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Items: 42

1.

Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study.

van Rheenen W, Diekstra FP, Harschnitz O, Westeneng HJ, van Eijk KR, Saris CGJ, Groen EJN, van Es MA, Blauw HM, van Vught PWJ, Veldink JH, van den Berg LH.

PLoS One. 2018 Jun 25;13(6):e0198874. doi: 10.1371/journal.pone.0198874. eCollection 2018.

2.

Temporal and tissue-specific variability of SMN protein levels in mouse models of spinal muscular atrophy.

Groen EJN, Perenthaler E, Courtney NL, Jordan CY, Shorrock HK, van der Hoorn D, Huang YT, Murray LM, Viero G, Gillingwater TH.

Hum Mol Genet. 2018 May 22. doi: 10.1093/hmg/ddy195. [Epub ahead of print]

PMID:
29790918
3.

Clinicopathological Risk Factors for an Invasive Breast Cancer Recurrence after Ductal Carcinoma In Situ-A Nested Case-Control Study.

Visser LL, Elshof LE, Schaapveld M, van de Vijver K, Groen EJ, Almekinders MM, Bierman C, van Leeuwen FE, Rutgers EJ, Schmidt MK, Lips EH, Wesseling J.

Clin Cancer Res. 2018 Apr 23. doi: 10.1158/1078-0432.CCR-18-0201. [Epub ahead of print]

PMID:
29685879
4.

Major Reduction in Axillary Lymph Node Dissections After Neoadjuvant Systemic Therapy for Node-Positive Breast Cancer by combining PET/CT and the MARI Procedure.

van der Noordaa MEM, van Duijnhoven FH, Straver ME, Groen EJ, Stokkel M, Loo CE, Elkhuizen PHM, Russell NS, Vrancken Peeters MTFD.

Ann Surg Oncol. 2018 Jun;25(6):1512-1520. doi: 10.1245/s10434-018-6404-y. Epub 2018 Mar 6.

PMID:
29511992
5.

Neurochondrin interacts with the SMN protein suggesting a novel mechanism for spinal muscular atrophy pathology.

Thompson LW, Morrison KD, Shirran SL, Groen EJN, Gillingwater TH, Botting CH, Sleeman JE.

J Cell Sci. 2018 Apr 17;131(8). pii: jcs211482. doi: 10.1242/jcs.211482.

6.

Advances in therapy for spinal muscular atrophy: promises and challenges.

Groen EJN, Talbot K, Gillingwater TH.

Nat Rev Neurol. 2018 Apr;14(4):214-224. doi: 10.1038/nrneurol.2018.4. Epub 2018 Feb 9. Review.

PMID:
29422644
7.

Overview of Current Drugs and Molecules in Development for Spinal Muscular Atrophy Therapy.

Shorrock HK, Gillingwater TH, Groen EJN.

Drugs. 2018 Mar;78(3):293-305. doi: 10.1007/s40265-018-0868-8.

8.

Breast conserving surgery for extensive DCIS using multiple radioactive seeds.

Janssen NNY, van la Parra RFD, Loo CE, Groen EJ, van den Berg MJ, Oldenburg HSA, Nijkamp J, Vrancken Peeters MTFD.

Eur J Surg Oncol. 2018 Jan;44(1):67-73. doi: 10.1016/j.ejso.2017.11.002. Epub 2017 Nov 20.

PMID:
29239733
9.

Long-term prognosis of young breast cancer patients (≤40 years) who did not receive adjuvant systemic treatment: protocol for the PARADIGM initiative cohort study.

Dackus GM, Ter Hoeve ND, Opdam M, Vreuls W, Varga Z, Koop E, Willems SM, Van Deurzen CH, Groen EJ, Cordoba A, Bart J, Mooyaart AL, van den Tweel JG, Zolota V, Wesseling J, Sapino A, Chmielik E, Ryska A, Amant F, Broeks A, Kerkhoven R, Stathonikos N, Veta M, Voogd A, Jozwiak K, Hauptmann M, Hoogstraat M, Schmidt MK, Sonke G, van der Wall E, Siesling S, van Diest PJ, Linn SC.

BMJ Open. 2017 Nov 14;7(11):e017842. doi: 10.1136/bmjopen-2017-017842.

10.

In Vivo Translatome Profiling in Spinal Muscular Atrophy Reveals a Role for SMN Protein in Ribosome Biology.

