ACNP - Italian Periodicals Catalogue

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Results: 176-200/227

GENETIC-MAPPING OF MICROSATELLITES SPANNING THE VHL REGION OF CHROMOSOME-3P25

Authors: VANCE JM LOEB DB WHISENANT E LUI W NUNES K STAJICH JS RIMMLER J HAINES J SMITH D DRABKIN H PERICAKVANCE MA

Citation: Jm. Vance et al., GENETIC-MAPPING OF MICROSATELLITES SPANNING THE VHL REGION OF CHROMOSOME-3P25, Cytogenetics and cell genetics, 65(1-2), 1994, pp. 47-48

APOLIPOPROTEIN-E TYPE-2 ALLELE DECREASES THE RISK OF LATE-ONSET ALZHEIMER-DISEASE

Authors: CORDER EH SAUNDERS AM RISCH NJ STRITTMATTER WJ SCHMECHEL DE GASKELL PC RIMMLER JB LOCKE PA CONNEALLY PM SCHMADER KE SMALL GW ROSES AD HAINES JL PERICAKVANCE MA

Citation: Eh. Corder et al., APOLIPOPROTEIN-E TYPE-2 ALLELE DECREASES THE RISK OF LATE-ONSET ALZHEIMER-DISEASE, Neurobiology of aging, 15, 1994, pp. 190000072-190000073

FAMILY STUDIES OF APOE IN EARLY AND LATE-ONSET ALZHEIMER DISEASES

Authors: HAINES JL LOCKE PA TANZI RE GUSELLA JF PERICAKVANCE MA CONNEALLY PN

Citation: Jl. Haines et al., FAMILY STUDIES OF APOE IN EARLY AND LATE-ONSET ALZHEIMER DISEASES, Neurobiology of aging, 15, 1994, pp. 190000131-190000131

GENOMIC SCREEN TO IDENTIFY ADDITIONAL ALZHEIMER-DISEASE EFFECTS IN LATE-ONSET DISEASE

Authors: PERICAKVANCE MA CORDER EH ROBINSON LC TERMISSIAN M SMALL GW SAUNDERS A LOCKE P TANZI TR CONNEALLY PM GUSELLA JF ROSES AD HAINES JL

Citation: Ma. Pericakvance et al., GENOMIC SCREEN TO IDENTIFY ADDITIONAL ALZHEIMER-DISEASE EFFECTS IN LATE-ONSET DISEASE, Neurobiology of aging, 15, 1994, pp. 190000134-190000134

APOLIPOPROTEIN-E AND ALZHEIMER-DISEASE

Authors: ROSES AD SAUNDERS AM CORDER EH RISCH NJ HAINES JL PERICAKVANCE MA HAN SH EINSTEIN G HULETTE C SCHMECHEL DE GOEDERT M JAKES R DONG LM WEISGRABER KH HOLSTI M HUANG D STRITTMATTER WJ

Citation: Ad. Roses et al., APOLIPOPROTEIN-E AND ALZHEIMER-DISEASE, Neurobiology of aging, 15, 1994, pp. 190000150-190000150

APOLIPOPROTEIN-E TYPE-4 ALLELE LOWERS CEREBRAL PARIETAL METABOLISM INRELATIVES AT RISK FOR FAMILIAL ALZHEIMER-DISEASE

Authors: SMALL GW COLLINS MT MAZZIOTTA JC BAXTER LR PHELPS ME MANDELKERN MA KAPLAN A ADAMSON CF CHANG L GUZE BH CORDER EH SAUNDERS AM CONNEALLY PM HAINES JL PERICAKVANCE MA ROSES AD

Citation: Gw. Small et al., APOLIPOPROTEIN-E TYPE-4 ALLELE LOWERS CEREBRAL PARIETAL METABOLISM INRELATIVES AT RISK FOR FAMILIAL ALZHEIMER-DISEASE, Neurobiology of aging, 15, 1994, pp. 190000155-190000155

DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY AND HAW-RIVER-SYNDROME

Authors: BURKE AR IKEUCHI T KOIDE R TSUJI S YAMADA M PERICAKVANCE MA VANCE JM

Citation: Ar. Burke et al., DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY AND HAW-RIVER-SYNDROME, Lancet, 344(8938), 1994, pp. 1711-1712

