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Results: 1-16 |
Results: 16
EXCLUSION STUDY OF FAD GENE-MUTATIONS IN A LARGE SWISS PEDIGREE WITH EARLY-ONSET ALZHEIMERS-DISEASE
Authors: LEUBA G SAVIOZ A LANNFELT L FORSELL C LILIUS L SAINI K
Citation: G. Leuba et al., EXCLUSION STUDY OF FAD GENE-MUTATIONS IN A LARGE SWISS PEDIGREE WITH EARLY-ONSET ALZHEIMERS-DISEASE, European journal of neuroscience, 10, 1998, pp. 3226-3226
TRACHEAL ADRENALINE IN INFANTS - REPLY
Authors: JONMARKER C OLSSON AK JOGI P FORSELL C
Citation: C. Jonmarker et al., TRACHEAL ADRENALINE IN INFANTS - REPLY, Acta anaesthesiologica Scandinavica, 42(3), 1998, pp. 386-387
A NOVEL PATHOGENIC MUTATION (LEU262PHE) FOUND IN THE PRESENILIN-1 GENE IN EARLY-ONSET ALZHEIMERS-DISEASE
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
MAPPING OF A DISEASE LOCUS FOR FAMILIAL RAPIDLY PROGRESSIVE FRONTOTEMPORAL DEMENTIA TO CHROMOSOME 17Q12-21
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
CLINICAL CHARACTERISTICS OF A CHROMOSOME 17-LINKED RAPIDLY PROGRESSIVE FAMILIAL FRONTOTEMPORAL DEMENTIA
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
ALLELIC ASSOCIATION BUT ONLY WEAK EVIDENCE FOR LINKAGE TO THE APOLIPOPROTEIN-E LOCUS IN LATE-ONSET SWEDISH ALZHEIMER FAMILIES
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
HEMODYNAMIC-EFFECTS OF TRACHEAL AND INTRAVENOUS ADRENALINE IN INFANTSWITH CONGENITAL HEART ANOMALIES
Authors: JONMARKER C OLSSON AK JOGI P FORSELL C
Citation: C. Jonmarker et al., HEMODYNAMIC-EFFECTS OF TRACHEAL AND INTRAVENOUS ADRENALINE IN INFANTSWITH CONGENITAL HEART ANOMALIES, Acta anaesthesiologica Scandinavica, 40(8), 1996, pp. 927-931
A MUTATION IN ALZHEIMERS-DISEASE DESTROYING A SPLICE ACCEPTOR SITE INTHE PRESENILIN-1 GENE
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
DIAGNOSIS OF ACUTE INTERMITTENT PORPHYRIA IN NORTHERN SWEDEN - AN EVALUATION OF MUTATION ANALYSIS AND BIOCHEMICAL METHODS
Authors: ANDERSSON C THUNELL S FLODERUS Y FORSELL C LUNDIN G ANVRET M LANNFELT L WETTERBERG L LITHNER F
Citation: C. Andersson et al., DIAGNOSIS OF ACUTE INTERMITTENT PORPHYRIA IN NORTHERN SWEDEN - AN EVALUATION OF MUTATION ANALYSIS AND BIOCHEMICAL METHODS, Journal of internal medicine, 237(3), 1995, pp. 301-308
AMYLOID PRECURSOR PROTEIN MUTATION AT CODON-713 (ALA-]VAL) DOES NOT CAUSE SCHIZOPHRENIA - NONPATHOGENIC VARIANT FOUND AT CODON-705 (SILENT)
Authors: FORSELL C LANNFELT L
Citation: C. Forsell et L. Lannfelt, AMYLOID PRECURSOR PROTEIN MUTATION AT CODON-713 (ALA-]VAL) DOES NOT CAUSE SCHIZOPHRENIA - NONPATHOGENIC VARIANT FOUND AT CODON-705 (SILENT), Neuroscience letters, 184(2), 1995, pp. 90-93
DEFINE CLIENT-SERVER
Authors: FORSELL C
Citation: C. Forsell, DEFINE CLIENT-SERVER, Datamation, 41(19), 1995, pp. 12-12
DIMINISHED [H-3] INOSITOL(1,4,5)P-3, BUT NOT [H-3] INOSITOL(1,3,4,5)P-4 BINDING IN ALZHEIMERS-DISEASE BRAIN
Authors: GARLIND A COWBURN RF FORSELL C RAVID R WINBLAD B FOWLER CJ
Citation: A. Garlind et al., DIMINISHED [H-3] INOSITOL(1,4,5)P-3, BUT NOT [H-3] INOSITOL(1,3,4,5)P-4 BINDING IN ALZHEIMERS-DISEASE BRAIN, Brain research, 681(1-2), 1995, pp. 160-166
SCHIZOPHRENIA AND APP GENE-MUTATIONS
Authors: JONSSON E FORSELL C LANNFELT L SEDVALL G
Citation: E. Jonsson et al., SCHIZOPHRENIA AND APP GENE-MUTATIONS, Biological psychiatry, 37(2), 1995, pp. 135-136
A NOVEL POLYMORPHISM AT CODON-705 IN THE AMYLOID PRECURSOR PROTEIN (APP) GENE FOUND WITH SINGLE-STRANDED CONFORMATION POLYMORPHISM (SSCP) ANALYSIS
Authors: FORSELL C LANNFELT L
Citation: C. Forsell et L. Lannfelt, A NOVEL POLYMORPHISM AT CODON-705 IN THE AMYLOID PRECURSOR PROTEIN (APP) GENE FOUND WITH SINGLE-STRANDED CONFORMATION POLYMORPHISM (SSCP) ANALYSIS, Neurobiology of aging, 15, 1994, pp. 190000131-190000131
NO LINKAGE TO CHROMOSOME-14 IN SWEDISH ALZHEIMERS-DISEASE FAMILIES
Authors: LANNFELT L LILIUS L APPELGREN H AXELMAN K FORSELL C LIU L JOHANSSON K
Citation: L. Lannfelt et al., NO LINKAGE TO CHROMOSOME-14 IN SWEDISH ALZHEIMERS-DISEASE FAMILIES, Nature genetics, 4(3), 1993, pp. 218-219
A CASE OF KEARNS-SAYRE SYNDROME WITH METAPHYSEAL DYSPLASIA
Authors: WILSON B CLAESSON I FORSELL C TULINIUS M HAGBERG B
Citation: B. Wilson et al., A CASE OF KEARNS-SAYRE SYNDROME WITH METAPHYSEAL DYSPLASIA, Pediatric radiology, 23(2), 1993, pp. 106-107
Risultati: 1-16 |