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Items: 1 to 50 of 55

1.

Dissecting the Heterogeneity in T-Cell Mediated Inflammation in IBD.

Tindemans I, Joosse ME, Samsom JN.

Cells. 2020 Jan 2;9(1). pii: E110. doi: 10.3390/cells9010110. Review.

2.

November consultation #3.

Joosse MV.

J Cataract Refract Surg. 2019 Nov;45(11):1687-1688. doi: 10.1016/j.jcrs.2019.08.026. No abstract available.

PMID:
31706526
3.

Deletion of IL-6 exacerbates colitis and induces systemic inflammation in IL-10-deficient mice.

Ye M, Joosse ME, Liu L, Sun Y, Dong Y, Cai C, Song Z, Zhang J, Brant SR, Lazarev M, Li X.

J Crohns Colitis. 2019 Nov 3. pii: jjz176. doi: 10.1093/ecco-jcc/jjz176. [Epub ahead of print]

PMID:
31679013
4.

IL-10 signaling in dendritic cells controls IL-1β-mediated IFNγ secretion by human CD4+ T cells: relevance to inflammatory bowel disease.

Veenbergen S, Li P, Raatgeep HC, Lindenbergh-Kortleve DJ, Simons-Oosterhuis Y, Farrel A, Costes LMM, Joosse ME, van Berkel LA, de Ruiter LF, van Leeuwen MA, Winter D, Holland SM, Freeman AF, Wakabayashi Y, Zhu J, de Ridder L, Driessen GJ, Escher JC, Leonard WJ, Samsom JN.

Mucosal Immunol. 2019 Sep;12(5):1201-1211. doi: 10.1038/s41385-019-0194-9. Epub 2019 Aug 15.

PMID:
31417161
5.

A randomized clinical trial using atropine, cyclopentolate, and tropicamide to compare refractive outcome in hypermetropic children with a dark iris; skin pigmentation and crying as significant factors for hypermetropic outcome.

van Minderhout HM, Joosse MV, Grootendorst DC, Schalij-Delfos NE.

Strabismus. 2019 Sep;27(3):127-138. doi: 10.1080/09273972.2019.1629466. Epub 2019 Jun 24.

PMID:
31234691
6.

Disease progression in paediatric- and adult-onset sclerosing cholangitis: Results from two independent Dutch registries.

Joosse ME, Haisma SM, Sterk MFM, van Munster KN, Ponsioen CIJ, Houwen RHJ, Koot BGP, de Meij T, van Rheenen PF, de Koning BAE.

Liver Int. 2019 Sep;39(9):1768-1775. doi: 10.1111/liv.14159. Epub 2019 Jun 26.

PMID:
31152478
7.

Tipping the balance: inhibitory checkpoints in intestinal homeostasis.

Joosse ME, Nederlof I, Walker LSK, Samsom JN.

Mucosal Immunol. 2019 Jan;12(1):21-35. doi: 10.1038/s41385-018-0113-5. Epub 2018 Nov 29. Review.

PMID:
30498201
8.

Refractive adaptation and efficacy of occlusion therapy in untreated amblyopic patients aged 12 to 40 years.

Simonsz-Tóth B, Joosse MV, Besch D.

Graefes Arch Clin Exp Ophthalmol. 2019 Feb;257(2):379-389. doi: 10.1007/s00417-018-4170-y. Epub 2018 Nov 5.

PMID:
30397791
9.

Clinical Evidence for Use of a Noninvasive Biosensor for Tear Glucose as an Alternative to Painful Finger-Prick for Diabetes Management Utilizing a Biopolymer Coating.

Kownacka AE, Vegelyte D, Joosse M, Anton N, Toebes BJ, Lauko J, Buzzacchera I, Lipinska K, Wilson DA, Geelhoed-Duijvestijn N, Wilson CJ.

Biomacromolecules. 2018 Nov 12;19(11):4504-4511. doi: 10.1021/acs.biomac.8b01429. Epub 2018 Oct 25.

10.

Frequencies of circulating regulatory TIGIT+CD38+ effector T cells correlate with the course of inflammatory bowel disease.