CLINICAL-APPLICATION OF APOLIPOPROTEIN-E GENOTYPING TO ALZHEIMERS-DISEASE

Authors: ROSES AD STRITTMATTER WJ PERICAKVANCE MA CORDER EH SAUNDERS AM SCHMECHEL DE

Citation: Ad. Roses et al., CLINICAL-APPLICATION OF APOLIPOPROTEIN-E GENOTYPING TO ALZHEIMERS-DISEASE, Lancet, 343(8912), 1994, pp. 1564-1565

ALZHEIMERS-DISEASE AND POSSIBLE GENE INTERACTION - RESPONSE

Authors: PERICAKVANCE MA CORDER EH SAUNDERS AM GASKILL PC STRITTMATTER WJ ROSES AD SCHMECHEL DE SMALL GW HAINES JL

Citation: Ma. Pericakvance et al., ALZHEIMERS-DISEASE AND POSSIBLE GENE INTERACTION - RESPONSE, Science, 263(5146), 1994, pp. 537-537

SPECTRUM OF THE PHENOTYPE IN FAMILIAL ALS WITH SOD1 MUTATIONS

Authors: SIDDIQUE T JUNEJA T CALIENDO J ROOS RP LAING NG RIMMLER J SMITH R PERICAKVANCE MA

Citation: T. Siddique et al., SPECTRUM OF THE PHENOTYPE IN FAMILIAL ALS WITH SOD1 MUTATIONS, Neurology, 44(4), 1994, pp. 10000165-10000165

AUTOSOMAL-DOMINANT CHARCOT-MARIE-TOOTH DISEASE TYPE-2 - INVESTIGATIONOF GENETIC-HETEROGENEITY AND MAPPING OF THE CMT2A LOCUS

Authors: VANCE JM DENTON VP OTHMANE KB LENNON F SLAJICH JM DENG H SIDDIQUE T ROSES AD PERICAKVANCE MA

Citation: Jm. Vance et al., AUTOSOMAL-DOMINANT CHARCOT-MARIE-TOOTH DISEASE TYPE-2 - INVESTIGATIONOF GENETIC-HETEROGENEITY AND MAPPING OF THE CMT2A LOCUS, Neurology, 44(4), 1994, pp. 10000293-10000293

FORE RECESSIVE FAMILIAL SPASTIC PARAPLEGIA - EVIDENCE OF LINKAGE TO CHROMOSOME-8 AND GENETIC-LOCUS HETEROGENEITY

Authors: HENTATI A PERICAKVANCE MA HUNG WY BELAL S LAING N BOUSTANY RM HENTATI F BENHAMIDA M SIDDIQUE T

Citation: A. Hentati et al., FORE RECESSIVE FAMILIAL SPASTIC PARAPLEGIA - EVIDENCE OF LINKAGE TO CHROMOSOME-8 AND GENETIC-LOCUS HETEROGENEITY, Neurology, 44(4), 1994, pp. 10000361-10000361

AUTOSOMAL RECESSIVE CHARCOT-MARIE-TOOTH DISEASE - CLASSIFICATION AND GENETIC-LINKAGE OF ONE FORM (CMT4A) TO CHROMOSOME 8Q

Authors: BENOTHMANE K HENTATI F LENNON F BENHAMIDA C BLEL S LOEB D RAO N ROSES AD PERICAKVANCE MA BENHAMIDA M VANCE JM

Citation: K. Benothmane et al., AUTOSOMAL RECESSIVE CHARCOT-MARIE-TOOTH DISEASE - CLASSIFICATION AND GENETIC-LINKAGE OF ONE FORM (CMT4A) TO CHROMOSOME 8Q, Neurology, 44(4), 1994, pp. 10000361-10000361

GENETIC-HETEROGENEITY IN HEREDITARY HEMORRHAGIC TELANGIECTASIA - POSSIBLE CORRELATION WITH CLINICAL PHENOTYPE

Authors: MCALLISTER KA LENNON F BOWLESBIESECKER B MCKINNON WC HELMBOLD EA MARKEL DS JACKSON CE GUTTMACHER AE PERICAKVANCE MA MARCHUK DA

