Citation: K. Axelman et al., WIDE-RANGE OF DISEASE ONSET IN A FAMILY WITH ALZHEIMER-DISEASE AND A HIS163TYR MUTATION IN THE PRESENILIN-1 GENE, Archives of neurology, 55(5), 1998, pp. 698-702
Authors:
FORSELL C
FROELICH S
AXELMAN K
VESTLING M
COWBURN RF
LILIUS L
JOHNSTON JA
ENGVALL B
JOHANSSON K
DAHLKILD A
INGELSON M
STGEORGEHYSLOP PH
LANNFELT L
Citation: C. Forsell et al., A NOVEL PATHOGENIC MUTATION (LEU262PHE) FOUND IN THE PRESENILIN-1 GENE IN EARLY-ONSET ALZHEIMERS-DISEASE, Neuroscience letters, 234(1), 1997, pp. 3-6
Authors:
FROELICH S
BASUN H
FORSELL C
LILIUS L
AXELMAN K
ANDREADIS A
LANNFELT L
Citation: S. Froelich et al., MAPPING OF A DISEASE LOCUS FOR FAMILIAL RAPIDLY PROGRESSIVE FRONTOTEMPORAL DEMENTIA TO CHROMOSOME 17Q12-21, American journal of medical genetics, 74(4), 1997, pp. 380-385
Authors:
BASUN H
ALMKVIST O
AXELMAN K
BRUN A
CAMPBELL TA
COLLINGE J
FORSELL C
FROELICH S
WAHLUND LO
WETTERBERG L
LANNFELT L
Citation: H. Basun et al., CLINICAL CHARACTERISTICS OF A CHROMOSOME 17-LINKED RAPIDLY PROGRESSIVE FAMILIAL FRONTOTEMPORAL DEMENTIA, Archives of neurology, 54(5), 1997, pp. 539-544
Authors:
LIU L
FORSELL C
LILIUS L
AXELMAN K
CORDER EH
LANNFELT L
Citation: L. Liu et al., ALLELIC ASSOCIATION BUT ONLY WEAK EVIDENCE FOR LINKAGE TO THE APOLIPOPROTEIN-E LOCUS IN LATE-ONSET SWEDISH ALZHEIMER FAMILIES, American journal of medical genetics, 67(3), 1996, pp. 306-311
Authors:
CLARK RF
HUTTON M
FULDNER RA
FROELICH S
KARRAN E
TALBOT C
CROOK R
LENDON C
PRIHAR G
HE C
KORENBLAT K
MARTINEZ A
WRAGG M
BUSFIELD F
BEHRENS MI
MYERS A
NORTON J
MORRIS J
MEHTA N
PEARSON C
LINCOLN S
BAKER M
DUFF K
ZEHR C
PEREZTUR J
HOULDEN H
RUIZ A
OSSA J
LOPERA F
ARCOS M
MADRIGAL L
COLLINGE J
HUMPHREYS C
ASHWORTH A
SARNER S
FOX N
HARVEY R
KENNEDY A
ROQUES P
CLINE RT
PHILLIPS CA
VENTER JC
FORSELL L
AXELMAN K
LILIUS L
JOHNSTON J
COWBURN R
VIITANEN M
WINBLAD B
KOSIK K
HALTIA M
POYHONEN M
DICKSON D
MANN D
NEARY D
SNOWDEN J
LANTOS P
LANNFELT L
ROSSOR M
ROBERTS GW
ADAMS MD
HARDY J
GOATE A
Citation: Rf. Clark et al., THE STRUCTURE OF THE PRESENILIN-1 (S182) GENE AND IDENTIFICATION OF 6NOVEL MUTATIONS IN EARLY-ONSET AD FAMILIES, Nature genetics, 11(2), 1995, pp. 219-222
Authors:
PEREZTUR J
FROELICH S
PRIHAR G
CROOK R
BAKER M
DUFF K
WRAGG M
BUSFIELD F
LENDON C
CLARK RF
ROQUES P
FULDNER RA
JOHNSTON J
COWBURN R
FORSELL C
AXELMAN K
LILIUS L
HOULDEN H
KARRAN E
ROBERTS GW
ROSSOR M
ADAMS MD
HARDY J
GOATE A
LANNFELT L
HUTTON M
