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1

Physiologic Effects of Dry Needling

Cagnie, Barbara, Dewitte, Vincent, Barbe, Tom, Timmermans, Frank, Delrue, Nicolas, Meeus, Mira

Journal:

Current Pain and Headache Reports

Year:

2013

Language:

english

File:

PDF, 241 KB

english, 2013

2

Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies

Sylvia Bort, E. Nelis, Vincent Timmerman, Teresa Sevilla, Antonio Cruz-Martínez, Francisco Martínez, José M. Millán, Javier Arpa, Juan J. Vílchez, Felix Prieto, Christine Van Broeckhoven, F. Palau

Journal:

Year:

1997

Language:

english

File:

PDF, 105 KB

english, 1997

3

Probiotic prophylaxis in patients with predicted severe acute pancreatitis (PROPATRIA): design and rationale of a double-blind, placebo-controlled randomised multicenter trial [ISRCTN38327949]

Marc GH Besselink, Harro M Timmerman, Erik Buskens, Vincent B Nieuwenhuijs, Louis MA Akkermans, Hein G Gooszen, the members of the Dutch Acute Pancreatitis Study Group

Journal:

Year:

2004

Language:

english

File:

PDF, 518 KB

english, 2004

4

Whole-exome sequencing in patients with inherited neuropathies: outcome and challenges

Schabhüttl, Maria, Wieland, Thomas, Senderek, Jan, Baets, Jonathan, Timmerman, Vincent, De Jonghe, Peter, Reilly, Mary M., Stieglbauer, Karl, Laich, Eva, Windhager, Reinhard, Erwa, Wolfgang, Trajanosk

Journal:

Journal of Neurology

Year:

2014

Language:

english

File:

PDF, 278 KB

english, 2014

5

Periaxin mutations cause a broad spectrum of demyelinating neuropathies

Hiroshi Takashima, Cornelius F. Boerkoel, Peter De Jonghe, Chantal Ceuterick, Jean-Jacques Martin, Thomas Voit, J.-Michael Schröder, Anna Williams, Peter J. Brophy, Vincent Timmerman, James R. Lupski

Journal:

Annals of Neurology

Year:

2002

Language:

english

File:

PDF, 900 KB

english, 2002

6

Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy

Gert Hünermund, Anja Schirmacher, Bernd Ringelstein, Peter Young, Giles D. Watts, Jan Meuleman, Eva Nelis, Phillip F. Chance, Vincent Timmerman, Florian Stögbauer, Gregor Kuhlenbäumer

Journal:

Year:

2004

Language:

english

File:

PDF, 75 KB

english, 2004

7

Determinants of folic acid use in early pregnancy in a multi-ethnic urban population in The Netherlands: The Generation R study

Sarah Timmermans, Vincent W.V. Jaddoe, Johan P. Mackenbach, Albert Hofman, Régine P.M. Steegers-Theunissen, Eric A.P. Steegers

Journal:

Preventive Medicine

Year:

2008

Language:

english

File:

PDF, 296 KB

english, 2008

8

Probiotic prophylaxis in predicted severe acute pancreatitis: a randomised, double-blind, placebo-controlled trial

Marc GH Besselink, Hjalmar C van Santvoort, Erik Buskens, Marja A Boermeester, Harry van Goor, Harro M Timmerman, Vincent B Nieuwenhuijs, Thomas L Bollen, Bert van Ramshorst, Ben JM Witteman, Camiel R

Journal:

Year:

2008

Language:

english

File:

PDF, 158 KB

english, 2008

9

A Comparison of Rate Control and Rhythm Control in Patients with Recurrent Persistent Atrial Fibrillation

Van Gelder, Isabelle C., Hagens, Vincent E., Bosker, Hans A., Kingma, J. Herre, Kamp, Otto, Kingma, Tsjerk, Said, Salah A., Darmanata, Julius I., Timmermans, Alphons J.M., Tijssen, Jan G.P., Crijns, H

Journal:

Boston Medical and Surgical Journal

Year:

2002

Language:

english

File:

PDF, 134 KB

english, 2002

10

Helicobacter pylori colonization and pregnancies complicated by preeclampsia, spontaneous prematurity, and small for gestational age birth

den Hollander, Wouter J., Schalekamp-Timmermans, Sarah, Holster, I. Lisanne, Jaddoe, Vincent W., Hofman, Albert, Moll, Henriëtte A., Perez-Perez, Guillermo I., Blaser, Martin J., Steegers, Eric A. P.,

