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Items: 1 to 50 of 89

1.

The External Genitalia Score (EGS): A European Multicenter Validation Study.

van der Straaten S, Springer A, Zecic A, Hebenstreit D, Tonnhofer U, Gawlik A, Baumert M, Szeliga K, Debulpaep S, Desloovere A, Tack L, Smets K, Wasniewska M, Corica D, Calafiore M, Ljubicic ML, Busch AS, Juul A, Nordenström A, Sigurdsson J, Flück CE, Haamberg T, Graf S, Hannema SE, Wolffenbuttel KP, Hiort O, Ahmed SF, Cools M.

J Clin Endocrinol Metab. 2020 Mar 1;105(3). pii: dgz142. doi: 10.1210/clinem/dgz142.

PMID:
31665438
2.

Congenital cytomegalovirus infection registry in flanders: opportunities and pitfalls.

Keymeulen A, De Leenheer E, Goderis J, Dhooge I, Smets K; Flemish Society of Pediatrics’ Neonatology and Perinatal Epidemiology Working Group for cCMV infection.

Acta Clin Belg. 2019 Oct 23:1-8. doi: 10.1080/17843286.2019.1683262. [Epub ahead of print]

PMID:
31645217
3.

Dose rationale and pharmacokinetics of dexmedetomidine in mechanically ventilated new-borns: impact of design optimisation.

van Dijkman SC, De Cock PAJG, Smets K, Decaluwe W, Smits A, Allegaert K, Vande Walle J, De Paepe P, Della Pasqua O.

Eur J Clin Pharmacol. 2019 Oct;75(10):1393-1404. doi: 10.1007/s00228-019-02708-y. Epub 2019 Jul 16.

PMID:
31312867
4.

FAHN/SPG35: a narrow phenotypic spectrum across disease classifications.

Rattay TW, Lindig T, Baets J, Smets K, Deconinck T, Söhn AS, Hörtnagel K, Eckstein KN, Wiethoff S, Reichbauer J, Döbler-Neumann M, Krägeloh-Mann I, Auer-Grumbach M, Plecko B, Münchau A, Wilken B, Janauschek M, Giese AK, De Bleecker JL, Ortibus E, Debyser M, Lopez de Munain A, Pujol A, Bassi MT, D'Angelo MG, De Jonghe P, Züchner S, Bauer P, Schöls L, Schüle R.

Brain. 2019 Jun 1;142(6):1561-1572. doi: 10.1093/brain/awz102.

PMID:
31135052
5.

Continuous infusion vs. intermittent flushing of peripheral cannulas in neonates using a needleless connector: a prospective cohort study.

Hoff R, Vervisch K, De Coen K, Smets K.

J Perinat Med. 2019 May 27;47(4):464-469. doi: 10.1515/jpm-2018-0285.

PMID:
30730844
6.

A case of Q fever with hepatitis and an atypical skin lesion.

Vanden Bussche S, Smets K, Steelandt T, Van Eyken P, Caenepeel P, Robaeys G.

Acta Gastroenterol Belg. 2018 Jul-Sep;81(3):441-442. No abstract available.

PMID:
30350538
7.

Occupational airborne allergic contact dermatitis caused by N-(4-hydroxyphenyl)benzenesulfonamide.

Aerts O, Mangodt E, Smets K, Mertens M, Constandt L, Goossens A.

Contact Dermatitis. 2019 Jan;80(1):71-73. doi: 10.1111/cod.13135. Epub 2018 Oct 17. No abstract available.

PMID:
30334269
8.

B-cell lymphomatoid contact dermatitis caused by methylisothiazolinone and methylchloroisothiazolinone.

Smets K, Busschots A, Hauben E, Goossens A.

Eur J Dermatol. 2018 Feb 1;28(1):91-93. doi: 10.1684/ejd.2017.3156. No abstract available.

PMID:
29141836
9.

Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trial.

Schöls L, Rattay TW, Martus P, Meisner C, Baets J, Fischer I, Jägle C, Fraidakis MJ, Martinuzzi A, Saute JA, Scarlato M, Antenora A, Stendel C, Höflinger P, Lourenco CM, Abreu L, Smets K, Paucar M, Deconinck T, Bis DM, Wiethoff S, Bauer P, Arnoldi A, Marques W, Jardim LB, Hauser S, Criscuolo C, Filla A, Züchner S, Bassi MT, Klopstock T, De Jonghe P, Björkhem I, Schüle R.

