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1

Regulating security on the Internet: control versus trust

van den Berg, Bibi, Keymolen, Esther

Journal:

International Review of Law Computers & Technology

Year:

2017

Language:

english

File:

PDF, 1.46 MB

english, 2017

2

Lists of Ethical, Legal, Societal and Economic Issues of Big Data Technologies

Custers, Bart, La Fors, Karolina, Jozwiak, Magdalena, Esther, Keymolen, Bachlechner, Daniel, Friedewald, Michael, Aguzzi, Stefania

Journal:

SSRN Electronic Journal

Year:

2017

Language:

english

File:

PDF, 1.44 MB

english, 2017

3

An ACVRL1 gene mutation presenting as vein of Galen malformation at prenatal diagnosis

De Luca, Caterina, Bevilacqua, Elisa, Badr, Dominique A., Cannie, Mieke M., Sanchez, Teresa C., Segers, ValÃ©rie, Keymolen, Kathelijn, Jani, Jacques C.

Journal:

American Journal of Medical Genetics Part A

Year:

2020

Language:

english

File:

PDF, 747 KB

english, 2020

4

Reliability and clinical correlates of 3D-accelerometry based gait analysis outcomes according to age and fall-risk

Ivan Bautmans, Bart Jansen, Bart Van Keymolen, Tony Mets

Journal:

Year:

2011

Language:

english

File:

PDF, 380 KB

english, 2011

5

Specific Congenital Malformations after Exposure to Cyclophosphamide, Epirubicin and 5-Fluorouracil during the First Trimester of Pregnancy

Leyder, Mina, Laubach, Monika, Breugelmans, Maria, Keymolen, Katelijn, De Greve, Jacques, Foulon, Walter

Journal:

Gynecologic and Obstetric Investigation

Year:

2011

Language:

english

File:

PDF, 121 KB

english, 2011

6

The Prevalence of Helicobacter pylori Positivity in Human Immunodeficiency Virus-Infected Children

Blecker, Uwe, Keymolen, Kathelijn, Lanciers, Sophie, Bahwere, Paluku, Souayah, Hicham, Levy, Jack, Vandenplas, Yvan

Journal:

Journal of Pediatric Gastroenterology & Nutrition

Year:

1994

File:

PDF, 355 KB

1994

7

Trunk inclination and hip extension mobility, but not thoracic kyphosis angle, are related to 3D-accelerometry based gait alterations and increased fall-risk in older persons

Demarteau, Jeroen, Jansen, Bart, Van Keymolen, Bart, Mets, Tony, Bautmans, Ivan

Journal:

Year:

2019

Language:

english

File:

PDF, 518 KB

english, 2019

8

iGovernment || Part II. Empirical Analysis

Keizer, Anne-Greet, Keymolen, Esther, Prins, Corien, Broeders, Dennis, Griffioen, Henk

Year:

2012

Language:

english

File:

PDF, 684 KB

english, 2012

9

iGovernment || Frontmatter

Keizer, Anne-Greet, Keymolen, Esther, Prins, Corien, Broeders, Dennis, Griffioen, Henk

Year:

2012

File:

PDF, 56 KB

2012

10

iGovernment || Preface

Keizer, Anne-Greet, Keymolen, Esther, Prins, Corien, Broeders, Dennis, Griffioen, Henk

Year:

2012

File:

PDF, 66 KB

2012

11

iGovernment || List of interviewees

Keizer, Anne-Greet, Keymolen, Esther, Prins, Corien, Broeders, Dennis, Griffioen, Henk

Year:

2012

File:

PDF, 92 KB

2012

12

iGovernment || Abbreviations and acronyms

Keizer, Anne-Greet, Keymolen, Esther, Prins, Corien, Broeders, Dennis, Griffioen, Henk

Year:

2012

File:

PDF, 70 KB

2012

13

iGovernment || References

Keizer, Anne-Greet, Keymolen, Esther, Prins, Corien, Broeders, Dennis, Griffioen, Henk

Year:

2012

File:

PDF, 202 KB

2012

14

Chromosomal abnormalities after ICSI in relation to semen parameters: results in 1114 fetuses and 1391 neonates from a single center