Bernabò P, Tebaldi T, Groen EJN, Lane FM, Perenthaler E, Mattedi F, Newbery HJ, Zhou H, Zuccotti P, Potrich V, Shorrock HK, Muntoni F, Quattrone A, Gillingwater TH, Viero G.

Cell Rep. 2017 Oct 24;21(4):953-965. doi: 10.1016/j.celrep.2017.10.010.

11.

Simplifying Breast Imaging Reporting and Data System classification of mammograms with pure suspicious calcifications.

Menezes GL, Winter-Warnars GA, Koekenbier EL, Groen EJ, Verkooijen HM, Pijnappel RM.

J Med Screen. 2018 Jun;25(2):82-87. doi: 10.1177/0969141317715281. Epub 2017 Jul 10.

12.

MRI predicts pathologic complete response in HER2-positive breast cancer after neoadjuvant chemotherapy.

van Ramshorst MS, Loo CE, Groen EJ, Winter-Warnars GH, Wesseling J, van Duijnhoven F, Peeters MTV, Sonke GS.

Breast Cancer Res Treat. 2017 Jul;164(1):99-106. doi: 10.1007/s10549-017-4254-0. Epub 2017 Apr 21.

PMID:
28432515
13.

Bioenergetic status modulates motor neuron vulnerability and pathogenesis in a zebrafish model of spinal muscular atrophy.

Boyd PJ, Tu WY, Shorrock HK, Groen EJN, Carter RN, Powis RA, Thomson SR, Thomson D, Graham LC, Motyl AAL, Wishart TM, Highley JR, Morton NM, Becker T, Becker CG, Heath PR, Gillingwater TH.

PLoS Genet. 2017 Apr 20;13(4):e1006744. doi: 10.1371/journal.pgen.1006744. eCollection 2017 Apr.

14.

Systemic restoration of UBA1 ameliorates disease in spinal muscular atrophy.

Powis RA, Karyka E, Boyd P, Côme J, Jones RA, Zheng Y, Szunyogova E, Groen EJ, Hunter G, Thomson D, Wishart TM, Becker CG, Parson SH, Martinat C, Azzouz M, Gillingwater TH.

JCI Insight. 2016 Jul 21;1(11):e87908.

15.

Finding the balance between over- and under-treatment of ductal carcinoma in situ (DCIS).

Groen EJ, Elshof LE, Visser LL, Rutgers EJT, Winter-Warnars HAO, Lips EH, Wesseling J.

Breast. 2017 Feb;31:274-283. doi: 10.1016/j.breast.2016.09.001. Epub 2016 Sep 23. Review.

16.

Restoration of SMN in Schwann cells reverses myelination defects and improves neuromuscular function in spinal muscular atrophy.

Hunter G, Powis RA, Jones RA, Groen EJ, Shorrock HK, Lane FM, Zheng Y, Sherman DL, Brophy PJ, Gillingwater TH.

Hum Mol Genet. 2016 Jul 1;25(13):2853-2861. Epub 2016 May 11.

17.

Comparative interactomics analysis of different ALS-associated proteins identifies converging molecular pathways.

Blokhuis AM, Koppers M, Groen EJ, van den Heuvel DM, Dini Modigliani S, Anink JJ, Fumoto K, van Diggelen F, Snelting A, Sodaar P, Verheijen BM, Demmers JA, Veldink JH, Aronica E, Bozzoni I, den Hertog J, van den Berg LH, Pasterkamp RJ.

Acta Neuropathol. 2016 Aug;132(2):175-96. doi: 10.1007/s00401-016-1575-8. Epub 2016 May 10.

18.

[Ductal carcinoma in situ: the balance between over- and undertreatment].

Groen EJ, Elshof LE, Rutgers EJ, Winter-Warnars HA, Lips EH, Wesseling J.

Ned Tijdschr Geneeskd. 2016;160:A9773. Review. Dutch.

PMID:
27071361
19.

UBA1: At the Crossroads of Ubiquitin Homeostasis and Neurodegeneration.

Groen EJN, Gillingwater TH.

Trends Mol Med. 2015 Oct;21(10):622-632. doi: 10.1016/j.molmed.2015.08.003. Review.

20.

Grading of neuroendocrine neoplasms: mitoses and Ki-67 are both essential.

van Velthuysen ML, Groen EJ, van der Noort V, van de Pol A, Tesselaar ME, Korse CM.

Neuroendocrinology. 2014;100(2-3):221-7. doi: 10.1159/000369275. Epub 2014 Oct 25.

PMID:
25358267
21.

Reliability of proliferation assessment by Ki-67 expression in neuroendocrine neoplasms: eyeballing or image analysis?

van Velthuysen ML, Groen EJ, Sanders J, Prins FA, van der Noort V, Korse CM.

Neuroendocrinology. 2014;100(4):288-92. doi: 10.1159/000367713. Epub 2014 Aug 25.

PMID:
25342217
22.

The intracellular redox protein MICAL-1 regulates the development of hippocampal mossy fibre connections.

Van Battum EY, Gunput RA, Lemstra S, Groen EJ, Yu KL, Adolfs Y, Zhou Y, Hoogenraad CC, Yoshida Y, Schachner M, Akhmanova A, Pasterkamp RJ.

Nat Commun. 2014 Jul 10;5:4317. doi: 10.1038/ncomms5317.

PMID:
25007825
23.

Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study.

van Doormaal PT, Ticozzi N, Gellera C, Ratti A, Taroni F, Chiò A, Calvo A, Mora G, Restagno G, Traynor BJ, Birve A, Lemmens R, van Es MA, Saris CG, Blauw HM, van Vught PW, Groen EJ, Corrado L, Mazzini L, Del Bo R, Corti S, Waibel S, Meyer T, Ludolph AC, Goris A, van Damme P, Robberecht W, Shatunov A, Fogh I, Andersen PM, D'Alfonso S, Hardiman O, Cronin S, Rujescu D, Al-Chalabi A, Landers JE, Silani V, van den Berg LH, Veldink JH.

Neurobiol Aging. 2014 Oct;35(10):2420.e13-4. doi: 10.1016/j.neurobiolaging.2014.04.014. Epub 2014 Apr 19.

24.

ALS-associated mutations in FUS disrupt the axonal distribution and function of SMN.

Groen EJ, Fumoto K, Blokhuis AM, Engelen-Lee J, Zhou Y, van den Heuvel DM, Koppers M, van Diggelen F, van Heest J, Demmers JA, Kirby J, Shaw PJ, Aronica E, Spliet WG, Veldink JH, van den Berg LH, Pasterkamp RJ.

Hum Mol Genet. 2013 Sep 15;22(18):3690-704. doi: 10.1093/hmg/ddt222. Epub 2013 May 15.

PMID:
23681068
25.

Protein aggregation in amyotrophic lateral sclerosis.

Blokhuis AM, Groen EJ, Koppers M, van den Berg LH, Pasterkamp RJ.

Acta Neuropathol. 2013 Jun;125(6):777-94. doi: 10.1007/s00401-013-1125-6. Epub 2013 May 15. Review.

26.

Gene expression profile of SOD1-G93A mouse spinal cord, blood and muscle.

Saris CG, Groen EJ, van Vught PW, van Es MA, Blauw HM, Veldink JH, van den Berg LH.

Amyotroph Lateral Scler Frontotemporal Degener. 2013 Apr;14(3):190-8. doi: 10.3109/21678421.2012.749914. Epub 2013 Jan 8.

PMID:
23298163
27.

Meta-analysis of gene expression profiling in amyotrophic lateral sclerosis: a comparison between transgenic mouse models and human patients.

Saris CG, Groen EJ, Koekkoek JA, Veldink JH, van den Berg LH.

Amyotroph Lateral Scler Frontotemporal Degener. 2013 Apr;14(3):177-89. doi: 10.3109/21678421.2012.729842. Epub 2013 Jan 4.

PMID:
23286751
28.

Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3.

Koppers M, Groen EJ, van Vught PW, van Rheenen W, Witteveen E, van Es MA, Pasterkamp RJ, van den Berg LH, Veldink JH.

Neurobiol Aging. 2013 May;34(5):1518.e5-7. doi: 10.1016/j.neurobiolaging.2012.09.018. Epub 2012 Nov 8.

PMID:
23141412
29.

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.

Ahmeti KB, Ajroud-Driss S, Al-Chalabi A, Andersen PM, Armstrong J, Birve A, Blauw HM, Brown RH, Bruijn L, Chen W, Chio A, Comeau MC, Cronin S, Diekstra FP, Soraya Gkazi A, Glass JD, Grab JD, Groen EJ, Haines JL, Hardiman O, Heller S, Huang J, Hung WY; ITALSGEN consortium, Jaworski JM, Jones A, Khan H, Landers JE, Langefeld CD, Leigh PN, Marion MC, McLaughlin RL, Meininger V, Melki J, Miller JW, Mora G, Pericak-Vance MA, Rampersaud E, Robberecht W, Russell LP, Salachas F, Saris CG, Shatunov A, Shaw CE, Siddique N, Siddique T, Smith BN, Sufit R, Topp S, Traynor BJ, Vance C, van Damme P, van den Berg LH, van Es MA, van Vught PW, Veldink JH, Yang Y, Zheng JG; ALSGEN Consortium.

Neurobiol Aging. 2013 Jan;34(1):357.e7-19. doi: 10.1016/j.neurobiolaging.2012.07.017. Epub 2012 Sep 5.

30.

Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.

Diekstra FP, Saris CG, van Rheenen W, Franke L, Jansen RC, van Es MA, van Vught PW, Blauw HM, Groen EJ, Horvath S, Estrada K, Rivadeneira F, Hofman A, Uitterlinden AG, Robberecht W, Andersen PM, Melki J, Meininger V, Hardiman O, Landers JE, Brown RH Jr, Shatunov A, Shaw CE, Leigh PN, Al-Chalabi A, Ophoff RA, van den Berg LH, Veldink JH.

PLoS One. 2012;7(4):e35333. doi: 10.1371/journal.pone.0035333. Epub 2012 Apr 11.

31.

CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis.

Groen EJ, van Rheenen W, Koppers M, van Doormaal PT, Vlam L, Diekstra FP, Dooijes D, Pasterkamp RJ, van den Berg LH, Veldink JH.

Neurobiol Aging. 2012 Aug;33(8):1852.e1-3. doi: 10.1016/j.neurobiolaging.2012.03.007. Epub 2012 Apr 15.

PMID:
22507827
32.

Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis.

van Es MA, Schelhaas HJ, van Vught PW, Ticozzi N, Andersen PM, Groen EJ, Schulte C, Blauw HM, Koppers M, Diekstra FP, Fumoto K, LeClerc AL, Keagle P, Bloem BR, Scheffer H, van Nuenen BF, van Blitterswijk M, van Rheenen W, Wills AM, Lowe PP, Hu GF, Yu W, Kishikawa H, Wu D, Folkerth RD, Mariani C, Goldwurm S, Pezzoli G, Van Damme P, Lemmens R, Dahlberg C, Birve A, Fernández-Santiago R, Waibel S, Klein C, Weber M, van der Kooi AJ, de Visser M, Verbaan D, van Hilten JJ, Heutink P, Hennekam EA, Cuppen E, Berg D, Brown RH Jr, Silani V, Gasser T, Ludolph AC, Robberecht W, Ophoff RA, Veldink JH, Pasterkamp RJ, de Bakker PI, Landers JE, van de Warrenburg BP, van den Berg LH.

Ann Neurol. 2011 Dec;70(6):964-73. doi: 10.1002/ana.22611. Review.

33.

VCP mutations in familial and sporadic amyotrophic lateral sclerosis.

Koppers M, van Blitterswijk MM, Vlam L, Rowicka PA, van Vught PW, Groen EJ, Spliet WG, Engelen-Lee J, Schelhaas HJ, de Visser M, van der Kooi AJ, van der Pol WL, Pasterkamp RJ, Veldink JH, van den Berg LH.

Neurobiol Aging. 2012 Apr;33(4):837.e7-13. doi: 10.1016/j.neurobiolaging.2011.10.006. Epub 2011 Nov 10.

PMID:
22078486
34.

Molecular diagnostics of Rickettsia africae infection in travelers returning from South Africa to The Netherlands.

Wieten RW, Hovius JW, Groen EJ, van der Wal AC, de Vries PJ, Beersma MF, Tijsse-Klasen E, Sprong H, Grobusch MP.

Vector Borne Zoonotic Dis. 2011 Dec;11(12):1541-7. doi: 10.1089/vbz.2011.0653. Epub 2011 Aug 25.

PMID:
21867422
35.

A large genome scan for rare CNVs in amyotrophic lateral sclerosis.

Blauw HM, Al-Chalabi A, Andersen PM, van Vught PW, Diekstra FP, van Es MA, Saris CG, Groen EJ, van Rheenen W, Koppers M, Van't Slot R, Strengman E, Estrada K, Rivadeneira F, Hofman A, Uitterlinden AG, Kiemeney LA, Vermeulen SH, Birve A, Waibel S, Meyer T, Cronin S, McLaughlin RL, Hardiman O, Sapp PC, Tobin MD, Wain LV, Tomik B, Slowik A, Lemmens R, Rujescu D, Schulte C, Gasser T, Brown RH Jr, Landers JE, Robberecht W, Ludolph AC, Ophoff RA, Veldink JH, van den Berg LH.

Hum Mol Genet. 2010 Oct 15;19(20):4091-9. doi: 10.1093/hmg/ddq323. Epub 2010 Aug 4.

PMID:
20685689
36.

FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.

Groen EJ, van Es MA, van Vught PW, Spliet WG, van Engelen-Lee J, de Visser M, Wokke JH, Schelhaas HJ, Ophoff RA, Fumoto K, Pasterkamp RJ, Dooijes D, Cuppen E, Veldink JH, van den Berg LH.

Arch Neurol. 2010 Feb;67(2):224-30. doi: 10.1001/archneurol.2009.329.

PMID:
20142531
37.

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.

van Es MA, Veldink JH, Saris CG, Blauw HM, van Vught PW, Birve A, Lemmens R, Schelhaas HJ, Groen EJ, Huisman MH, van der Kooi AJ, de Visser M, Dahlberg C, Estrada K, Rivadeneira F, Hofman A, Zwarts MJ, van Doormaal PT, Rujescu D, Strengman E, Giegling I, Muglia P, Tomik B, Slowik A, Uitterlinden AG, Hendrich C, Waibel S, Meyer T, Ludolph AC, Glass JD, Purcell S, Cichon S, Nöthen MM, Wichmann HE, Schreiber S, Vermeulen SH, Kiemeney LA, Wokke JH, Cronin S, McLaughlin RL, Hardiman O, Fumoto K, Pasterkamp RJ, Meininger V, Melki J, Leigh PN, Shaw CE, Landers JE, Al-Chalabi A, Brown RH Jr, Robberecht W, Andersen PM, Ophoff RA, van den Berg LH.

Nat Genet. 2009 Oct;41(10):1083-7. doi: 10.1038/ng.442. Epub 2009 Sep 6.

PMID:
19734901
38.

Cushing's syndrome due to unilateral multiple adrenal adenomas as an extraintestinal manifestation of familial adenomatous polyposis.

Roos A, Groen EJ, van Beek AP.

Int J Colorectal Dis. 2009 Feb;24(2):239. doi: 10.1007/s00384-008-0558-1. Epub 2008 Aug 22. No abstract available.

PMID:
18719925
39.

Extra-intestinal manifestations of familial adenomatous polyposis.

Groen EJ, Roos A, Muntinghe FL, Enting RH, de Vries J, Kleibeuker JH, Witjes MJ, Links TP, van Beek AP.

Ann Surg Oncol. 2008 Sep;15(9):2439-50. doi: 10.1245/s10434-008-9981-3. Epub 2008 Jul 9. Review.

40.

Rate-difference method proved satisfactory in estimating the influenza burden in primary care visits.

Jansen AG, Sanders EA, Wallinga J, Groen EJ, van Loon AM, Hoes AW, Hak E.

J Clin Epidemiol. 2008 Aug;61(8):803-12. doi: 10.1016/j.jclinepi.2007.08.017. Epub 2008 May 20.

PMID:
18495428
41.

Analysis of the UK diagnostic strategy for limb girdle muscular dystrophy 2A.

Groen EJ, Charlton R, Barresi R, Anderson LV, Eagle M, Hudson J, Koref MS, Straub V, Bushby KM.

Brain. 2007 Dec;130(Pt 12):3237-49.

PMID:
18055493
42.

The m.5650G>A mitochondrial tRNAAla mutation is pathogenic and causes a phenotype of pure myopathy.

McFarland R, Swalwell H, Blakely EL, He L, Groen EJ, Turnbull DM, Bushby KM, Taylor RW.

Neuromuscul Disord. 2008 Jan;18(1):63-7. Epub 2007 Sep 6.

PMID:
17825557

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