Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 74


Health Related Quality of Life and Physical Activity after Multiple-surgeries in Patients with Early Onset Scoliosis.

Molland RS, Brox JI, Stuge B, Holm I, Riise RB, Kibsgård TJ.

Spine Deform. 2019 Nov;7(6):1010. doi: 10.1016/j.jspd.2019.09.016. No abstract available.


Bleomycin hydrolase regulates the release of chemokines important for inflammation and wound healing by keratinocytes.

Riise R, Odqvist L, Mattsson J, Monkley S, Abdillahi SM, Tyrchan C, Muthas D, Yrlid LF.

Sci Rep. 2019 Dec 31;9(1):20407. doi: 10.1038/s41598-019-56667-6.


Genetic variations in A20 DUB domain provide a genetic link to citrullination and neutrophil extracellular traps in systemic lupus erythematosus.

Odqvist L, Jevnikar Z, Riise R, Öberg L, Rhedin M, Leonard D, Yrlid L, Jackson S, Mattsson J, Nanda S, Cohen P, Knebel A, Arthur S, Thörn K, Svenungsson E, Jönsen A, Gunnarsson I, Tandre K, Alexsson A, Kastbom A, Rantapää-Dahlqvist S, Eloranta ML, Syvänen AC, Bengtsson A, Johansson P, Sandling JK, Sjöwall C, Rönnblom L, Collins B, Vaarala O.

Ann Rheum Dis. 2019 Oct;78(10):1363-1370. doi: 10.1136/annrheumdis-2019-215434. Epub 2019 Jul 12.


GM1 ganglioside-independent intoxication by Cholera toxin.

Cervin J, Wands AM, Casselbrant A, Wu H, Krishnamurthy S, Cvjetkovic A, Estelius J, Dedic B, Sethi A, Wallom KL, Riise R, Bäckström M, Wallenius V, Platt FM, Lebens M, Teneberg S, Fändriks L, Kohler JJ, Yrlid U.

PLoS Pathog. 2018 Feb 12;14(2):e1006862. doi: 10.1371/journal.ppat.1006862. eCollection 2018 Feb.


Role of regulatory T cells in acute myeloid leukemia patients undergoing relapse-preventive immunotherapy.

Sander FE, Nilsson M, Rydström A, Aurelius J, Riise RE, Movitz C, Bernson E, Kiffin R, Ståhlberg A, Brune M, Foà R, Hellstrand K, Thorén FB, Martner A.

Cancer Immunol Immunother. 2017 Nov;66(11):1473-1484. doi: 10.1007/s00262-017-2040-9. Epub 2017 Jul 18.


NOX2-dependent immunosuppression in chronic myelomonocytic leukemia.

Aurelius J, Hallner A, Werlenius O, Riise R, Möllgård L, Brune M, Hansson M, Martner A, Thorén FB, Hellstrand K.

J Leukoc Biol. 2017 Aug;102(2):459-466. doi: 10.1189/jlb.5VMA1116-454R. Epub 2017 Mar 14.


"Ant-egg" cataract revisited.

Clemmensen K, Enghild JJ, Ivarsen A, Riise R, Vorum H, Heegaard S.

Graefes Arch Clin Exp Ophthalmol. 2017 Jan;255(1):119-125. doi: 10.1007/s00417-016-3539-z. Epub 2016 Nov 5.


A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect.

McEntagart M, Williamson KA, Rainger JK, Wheeler A, Seawright A, De Baere E, Verdin H, Bergendahl LT, Quigley A, Rainger J, Dixit A, Sarkar A, López Laso E, Sanchez-Carpintero R, Barrio J, Bitoun P, Prescott T, Riise R, McKee S, Cook J, McKie L, Ceulemans B, Meire F, Temple IK, Prieur F, Williams J, Clouston P, Németh AH, Banka S, Bengani H, Handley M, Freyer E, Ross A; DDD Study, van Heyningen V, Marsh JA, Elmslie F, FitzPatrick DR.

Am J Hum Genet. 2016 May 5;98(5):981-992. doi: 10.1016/j.ajhg.2016.03.018. Epub 2016 Apr 21.


Role of natural killer cell subsets and natural cytotoxicity receptors for the outcome of immunotherapy in acute myeloid leukemia.

Martner A, Rydström A, Riise RE, Aurelius J, Anderson H, Brune M, Foà R, Hellstrand K, Thorén FB.

Oncoimmunology. 2015 May 5;5(1):e1041701. doi: 10.1080/2162402X.2015.1041701. eCollection 2016.


Dynamics of cytotoxic T cell subsets during immunotherapy predicts outcome in acute myeloid leukemia.

Sander FE, Rydström A, Bernson E, Kiffin R, Riise R, Aurelius J, Anderson H, Brune M, Foà R, Hellstrand K, Thorén FB, Martner A.

Oncotarget. 2016 Feb 16;7(7):7586-96. doi: 10.18632/oncotarget.7210.


NK cell expression of natural cytotoxicity receptors may determine relapse risk in older AML patients undergoing immunotherapy for remission maintenance.

Martner A, Rydström A, Riise RE, Aurelius J, Brune M, Foà R, Hellstrand K, Thorén FB.

Oncotarget. 2015 Dec 15;6(40):42569-74. doi: 10.18632/oncotarget.5559.


TLR-Stimulated Neutrophils Instruct NK Cells To Trigger Dendritic Cell Maturation and Promote Adaptive T Cell Responses.

Riise RE, Bernson E, Aurelius J, Martner A, Pesce S, Della Chiesa M, Marcenaro E, Bylund J, Hellstrand K, Moretta L, Moretta A, Thorén FB.

