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    Results: 1 to 50 of 52

    1.

    Rieger syndrome is not associated with PAX6 deletion: a correction to Acta Ophthalmol Scand 2001: 79: 201-203.

    Riise R, D'haene B, De Baere E, Grønskov K, Brøndum-Nielsen K.

    Acta Ophthalmol. 2009 Sep 18. [Epub ahead of print] No abstract available. PMID: 19764918 [PubMed - as supplied by publisher]Related articles

    2.

    X-linked cataract and Nance-Horan syndrome are allelic disorders.

    Coccia M, Brooks SP, Webb TR, Christodoulou K, Wozniak IO, Murday V, Balicki M, Yee HA, Wangensteen T, Riise R, Saggar AK, Park SM, Kanuga N, Francis PJ, Maher ER, Moore AT, Russell-Eggitt IM, Hardcastle AJ.

    Hum Mol Genet. 2009 Jul 15;18(14):2643-55. Epub 2009 May 4.PMID: 19414485 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Autosomal dominant pericentral retinal dystrophy caused by a novel missense mutation in the TOPORS gene.

    Selmer KK, Grøndahl J, Riise R, Brandal K, Braaten O, Bragadottir R, Undlien DE.

    Acta Ophthalmol. 2009 Jan 30. [Epub ahead of print]PMID: 19183411 [PubMed - as supplied by publisher]Related articles

    4.

    Functional outcome after lumbar closing wedge osteotomy in ankylosing spondylitis.

    Brox JI, Helle A, Sørensen R, Gunderson R, Riise R, Reikerås O.

    Int Orthop. 2009 Aug;33(4):1049-53. Epub 2008 May 28.PMID: 18506442 [PubMed - indexed for MEDLINE]Related articles

    5.

    Epidemiology of aniridia in Sweden and Norway.

    Edén U, Iggman D, Riise R, Tornqvist K.

    Acta Ophthalmol. 2008 Nov;86(7):727-9. Epub 2008 May 19.PMID: 18494745 [PubMed - indexed for MEDLINE]Related articles

    6.

    Aniridia among children and teenagers in Sweden and Norway.

    Edén U, Beijar C, Riise R, Tornqvist K.

    Acta Ophthalmol. 2008 Nov;86(7):730-4. Epub 2008 May 19. Erratum in: Acta Ophthalmol. 2009 Mar;87(2):242. PMID: 18494744 [PubMed - indexed for MEDLINE]Related articles

    7.

    Autosomal dominant retinitis pigmentosa in Norway: a 20-year clinical follow-up study with molecular genetic analysis. Two novel rhodopsin mutations: 1003delG and I179F.

    Grøndahl J, Riise R, Heiberg A, Leren T, Christoffersen T, Bragadottir R.

    Acta Ophthalmol Scand. 2007 May;85(3):287-97.PMID: 17488458 [PubMed - indexed for MEDLINE]Related articles

    8.

    Ocular findings in Norwegian patients with ataxia-telangiectasia: a 5 year prospective cohort study.

    Riise R, Ygge J, Lindman C, Stray-Pedersen A, Bek T, Rødningen OK, Heiberg A.

    Acta Ophthalmol Scand. 2007 Aug;85(5):557-62. Epub 2007 Mar 22.PMID: 17376192 [PubMed - indexed for MEDLINE]Related articles

    9.

    The congenital "ant-egg" cataract phenotype is caused by a missense mutation in connexin46.

    Hansen L, Yao W, Eiberg H, Funding M, Riise R, Kjaer KW, Hejtmancik JF, Rosenberg T.

    Mol Vis. 2006 Sep 1;12:1033-9.PMID: 16971895 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Nordic research in ophthalmology.

    Heijl A, Algvere PV, Alm A, Andersen N, Bauer B, Carlsson JO, Ehinger B, Eide N, Fledelius H, Foerster M, Hjortdal J, Holmström G, Høvding G, Kivelä T, la Cour M, Lindblom B, Møller-Pedersen T, Nikoskelainen E, Prause JU, Riise R, Rosenberg T, Seregard S, Stefánsson E, Tarkkanen A, Tervo T, Tornqvist K, Zetterström C.

    Acta Ophthalmol Scand. 2005 Jun;83(3):278-88. Review.PMID: 15948777 [PubMed - indexed for MEDLINE]Related articles

    11.