Joosse ME, Menckeberg CL, de Ruiter LF, Raatgeep HRC, van Berkel LA, Simons-Oosterhuis Y, Tindemans I, Muskens AFM, Hendriks RW, Hoogenboezem RM, Cupedo T, de Ridder L, Escher JC, Veenbergen S, Samsom JN.

Mucosal Immunol. 2019 Jan;12(1):154-163. doi: 10.1038/s41385-018-0078-4. Epub 2018 Aug 20.

PMID:
30127383
11.

Randomized controlled European multicenter trial on the prevention of cystoid macular edema after cataract surgery in diabetics: ESCRS PREMED Study Report 2.

Wielders LHP, Schouten JSAG, Winkens B, van den Biggelaar FJHM, Veldhuizen CA, Murta JCN, Goslings WRO, Kohnen T, Tassignon MJ, Joosse MV, Henry YP, Nagy ZZ, Rulo AHF, Findl O, Amon M, Nuijts RMMA; ESCRS PREMED study group.

J Cataract Refract Surg. 2018 Jul;44(7):836-847. doi: 10.1016/j.jcrs.2018.05.015.

PMID:
30055692
12.

Malignancy and mortality in paediatric-onset inflammatory bowel disease: a 3-year prospective, multinational study from the paediatric IBD Porto group of ESPGHAN.

Joosse ME, Aardoom MA, Kemos P, Turner D, Wilson DC, Koletzko S, Martin-de-Carpi J, Fagerberg UL, Spray C, Tzivinikos C, Sladek M, Shaoul R, Roma-Giannikou E, Bronsky J, Serban DE, Ruemmele FM, Garnier-Lengline H, Veres G, Hojsak I, Kolho KL, Davies IH, Aloi M, Lionetti P, Hussey S, Veereman G, Braegger CP, Trindade E, Wewer AV, Hauer AC, de Vries ACH, Sigall Boneh R, Sarbagili Shabat C, Levine A, de Ridder L; Paediatric IBD Porto group of ESPGHAN.

Aliment Pharmacol Ther. 2018 Sep;48(5):523-537. doi: 10.1111/apt.14893. Epub 2018 Jul 8.

PMID:
29984520
13.

European multicenter trial of the prevention of cystoid macular edema after cataract surgery in nondiabetics: ESCRS PREMED study report 1.

Wielders LHP, Schouten JSAG, Winkens B, van den Biggelaar FJHM, Veldhuizen CA, Findl O, Murta JCN, Goslings WRO, Tassignon MJ, Joosse MV, Henry YP, Rulo AHF, Güell JL, Amon M, Kohnen T, Nuijts RMMA; ESCRS PREMED Study Group.

J Cataract Refract Surg. 2018 Apr;44(4):429-439. doi: 10.1016/j.jcrs.2018.01.029. Erratum in: J Cataract Refract Surg. 2018 Sep;44(9):1166.

PMID:
29778106
14.

Malignancy and Mortality in Pediatric-onset Inflammatory Bowel Disease: A Systematic Review.

Aardoom MA, Joosse ME, de Vries ACH, Levine A, de Ridder L.

Inflamm Bowel Dis. 2018 Mar 19;24(4):732-741. doi: 10.1093/ibd/izx104.

PMID:
29522170
15.

Consultation Section: Cataract. November consultation #3.

Joosse MV.

J Cataract Refract Surg. 2017 Nov;43(11):1479-1480. doi: 10.1016/j.jcrs.2017.10.022. No abstract available.

PMID:
29223243
16.

A translucent vascularised iris granuloma in a patient with secondary syphilis.

de Jong Y, Haverkort ME, van Sorge AJ, Jansen C, Luyten GP, Joosse M.

Lancet Infect Dis. 2017 Mar;17(3):255-256. doi: 10.1016/S1473-3099(17)30071-3. Epub 2017 Feb 23. No abstract available.

PMID:
28244379
17.

The Pathogenic Role of NLRP3 Inflammasome Activation in Inflammatory Bowel Diseases of Both Mice and Humans.