Brain. 2017 Dec 1;140(12):3112-3127. doi: 10.1093/brain/awx273.

10.

Rapeseed and Raspberry Seed Cakes as Inexpensive Raw Materials in the Production of Activated Carbon by Physical Activation: Effect of Activation Conditions on Textural and Phenol Adsorption Characteristics.

Smets K, De Jong M, Lupul I, Gryglewicz G, Schreurs S, Carleer R, Yperman J.

Materials (Basel). 2016 Jul 12;9(7). pii: E565. doi: 10.3390/ma9070565.

11.

STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations.

Hayer SN, Deconinck T, Bender B, Smets K, Züchner S, Reich S, Schöls L, Schüle R, De Jonghe P, Baets J, Synofzik M.

Orphanet J Rare Dis. 2017 Feb 13;12(1):31. doi: 10.1186/s13023-017-0580-x.

12.

Sensitization from ketotifen fumarate in eye drops presenting as chronic conjunctivitis.

Smets K, Werbrouck J, Goossens A, Gilissen L.

Contact Dermatitis. 2017 Feb;76(2):124-126. doi: 10.1111/cod.12695. No abstract available.

PMID:
28095628
13.

TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.

van der Zee J, Gijselinck I, Van Mossevelde S, Perrone F, Dillen L, Heeman B, Bäumer V, Engelborghs S, De Bleecker J, Baets J, Gelpi E, Rojas-García R, Clarimón J, Lleó A, Diehl-Schmid J, Alexopoulos P, Perneczky R, Synofzik M, Just J, Schöls L, Graff C, Thonberg H, Borroni B, Padovani A, Jordanova A, Sarafov S, Tournev I, de Mendonça A, Miltenberger-Miltényi G, Simões do Couto F, Ramirez A, Jessen F, Heneka MT, Gómez-Tortosa E, Danek A, Cras P, Vandenberghe R, De Jonghe P, De Deyn PP, Sleegers K, Cruts M, Van Broeckhoven C, Goeman J, Nuytten D, Smets K, Robberecht W, Damme PV, Bleecker J, Santens P, Dermaut B, Versijpt J, Michotte A, Ivanoiu A, Deryck O, Bergmans B, Delbeck J, Bruyland M, Willems C, Salmon E, Pastor P, Ortega-Cubero S, Benussi L, Ghidoni R, Binetti G, Hernández I, Boada M, Ruiz A, Sorbi S, Nacmias B, Bagnoli S, Sorbi S, Sanchez-Valle R, Llado A, Santana I, Rosário Almeida M, Frisoni GB, Maetzler W, Matej R, Fraidakis MJ, Kovacs GG, Fabrizi GM, Testi S.

Hum Mutat. 2017 Mar;38(3):297-309. doi: 10.1002/humu.23161. Epub 2017 Jan 19.

14.

Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48).

Hirst J, Madeo M, Smets K, Edgar JR, Schols L, Li J, Yarrow A, Deconinck T, Baets J, Van Aken E, De Bleecker J, Datiles MB 3rd, Roda RH, Liepert J, Züchner S, Mariotti C, De Jonghe P, Blackstone C, Kruer MC.

Neurol Genet. 2016 Aug 25;2(5):e98. doi: 10.1212/NXG.0000000000000098. eCollection 2016 Oct. Erratum in: Neurol Genet. 2016 Oct 06;2(5):e111.

15.

Automated non-EEG based seizure detection: Do users have a say?

Van de Vel A, Smets K, Wouters K, Ceulemans B.

Epilepsy Behav. 2016 Sep;62:121-8. doi: 10.1016/j.yebeh.2016.06.029. Epub 2016 Jul 25.

PMID:
27454332
16.

SYNE1 ataxia is a common recessive ataxia with major non-cerebellar features: a large multi-centre study.

Synofzik M, Smets K, Mallaret M, Di Bella D, Gallenmüller C, Baets J, Schulze M, Magri S, Sarto E, Mustafa M, Deconinck T, Haack T, Züchner S, Gonzalez M, Timmann D, Stendel C, Klopstock T, Durr A, Tranchant C, Sturm M, Hamza W, Nanetti L, Mariotti C, Koenig M, Schöls L, Schüle R, de Jonghe P, Anheim M, Taroni F, Bauer P.

Brain. 2016 May;139(Pt 5):1378-93. doi: 10.1093/brain/aww079. Epub 2016 Apr 17.

