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1

Embryo implantation after biopsy of one or two cells from cleavage-stage embryos with a view to preimplantation genetic diagnosis

Hilde Van de Velde, Anick De Vos, Karen Sermon, Catherine Staessen, Martine De Rycke, Elvire Van Assche, Willy Lissens, Mark Vandervorst, Heidi Van Ranst, Inge Liebaers, André Van Steirteghem

Journal:

Prenatal Diagnosis

Year:

2000

Language:

english

File:

PDF, 93 KB

english, 2000

2

Proteomic analysis in giant axonal neuropathy: New insights into disease mechanisms

Silke Mussche, Boel De Paepe, Joél Smet, Katrien Devreese, Willy Lissens, Vedrana Milic Rasic, Matthew Murnane, Bart Devreese, Rudy Van Coster

Journal:

Year:

2012

Language:

english

File:

PDF, 1.30 MB

english, 2012

3

Mutations c.459 + 1G > A and p.P426L in the ARSA gene: Prevalence in metachromatic leukodystrophy patients from European countries

Agnieszka Lugowska, Olga Amaral, Johannes Berger, Linda Berna, Nils U. Bosshard, Amparo Chabas, Anthony Fensom, Volkmar Gieselmann, Natalia G. Gorovenko, Willy Lissens, Jan-Eric Mansson, Ana Marcao, H

Journal:

Molecular Genetics and Metabolism

Year:

2005

Language:

english

File:

PDF, 331 KB

english, 2005

4

PGD in the lab for triplet repeat diseases — myotonic dystrophy, Huntington's disease and Fragile-X syndrome

Karen Sermon, Sara Seneca, Martine De Rycke, Veerle Goossens, Hilde Van de Velde, Anick De Vos, Peter Platteau, Willy Lissens, André Van Steirteghem, Inge Liebaers

Journal:

Molecular and Cellular Endocrinology

Year:

2001

Language:

english

File:

PDF, 344 KB

english, 2001

5

Mutation analysis of the pyruvate dehydrogenase E1α gene in eight patients with a pyruvate dehydrogenase complex deficiency

Willy Lissens, Linda De Meirleir, Sara Seneca, Chantal Benelli, Cécile Marsac, Bwee Tien Poll-The, Paz Briones, Wim Ruitenbeek, Otto van Diggelen, Denis Chaigne, Vincent Ramaekers, Ingeborg Liebaers

Journal:

Year:

1996

Language:

english

File:

PDF, 598 KB

english, 1996

6

Mutations in the X-linked pyruvate dehydrogenase (E1) α subunit gene (PDHA1) in patients with a pyruvate dehydrogenase complex deficiency

Willy Lissens, Linda De Meirleir, Sara Seneca, Inge Liebaers, Garry K. Brown, Ruth M. Brown, Michinori Ito, Etsuo Naito, Yasuhiro Kuroda, Douglas S. Kerr, Isaiah D. Wexler, Mulchand S. Patel, Brian H.

Journal:

Year:

2000

Language:

english

File:

PDF, 290 KB

english, 2000

7

Clinical and diagnostic characteristics of complex III deficiency due to mutations in the BCS1L gene

Linda De Meirleir, Sara Seneca, Eliane Damis, Brigitte Sepulchre, Anne Hoorens, Erik Gerlo, M. Teres García Silva, Elena Martín Hernandez, Willy Lissens, Rudy Van Coster

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 219 KB

english, 2003

8

Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene

Karen Buysse, Sarah Vergult, Silke Mussche, Chantal Ceuterick-de Groote, Frank Speleman, Björn Menten, Willy Lissens, Rudy Van Coster

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 107 KB

english, 2010

9

Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNA

Joél Smet, Sara Seneca, Boel De Paepe, Ann Meulemans, Helene Verhelst, Jules Leroy, Linda De Meirleir, Willy Lissens, Rudy Van Coster

Journal:

ELECTROPHORESIS

Year:

2009

Language:

english

File:

PDF, 203 KB

english, 2009

10

Genetically heterogeneous selective intestinal malabsorption of vitamin B12: Founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East

Stephan M. Tanner, Zhongyuan Li, Ryan Bisson, Ceren Acar, Cihan Öner, Reyhan Öner, Mualla Çetin, Mohamed A. Abdelaal, Essam A. Ismail, Willy Lissens, Ralf Krahe, Harald Broch, Ralph Gräsbeck, Albert d

Journal:

Year:

2004

Language:

english

File:

PDF, 286 KB

english, 2004

11

Cancer predisposing missense and protein truncating BARD1 mutations in non-BRCA1 or BRCA2 breast cancer families

Sylvia De Brakeleer, Jacques De Grève, Remy Loris, Nicolas Janin, Willy Lissens, Erica Sermijn, Erik Teugels

Journal:

Year:

2010

Language:

english

File:

PDF, 321 KB

english, 2010

12

De novo Alu element insertions targeted to a sequence common to the BRCA1 and BRCA2 genes

Erik Teugels, Sylvia De Brakeleer, Guido Goelen, Willy Lissens, Erica Sermijn, Jacques De Grève

Journal:

Year:

2005

Language:

english

File:

PDF, 342 KB

english, 2005

13

A single mutation in the GALC gene is responsible for the majority of late onset Krabbe disease patients in the Catania (Sicily, Italy) region

Willy Lissens, Alessia Arena, Sara Seneca, Mohammad Rafi, Giovanni Sorge, Inge Liebaers, David Wenger, Agata Fiumara

Journal:

Year:

2007

Language:

english

File:

PDF, 56 KB

english, 2007

14

Wet oxidation pre-treatment of woody yard waste: parameter optimization and enzymatic digestibility for ethanol production

Geert Lissens, Helene Klinke, Willy Verstraete, Birgitte Ahring, Anne Belinda Thomsen

Journal:

Journal of Chemical Technology & Biotechnology

Year:

2004

Language:

english

File:

PDF, 129 KB

english, 2004

15

Electrochemical decomplexing and oxidation of organic (chelating) additives in effluents from surface treatment and metal finishing

Geert Lissens, Marc Verhaege, Luc Pinoy, Willy Verstraete

Journal:

Journal of Chemical Technology & Biotechnology

Year:

2003

Language:

english

File:

PDF, 180 KB

english, 2003

16

Gas chromatographic–mass spectrometric analysis of N-acetylated amino acids: The first case of aminoacylase I deficiency

Erik Gerlo, Rudy Van Coster, Willy Lissens, Gerda Winckelmans, Linda De Meirleir, Ron Wevers

Journal:

Analytica Chimica Acta

Year:

2006

Language:

english

File:

PDF, 189 KB

english, 2006

17

Imprinting analysis in spermatozoa prepared for intracytoplasmic sperm injection (ICSI)

Martina Manning, Willy Lissens, Inge Liebaers, André Van Steirteghem, Wolfgang Weidner

Journal:

International Journal of Andrology

Year:

2001

Language:

english

File:

PDF, 1.23 MB

english, 2001

18

Idiopathic non-obstructive azoospermia or severe oligozoospermia: a cross-sectional study in 61 Greek men

Chariklia Giannouli, Dimitrios G. Goulis, Alexander Lambropoulos, Willy Lissens, Basil C. Tarlatzis, John N. Bontis, John Papadimas

Journal:

International Journal of Andrology

Year:

2004

Language:

english

File:

PDF, 151 KB

english, 2004

19

Polymerase chain reaction analysis of the cystic fibrosis ΔF508 mutation in human blastomeres following oocyte injection of a single sperm from a carrier

Jiaen Liu, Dr Willy Lissens, Paul Devroey, Andre Van Steirteghem, Ingeborg Liebaers

Journal:

Prenatal Diagnosis

Year:

1993

Language:

english

File:

PDF, 503 KB

english, 1993

20

Normal pregnancy after preimplantation DNA diagnosis of a dystrophin gene deletion

Jiaen Liu, Dr. Willy Lissens, Christine Van Broeckhoven, Ann Löfgren, Michel Camus, Ingeborg Liebaers, André Van Steirteghem

Journal:

Prenatal Diagnosis

Year:

1995

Language:

english

File:

PDF, 843 KB

english, 1995

21

A novel L1CAM mutation with L1 spectrum disorders

Fatma Silan, Ismail Ozdemir, Willy Lissens

Journal:

Prenatal Diagnosis

Year:

2005

Language:

english

File:

PDF, 136 KB

english, 2005

22

Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the Elα subunit

Linda De Meirleir, Willy Lissens, Esther Vamos, Inge Liebaers

Journal:

Year:

1992

Language:

english

File:

PDF, 591 KB

english, 1992

23

The deletion F508 is the major gene mutation in a representative Belgian cystic fibrosis population

Maryse Bonduelle, Willy Lissens, Anne Malfroot, Isi Dab, Inge Liebaers

Journal:

Year:

1990

Language:

english

File:

PDF, 203 KB

english, 1990

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

A family with pyruvate dehydrogenase complex deficiency due to a novel C>T substitution at nucleotide position 407 in exon 4 of the X-linked Ε1α gene

Már Tulinius, Niklas Darin, Lars-Martin Wiklund, Eva Holmberg, Jan Erik Eriksson, Willy Lissens, Linda De Meirleir, Elisabeth Holme

Journal:

European Journal of Pediatrics

Year:

2005

Language:

english

File:

PDF, 416 KB

english, 2005

26

Two pregnancies after preimplantation genetic diagnosis for osteogenesis imperfecta type I and type IV

Anick De Vos, Karen Sermon, Hilde Van de Velde, Hubert Joris, Mark Vandervorst, Willy Lissens, Anne De Paepe, Inge Liebaers, André Van Steirteghem

Journal:

Year:

2000

Language:

english

File:

PDF, 81 KB

english, 2000

27

β-Glucuronidase P408S, P415L mutations: evidence that both mutations combine to produce an MPS VII allele in certain Mexican patients

M. Rafiqul Islam, R. Vervoort, Willy Lissens, Joe J. Hoo, Leonard A. Valentino, W. S. Sly

Journal:

Year:

1996

Language:

english

File:

PDF, 80 KB

english, 1996

28

Preimplantation genetic diagnosis for spinal and bulbar muscular atrophy (SBMA)

Ioannis Georgiou, Karen Sermon, Willy Lissens, Anick De Vos, Peter Platteau, Dimitrios Lolis, Andre Van Steirteghem, Inge Liebaers

Journal:

Year:

2001

Language:

english

File:

PDF, 57 KB

english, 2001

29

Complex III staining in blue native polyacrylamide gels

Joél Smet, Boel De Paepe, Sara Seneca, Willy Lissens, Heike Kotarsky, Linda De Meirleir, Vineta Fellman, Rudy Van Coster

Journal:

Journal of Inherited Metabolic Disease

Year:

2011

Language:

english

File:

PDF, 333 KB

english, 2011

30

Electrochemical degradation of surfactants by intermediates of water discharge at carbon-based electrodes

Geert Lissens, Jan Pieters, Marc Verhaege, Luc Pinoy, Willy Verstraete

Journal:

Electrochimica Acta

Year:

2003

Language:

english

File:

PDF, 371 KB

english, 2003

31

A homozygous inactivating calcium-sensing receptor mutation, Pro339Thr, is associated with isolated primary hyperparathyroidism: correlation between location of mutations and severity of hypercalcaemia

Fadil M. Hannan, M. A. Nesbit, Paul T. Christie, Willy Lissens, Bart Van der Schueren, Marie Bex, Roger Bouillon, Rajesh V. Thakker

Journal:

Clinical Endocrinology

Year:

2010

Language:

english

File:

PDF, 180 KB

english, 2010

32

Alterations of the USP26 gene in Caucasian men

Katrien Stouffs, Willy Lissens, Herman Tournaye, André Van Steirteghem, Inge Liebaers

Journal:

International Journal of Andrology

Year:

2006

Language:

english

File:

PDF, 845 KB

english, 2006

33

Pearson marrow pancreas syndrome: a molecular study and clinical management

Sara Seneca, Linda De Meirleir, Jean De Scbepper, Nadine Balduck, Kristin Jochmans, Inge Liebaers, Willy Lissens

Journal:

Clinical Genetics

Year:

1997

Language:

english

File:

PDF, 574 KB

english, 1997

34

10.1038/81563

Van Hul, Wim, Janssens, Katrien, Gershoni-Baruch, Ruth, Guañabens, Nuria, Migone, Nicola, Ralston, Stuart, Bonduelle, Maryse, Lissens, Willy, Van Maldergem, Lionel, Vanhoenacker, Filip, Verbruggen, Le

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 293 KB

english, 2000

35

Preimplantation genetic diagnosis for Huntington's disease with exclusion testing

Sermon, Karen, De Rijcke, Martine, Lissens, Willy, De Vos, Anick, Platteau, Peter, Bonduelle, Maryse, Devroey, Paul, Van Steirteghem, André, Liebaers, Inge

Journal:

European Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 119 KB

english, 2002

36

Possible role of USP26 in patients with severely impaired spermatogenesis

Stouffs, Katrien, Lissens, Willy, Tournaye, Herman, Van Steirteghem, André, Liebaers, Inge

Journal:

European Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 105 KB

english, 2004

37

Demonstration of human α-l-fucosidase polymorphism by means of monoclonal antibodies