    [Visual problems in cerebral stroke]

    Riise R, Gundersen B, Brodal S, Bjerke P.

    Tidsskr Nor Laegeforen. 2005 Jan 20;125(2):176-7. Norwegian. PMID: 15665892 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Re: Hägg O, Fritzell P. Letter. Spine 2003; 29: 1160-1.

    Brox JI, Reikerås O, Sørensen R, Riise R, Nygård Ø, Ingebrigtsen T, Keller A, Indahl A, Holm I, Friis A, Koller AK, Eriksen H.

    Spine (Phila Pa 1976). 2004 Sep 15;29(18):2088-9. No abstract available. PMID: 15371716 [PubMed - indexed for MEDLINE]Related articles

    13.

    Tranexamic acid given into the wound reduces postoperative blood loss by half in major orthopaedic surgery.

    Krohn CD, Sørensen R, Lange JE, Riise R, Bjørnsen S, Brosstad F.

    Eur J Surg Suppl. 2003 Jul;(588):57-61.PMID: 15200045 [PubMed - indexed for MEDLINE]Related articles

    14.

    [Ocular changes in Down syndrome]

    Haugen OH, Høvding G, Riise R.

    Tidsskr Nor Laegeforen. 2004 Jan 22;124(2):186-8. Review. Norwegian. PMID: 14743234 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Randomized clinical trial of lumbar instrumented fusion and cognitive intervention and exercises in patients with chronic low back pain and disc degeneration.

    Brox JI, Sørensen R, Friis A, Nygaard Ø, Indahl A, Keller A, Ingebrigtsen T, Eriksen HR, Holm I, Koller AK, Riise R, Reikerås O.

    Spine (Phila Pa 1976). 2003 Sep 1;28(17):1913-21.PMID: 12973134 [PubMed - indexed for MEDLINE]Related articles

    16.

    Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1).

    Mykytyn K, Nishimura DY, Searby CC, Beck G, Bugge K, Haines HL, Cornier AS, Cox GF, Fulton AB, Carmi R, Iannaccone A, Jacobson SG, Weleber RG, Wright AF, Riise R, Hennekam RC, Lüleci G, Berker-Karauzum S, Biesecker LG, Stone EM, Sheffield VC.

    Am J Hum Genet. 2003 Feb;72(2):429-37. Epub 2003 Jan 10.PMID: 12524598 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    The phenotype in Norwegian patients with Bardet-Biedl syndrome with mutations in the BBS4 gene.

    Riise R, Tornqvist K, Wright AF, Mykytyn K, Sheffield VC.

    Arch Ophthalmol. 2002 Oct;120(10):1364-7.PMID: 12365916 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Identification of the gene that, when mutated, causes the human obesity syndrome BBS4.

    Mykytyn K, Braun T, Carmi R, Haider NB, Searby CC, Shastri M, Beck G, Wright AF, Iannaccone A, Elbedour K, Riise R, Baldi A, Raas-Rothschild A, Gorman SW, Duhl DM, Jacobson SG, Casavant T, Stone EM, Sheffield VC.

    Nat Genet. 2001 Jun;28(2):188-91.PMID: 11381270 [PubMed - indexed for MEDLINE]Related articles

    19.

    Rieger syndrome is associated with PAX6 deletion.

    Riise R, Storhaug K, Brøndum-Nielsen K.

    Acta Ophthalmol Scand. 2001 Apr;79(2):201-3.PMID: 11284764 [PubMed - indexed for MEDLINE]Related articles

    20.

    Bardet-Biedl and Cohen syndromes: differential diagnostic criteria.

    Warburg M, Riise R.

    J Med Genet. 2000 Dec;37(12):E46. No abstract available. PMID: 11106364 [PubMed - indexed for MEDLINE]Related articlesFree article

    21.

    Laurence-Moon-Bardet-Biedl syndrome. Clinical, electrophysiological and genetic aspects.

    Riise R.

    Acta Ophthalmol Scand Suppl. 1998;(226):1-28. No abstract available. PMID: 9645236 [PubMed - indexed for MEDLINE]Related articles

    22.

    Intrafamilial variation of the phenotype in Bardet-Biedl syndrome.

    Riise R, Andréasson S, Borgaström MK, Wright AF, Tommerup N, Rosenberg T, Tornqvist K.

    Br J Ophthalmol. 1997 May;81(5):378-85. Erratum in: Br J Ophthalmol 1997 Aug;81(8):711. PMID: 9227203 [PubMed - indexed for MEDLINE]Related articlesFree article

    23.

    Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.

    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.

    Genomics. 1997 Apr 1;41(1):93-9.PMID: 9126487 [PubMed - indexed for MEDLINE]Related articles

    24.

    Full-field electroretinograms in individuals with the Laurence-Mood-Bardet-Biedl syndrome.

    Riise R, Andréasson S, Tornqvist K.

    Acta Ophthalmol Scand. 1996 Dec;74(6):618-20.PMID: 9017054 [PubMed - indexed for MEDLINE]Related articles

    25.

    Ocular findings in the Laurence-Moon-Bardet-Biedl syndrome.

    Riise R, Andréasson S, Wright AF, Tornqvist K.

    Acta Ophthalmol Scand. 1996 Dec;74(6):612-7.PMID: 9017053 [PubMed - indexed for MEDLINE]Related articles

    26.

    Skeletal abnormalities of hands and feet in Laurence-Moon-Bardet-Biedl (LMBB) syndrome: a radiographic study.

    Rudling O, Riise R, Tornqvist K, Jonsson K.

    Skeletal Radiol. 1996 Oct;25(7):655-60.PMID: 8915050 [PubMed - indexed for MEDLINE]Related articles

    27.

    Anomalies in the permanent dentition and other oral findings in 29 individuals with Laurence-Moon-Bardet-Biedl syndrome.

    Borgström MK, Riise R, Tornqvist K, Granath L.

    J Oral Pathol Med. 1996 Feb;25(2):86-9.PMID: 8667262 [PubMed - indexed for MEDLINE]Related articles

    28.

    The cause of death in Laurence-Moon-Bardet-Biedl syndrome.

    Riise R.

    Acta Ophthalmol Scand Suppl. 1996;(219):45-7.PMID: 8741118 [PubMed - indexed for MEDLINE]Related articles

    29.

    Incidence of registered visual impairment in the Nordic child population.

    Rosenberg T, Flage T, Hansen E, Riise R, Rudanko SL, Viggosson G, Tornqvist K.

    Br J Ophthalmol. 1996 Jan;80(1):49-53.PMID: 8664232 [PubMed - indexed for MEDLINE]Related articlesFree article

    30.

    [Ophthalmological services to mentally retarded persons. A review and recommendations]

    Warburg M, Riise R.

    Ugeskr Laeger. 1994 Oct 24;156(43):6366-9. Review. Danish. PMID: 7810010 [PubMed - indexed for MEDLINE]Related articles

    31.

    [The best may become the enemy of good. On physician-patient relations and the EDP medical record]

    Trolle D, Riise R.

    Tidsskr Nor Laegeforen. 1994 Sep 10;114(21):2534-5. Norwegian. No abstract available. PMID: 7940463 [PubMed - indexed for MEDLINE]Related articles

    32.

    Visual impairment in Nordic children. V. X-linked juvenile retinoschisis.

    Rudanko SL, Flage T, Hansen E, Rosenberg T, Viggosson G, Riise R.

    Acta Ophthalmol (Copenh). 1993 Oct;71(5):586-9.PMID: 8109204 [PubMed - indexed for MEDLINE]Related articles

    33.

    Nordic registers of visually impaired children.

    Riise R.

    Scand J Soc Med. 1993 Jun;21(2):66-8.PMID: 8367684 [PubMed - indexed for MEDLINE]Related articles

    34.

    [Causes of visual impairment among Scandinavian children]

    Rosenberg T, Flage T, Hansen E, Rudanko SL, Viggosson G, Riise R.

    Ugeskr Laeger. 1993 Mar 22;155(12):874-6. Danish. No abstract available. PMID: 8480385 [PubMed - indexed for MEDLINE]Related articles

    35.

    High-resolution chromosome analysis in autosomal recessive disorders: Laurence-Moon-Bardet-Biedl syndrome.

    Fannemel M, Riise R, Lofterød B, Tommerup N.

    Clin Genet. 1993 Feb;43(2):111-2. Review. No abstract available. PMID: 8448900 [PubMed - indexed for MEDLINE]Related articles

    36.

    Visual impairment due to retinopathy of prematurity in Nordic children.

    Riise R, Flage T, Hansen E, Rosenberg T, Rudanko SL, Viggosson G.