Belva, F, Bonduelle, M, Buysse, A, Van den Bogaert, A, Hes, F, Roelants, M, Verheyen, G, Tournaye, H, Keymolen, K

Journal:

Human Reproduction

Year:

2020

File:

PDF, 206 KB

2020

15

iGovernment || Summary

Prins, Corien, Broeders, Dennis, Griffioen, Henk, Keizer, Anne-Greet, Keymolen, Esther

Year:

2012

File:

PDF, 59 KB

2012

16

Distal limb deficiencies, oral involvement, and renal defect: Report of a third patient and confirmation of a distinct entity

K. Keymolen, R. Van Damme-Lombaerts, A. Verloes, J.P. Fryns

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 211 KB

english, 2000

17

Glypican 1 gene: Good candidate for brachydactyly type E

Maria Syrrou, Katelÿne Keymolen, Koen Devriendt, Maureen Holvoet, Reinhilde Thoelen, K. Verhofstadt, Jean-Pierre Fryns

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 218 KB

english, 2002

18

Phenotype and 244k array-CGH characterization of chromosome 13q deletions: An update of the phenotypic map of 13q21.1-qter

Maria Kirchhoff, Anne-Marie Bisgaard, Radka Stoeva, Boyan Dimitrov, Gabriele Gillessen-Kaesbach, Jean-Pierre Fryns, Hanne Rose, Liliana Grozdanova, Ivan Ivanov, Kathelijn Keymolen, Christina Fagerberg

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 356 KB

english, 2009

19

Floating-Harbor syndrome associated with middle ear abnormalities

Jan-Jaap Hendrickx, Kathelijn Keymolen, Brigitte Desprechins, Jan Casselman, Frans Gordts

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 150 KB

english, 2010

20

Pregnancy outcome in carriers of Robertsonian translocations

Kathelijn Keymolen, Kim Van Berkel, Anniek Vorsselmans, Catherine Staessen, Inge Liebaers

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 85 KB

english, 2011

21

Observations on intelligence and behavior in 15 patients with Legius syndrome

Ellen Denayer, Mie-Jef Descheemaeker, Douglas R. Stewart, Kathelijn Keymolen, Ellen Plasschaert, Sarah L. Ruppert, Joseph Snow, Audrey E. Thurm, Lisa A. Joseph, Jean-Pierre Fryns, Eric Legius

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Year:

2011

Language:

english

File:

PDF, 91 KB

english, 2011

22

Investigation of the polymorphic transformations from glassy nifedipine

Bram Keymolen, James L Ford, Mark W Powell, Ali R Rajabi-Siahboomi

Journal:

Thermochimica Acta

Year:

2003

Language:

english

File:

PDF, 470 KB

english, 2003

23

Post-zygotic origin of isochromosome 12p

Dr Thomy J. L. de Ravel, Kathelijn Keymolen, Elvire van Assche, Ingrid Wittevronghel, Philippe Moerman, Ivo Salden, Gert Matthijs, Jean-Pierre Fryns, Joris R. Vermeesch

Journal:

Prenatal Diagnosis

Year:

2004

Language:

english

File:

PDF, 133 KB

english, 2004

24

Early onset Huntington disease: a neuronal degeneration syndrome

Sara Seneca, Dominique Fagnart, Kathelijn Keymolen, Willy Lissens, Daniele Hasaerts, Sara Debulpaep, Brigitte Desprechins, Inge Liebaers, Linda De Meirleir

Journal:

European Journal of Pediatrics

Year:

2004

Language:

english

File:

PDF, 246 KB

english, 2004

25

Intervention during pregnancy and allergic disease in the offspring

S. Salvatore, K. Keymolen, B. Hauser, Y. Vandenplas

Journal:

Pediatric Allergy and Immunology

Year:

2005

Language:

english

File:

PDF, 125 KB

english, 2005

26

Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders

Vogels, Annick, Van Den Ende, Jenneke, Keymolen, Kathelijne, Mortier, Geert, Devriendt, Koen, Legius, E, Fryns, J P

Journal:

European Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 75 KB

english, 2003

27

Clinical outcome of preimplantation genetic diagnosis for cystic fibrosis: the Brussels' experience

Keymolen, Kathelijn, Goossens, Veerle, De rycke, Martine, Sermon, Karen, Boelaert, Kristel, Bonduelle, Maryse, Van Steirteghem, André, Liebaers, Inge

Journal:

European Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 89 KB

english, 2007

28

A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia

Morava, Eva, Zeevaert, Renate, Korsch, Eckhard, Huijben, Karin, Wopereis, Suzan, Matthijs, Gert, Keymolen, Kathelijn, Lefeber, Dirk J, De Meirleir, Linda, Wevers, Ron A

Journal:

European Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 218 KB

english, 2007

29

A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia

Morava, Eva, Zeevaert, Renate, Korsch, Eckhard, Huijben, Karin, Wopereis, Suzan, Matthijs, Gert, Keymolen, Kathelijn, Lefeber, Dirk J, De Meirleir, Linda, Wevers, Ron A

Journal:

European Journal of Human Genetics

Year:

2007

File:

PDF, 59 KB

2007

30

P14.74: Achondroplasia: evaluation of the phenotypic expression by 3D ultrasound

L. De Catte, E. Sleurs, K. Keymolen

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2004

Language:

english

File:

PDF, 41 KB

english, 2004

31

Adrenal secretion of estrogens, glucocorticosteroids and mineralocorticosteroids in the dog

Pierre Dor, Viviane Keymolen, Monique de Rood, Sam Levin, Abraham Borkowski

Journal:

European Journal of Cancer (1965)

Year:

1965

Language:

english

File:

PDF, 346 KB

english, 1965

32

Two different infantile phenotypes of Rett syndromes

S. Voets, S. Seneca, F. Roelens, M. De Rademaeker, W. Lissens, K. Keymolen, L. De Meirleir

Journal:

European Journal of Paediatric Neurology

Year:

2008

Language:

english

File:

PDF, 43 KB

english, 2008

33

CPP012 X-linked Hydrocephalus due to a new missense mutation: a cause of cerebral palsy

D. Amrom, M.-L. Leclercq, K. Keymolen, I. Liebaers, S. Seneca, W. Lissens

Journal:

European Journal of Paediatric Neurology

Year:

2007

Language:

english

File:

PDF, 46 KB

english, 2007

34

MLP023 CDG phenotype characterized by failure to thrive, hypotonia, microcephaly and hyperthermia in two infants of North African origin

A. Jansen, K. Keymolen, R. Zeevaert, G. Matthijs, H. Carchon, J. Jaeken, L. De Meirleir

Journal:

European Journal of Paediatric Neurology

Year:

2007

Language:

english

File:

PDF, 42 KB

english, 2007

35

NMP033 Molecular analysis in congenital muscular dystrophy

L. De Meirleir, D. Hasaerts, K. Keymolen, S. Voets, M. De Rademaeker, W. Lissens, S. Seneca, S. Lamande, S. Quijano-Roy, A. Michotte

Journal:

European Journal of Paediatric Neurology

Year:

2007

Language:

english

File:

PDF, 43 KB

english, 2007

36

Symptomatology of Helicobacter pylori infection in children

U. Blecker, B. Hauser, S. Lanciers, K. Keymolen, Y. Vandenplas

Journal:

Acta Paediatrica

Year:

1996

Language:

english

File:

PDF, 234 KB

english, 1996

37

Osteopathia striata with cranial sclerosis due to mutations in the WTX gene

B. Perdu, F. De Freitas, S. Frints, M. Schouten, C. Schrander-Stumpel, M. Barbosa, J. Pinto-Basto, M. Reis-Lima, M. de Vernejoul, K. Becker, M. Freckmann, K. Keymolen, E. Haan, R. Savarirayan, R. Köni

Journal:

Year:

2009

Language:

english

File:

PDF, 65 KB

english, 2009

38

Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV

Nathalie Verpoorten, Kristl G. Claeys, Liesbet Deprez, An Jacobs, Veerle Van Gerwen, Lieven Lagae, Willem Frans Arts, Linda De Meirleir, Kathelijn Keymolen, Chantal Ceuterick-de Groote, Peter De Jongh

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 345 KB

english, 2006

39

Late onset painful cold-aggravated myotonia: Three families with SCN4A L1436P mutation

Véronique Bissay, Kathelijn Keymolen, Willy Lissens, Guy Laureys, Eric Schmedding, Jacques De Keyser