Willy Lissens, Raf Vrijsen, Robert Jan Sijens, Inge Liebaers, Albert Boeyé

Journal:

Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology

Year:

1985

Language:

english

File:

PDF, 523 KB

english, 1985

38

Analysis of the mitochondrial encoded subunits of complex I in 20 patients with a complex I deficiency

Ann Meulemans, Willy Lissens, Rudy Van Coster, Linda De Meirleir, Joél Smet, Marie-Cécile Nassogne, Inge Liebaers, Sara Seneca

Journal:

European Journal of Paediatric Neurology

Year:

2004

Language:

english

File:

PDF, 107 KB

english, 2004

39

A new family with the mitochondrial tRNAGLU gene mutation m.14709T>C presenting with hydrops fetalis

Ann Meulemans, Sara Seneca, Joel Smet, Boel De Paepe, Willy Lissens, Rudy Van Coster, Anne Debeer, Linda De Meirleir, Jaak Jaeken

Journal:

European Journal of Paediatric Neurology

Year:

2007

Language:

english

File:

PDF, 350 KB

english, 2007

40

Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 gene

Linda De Meirleir, Sara Seneca, Willy Lissens, Eric Schoentjes, Brigette Desprechins

Journal:

Pediatric Neurology

Year:

1995

Language:

english

File:

PDF, 1.82 MB

english, 1995

41

A case of thyroid hormone resistance: Prospective follow-up during pregnancy and obstetric outcome

Dany Massaad, Kris Poppe, Willy Lissens, Brigitte Velkeniers

Journal:

European Journal of Internal Medicine

Year:

2007

Language:

english

File:

PDF, 156 KB

english, 2007

42

Preimplantation genetic diagnosis for Marfan syndrome

Claudia Spits, Martine De Rycke, Willem Verpoest, Willy Lissens, Andre Van Steirteghem, Inge Liebaers, Karen Sermon

Journal:

Fertility and Sterility

Year:

2006

Language:

english

File:

PDF, 133 KB

english, 2006

43

Is there a role for the nuclear export factor 2 gene in male infertility?

Katrien Stouffs, Herman Tournaye, Josiane Van der Elst, Inge Liebaers, Willy Lissens

Journal:

Fertility and Sterility

Year:

2008

Language:

english

File:

PDF, 98 KB

english, 2008

44

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

45

8b The genetics of male infertility in relation to cystic fibrosis

Willy Lissens, Inge Liebaers

Journal:

Baillière's Clinical Obstetrics and Gynaecology

Year:

1997

Language:

english

File:

PDF, 1.70 MB

english, 1997

46

Evaluation of Parental Mitochondrial Inheritance in Neonates Born after Intracytoplasmic Sperm Injection

Claude Danan, Damien Sternberg, André Van Steirteghem, Cécile Cazeneuve, Philippe Duquesnoy, Claude Besmond, Michel Goossens, Willy Lissens, Serge Amselem

Journal:

The American Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 296 KB

english, 1999

47

Intergenerational Instability of the Expanded CTG Repeat in the DMPK Gene: Studies in Human Gametes and Preimplantation Embryos

Nele De Temmerman, Karen Sermon, Sara Seneca, Martine De Rycke, Pierre Hilven, Willy Lissens, André Van Steirteghem, Inge Liebaers

Journal:

The American Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 282 KB

english, 2004

48

SYCP3 mutations are uncommon in patients with azoospermia

Katrien Stouffs, Willy Lissens, Herman Tournaye, André Van Steirteghem, Inge Liebaers

Journal:

Fertility and Sterility

Year:

2005

Language:

english

File:

PDF, 50 KB

english, 2005

49

Serine Protease Activity and Residual LEKTI Expression Determine Phenotype in Netherton Syndrome

Hachem, Jean-Pierre, Wagberg, Fredrik, Schmuth, Matthias, Crumrine, Debra, Lissens, Willy, Jayakumar, Arumugam, Houben, Evi, Mauro, Theodora M, Leonardsson, Göran, Brattsand, Maria, Egelrud, Torbjorn,

Journal:

The Journal of Investigative Dermatology

Year:

2006

Language:

english

File:

PDF, 610 KB

english, 2006

50

CarP, a novel gene regulating the transcription of the carbamoylphosphate synthetase operon of Escherichia coli

Martine Roovers, Daniel Charlier, André Feller, Daniel Gigot, Frank Holemans, Willy Lissens, André Piérard, Nicolas Glansdorff

Journal:

Journal of Molecular Biology

Year:

1988

Language:

english

File:

PDF, 1.80 MB

english, 1988

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