17.

A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype.

Beunders G, van de Kamp J, Vasudevan P, Morton J, Smets K, Kleefstra T, de Munnik SA, Schuurs-Hoeijmakers J, Ceulemans B, Zollino M, Hoffjan S, Wieczorek S, So J, Mercer L, Walker T, Velsher L; DDD study, Parker MJ, Magee AC, Elffers B, Kooy RF, Yntema HG, Meijers-Heijboer EJ, Sistermans EA.

J Med Genet. 2016 Aug;53(8):523-32. doi: 10.1136/jmedgenet-2015-103601. Epub 2016 Apr 13.

PMID:
27075013
18.

Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions.

Denora PS, Smets K, Zolfanelli F, Ceuterick-de Groote C, Casali C, Deconinck T, Sieben A, Gonzales M, Zuchner S, Darios F, Peeters D, Brice A, Malandrini A, De Jonghe P, Santorelli FM, Stevanin G, Martin JJ, El Hachimi KH.

Brain. 2016 Jun;139(Pt 6):1723-34. doi: 10.1093/brain/aww061. Epub 2016 Mar 25.

19.

Effects of Presentation Type and Visual Control in Numerosity Discrimination: Implications for Number Processing?

Smets K, Moors P, Reynvoet B.

Front Psychol. 2016 Feb 1;7:66. doi: 10.3389/fpsyg.2016.00066. eCollection 2016.

20.

Hearing in Children with Congenital Cytomegalovirus Infection: Results of a Longitudinal Study.

Goderis J, Keymeulen A, Smets K, Van Hoecke H, De Leenheer E, Boudewyns A, Desloovere C, Kuhweide R, Muylle M, Royackers L, Schatteman I, Dhooge I.

J Pediatr. 2016 May;172:110-115.e2. doi: 10.1016/j.jpeds.2016.01.024. Epub 2016 Feb 5. Erratum in: J Pediatr. 2016 Oct;177:335.

PMID:
26858192
21.

First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy.

Smets K, Duarri A, Deconinck T, Ceulemans B, van de Warrenburg BP, Züchner S, Gonzalez MA, Schüle R, Synofzik M, Van der Aa N, De Jonghe P, Verbeek DS, Baets J.

BMC Med Genet. 2015 Jul 21;16:51. doi: 10.1186/s12881-015-0200-3.

22.

The spectrum of epilepsy caused by POLG mutations.

Janssen W, Quaegebeur A, Van Goethem G, Ann L, Smets K, Vandenberghe R, Van Paesschen W.

Acta Neurol Belg. 2016 Mar;116(1):17-25. doi: 10.1007/s13760-015-0499-8. Epub 2015 Jun 24.

PMID:
26104464
23.

Hearing loss and congenital CMV infection: a systematic review.

Goderis J, De Leenheer E, Smets K, Van Hoecke H, Keymeulen A, Dhooge I.

Pediatrics. 2014 Nov;134(5):972-82. doi: 10.1542/peds.2014-1173. Review.

PMID:
25349318
24.

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.

van der Zee J, Van Langenhove T, Kovacs GG, Dillen L, Deschamps W, Engelborghs S, Matěj R, Vandenbulcke M, Sieben A, Dermaut B, Smets K, Van Damme P, Merlin C, Laureys A, Van Den Broeck M, Mattheijssens M, Peeters K, Benussi L, Binetti G, Ghidoni R, Borroni B, Padovani A, Archetti S, Pastor P, Razquin C, Ortega-Cubero S, Hernández I, Boada M, Ruiz A, de Mendonça A, Miltenberger-Miltényi G, do Couto FS, Sorbi S, Nacmias B, Bagnoli S, Graff C, Chiang HH, Thonberg H, Perneczky R, Diehl-Schmid J, Alexopoulos P, Frisoni GB, Bonvicini C, Synofzik M, Maetzler W, vom Hagen JM, Schöls L, Haack TB, Strom TM, Prokisch H, Dols-Icardo O, Clarimón J, Lleó A, Santana I, Almeida MR, Santiago B, Heneka MT, Jessen F, Ramirez A, Sanchez-Valle R, Llado A, Gelpi E, Sarafov S, Tournev I, Jordanova A, Parobkova E, Fabrizi GM, Testi S, Salmon E, Ströbel T, Santens P, Robberecht W, De Jonghe P, Martin JJ, Cras P, Vandenberghe R, De Deyn PP, Cruts M, Sleegers K, Van Broeckhoven C.

