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Results: 1-16 |
Results: 16
LAURENCE-MOON-BARDET-BIEDL-SYNDROME - CLINICAL, ELECTROPHYSIOLOGICAL AND GENETIC-ASPECTS - INTRODUCTION
Authors: RIISE R
Citation: R. Riise, LAURENCE-MOON-BARDET-BIEDL-SYNDROME - CLINICAL, ELECTROPHYSIOLOGICAL AND GENETIC-ASPECTS - INTRODUCTION, Acta ophthalmologica Scandinavica, 76, 1998, pp. 7-28
LINKAGE MAPPING IN 29 BARDET-BIEDL-SYNDROME FAMILIES CONFIRMS LOCI INCHROMOSOMAL REGIONS 11Q13, 15Q22.3-Q23, AND 16Q21
Authors: BRUFORD EA RIISE R TEAGUE PW PORTER K THOMSON KL MOORE AT JAY M WARBURG M SCHINZEL A TOMMERUP N TORNQVIST K ROSENBERG T PATTON M MANSFIELD DC WRIGHT AF
Citation: Ea. Bruford et al., LINKAGE MAPPING IN 29 BARDET-BIEDL-SYNDROME FAMILIES CONFIRMS LOCI INCHROMOSOMAL REGIONS 11Q13, 15Q22.3-Q23, AND 16Q21, Genomics, 41(1), 1997, pp. 93-99
INTRAFAMILIAL VARIATION OF THE PHENOTYPE IN BARDET-BIEDL SYNDROME
Authors: RIISE R ANDREASSON S BORGSTROM MK WRIGHT AF TOMMERUP N ROSENBERG T TORNQVIST K
Citation: R. Riise et al., INTRAFAMILIAL VARIATION OF THE PHENOTYPE IN BARDET-BIEDL SYNDROME, British journal of ophthalmology, 81(5), 1997, pp. 378-385
OCULAR FINDINGS IN THE LAURENCE-MOON-BARDET-BIEDL SYNDROME
Authors: RIISE R ANDREASSON S WRIGHT AF TORNQVIST K
Citation: R. Riise et al., OCULAR FINDINGS IN THE LAURENCE-MOON-BARDET-BIEDL SYNDROME, Acta ophthalmologica Scandinavica, 74(6), 1996, pp. 612-617
FULL-FIELD ELECTRORETINOGRAMS IN INDIVIDUALS WITH THE LAURENCE-MOON-BARDET-BIEDL SYNDROME
Authors: RIISE R ANDREASSON S TORNQVIST K
Citation: R. Riise et al., FULL-FIELD ELECTRORETINOGRAMS IN INDIVIDUALS WITH THE LAURENCE-MOON-BARDET-BIEDL SYNDROME, Acta ophthalmologica Scandinavica, 74(6), 1996, pp. 618-620
THE CAUSE OF DEATH IN LAURENCE-MOON-BARDET-BIEDL SYNDROME
Authors: RIISE R
Citation: R. Riise, THE CAUSE OF DEATH IN LAURENCE-MOON-BARDET-BIEDL SYNDROME, Acta ophthalmologica Scandinavica, 74, 1996, pp. 45-47
ANOMALIES IN THE PERMANENT DENTITION AND OTHER ORAL FINDINGS IN 29 INDIVIDUALS WITH LAURENCE-MOON-BARDET-BIEDL SYNDROME
Authors: BORGSTROM MK RIISE R TORNQVIST K GRANATH L
Citation: Mk. Borgstrom et al., ANOMALIES IN THE PERMANENT DENTITION AND OTHER ORAL FINDINGS IN 29 INDIVIDUALS WITH LAURENCE-MOON-BARDET-BIEDL SYNDROME, Journal of oral pathology & medicine, 25(2), 1996, pp. 86-89
SKELETAL ABNORMALITIES OF HANDS AND FEET IN LAURENCE-MOON-BARDET-BIEDL (LMBB) SYNDROME - A RADIOGRAPHIC STUDY
Authors: RUDLING O RIISE R TORNQVIST K JONSSON K
Citation: O. Rudling et al., SKELETAL ABNORMALITIES OF HANDS AND FEET IN LAURENCE-MOON-BARDET-BIEDL (LMBB) SYNDROME - A RADIOGRAPHIC STUDY, Skeletal radiology, 25(7), 1996, pp. 655-660
INCIDENCE OF REGISTERED VISUAL IMPAIRMENT IN THE NORDIC CHILD POPULATION
Authors: ROSENBERG T FLAGE T HANSEN E RIISE R RUDANKO SL VIGGOSSON G TORNQVIST K