Citation: Ka. Mcallister et al., GENETIC-HETEROGENEITY IN HEREDITARY HEMORRHAGIC TELANGIECTASIA - POSSIBLE CORRELATION WITH CLINICAL PHENOTYPE, Journal of Medical Genetics, 31(12), 1994, pp. 927-932

HYPOTHESIS - MICROTUBULE INSTABILITY AND PAIRED HELICAL FILAMENT FORMATION IN THE ALZHEIMER-DISEASE BRAIN ARE RELATED TO APOLIPOPROTEIN-E GENOTYPE

Authors: STRITTMATTER WJ WEISGRABER KH GOEDERT M SAUNDERS AM HUANG D CORDER EH DONG LM JAKES R ALBERTS MJ GILBERT JR HAN SH HULETTE C EINSTEIN G SCHMECHEL DE PERICAKVANCE MA ROSES AD

Citation: Wj. Strittmatter et al., HYPOTHESIS - MICROTUBULE INSTABILITY AND PAIRED HELICAL FILAMENT FORMATION IN THE ALZHEIMER-DISEASE BRAIN ARE RELATED TO APOLIPOPROTEIN-E GENOTYPE, Experimental neurology, 125(2), 1994, pp. 163-171

COMPLEX GENETIC-DISEASE - CAN GENETIC STRATEGIES IN ALZHEIMERS-DISEASE AND NEW GENETIC MECHANISMS BE APPLIED TO EPILEPSY

Authors: ROSES AD PERICAKVANCE MA SAUNDERS AM SCHMECHEL D GOLDGABER D STRITTMATTER W

Citation: Ad. Roses et al., COMPLEX GENETIC-DISEASE - CAN GENETIC STRATEGIES IN ALZHEIMERS-DISEASE AND NEW GENETIC MECHANISMS BE APPLIED TO EPILEPSY, Epilepsia, 35, 1994, pp. 190000020-190000028

LINKAGE OF A LOCUS (CMT4A) FOR AUTOSOMAL RECESSIVE CHARCOT-MARIE-TOOTH DISEASE TO CHROMOSOME-8Q

Authors: OTHMANE KB HENTATI F LENNON F HAMIDA CB BLEL S ROSES AD PERICAKVANCE MA HAMIDA MB VANCE JM

Citation: Kb. Othmane et al., LINKAGE OF A LOCUS (CMT4A) FOR AUTOSOMAL RECESSIVE CHARCOT-MARIE-TOOTH DISEASE TO CHROMOSOME-8Q, Human molecular genetics, 2(10), 1993, pp. 1625-1628

LOCALIZATION OF A GENE (CMT2A) FOR AUTOSOMAL-DOMINANT CHARCOT-MARIE-TOOTH DISEASE TYPE-2 TO CHROMOSOME-1P AND EVIDENCE OF GENETIC-HETEROGENEITY

Authors: BENOTHMANE K MIDDLETON LT LOPREST LJ WILKINSON KM LENNON F ROZEAR MP STAJICH JM GASKELL PC ROSES AD PERICAKVANCE MA VANCE JM

Citation: K. Benothmane et al., LOCALIZATION OF A GENE (CMT2A) FOR AUTOSOMAL-DOMINANT CHARCOT-MARIE-TOOTH DISEASE TYPE-2 TO CHROMOSOME-1P AND EVIDENCE OF GENETIC-HETEROGENEITY, Genomics, 17(2), 1993, pp. 370-375

FLANKING MARKERS DEFINE THE X-LINKED HYPOPHOSPHATEMIC RICKETS GENE LOCUS

Authors: ECONS MJ FAIN PR NORMAN M SPEER MC PERICAKVANCE MA BECKER PA BARKER DF TAYLOR A DREZNER MK

Citation: Mj. Econs et al., FLANKING MARKERS DEFINE THE X-LINKED HYPOPHOSPHATEMIC RICKETS GENE LOCUS, Journal of bone and mineral research, 8(9), 1993, pp. 1149-1152