Acta Neuropathol. 2014 Sep;128(3):397-410. doi: 10.1007/s00401-014-1298-7. Epub 2014 Jun 5.

25.

Concurrent validity of approximate number sense tasks in adults and children.

Smets K, Gebuis T, Defever E, Reynvoet B.

Acta Psychol (Amst). 2014 Jul;150:120-8. doi: 10.1016/j.actpsy.2014.05.001. Epub 2014 May 27.

PMID:
24875582
26.

Partial deletion of AFG3L2 causing spinocerebellar ataxia type 28.

Smets K, Deconinck T, Baets J, Sieben A, Martin JJ, Smouts I, Wang S, Taroni F, Di Bella D, Van Hecke W, Parizel PM, Jadoul C, De Potter R, Couvreur F, Rugarli E, De Jonghe P.

Neurology. 2014 Jun 10;82(23):2092-100. doi: 10.1212/WNL.0000000000000491. Epub 2014 May 9.

PMID:
24814845
27.

The power of emotion versus the power of suggestion: memory for emotional events in the misinformation paradigm.

Van Damme I, Smets K.

Emotion. 2014 Apr;14(2):310-20. doi: 10.1037/a0034629. Epub 2013 Nov 11.

PMID:
24219394
28.

Practitioner review: evidence-based practice guidelines on alcohol and drug misuse among adolescents: a systematic review.

Bekkering GE, Aertgeerts B, Asueta-Lorente JF, Autrique M, Goossens M, Smets K, van Bussel JC, Vanderplasschen W, Van Royen P, Hannes K.

J Child Psychol Psychiatry. 2014 Jan;55(1):3-21. doi: 10.1111/jcpp.12145. Epub 2013 Oct 7. Review.

PMID:
24117606
29.

PRRT2 mutations: exploring the phenotypical boundaries.

Djémié T, Weckhuysen S, Holmgren P, Hardies K, Van Dyck T, Hendrickx R, Schoonjans AS, Van Paesschen W, Jansen AC, De Meirleir L, Selim LA, Girgis MY, Buyse G, Lagae L, Smets K, Smouts I, Claeys KG, Van den Bergh V, Grisar T, Blatt I, Shorer Z, Roelens F, Afawi Z, Helbig I, Ceulemans B, De Jonghe P, Suls A.

J Neurol Neurosurg Psychiatry. 2014 Apr;85(4):462-5. doi: 10.1136/jnnp-2013-305122. Epub 2013 Oct 7.

PMID:
24101679
30.

First line management of prolonged convulsive seizures in children and adults: good practice points.

De Waele L, Boon P, Ceulemans B, Dan B, Jansen A, Legros B, Leroy P, Delmelle F, Ossemann M, De Raedt S, Smets K, Van De Voorde P, Verhelst H, Lagae L; Belgium League against Epilepsy; Belgium Society for Emergengy and Disaster Medicine.

Acta Neurol Belg. 2013 Dec;113(4):375-80. doi: 10.1007/s13760-013-0247-x. Epub 2013 Sep 10.

PMID:
24019121
31.

Neonatal blood pressure monitoring: visual assessment is an unreliable method for selecting cuff sizes.

Devinck A, Keukelier H, De Savoye I, Desmet L, Smets K.

Acta Paediatr. 2013 Oct;102(10):961-4. doi: 10.1111/apa.12328. Epub 2013 Jul 16.

PMID:
23799976
32.

Comparing the neural distance effect derived from the non-symbolic comparison and the same-different task.

Smets K, Gebuis T, Reynvoet B.

Front Hum Neurosci. 2013 Feb 14;7:28. doi: 10.3389/fnhum.2013.00028. eCollection 2013.

33.

Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia.

Martin E, Schüle R, Smets K, Rastetter A, Boukhris A, Loureiro JL, Gonzalez MA, Mundwiller E, Deconinck T, Wessner M, Jornea L, Oteyza AC, Durr A, Martin JJ, Schöls L, Mhiri C, Lamari F, Züchner S, De Jonghe P, Kabashi E, Brice A, Stevanin G.

Am J Hum Genet. 2013 Feb 7;92(2):238-44. doi: 10.1016/j.ajhg.2012.11.021. Epub 2013 Jan 17.

34.