Citation: J. Pereztur et al., A MUTATION IN ALZHEIMERS-DISEASE DESTROYING A SPLICE ACCEPTOR SITE INTHE PRESENILIN-1 GENE, NeuroReport, 7(1), 1995, pp. 297-301
Authors:
LANNFELT L
PEDERSEN NL
LILIUS L
AXELMAN K
JOHANSSON K
VIITANEN M
GATZ M
Citation: L. Lannfelt et al., APOLIPOPROTEIN EPSILON-4 ALLELE IN SWEDISH TWINS AND SIBLINGS WITH ALZHEIMER-DISEASE, Alzheimer disease and associated disorders, 9(3), 1995, pp. 166-169
Citation: L. Lannfelt et al., GENETIC-COUNSELING IN A SWEDISH ALZHEIMER FAMILY WITH AMYLOID PRECURSOR PROTEIN MUTATION, American journal of human genetics, 56(1), 1995, pp. 332-335
Authors:
HALTIA M
VIITANEN M
SULKAVA R
ALAHURULA V
POYHONEN M
GOLDFARB L
BROWN P
LEVY E
HOULDEN H
CROOK R
GOATE A
CLARK R
KORENBLAT K
PANDIT S
KELLER HD
LILIUS L
LIU L
AXELMAN K
FORSELL L
WINBLAD B
LANNFELT L
HARDY J
Citation: M. Haltia et al., CHROMOSOME 14-ENCODED ALZHEIMERS-DISEASE - GENETIC AND CLINICOPATHOLOGICAL DESCRIPTION, Annals of neurology, 36(3), 1994, pp. 362-367
Authors:
LANNFELT L
BOGDANOVIC N
APPELGREN H
AXELMAN K
LILIUS L
HANSSON G
SCHENK D
HARDY J
WINBLAD B
Citation: L. Lannfelt et al., AMYLOID PRECURSOR PROTEIN MUTATION CAUSES ALZHEIMERS-DISEASE IN A SWEDISH FAMILY, Neuroscience letters, 168(1-2), 1994, pp. 254-255
Citation: K. Axelman et al., FAMILIAL ALZHEIMERS-DISEASE, DESCRIPTION OF A PEDIGREE SEGREGATING THE APP-670 671 MUTATION/, Neurobiology of aging, 15, 1994, pp. 190000009-190000009
Authors:
LIU L
LILIUS L
FORSELL L
AXELMAN K
LANNFELT L
Citation: L. Liu et al., NO LINKAGE TO THE APOLIPOPROTEIN-E GENE IN SWEDISH ALZHEIMER-DISEASE FAMILIES, Neurobiology of aging, 15, 1994, pp. 190000133-190000133
Citation: K. Axelman et al., A LARGE SWEDISH FAMILY WITH ALZHEIMERS-DISEASE WITH A CODON-670 671 AMYLOID PRECURSOR PROTEIN MUTATION - A CLINICAL AND GENEALOGICAL INVESTIGATION/, Archives of neurology, 51(12), 1994, pp. 1193-1197
Authors:
JOHNSTON J
LILIUS L
AXELMAN K
COWBURN R
JOHANSSON K
VIITANEN M
WINBLAD B
LANNFELT L
Citation: J. Johnston et al., SEQUENCING OF EXON-16 AND EXON-17 OF THE BETA-AMYLOID PRECURSOR PROTEIN GENE FAILS TO IDENTIFY NEW MUTATIONS IN SWEDISH ALZHEIMERS-DISEASE PATIENTS, Human molecular genetics, 2(7), 1993, pp. 1045-1046
Authors:
ALMQVIST E
LAKE S
AXELMAN K
JOHANSSON K
WINBLAD B
Citation: E. Almqvist et al., SCREENING OF AMYLOID PRECURSOR PROTEIN GENE MUTATION (APP717VAL-]ILE)IN SWEDISH FAMILIES WITH ALZHEIMERS-DISEASE, Journal of neural transmission. Parkinson's disease and dementia section, 6(2), 1993, pp. 151-156