FINE-STRUCTURE MAPPING OF THE HUMAN X-LINKED HYPOPHOSPHATEMIC RICKETSGENE

Authors: ECONS MJ ROWE PSN FRANCIS F BARKER DF SPEER MC NORMAN M PERICAKVANCE MA FAIN PR WEISSENBACH J READ A BECKER PA LEHRACH H ORIORDAN J DREZNER MK

Citation: Mj. Econs et al., FINE-STRUCTURE MAPPING OF THE HUMAN X-LINKED HYPOPHOSPHATEMIC RICKETSGENE, Journal of bone and mineral research, 8, 1993, pp. 190000137-190000137

LINKAGE ANALYSIS IN FAMILIAL ALZHEIMER-DISEASE - DESCRIPTION OF THE DUKE AND BOSTON DATA SETS

Authors: PERICAKVANCE MA STGEORGEHYSLOP PH GASKELL PC GROWDON J CRAIN BJ HULETTE C GUSELLA JF YAMAOKA L TANZI RE ROSES AD HAINES JL

Citation: Ma. Pericakvance et al., LINKAGE ANALYSIS IN FAMILIAL ALZHEIMER-DISEASE - DESCRIPTION OF THE DUKE AND BOSTON DATA SETS, Genetic epidemiology, 10(6), 1993, pp. 361-364

GENETIC-ANALYSIS WORKSHOP-8 - ISSUES IN THE ANALYSIS OF COMPLEX DISEASES AND THEIR RISK-FACTORS - PREFACE

Authors: ELSTON RC SPENCE MA HAINES JL MARAZITA ML PERICAKVANCE MA SIERVOGEL RM MACCLUER JW

Citation: Rc. Elston et al., GENETIC-ANALYSIS WORKSHOP-8 - ISSUES IN THE ANALYSIS OF COMPLEX DISEASES AND THEIR RISK-FACTORS - PREFACE, Genetic epidemiology, 10(6), 1993, pp. 180000019-180000020

MUTATIONS IN THE CU-ZN SUPEROXIDE-DISMUTASE GENE IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS

Authors: SIDDIQUE T DENG HX HENTATI A TANDON R PERICAKVANCE MA LAING NG ROOS RP CAYABYAB A GERZFELDT B HUNG WY DENG G NEARING R WARNER C MITSUMOTO H SORIANO E SMYTH C

Citation: T. Siddique et al., MUTATIONS IN THE CU-ZN SUPEROXIDE-DISMUTASE GENE IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS, Annals of neurology, 34(2), 1993, pp. 303-304

AUTOSOMAL RECESSIVE CHARCOT-MARIE-TOOTH DISEASE TYPE-A - EVIDENCE OF GENETIC-LINKAGE OF CMT4 TO CHROMOSOME-8Q

Authors: BENOTHMANE K BENHAMIDA M HENTATI F LENNON F BENHAMIDA C BLEL S ROSES AD PERICAKVANCE MA VANCE JM

Citation: K. Benothmane et al., AUTOSOMAL RECESSIVE CHARCOT-MARIE-TOOTH DISEASE TYPE-A - EVIDENCE OF GENETIC-LINKAGE OF CMT4 TO CHROMOSOME-8Q, Cytogenetics and cell genetics, 64(3-4), 1993, pp. 142-142

THE GENE LOCUS FOR ONE FORM OF JUVENILE AMYOTROPHIC-LATERAL-SCLEROSISMAPS TO CHROMOSOME 2Q33-Q35

Authors: HENTATI A BEJAOUI K PERICAKVANCE MA HENTAT F YENHUNG W FIGLEWICZ DA BENHAMIDA C BENHAMIDA M BROWN RH SIDDIQUE T

Citation: A. Hentati et al., THE GENE LOCUS FOR ONE FORM OF JUVENILE AMYOTROPHIC-LATERAL-SCLEROSISMAPS TO CHROMOSOME 2Q33-Q35, Cytogenetics and cell genetics, 64(2), 1993, pp. 89-89

Risultati: << | 101-125 | 126-150 | 151-175 | 176-200 | >>