Keymolen, K : rechercher sur Z-Library

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

Année:

2020

Langue:

english

Fichier:

PDF, 747 KB

english, 2020

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:

Gait & Posture

Année:

2011

Langue:

english

Fichier:

PDF, 380 KB

english, 2011

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

Journal:

Gynecologic and Obstetric Investigation

Année:

2011

Langue:

english

Fichier:

PDF, 121 KB

english, 2011

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

Année:

1994

Fichier:

PDF, 355 KB

1994

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:

Gait & Posture

Année:

2019

Langue:

english

Fichier:

PDF, 518 KB

english, 2019

iGovernment || Part II. Empirical Analysis

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

Année:

2012

Langue:

english

Fichier:

PDF, 684 KB

english, 2012

iGovernment || Frontmatter

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

Année:

2012

Fichier:

PDF, 56 KB

2012

iGovernment || Preface

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

Année:

2012

Fichier:

PDF, 66 KB

2012

iGovernment || List of interviewees

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

Année:

2012

Fichier:

PDF, 92 KB

2012

iGovernment || Abbreviations and acronyms

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

Année:

2012

Fichier:

PDF, 70 KB

2012

iGovernment || References

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

Année:

2012

Fichier:

PDF, 202 KB

2012

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

Année:

2020

Fichier:

PDF, 206 KB

2020

iGovernment || Summary

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

Année:

2012

Fichier:

PDF, 59 KB

2012

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:

Année:

2000

Langue:

english

Fichier:

PDF, 211 KB

english, 2000

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:

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

Année:

2002

Langue:

english

Fichier:

PDF, 218 KB

english, 2002

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

Journal:

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

Année:

2009

Langue:

english

Fichier:

PDF, 356 KB

english, 2009

Floating-Harbor syndrome associated with middle ear abnormalities

Journal:

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

Année:

2010

Langue:

english

Fichier:

PDF, 150 KB

english, 2010

Pregnancy outcome in carriers of Robertsonian translocations

Journal:

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

Année:

2011

Langue:

english

Fichier:

PDF, 85 KB

english, 2011

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:

Année:

2011

Langue:

english

Fichier:

PDF, 91 KB

english, 2011

Investigation of the polymorphic transformations from glassy nifedipine

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

Journal:

Thermochimica Acta

Année:

2003

Langue:

english

Fichier:

PDF, 470 KB

english, 2003

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

Année:

2004

Langue:

english

Fichier:

PDF, 133 KB

english, 2004

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

Année:

2004

Langue:

english

Fichier:

PDF, 246 KB

english, 2004

Intervention during pregnancy and allergic disease in the offspring

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

Journal:

Pediatric Allergy and Immunology

Année:

2005

Langue:

english

Fichier:

PDF, 125 KB

english, 2005

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:

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

Année:

2003

Langue:

english

Fichier:

PDF, 75 KB

english, 2003

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

Journal:

Année:

2007

Langue:

english

Fichier:

PDF, 89 KB

english, 2007

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:

Année:

2007

Langue:

english

Fichier:

PDF, 218 KB

english, 2007

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:

Ultrasound in Obstetrics & Gynecology

Année:

2007

Fichier:

PDF, 59 KB

2007

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

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

Journal:

Année:

2004

Langue:

english

Fichier:

PDF, 41 KB

english, 2004

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)

Année:

1965

Langue:

english

Fichier:

PDF, 346 KB

english, 1965

Two different infantile phenotypes of Rett syndromes

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

Journal:

Année:

2008

Langue:

english

Fichier:

PDF, 43 KB

english, 2008

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:

Année:

2007

Langue:

english

Fichier:

PDF, 46 KB

english, 2007

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:

Année:

2007

Langue:

english

Fichier:

PDF, 42 KB

english, 2007

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:

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

Année:

2007

Langue:

english

Fichier:

PDF, 43 KB

english, 2007

Symptomatology of Helicobacter pylori infection in children

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

Journal:

Acta Paediatrica

Année:

1996

Langue:

english

Fichier:

PDF, 234 KB

english, 1996

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:

Bone

Année:

2009

Langue:

english

Fichier:

PDF, 65 KB

english, 2009

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

Journal:

Neuromuscular Disorders

Année:

2006

Langue:

english

Fichier:

PDF, 345 KB

english, 2006

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

Année:

2011

Langue:

english

Fichier:

PDF, 156 KB

english, 2011

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

Année:

2010

Langue:

english

Fichier:

PDF, 46 KB

english, 2010

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

Année:

2011

Langue:

english

Fichier:

PDF, 176 KB

english, 2011

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

Année:

2002

Langue:

english

Fichier:

PDF, 209 KB

english, 2002

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

Année:

2014

Langue:

english

Fichier:

PDF, 732 KB

english, 2014

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

Année:

2012

Langue:

english

Fichier:

PDF, 1.22 MB

english, 2012

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:

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

Année:

2014

Langue:

english

Fichier:

PDF, 1.15 MB

english, 2014

PP6.5 – 1922 Incidental findings in array CGH

Journal: