG J FIZAMES C LINCOLN R PERICAKVANCE MA GUSELLA JF ROSES AD WEISSENBACH J DAUTIGNY A HAUSER SL
Citation: E. Seboun et al., GENETIC SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS - THE ROLE OF MAG, MBP, MOG, OMGP, AND PLP, Neurology, 46(2), 1996, pp. 34004-34004
APOLIPOPROTEIN IS A SUSCEPTIBILITY GENETIC-LOCUS THAT AFFECTS THE EXPRESSION OF LATE-ONSET FAMILIAL AND SPORADIC ALZHEIMERS-DISEASE
Authors: ROSES AD SAUNDERS AM PERICAKVANCE MA EINSTEIN G HULETTE C SCHMECHEL DE HUANG D STRITTMATTER WJ
Citation: Ad. Roses et al., APOLIPOPROTEIN IS A SUSCEPTIBILITY GENETIC-LOCUS THAT AFFECTS THE EXPRESSION OF LATE-ONSET FAMILIAL AND SPORADIC ALZHEIMERS-DISEASE, Biological psychiatry, 39(7), 1996, pp. 217-217
PERIODIC VESTIBULOCEREBELLAR ATAXIA, AN AUTOSOMAL-DOMINANT ATAXIA WITH DEFECTIVE SMOOTH-PURSUIT, IS GENETICALLY DISTINCT FROM OTHER AUTOSOMAL-DOMINANT ATAXIAS
Authors: DAMJI KF ALLINGHAM RR POLLOCK SC SMALL K LEWIS KE STAJICH JM YAMAOKA LH VANCE JM PERICAKVANCE MA
Citation: Kf. Damji et al., PERIODIC VESTIBULOCEREBELLAR ATAXIA, AN AUTOSOMAL-DOMINANT ATAXIA WITH DEFECTIVE SMOOTH-PURSUIT, IS GENETICALLY DISTINCT FROM OTHER AUTOSOMAL-DOMINANT ATAXIAS, Archives of neurology, 53(4), 1996, pp. 338-344
LINKAGE OF FRONTOTEMPORAL DEMENTIA TO CHROMOSOME-17 - CLINICAL AND NEUROPATHOLOGICAL CHARACTERIZATION OF PHENOTYPE
Authors: YAMAOKA LH WELSHBOHMER KA HULETTE CM GASKELL PC MURRAY M RIMMLER JL HELMS BR GUERRA M ROSES AD SCHMECHEL DE PERICAKVANCE MA
Citation: Lh. Yamaoka et al., LINKAGE OF FRONTOTEMPORAL DEMENTIA TO CHROMOSOME-17 - CLINICAL AND NEUROPATHOLOGICAL CHARACTERIZATION OF PHENOTYPE, American journal of human genetics, 59(6), 1996, pp. 1306-1312
LINKAGE OF A GENE FOR MACULAR CORNEAL-DYSTROPHY TO CHROMOSOME-16
Authors: VANCE JM JONASSON F LENNON F SARRICA J DAMJI KF STAUFFER J PERICAKVANCE MA KLINTWORTH GK
Citation: Jm. Vance et al., LINKAGE OF A GENE FOR MACULAR CORNEAL-DYSTROPHY TO CHROMOSOME-16, American journal of human genetics, 58(4), 1996, pp. 757-762
THE DISTINCTION BETWEEN JUVENILE AND ADULT-ONSET PRIMARY OPEN-ANGLE GLAUCOMA
Authors: WIGGS JL DAMJI KF HAINES JL PERICAKVANCE MA ALLINGHAM RR
Citation: Jl. Wiggs et al., THE DISTINCTION BETWEEN JUVENILE AND ADULT-ONSET PRIMARY OPEN-ANGLE GLAUCOMA, American journal of human genetics, 58(1), 1996, pp. 243-244
A DE-NOVO FRAME-SHIFT MUTATION IN THE TUBERIN GENE
Authors: KUMAR A WOLPERT C KANDT RS SEGAL J PUFKY J ROSES AD PERICAKVANCE MA GILBERT JR
Citation: A. Kumar et al., A DE-NOVO FRAME-SHIFT MUTATION IN THE TUBERIN GENE, Human molecular genetics, 4(8), 1995, pp. 1471-1472
BLEPHAROPHIMOSIS SYNDROME IS LINKED TO CHROMOSOME 3Q
Authors: SMALL KW STALVEY M FISHER L MULLEN L DICKEL C BEADLES K REIMER R LESSNER A LEWIS K PERICAKVANCE MA
Citation: Kw. Small et al., BLEPHAROPHIMOSIS SYNDROME IS LINKED TO CHROMOSOME 3Q, Human molecular genetics, 4(3), 1995, pp. 443-448
MUTATION ANALYSIS OF THE TSC2 GENE IN AN AFRICAN-AMERICAN FAMILY
Authors: KUMAR A KANDT RS WOLPERT C ROSES AD PERICAKVANCE MA GILBERT JR
Citation: A. Kumar et al., MUTATION ANALYSIS OF THE TSC2 GENE IN AN AFRICAN-AMERICAN FAMILY, Human molecular genetics, 4(12), 1995, pp. 2295-2298
PHYSICAL AND GENETIC-MAPPING OF THE CMT4A LOCUS AND EXCLUSION OF PMP-2 AS THE DEFECT IN CMT4A
Authors: BENOTHMANE K LOEB D HAYWORTHHODGTE R HENTATI F RAO N ROSES AD BENHAMIDA M PERICAKVANCE MA VANCE JM
Citation: K. Benothmane et al., PHYSICAL AND GENETIC-MAPPING OF THE CMT4A LOCUS AND EXCLUSION OF PMP-2 AS THE DEFECT IN CMT4A, Genomics, 28(2), 1995, pp. 286-290