Liu L, Dong Y, Ye M, Jin S, Yang J, Joosse ME, Sun Y, Zhang J, Lazarev M, Brant SR, Safar B, Marohn M, Mezey E, Li X.

J Crohns Colitis. 2017 Jun 1;11(6):737-750. doi: 10.1093/ecco-jcc/jjw219.

18.

Adverse reactions following routine anticholinergic eye drops in a paediatric population: an observational cohort study.

van Minderhout HM, Joosse MV, Grootendorst DC, Schalij-Delfos NE.

BMJ Open. 2015 Dec 23;5(12):e008798. doi: 10.1136/bmjopen-2015-008798.

19.

The Role of Therapeutic Drug Monitoring of Anti-Tumor Necrosis Factor Alpha Agents in Children and Adolescents with Inflammatory Bowel Disease.

Joosse ME, Samsom JN, van der Woude CJ, Escher JC, van Gelder T.

Inflamm Bowel Dis. 2015 Sep;21(9):2214-21. doi: 10.1097/MIB.0000000000000420. Review.

PMID:
26284297
20.

May consultation #3.

Joosse MV.

J Cataract Refract Surg. 2015 May;41(5):1115-6. doi: 10.1016/j.jcrs.2015.04.012. No abstract available.

PMID:
26049843
21.

Recurrent cholangitis in a 65-year-old man. Biliary papillomatosis.

Joosse ME, Schipper ME, Libbrecht L, van Buuren HR, de Man RA.

Gut. 2015 Jun;64(6):883, 910. doi: 10.1136/gutjnl-2014-308726. Epub 2014 Dec 22. No abstract available.

PMID:
25533647
22.

May consultation #8.

Joosse MV.

J Cataract Refract Surg. 2014 May;40(5):848-9. doi: 10.1016/j.jcrs.2014.03.016. No abstract available.

PMID:
24767927
23.

Implantation of phakic intraocular lens in 3 patients with oculocutaneous albinism.

van Rijn GA, Snoek C, Joosse M, Saxena R, Luyten GP.

J Cataract Refract Surg. 2013 Oct;39(10):1604-8. doi: 10.1016/j.jcrs.2013.08.008.

PMID:
24075162
24.

Physiological and behavioral reactions elicited by simulated and real-life visual and acoustic helicopter stimuli in dairy goats.

van der Staay FJ, Joosse M, van Dijk H, Schuurman T, van der Meulen J.

BMC Vet Res. 2011 Apr 15;7:16. doi: 10.1186/1746-6148-7-16.

25.

Comparison of wavefront-guided photorefractive keratectomy and foldable iris-fixated phakic intraocular lens implantation for low to moderate myopia.

Joosse MV, Snoek C, van Minderhout HM.

J Cataract Refract Surg. 2011 Feb;37(2):370-7. doi: 10.1016/j.jcrs.2010.08.051.

PMID:
21241923
26.

Visual evoked potentials during suppression in exotropic and esotropic strabismics: strabismic suppression objectified.

Joosse MV, Esme DL, Schimsheimer RJ, Verspeek SA, Vermeulen MH, van Minderhout EM.

Graefes Arch Clin Exp Ophthalmol. 2005 Feb;243(2):142-50. Epub 2005 Jan 14.

PMID:
15650853
27.

Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study.

Rosso SM, Donker Kaat L, Baks T, Joosse M, de Koning I, Pijnenburg Y, de Jong D, Dooijes D, Kamphorst W, Ravid R, Niermeijer MF, Verheij F, Kremer HP, Scheltens P, van Duijn CM, Heutink P, van Swieten JC.

Brain. 2003 Sep;126(Pt 9):2016-22. Epub 2003 Jul 22.

PMID:
12876142
28.

CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder.

Verkerk AJ, Mathews CA, Joosse M, Eussen BH, Heutink P, Oostra BA; Tourette Syndrome Association International Consortium for Genetics.

Genomics. 2003 Jul;82(1):1-9.

PMID:
12809671
29.

A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer disease.

Bertoli Avella AM, Marcheco Teruel B, Llibre Rodriguez JJ, Gomez Viera N, Borrajero Martinez I, Severijnen EA, Joosse M, van Duijn CM, Heredero Baute L, Heutink P.

Neurogenetics. 2002 Oct;4(2):97-104.

PMID:
12484344
30.

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism.

Bonifati V, Rizzu P, van Baren MJ, Schaap O, Breedveld GJ, Krieger E, Dekker MC, Squitieri F, Ibanez P, Joosse M, van Dongen JW, Vanacore N, van Swieten JC, Brice A, Meco G, van Duijn CM, Oostra BA, Heutink P.

Science. 2003 Jan 10;299(5604):256-9. Epub 2002 Nov 21.

31.

Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly.

Lettice LA, Horikoshi T, Heaney SJ, van Baren MJ, van der Linde HC, Breedveld GJ, Joosse M, Akarsu N, Oostra BA, Endo N, Shibata M, Suzuki M, Takahashi E, Shinka T, Nakahori Y, Ayusawa D, Nakabayashi K, Scherer SW, Heutink P, Hill RE, Noji S.

Proc Natl Acad Sci U S A. 2002 May 28;99(11):7548-53.

32.

Mutations in TITF-1 are associated with benign hereditary chorea.

Breedveld GJ, van Dongen JW, Danesino C, Guala A, Percy AK, Dure LS, Harper P, Lazarou LP, van der Linde H, Joosse M, Grüters A, MacDonald ME, de Vries BB, Arts WF, Oostra BA, Krude H, Heutink P.

Hum Mol Genet. 2002 Apr 15;11(8):971-9.

PMID:
11971878
33.

Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3.

Ophoff RA, DeYoung J, Service SK, Joosse M, Caffo NA, Sandkuijl LA, Terwindt GM, Haan J, van den Maagdenberg AM, Jen J, Baloh RW, Barilla-LaBarca ML, Saccone NL, Atkinson JP, Ferrari MD, Freimer NB, Frants RR.

Am J Hum Genet. 2001 Aug;69(2):447-53. Epub 2001 Jun 28.

34.

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.

Njajou OT, Vaessen N, Joosse M, Berghuis B, van Dongen JW, Breuning MH, Snijders PJ, Rutten WP, Sandkuijl LA, Oostra BA, van Duijn CM, Heutink P.

Nat Genet. 2001 Jul;28(3):213-4.

PMID:
11431687
35.

The optimal stimulus to elicit suppression in small-angle convergent strabismus.

Joosse MV, Simonsz HJ, Spekreijse H, Mulder PG, van Minderhout HM.

Strabismus. 2000 Dec;8(4):233-42.

PMID:
11262683
36.

Hemimelic extra toes and Hammer toe are distinct mutations that show a genetic interaction.

Heus HC, Luijsterburg AJ, van Baren MJ, Breedveld GJ, Joosse MN, Nieuwenhuizen IM, Vermeij-Keers C, Oostra BA, Heutink P.

Mamm Genome. 2001 Jan;12(1):77-9. No abstract available.

PMID:
11178748
37.

Mutation-dependent aggregation of tau protein and its selective depletion from the soluble fraction in brain of P301L FTDP-17 patients.

Rizzu P, Joosse M, Ravid R, Hoogeveen A, Kamphorst W, van Swieten JC, Willemsen R, Heutink P.

Hum Mol Genet. 2000 Dec 12;9(20):3075-82.

PMID:
11115852
38.

A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases.

Verheijen FW, Verbeek E, Aula N, Beerens CE, Havelaar AC, Joosse M, Peltonen L, Aula P, Galjaard H, van der Spek PJ, Mancini GM.

Nat Genet. 1999 Dec;23(4):462-5.

PMID:
10581036
39.

FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation.

Sperfeld AD, Collatz MB, Baier H, Palmbach M, Storch A, Schwarz J, Tatsch K, Reske S, Joosse M, Heutink P, Ludolph AC.

Ann Neurol. 1999 Nov;46(5):708-15.

PMID:
10553987
40.

The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian cases.

Bonifati V, Joosse M, Nicholl DJ, Vanacore N, Bennett P, Rizzu P, Fabbrini G, Marconi R, Colosimo C, Locuratolo N, Stocchi F, Bonuccelli U, De Mari M, Wenning G, Vieregge P, Oostra B, Meco G, Heutink P.

Neurosci Lett. 1999 Oct 15;274(1):61-5.

PMID:
10530520
41.

Phenotypic variation in hereditary frontotemporal dementia with tau mutations.

van Swieten JC, Stevens M, Rosso SM, Rizzu P, Joosse M, de Koning I, Kamphorst W, Ravid R, Spillantini MG, Niermeijer, Heutink P.

Ann Neurol. 1999 Oct;46(4):617-26.

PMID:
10514099
42.

Quantitative visual fields under binocular viewing conditions in primary and consecutive divergent strabismus.

Joosse MV, Simonsz HJ, van Minderhout EM, Mulder PG, de Jong PT.

Graefes Arch Clin Exp Ophthalmol. 1999 Jul;237(7):535-45.

PMID:
10424303
43.

A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36.

Heus HC, Hing A, van Baren MJ, Joosse M, Breedveld GJ, Wang JC, Burgess A, Donnis-Keller H, Berglund C, Zguricas J, Scherer SW, Rommens JM, Oostra BA, Heutink P.

Genomics. 1999 May 1;57(3):342-51.

PMID:
10329000
44.

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands.

Rizzu P, Van Swieten JC, Joosse M, Hasegawa M, Stevens M, Tibben A, Niermeijer MF, Hillebrand M, Ravid R, Oostra BA, Goedert M, van Duijn CM, Heutink P.

Am J Hum Genet. 1999 Feb;64(2):414-21.

45.

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17.

Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, Pickering-Brown S, Chakraverty S, Isaacs A, Grover A, Hackett J, Adamson J, Lincoln S, Dickson D, Davies P, Petersen RC, Stevens M, de Graaff E, Wauters E, van Baren J, Hillebrand M, Joosse M, Kwon JM, Nowotny P, Che LK, Norton J, Morris JC, Reed LA, Trojanowski J, Basun H, Lannfelt L, Neystat M, Fahn S, Dark F, Tannenberg T, Dodd PR, Hayward N, Kwok JB, Schofield PR, Andreadis A, Snowden J, Craufurd D, Neary D, Owen F, Oostra BA, Hardy J, Goate A, van Swieten J, Mann D, Lynch T, Heutink P.

Nature. 1998 Jun 18;393(6686):702-5.

PMID:
9641683
46.

Quantitative perimetry under binocular viewing conditions in microstrabismus.

Joosse MV, Simonsz HJ, van Minderhout HM, de Jong PT, Noordzij B, Mulder PG.

Vision Res. 1997 Oct;37(19):2801-12.

47.

A novel acid alpha-glucosidase mutation identified in a Pakistani family with glycogen storage disease type II.

Kroos MA, Waitfield AE, Joosse M, Winchester B, Reuser AJ, MacDermot KD.

J Inherit Metab Dis. 1997 Aug;20(4):556-8.

PMID:
9266392
48.

The effect of a single base pair deletion (delta T525) and a C1634T missense mutation (pro545leu) on the expression of lysosomal alpha-glucosidase in patients with glycogen storage disease type II.

Hermans MM, De Graaff E, Kroos MA, Mohkamsing S, Eussen BJ, Joosse M, Willemsen R, Kleijer WJ, Oostra BA, Reuser AJ.

Hum Mol Genet. 1994 Dec;3(12):2213-8.

PMID:
7881422
49.

[Cortical blindness during treatment with cyclosporin].

Vlasveld LT, Cornelissen JJ, Dellemijn PL, Joosse MV, van den Bent MJ.

Ned Tijdschr Geneeskd. 1994 Oct 8;138(41):2057-61. Review. Dutch.

PMID:
7935970
50.

Deletion of exon 18 is a frequent mutation in glycogen storage disease type II.

Van der Kraan M, Kroos MA, Joosse M, Bijvoet AG, Verbeet MP, Kleijer WJ, Reuser AJ.

Biochem Biophys Res Commun. 1994 Sep 30;203(3):1535-41.

PMID:
7945303

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