NEOREG: design and implementation of an online Neonatal Registration System to access, follow and analyse the data of newborns with congenital cytomegalovirus infection.

Steurbaut K, De Backere F, Keymeulen A, De Leenheer M, Smets K, De Turck F.

Inform Health Soc Care. 2013 Sep;38(3):223-35. doi: 10.3109/17538157.2012.741166. Epub 2013 Jan 16.

PMID:
23323747
35.

Approximate number sense, symbolic number processing, or number-space mappings: what underlies mathematics achievement?

Sasanguie D, Göbel SM, Moll K, Smets K, Reynvoet B.

J Exp Child Psychol. 2013 Mar;114(3):418-31. doi: 10.1016/j.jecp.2012.10.012. Epub 2012 Dec 25.

PMID:
23270796
36.

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

EPICURE Consortium; EMINet Consortium, Steffens M, Leu C, Ruppert AK, Zara F, Striano P, Robbiano A, Capovilla G, Tinuper P, Gambardella A, Bianchi A, La Neve A, Crichiutti G, de Kovel CG, Kasteleijn-Nolst Trenité D, de Haan GJ, Lindhout D, Gaus V, Schmitz B, Janz D, Weber YG, Becker F, Lerche H, Steinhoff BJ, Kleefuß-Lie AA, Kunz WS, Surges R, Elger CE, Muhle H, von Spiczak S, Ostertag P, Helbig I, Stephani U, Møller RS, Hjalgrim H, Dibbens LM, Bellows S, Oliver K, Mullen S, Scheffer IE, Berkovic SF, Everett KV, Gardiner MR, Marini C, Guerrini R, Lehesjoki AE, Siren A, Guipponi M, Malafosse A, Thomas P, Nabbout R, Baulac S, Leguern E, Guerrero R, Serratosa JM, Reif PS, Rosenow F, Mörzinger M, Feucht M, Zimprich F, Kapser C, Schankin CJ, Suls A, Smets K, De Jonghe P, Jordanova A, Caglayan H, Yapici Z, Yalcin DA, Baykan B, Bebek N, Ozbek U, Gieger C, Wichmann HE, Balschun T, Ellinghaus D, Franke A, Meesters C, Becker T, Wienker TF, Hempelmann A, Schulz H, Rüschendorf F, Leber M, Pauck SM, Trucks H, Toliat MR, Nürnberg P, Avanzini G, Koeleman BP, Sander T.

Hum Mol Genet. 2012 Dec 15;21(24):5359-72. doi: 10.1093/hmg/dds373. Epub 2012 Sep 4.

PMID:
22949513
37.

Implementation and results of bedside hearing screening with automated auditory brainstem response in the neonatal intensive care unit.

Smets K, Verrue N, Dhooge I.

Acta Paediatr. 2012 Sep;101(9):e392-8. doi: 10.1111/j.1651-2227.2012.02736.x. Epub 2012 Jun 12.

PMID:
22591124
38.

Recommendations for the treatment of epilepsy in adult patients in general practice in Belgium: an update.

Boon P, Engelborghs S, Hauman H, Jansen A, Lagae L, Legros B, Ossemann M, Sadzot B, Smets K, Urbain E, van Rijckevorsel K.

Acta Neurol Belg. 2012 Jun;112(2):119-31. doi: 10.1007/s13760-012-0070-9. Epub 2012 Apr 28.

39.

KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy.

Weckhuysen S, Mandelstam S, Suls A, Audenaert D, Deconinck T, Claes LR, Deprez L, Smets K, Hristova D, Yordanova I, Jordanova A, Ceulemans B, Jansen A, Hasaerts D, Roelens F, Lagae L, Yendle S, Stanley T, Heron SE, Mulley JC, Berkovic SF, Scheffer IE, de Jonghe P.

Ann Neurol. 2012 Jan;71(1):15-25. doi: 10.1002/ana.22644.

PMID:
22275249
40.

An integrated workflow for robust alignment and simplified quantitative analysis of NMR spectrometry data.

Vu TN, Valkenborg D, Smets K, Verwaest KA, Dommisse R, Lemière F, Verschoren A, Goethals B, Laukens K.

BMC Bioinformatics. 2011 Oct 20;12:405. doi: 10.1186/1471-2105-12-405.

41.

Unraveling tobacco BY-2 protein complexes with BN PAGE/LC-MS/MS and clustering methods.