MOLECULAR PATHOLOGY OF TUBEROUS SCLEROSIS COMPLEX
Authors: KANDT RS KUMAR A WOLPERT C ROSES AD PERICAKVANCE MA GILBERT JR
Citation: Rs. Kandt et al., MOLECULAR PATHOLOGY OF TUBEROUS SCLEROSIS COMPLEX, Annals of neurology, 38(3), 1995, pp. 537-537
GENETIC AND PHYSICAL MAPPING OF THE GENOMIC REGION SPANNING CMT4A
Authors: BENOTHMANE K LOEB D RAO N HAYWORTHHOTGE R ROSES AD PERICAKVANCE MA BENHAMIDA M VANCE JM
Citation: K. Benothmane et al., GENETIC AND PHYSICAL MAPPING OF THE GENOMIC REGION SPANNING CMT4A, Cytogenetics and cell genetics, 68(3-4), 1995, pp. 156-156
DELAYED-ONSET OF ALZHEIMERS-DISEASE WITH NONSTEROIDAL ANTIINFLAMMATORY AND HISTAMINE-H2 BLOCKING-DRUGS
Authors: BREITNER JCS WELSH KA HELMS MJ GASKELL PC GAU BA ROSES AD PERICAKVANCE MA SAUNDERS AM
Citation: Jcs. Breitner et al., DELAYED-ONSET OF ALZHEIMERS-DISEASE WITH NONSTEROIDAL ANTIINFLAMMATORY AND HISTAMINE-H2 BLOCKING-DRUGS, Neurobiology of aging, 16(4), 1995, pp. 523-530
GENETIC SUSCEPTIBILITY TO ALZHEIMER-DISEASE
Authors: PERICAKVANCE MA HAINES JL
Citation: Ma. Pericakvance et Jl. Haines, GENETIC SUSCEPTIBILITY TO ALZHEIMER-DISEASE, Trends in genetics, 11(12), 1995, pp. 504-508
CONFIRMATION OF LOCUS HETEROGENEITY IN THE PURE FORM OF FAMILIAL SPASTIC PARAPLEGIA
Authors: SPEER MC KINGSTON HM BOUSTANY RMN GASKELL PC ROBINSON LC LENNON F WOLPERT CM YAMAOKA LH KAHLER SG HOGAN EL CUMMING WJK PERICAKVANCE MA
Citation: Mc. Speer et al., CONFIRMATION OF LOCUS HETEROGENEITY IN THE PURE FORM OF FAMILIAL SPASTIC PARAPLEGIA, American journal of medical genetics, 60(4), 1995, pp. 307-311
BETHLEM MYOPATHY IS NOT ALLELIC TO LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 1A
Authors: SPEER MC YAMAOKA LH STAJICH J LEWIS K PERICAKVANCE MA STACY R TANDAN R FRIES TJ
Citation: Mc. Speer et al., BETHLEM MYOPATHY IS NOT ALLELIC TO LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 1A, American journal of medical genetics, 58(2), 1995, pp. 197-198
PERIODIC VESTIBULOCEREBELLAR ATAXIA IS GENETICALLY DISTINCT FROM OTHER AUTOSOMAL-DOMINANT ATAXIAS
Authors: DAMJI KF ALLINGHAM RR POLLOCK S SMALL K LEWIS K YAMAOKA L VANCE JW PERICAKVANCE MA
Citation: Kf. Damji et al., PERIODIC VESTIBULOCEREBELLAR ATAXIA IS GENETICALLY DISTINCT FROM OTHER AUTOSOMAL-DOMINANT ATAXIAS, Investigative ophthalmology & visual science, 36(4), 1995, pp. 227-227
BELIZE MACULAR DYSTROPHY MAPS TO CHROMOSOME-6Q16 (THE NORTH-CAROLINA MACULAR DYSTROPHY LOCUS, MCDR1)
Authors: RABB M MULLEN L YELCHITS S LEWIS K PERICAKVANCE MA SMALL KW
Citation: M. Rabb et al., BELIZE MACULAR DYSTROPHY MAPS TO CHROMOSOME-6Q16 (THE NORTH-CAROLINA MACULAR DYSTROPHY LOCUS, MCDR1), Investigative ophthalmology & visual science, 36(4), 1995, pp. 892-892
NORTH-CAROLINA MACULAR DYSTROPHY (MCDR1) - EVIDENCE OF LINKAGE DISEQUILIBRIUM IN MULTIPLE DIFFERENT FAMILIES AND GENETIC-HETEROGENEITY
Authors: SMALL KW YELCHITS S MULLEN L GARCIA CA RABB M KLEIN R PANGALINI R FLAXEL C PUECH B LEWIS K PERICAKVANCE MA
Citation: Kw. Small et al., NORTH-CAROLINA MACULAR DYSTROPHY (MCDR1) - EVIDENCE OF LINKAGE DISEQUILIBRIUM IN MULTIPLE DIFFERENT FAMILIES AND GENETIC-HETEROGENEITY, Investigative ophthalmology & visual science, 36(4), 1995, pp. 1064-1064
APOLIPOPROTEIN-E IN CREUTZFELDT-JAKOB-DISEASE
Authors: ROSES AD SAUNDERS AM STRITTMATTER WJ SCHMECHEL DE PERICAKVANCE MA HYMAN B
Citation: Ad. Roses et al., APOLIPOPROTEIN-E IN CREUTZFELDT-JAKOB-DISEASE, Lancet, 345(8941), 1995, pp. 69-69
Risultati: << | 101-125 | 126-150 | 151-175 | 176-200 | >>