Citation: T. Rosenberg et al., INCIDENCE OF REGISTERED VISUAL IMPAIRMENT IN THE NORDIC CHILD POPULATION, British journal of ophthalmology, 80(1), 1996, pp. 49-53
THE NORWEGIAN-OPHTHALMOLOGICAL-SOCIETY SPRING MEETING, BERGEN, NORWAY, 1995 - USE OF MITOMYCIN IN TRABECULECTOMIES
Authors: ODBERG T PEDERSEN OO FLAGE T FINNE PH WHITELAW A RIISE R ARNESTAD J SKUESETH T ANDREASSON S BORGSTROM M RUDLING O TOMMERUP N WRIGHT A KNUDTZON J LOFTEROD B STORHAUG K SKUESETH T ROSENBERG T TORNQVIST K KLYVE P
Citation: T. Odberg et al., THE NORWEGIAN-OPHTHALMOLOGICAL-SOCIETY SPRING MEETING, BERGEN, NORWAY, 1995 - USE OF MITOMYCIN IN TRABECULECTOMIES, Acta ophthalmologica Scandinavica, 73(5), 1995, pp. 478-479
GENETIC-LINKAGE ANALYSIS IN 26 FAMILIES WITH BARDET-BIEDL SYNDROME
Authors: WRIGHT AF BRUFORD EA THOMSON KL RIISE R JAY M PATTON MA JEFFERY S SCHINZEL A TOMMERUP N TEAGUE PW MANSFIELD DC
Citation: Af. Wright et al., GENETIC-LINKAGE ANALYSIS IN 26 FAMILIES WITH BARDET-BIEDL SYNDROME, Investigative ophthalmology & visual science, 36(4), 1995, pp. 774-774
INTERFAMILIAL AND INTRAFAMILIAL VARIATION IN THE PHENOTYPE IN LAURENCE-MOON-BARDET-BIEDL (LMBB) SYNDROME
Authors: RIISE R TORNQVIST K ANDREASSON S BORGSTROM M RYDLING O EHINGER B
Citation: R. Riise et al., INTERFAMILIAL AND INTRAFAMILIAL VARIATION IN THE PHENOTYPE IN LAURENCE-MOON-BARDET-BIEDL (LMBB) SYNDROME, Investigative ophthalmology & visual science, 36(4), 1995, pp. 874-874
NORDIC REGISTERS OF VISUALLY-IMPAIRED CHILDREN
Authors: RIISE R
Citation: R. Riise, NORDIC REGISTERS OF VISUALLY-IMPAIRED CHILDREN, Scandinavian journal of social medicine, 21(2), 1993, pp. 66-68
THE USE OF AUTOMATED LINKAGE ANALYSIS IN GENETIC-MAPPING OF AUTOSOMALRECESSIVE RETINITIS-PIGMENTOSA (ARRP) AND BARDET-BIEDL (BB) SYNDROME GENES
Authors: WRIGHT AF MANSFIELD DC GREEN DK MOONEY K BROWN A FOSSARELLO M JAY M JEFFERY S PATTON MA TOMMERUP N RIISE R SCHINZEL A EVANS HJ
Citation: Af. Wright et al., THE USE OF AUTOMATED LINKAGE ANALYSIS IN GENETIC-MAPPING OF AUTOSOMALRECESSIVE RETINITIS-PIGMENTOSA (ARRP) AND BARDET-BIEDL (BB) SYNDROME GENES, American journal of human genetics, 53(3), 1993, pp. 1106-1106
VISUAL IMPAIRMENT IN NORDIC CHILDREN .5. X-LINKED JUVENILE RETINOSCHISIS
Authors: RUDANKO SL FLAGE T HANSEN E ROSENBERG T VIGGOSSON G RIISE R
Citation: Sl. Rudanko et al., VISUAL IMPAIRMENT IN NORDIC CHILDREN .5. X-LINKED JUVENILE RETINOSCHISIS, Acta ophthalmologica, 71(5), 1993, pp. 586-589
VISUAL IMPAIRMENT DUE TO RETINOPATHY OF PREMATURITY IN NORDIC CHILDREN
Authors: RIISE R FLAGE T HANSEN E ROSENBERG T RUDANKO SL VIGGOSSON G
Citation: R. Riise et al., VISUAL IMPAIRMENT DUE TO RETINOPATHY OF PREMATURITY IN NORDIC CHILDREN, Acta ophthalmologica, 71, 1993, pp. 9-11
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