Remmerie N, De Vijlder T, Valkenborg D, Laukens K, Smets K, Vreeken J, Mertens I, Carpentier SC, Panis B, De Jaeger G, Blust R, Prinsen E, Witters E.

J Proteomics. 2011 Aug 12;74(8):1201-17. doi: 10.1016/j.jprot.2011.03.023. Epub 2011 Apr 2.

PMID:
21443973
42.

Neonatal pulmonary interstitial glycogenosis in a patient with Hunter syndrome.

Smets K, Van Daele S.

Eur J Pediatr. 2011 Aug;170(8):1083-4. doi: 10.1007/s00431-011-1444-3. Epub 2011 Mar 22. No abstract available.

PMID:
21424671
43.

Mutations in SACS cause atypical and late-onset forms of ARSACS.

Baets J, Deconinck T, Smets K, Goossens D, Van den Bergh P, Dahan K, Schmedding E, Santens P, Rasic VM, Van Damme P, Robberecht W, De Meirleir L, Michielsens B, Del-Favero J, Jordanova A, De Jonghe P.

Neurology. 2010 Sep 28;75(13):1181-8. doi: 10.1212/WNL.0b013e3181f4d86c.

PMID:
20876471
44.

Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C.

Dermaut B, Seneca S, Dom L, Smets K, Ceulemans L, Smet J, De Paepe B, Tousseyn S, Weckhuysen S, Gewillig M, Pals P, Parizel P, De Bleecker JL, Boon P, De Meirleir L, De Jonghe P, Van Coster R, Van Paesschen W, Santens P.

J Neurol Neurosurg Psychiatry. 2010 Jan;81(1):90-3. doi: 10.1136/jnnp.2008.157354.

PMID:
20019223
45.

Treatment of cranial epidural hematoma in a neonate by needle aspiration of a communicating cephalhematoma.

Smets KJ, Vanhauwaert D.

Eur J Pediatr. 2010 May;169(5):617-9. doi: 10.1007/s00431-009-1071-4. Epub 2009 Oct 16.

PMID:
19834739
46.

Cytomegalovirus DNA detection in Guthrie cards: role in the diagnostic work-up of childhood hearing loss.

Boudewyns A, Declau F, Smets K, Ursi D, Eyskens F, Van den Ende J, Van de Heyning P.

Otol Neurotol. 2009 Oct;30(7):943-9. doi: 10.1097/MAO.0b013e3181b76b22.

PMID:
19730140
47.

The SCN1A variant database: a novel research and diagnostic tool.

Claes LR, Deprez L, Suls A, Baets J, Smets K, Van Dyck T, Deconinck T, Jordanova A, De Jonghe P.

Hum Mutat. 2009 Oct;30(10):E904-20. doi: 10.1002/humu.21083.

PMID:
19585586
48.

A pan-European survey of antimicrobial susceptibility towards human-use antimicrobial drugs among zoonotic and commensal enteric bacteria isolated from healthy food-producing animals.

de Jong A, Bywater R, Butty P, Deroover E, Godinho K, Klein U, Marion H, Simjee S, Smets K, Thomas V, Vallé M, Wheadon A.

J Antimicrob Chemother. 2009 Apr;63(4):733-44. doi: 10.1093/jac/dkp012. Epub 2009 Feb 20.

PMID:
19233897
49.

REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31.

Beetz C, Schüle R, Deconinck T, Tran-Viet KN, Zhu H, Kremer BP, Frints SG, van Zelst-Stams WA, Byrne P, Otto S, Nygren AO, Baets J, Smets K, Ceulemans B, Dan B, Nagan N, Kassubek J, Klimpe S, Klopstock T, Stolze H, Smeets HJ, Schrander-Stumpel CT, Hutchinson M, van de Warrenburg BP, Braastad C, Deufel T, Pericak-Vance M, Schöls L, de Jonghe P, Züchner S.

Brain. 2008 Apr;131(Pt 4):1078-86. doi: 10.1093/brain/awn026. Epub 2008 Mar 5.

50.

Detection of enteroviral RNA on Guthrie card dried blood of a neonate with fatal Coxsackie B3 myocarditis on day 17.

Smets K, Keymeulen A, Wollants E, Lagrou K, Van Ranst M, Padalko E.

J Clin Virol. 2008 Jun;42(2):207-10. doi: 10.1016/j.jcv.2008.01.004. Epub 2008 Mar 7.

PMID:
18316244

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