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 156 KB

english, 2011

40

237 AN ALTERNATIVE CORRELATION BASED FEATURE FOR MEASURING STEP SYMMETRY FOR ASSESSING FALL RISK IN ELDERLY PERSONS

B. Jansen, I. Bautmans, B. Van Keymolen, R. Deklerck, T. Mets

Journal:

Parkinsonism & Related Disorders

Year:

2010

Language:

english

File:

PDF, 46 KB

english, 2010

41

A novel mutation in the SCN4A responsible for cold-induced myotonia with normal electromyography findings on room temperature

Véronique Bissay, Kathelijn Keymolen, Willy Lissens, Eric Schmedding, Jacques De Keyser

Journal:

Journal of the Neurological Sciences

Year:

2011

Language:

english

File:

PDF, 176 KB

english, 2011

42

O-39. PGD for reciprocal and Robertsonian translocations in 41 treatment cycles

E Van Assche, C Staessen, G Ogur, A Michiels, K Keymolen, P Devroey, A Van Steirteghem, I Liebaers

Journal:

Reproductive BioMedicine Online

Year:

2002

Language:

english

File:

PDF, 209 KB

english, 2002

43

A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors

Brady, Paul Daniel, Delle Chiaie, Barbara, Christenhusz, Gabrielle, Dierickx, Kris, Van Den Bogaert, Kris, Menten, Bjorn, Janssens, Sandra, Defoort, Paul, Roets, Ellen, Sleurs, Elke, Keymolen, Katheli

Journal:

Genetics in Medicine

Year:

2014

Language:

english

File:

PDF, 732 KB

english, 2014

44

Reliable and Sensitive Detection of Fragile X (Expanded) Alleles in Clinical Prenatal DNA Samples with a Fast Turnaround Time

Seneca, Sara, Lissens, Willy, Endels, Kristof, Caljon, Ben, Bonduelle, Maryse, Keymolen, Kathleen, De Rademaeker, Marjan, Ullmann, Urielle, Haentjens, Patrick, Van Berkel, Kim, Van Dooren, Sonia

Journal:

The Journal of Molecular Diagnostics

Year:

2012

Language:

english

File:

PDF, 1.22 MB

english, 2012

45

Thin genu of the corpus callosum points to mutation in FOXG1 in a child with acquired microcephaly, trigonocephaly, and intellectual developmental disorder: A case report and review of literature

De Bruyn, Caroline, Vanderhasselt, Tim, Tanyalçin, Ibrahim, Keymolen, Kathelijn, Van Rompaey, Katrijn L., De Meirleir, Linda, Jansen, Anna C.

Journal:

European Journal of Paediatric Neurology

Year:

2014

Language:

english

File:

PDF, 1.15 MB

english, 2014

46

PP6.5 – 1922 Incidental findings in array CGH

Keymolen, K, De Rademaeker, M, Van Den Bogaert, A

Journal:

European Journal of Paediatric Neurology

Year:

2013

Language:

english

File:

PDF, 60 KB

english, 2013

47

Role of CGH array in the diagnosis of autosomal recessive disease: a case of Ellis-van Creveld syndrome

D'Ambrosio, Valentina, Votino, Carmela, Cos, Teresa, Boulanger, Sebastien, Dheedene, Annelies, Jani, Jacques, Keymolen, Kathelijn

Journal:

Prenatal Diagnosis

Year:

2015

Language:

english

File:

PDF, 390 KB

english, 2015

48

The annual incidence of DiGeorge/velocardiofacial syndrome.

Devriendt, K, Fryns, J P, Mortier, G, van Thienen, M N, Keymolen, K

Journal:

Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 577 KB

english, 1998

49

HYPO-ALLERGENIC INTERVENTIONS DURING PREGNANCY

SALVATORE, S, KEYMOLEN, K, HAUSER, B, VANDENPLAS, Y

Journal:

Fetal and Maternal Medicine Review

Year:

2006

Language:

english

File:

PDF, 341 KB

english, 2006

50

Innocence Lost: Care and Control in Dutch Digital Youth Care

Keymolen, E., Broeders, D.

Journal:

British Journal of Social Work

Year:

2013

Language:

english

File:

PDF, 168 KB

english, 2013

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