J Immunol. 2015 Aug 1;195(3):1121-8. doi: 10.4049/jimmunol.1500709. Epub 2015 Jun 17.


CD20 antibodies induce production and release of reactive oxygen species by neutrophils.

Werlenius O, Riise RE, Simpanen M, Aurelius J, Thorén FB.

Blood. 2014 Jun 19;123(25):4001-2. doi: 10.1182/blood-2014-05-574285. No abstract available.


Extraspinal ossifications after implantation of vertical expandable prosthetic titanium ribs (VEPTRs).

Zivkovic V, Büchler P, Ovadia D, Riise R, Stuecker R, Hasler C.

J Child Orthop. 2014 May;8(3):237-44. doi: 10.1007/s11832-014-0585-0. Epub 2014 Apr 22.


In vivo morphology of the limbal palisades of vogt correlates with progressive stem cell deficiency in aniridia-related keratopathy.

Lagali N, Edén U, Utheim TP, Chen X, Riise R, Dellby A, Fagerholm P.

Invest Ophthalmol Vis Sci. 2013 Aug 7;54(8):5333-42. doi: 10.1167/iovs.13-11780.


Cataract development in Norwegian patients with congenital aniridia.

Edén U, Lagali N, Dellby A, Utheim TP, Riise R, Chen X, Fagerholm P.

Acta Ophthalmol. 2014 Mar;92(2):e165-7. doi: 10.1111/aos.12225. Epub 2013 Jul 4. No abstract available.


Scoliosis detection, patient characteristics, referral patterns and treatment in the absence of a screening program in Norway.

Adobor RD, Riise RB, Sørensen R, Kibsgård TJ, Steen H, Brox JI.

Scoliosis. 2012 Oct 25;7(1):18. doi: 10.1186/1748-7161-7-18.


Chronic myeloid leukemic cells trigger poly(ADP-ribose) polymerase-dependent inactivation and cell death in lymphocytes.

Aurelius J, Martner A, Riise RE, Romero AI, Palmqvist L, Brune M, Hellstrand K, Thorén FB.

J Leukoc Biol. 2013 Jan;93(1):155-60. doi: 10.1189/jlb.0512257. Epub 2012 Oct 16.


Human NK Cells induce neutrophil apoptosis via an NKp46- and Fas-dependent mechanism.

Thorén FB, Riise RE, Ousbäck J, Della Chiesa M, Alsterholm M, Marcenaro E, Pesce S, Prato C, Cantoni C, Bylund J, Moretta L, Moretta A.

J Immunol. 2012 Feb 15;188(4):1668-74. doi: 10.4049/jimmunol.1102002. Epub 2012 Jan 9.


Spinal deformity and disability in patients with Rett syndrome.

Riise R, Brox JI, Sorensen R, Skjeldal OH.

Dev Med Child Neurol. 2011 Jul;53(7):653-7. doi: 10.1111/j.1469-8749.2011.03935.x. Epub 2011 Apr 18.


Corneal involvement in congenital aniridia.

Edén U, Riise R, Tornqvist K.

Cornea. 2010 Oct;29(10):1096-102. doi: 10.1097/ICO.0b013e3181d20493.


Bardet-Biedl syndrome in Denmark--report of 13 novel sequence variations in six genes.

Hjortshøj TD, Grønskov K, Philp AR, Nishimura DY, Riise R, Sheffield VC, Rosenberg T, Brøndum-Nielsen K.

Hum Mutat. 2010 Apr;31(4):429-36. doi: 10.1002/humu.21204.


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 Nov;87(8):923. doi: 10.1111/j.1755-3768.2009.01696.x. No abstract available.


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. doi: 10.1093/hmg/ddp206. Epub 2009 May 4.


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. 2010 May;88(3):323-8. doi: 10.1111/j.1755-3768.2008.01465.x. Epub 2009 Jan 30.


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. doi: 10.1007/s00264-008-0590-3. Epub 2008 May 28.


Epidemiology of aniridia in Sweden and Norway.

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

Acta Ophthalmol. 2008 Nov;86(7):727-9. doi: 10.1111/j.1755-3768.2008.01309.x. Epub 2008 May 19.


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. doi: 10.1111/j.1755-3768.2008.01310.x. Epub 2008 May 19. Erratum in: Acta Ophthalmol. 2009 Mar;87(2):242.


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.


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.


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.


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.


[Visual problems in cerebral stroke].

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

Tidsskr Nor Laegeforen. 2005 Jan 20;125(2):176-7. Norwegian.


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.


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.


[Ocular changes in Down syndrome].

Haugen OH, Høvding G, Riise R.

Tidsskr Nor Laegeforen. 2004 Jan 22;124(2):186-8. Review. Norwegian.


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.


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.


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.


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.


Rieger syndrome is associated with PAX6 deletion.

Riise R, Storhaug K, Brøndum-Nielsen K.

Acta Ophthalmol Scand. 2001 Apr;79(2):201-3. Erratum in: Acta Ophthalmol. 2009 Nov;87(8):923.


Bardet-Biedl and Cohen syndromes: differential diagnostic criteria.

Warburg M, Riise R.

J Med Genet. 2000 Dec;37(12):E46. No abstract available.


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

Riise R.

Acta Ophthalmol Scand Suppl. 1998;(226):1-28. No abstract available.


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.


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.


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.


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.


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.


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.


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

Riise R.

Acta Ophthalmol Scand Suppl. 1996;(219):45-7.


Supplemental Content

Support Center