    Acta Ophthalmol Suppl. 1993;(210):9-11.PMID: 8329963 [PubMed - indexed for MEDLINE]Related articles

    37.

    Visual impairment in Nordic children. IV. Sex distribution.

    Riise R, Flage T, Hansen E, Rosenberg T, Rudanko SL, Viggosson G.

    Acta Ophthalmol (Copenh). 1992 Oct;70(5):605-9.PMID: 1471483 [PubMed - indexed for MEDLINE]Related articles

    38.

    Visual impairment in Nordic children. III. Diagnoses.

    Hansen E, Flage T, Rosenberg T, Rudanko SL, Viggosson G, Riise R.

    Acta Ophthalmol (Copenh). 1992 Oct;70(5):597-604.PMID: 1471482 [PubMed - indexed for MEDLINE]Related articles

    39.

    Visual impairment in Nordic children. II. Aetiological factors.

    Rosenberg T, Flage T, Hansen E, Rudanko SL, Viggosson G, Riise R.

    Acta Ophthalmol (Copenh). 1992 Apr;70(2):155-64.PMID: 1609563 [PubMed - indexed for MEDLINE]Related articles

    40.

    Visual impairment in Nordic children. I. Nordic registers and prevalence data.

    Riise R, Flage T, Hansen E, Rosenberg T, Rudanko SL, Viggosson G, Warburg M.

    Acta Ophthalmol (Copenh). 1992 Apr;70(2):145-54.PMID: 1609562 [PubMed - indexed for MEDLINE]Related articles

    41.

    [Laurence-Moon-Bardet-Biedl syndrome]

    Lofterød B, Riise R, Skuseth T, Storhaug K.

    Nord Med. 1990;105(5):146-8. Norwegian. PMID: 2349067 [PubMed - indexed for MEDLINE]Related articles

    42.

    Comparison of spiramycin and doxycycline in the treatment of lower respiratory infections in general practice.

    Biermann C, Løken A, Riise R.

    J Antimicrob Chemother. 1988 Jul;22 Suppl B:155-8.PMID: 3053569 [PubMed - indexed for MEDLINE]Related articles

    43.

    [Use of vision aids in the elderly]

    Riise R, Skuseth T, Arnestad JE, Hultgren SJ.

    Tidsskr Nor Laegeforen. 1988 Jun 10;108(16):1313-6. Norwegian. No abstract available. PMID: 3388360 [PubMed - indexed for MEDLINE]Related articles

    44.

    Myopia as cause of blindness.

    Riise R.

    Acta Ophthalmol Suppl. 1988;185:109-10. No abstract available. PMID: 2853513 [PubMed - indexed for MEDLINE]Related articles

    45.

    Visual function in Laurence-Moon-Bardet-Biedl syndrome. A survey of 26 cases.

    Riise R.

    Acta Ophthalmol Suppl. 1987;182:128-31.PMID: 2837047 [PubMed - indexed for MEDLINE]Related articles

    46.

    [Visual function in Down's syndrome]

    Riise R.

    Tidsskr Nor Laegeforen. 1986 Feb 10;106(4):317-9. Norwegian. No abstract available. PMID: 2938304 [PubMed - indexed for MEDLINE]Related articles

    47.

    [Who will take care of patients with eye problems?]

    Grini-Johansen W, Bruusgaard D, Riise R.

    Tidsskr Nor Laegeforen. 1981 Sep 20;101(26):1472-5. Norwegian. No abstract available. PMID: 7336397 [PubMed - indexed for MEDLINE]Related articles

    48.

    [Visual screening of the elderly inside and outside homes and hospitals]

    Riise R.

    Tidsskr Nor Laegeforen. 1978 Nov 10;98(31):1572-3. Norwegian. No abstract available. PMID: 715748 [PubMed - indexed for MEDLINE]Related articles

    49.

    The use of contact lenses in children with unilateral traumatic aphakia.

    Riise R, Kolstad A, Bruun S, Espeland A.

    Acta Ophthalmol (Copenh). 1977 Jun;55(3):386-94.PMID: 577349 [PubMed - indexed for MEDLINE]Related articles

    50.

    Long-term prognosis in malignant exophthalmos.

    Riise R.

    Acta Ophthalmol (Copenh). 1970;48(4):634-43. No abstract available. PMID: 5536710 [PubMed - indexed for MEDLINE]Related articles

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