Journal:

Year:

2016

Language:

english

File:

PDF, 357 KB

english, 2016

11

Innovation Systems for Transformations towards Sustainability? Taking the Normative Dimension Seriously

Schlaile, Michael, Urmetzer, Sophie, Blok, Vincent, Andersen, Allan, Timmermans, Job, Mueller, Matthias, Fagerberg, Jan, Pyka, Andreas

Journal:

Year:

2017

Language:

english

File:

PDF, 288 KB

english, 2017

12

Social labs as an inclusive methodology to implement and study social change: the case of responsible research and innovation

Timmermans, Job, Blok, Vincent, Braun, Robert, Wesselink, Renate, Nielsen, Rasmus Ãjvind

Journal:

Journal of Responsible Innovation

Year:

2020

File:

PDF, 1.99 MB

2020

13

A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine—Sottas syndrome patients

Kaisa Silander, Päivi Meretoja, Eva Nelis, Vincent Timmerman, Christine Van Broeckhoven, Pertti Aula, Marja-Liisa Savontaus

Journal:

Year:

1996

Language:

english

File:

PDF, 742 KB

english, 1996

14

Mutation analysis of the connexin 32 (Cx32) gene in charcot-marie-tooth neuropathy type 1: Identification of five new mutations

Eva Nelis, Sandra Simokovic, Vincent Timmerman, Ann Löfgren, Hubert Backhovens, Peter De Jonghe, Jean-Jacques Martin, Christine Van Broeckhoven

Journal:

Year:

1997

Language:

english

File:

PDF, 171 KB

english, 1997

15

Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients

Irina V. Mersiyanova, Sookhrat M. Ismailov, Alexandr V. Polyakov, Elena L. Dadali, Valeriy P. Fedotov, Eva Nelis, Ann Löfgren, Vincent Timmerman, Christine Van Broeckhoven, Oleg V. Evgrafov

Journal:

Year:

2000

Language:

english

File:

PDF, 255 KB

english, 2000

16

Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E

Peter De Jonghe, Irina Mersivanova, Eva Nelis, Jurgen Del Favero, Jean-Jacques Martin, Christine Van Broeckhoven, Oleg Evgrafov, Vincent Timmerman

Journal:

Annals of Neurology

Year:

2001

Language:

english

File:

PDF, 7.87 MB

english, 2001

17

Toll-like receptor expression in the peripheral nerve

Sofie Goethals, Elke Ydens, Vincent Timmerman, Sophie Janssens

Journal:

Year:

2010

Language:

english

File:

PDF, 447 KB

english, 2010

18

Characterization of two mutations in the SPTLC1 subunit of serine palmitoyltransferase associated with hereditary sensory and autonomic neuropathy type I

Annelies Rotthier, Anke Penno, Bernd Rautenstrauss, Michaela Auer-Grumbach, Georg M. Stettner, Bob Asselbergh, Kim Van Hoof, Heinrich Sticht, Nicolas Lévy, Vincent Timmerman, Thorsten Hornemann, Katri

Journal:

Year:

2011

Language:

english

File:

PDF, 615 KB

english, 2011

19

Mutation analysis of 12 candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3

Joy Irobi, Eva Nelis, Kristien Verhoeven, Els De Vriendt, Ines Dierick, Peter De Jonghe, Christine Van Broeckhoven, Vincent Timmerman

Journal:

Journal of the Peripheral Nervous System

Year:

2002

Language:

english

File:

PDF, 154 KB

english, 2002

20

Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0gene

Eva Nelis, Vincent Timmerman, Peter Jonghe, Antoon Vandenberghe, Danielle Pham-Dinh, André Dautigny, Jean-Jacques Martin, Christine Broeckhoven

Journal:

Year:

1994

Language:

english

File:

PDF, 525 KB

english, 1994

21

Reduced penetrance in hereditary motor neuropathy caused byTRPV4Arg269Cys mutation

José Berciano, Jonathan Baets, Elena Gallardo, Magdalena Zimoń, Antonio García, Eduardo López-Laso, Onofre Combarros, Jon Infante, Vincent Timmerman, Albena Jordanova, Peter De Jonghe

Journal:

Journal of Neurology

Year:

2011

Language:

english

File:

PDF, 395 KB

english, 2011

22

Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous

Gregor Kuhlenbäumer, Jan Meuleman, Peter De Jonghe, Björn Falck, Peter Young, Gert Hünermund, Christine Van Broeckhoven, Vincent Timmerman, Florian Stögbauer

Journal:

Journal of Neurology

Year:

2001

Language:

english

File:

PDF, 218 KB

english, 2001

23

Refinement of the hereditary neuralgic amyotrophy (HNA) locus to chromosome 17q24–q25

F. Stögbauer, Peter Young, Vincent Timmerman, Petra Spoelders, E. Bernd Ringelstein, Christine Van Broeckhoven, Gerd Kurlemann

Journal:

Year:

1997

Language:

english

File:

PDF, 43 KB

english, 1997

24

Juvenile open angle glaucoma: fine mapping of the TIGR gene to 1q24.3–q25.2 and mutation analysis

Karin G. Michels-Rautenstrauss, Christian Y. Mardin, Wido M. Budde, Thomas Liehr, J. Polansky, Thai Nguyen, Vincent Timmerman, C. Van Broeckhoven, Gottfried O. H. Naumann, Rudolf A. Pfeiffer, B. W. Ra

Journal:

Year:

1998

Language:

english

File:

PDF, 132 KB

english, 1998

25

Humoral immunodeficiency in congenital insensitivity to pain with anhidrosis

Sara Sebnem Kilic, Rifatcan Ozturk, Bartu Sarisozen, Annelies Rotthier, Jonathan Baets, Vincent Timmerman

Journal:

Year:

2009

Language:

english

File:

PDF, 145 KB

english, 2009

26

A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associated

Thorsten Hornemann, Anke Penno, Stephane Richard, Garth Nicholson, Fleur S. van Dijk, Annelies Rotthier, Vincent Timmerman, Arnold von Eckardstein

Journal:

Year:

2009

Language:

english

File:

PDF, 238 KB

english, 2009

27

L239F founder mutation inGDAP1is associated with a mild Charcot–Marie–Tooth type 4C4 (CMT4C4) phenotype

Dagmara Kabzińska, Halina Strugalska-Cynowska, Anna Kostera-Pruszczyk, Barbara Ryniewicz, Renata Posmyk, Alina Midro, Pavel Seeman, Lucia Báranková, Magdalena Zimoń, Jonathan Baets, Vincent Timmerman,

Journal:

Year:

2010

Language:

english

File:

PDF, 417 KB

english, 2010

28

Hereditary neuralgic amyotrophy

Jan Meuleman, Vincent Timmerman, Christine Van Broeckhoven, Peter De Jonghe

Journal:

Year:

2001

Language:

english

File:

PDF, 30 KB

english, 2001

29

Genetics of motor neuron disease

Ludo Van Den Bosch, Vincent Timmerman

Journal:

Current Neurology and Neuroscience Reports

Year:

2006

Language:

english

File:

PDF, 213 KB

english, 2006

30

Increased axonal ribosome numbers in CMT diseases

Mark H. G. Verheijen, Martin Lammens, Chantal Ceuterick-de Groote, Vincent Timmerman, Peter De Jonghe, Rosalind H. M. King, August B. Smit, Jan van Minnen

Journal:

Journal of the Peripheral Nervous System

Year:

2011

Language:

english

File:

PDF, 554 KB

english, 2011

31

Construction of a PAC Contig within the Distal Hereditary Motor Neuropathy Type II Candidate Region at 12q24

JOY IROBI, VINCENT TIMMERMAN, PETER De JONGHE, ELS De VRIENDT, CHRISTINE VAN BROECKHOVEN, J. BEUTEN

Journal:

Annals of the New York Academy of Sciences

Year:

1999

File:

PDF, 207 KB

1999

32

Charcot-Marie-Tooth Neuropathy Type 2 and P0 Point Mutations: Two Novel Amino Acid Substitutions (Asp61Gly; Tyr119Cys) and a Possible “Hotspot” on Thr124Met

Jan Senderek, Benita Hermanns, Ute Lehmann, Carsten Bergmann, Georg Marx, Christian Kabus, Vincent Timmerman, Gisela Stoltenburg-Didinger, J. Michael Schröder

Journal:

Brain Pathology

Year:

2000

Language:

english

File:

PDF, 264 KB

english, 2000

33

10.1038/81521

Timmerman, Vincent, De Jonghe, Peter, Van Broeckhoven, Christine

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 291 KB

english, 2000

34

Clinical utility gene card for: HMSN/HNPP HMSN types 1, 2, 3, 6 (CMT1,2,4, DSN, CHN, GAN, CCFDN, HNA); HNPP

Aretz, Stefan, Rautenstrauß, Bernd, Timmerman, Vincent

Journal:

European Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 150 KB

english, 2010

35

Anti-steroid takes aim at neuropathy

De Jonghe, Peter, Timmerman, Vincent

Journal:

Nature Medicine

Year:

2003

Language:

english

File:

PDF, 245 KB

english, 2003

36

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21

Ismailov, Shoukhrat M, Fedotov, Valeriy P, Dadali, Elena L, Polyakov, Alexander V, Van Broeckhoven, Christine, Ivanov, Vladimir I, De Jonghe, Peter, Timmerman, Vincent, Evgrafov, Oleg V

Journal:

European Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 113 KB

english, 2001

37

Unraveling the genetics of distal hereditary motor neuronopathies

Joy Irobi, Ines Dierick, Albena Jordanova, Kristl G. Clayes, Peter De Jonghe, Vincent Timmerman

Journal:

NeuroMolecular Medicine

Year:

2006

Language:

english

File:

PDF, 281 KB

english, 2006

38

Molecular genetics, biology, and therapy for inherited peripheral neuropathies

Vincent Timmerman, James R. Lupski, Peter De Jonghe

Journal:

NeuroMolecular Medicine

Year:

2006

Language:

english

File:

PDF, 49 KB

english, 2006

39

Microtubule dynamics in the peripheral nervous system: A matter of balance

Almeida-Souza, Leonardo, Timmerman, Vincent, Janssens, Sophie

Journal:

BioArchitecture

Year:

2011

Language:

english

File:

PDF, 864 KB

english, 2011

40

HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1–induced Charcot-Marie-Tooth disease

d'Ydewalle, Constantin, Krishnan, Jyothsna, Chiheb, Driss M, Van Damme, Philip, Irobi, Joy, Kozikowski, Alan P, Berghe, Pieter Vanden, Timmerman, Vincent, Robberecht, Wim, Van Den Bosch, Ludo

Journal:

Nature Medicine

Year:

2011

Language:

english

File:

PDF, 1.00 MB

english, 2011

41

Drosophilaas a platform to predict the pathogenicity of novel aminoacyl-tRNA synthetase mutations in CMT

Ricardo Leitão-Gonçalves, Biljana Ermanoska, An Jacobs, Els De Vriendt, Vincent Timmerman, James R. Lupski, Patrick Callaerts, Albena Jordanova

Journal:

Year:

2012

Language:

english

File:

PDF, 539 KB

english, 2012

42

Search for mutations in the EGR2 corepressor proteins, NAB1 and NAB2, in human peripheral neuropathies

Timmerman, Vincent, De Jonghe, Peter, Bellone, Emilia, Mandich, Paola, Cassandrini, Denise, Venken, Koen, Balestra, Piercesare, Di Maria, Emilio, Svaren, John

Journal:

Year:

2002

Language:

english

File:

PDF, 38 KB

english, 2002

43

Autosomal-Dominant Striatal Degeneration Is Caused by a Mutation in the Phosphodiesterase 8B Gene

Silke Appenzeller, Anja Schirmacher, Hartmut Halfter, Sebastian Bäumer, Manuela Pendziwiat, Vincent Timmerman, Peter De Jonghe, Klára Fekete, Florian Stögbauer, Peter Lüdemann, Margret Hund, Elgar Sus

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 448 KB

english, 2010

44

Major dietary patterns and blood pressure patterns during pregnancy: the Generation R Study

Sarah Timmermans, Régine P.M. Steegers-Theunissen, Marijana Vujkovic, Rachel Bakker, Hanneke den Breeijen, Hein Raat, Henk Russcher, Jan Lindemans, Albert Hofman, Vincent W.V. Jaddoe, Eric A.P. Steege

Journal:

American Journal of Obstetrics and Gynecology

Year:

2011

Language:

english

File:

PDF, 914 KB

english, 2011

45

Disease mechanisms in hereditary sensory and autonomic neuropathies

Nathalie Verpoorten, Peter De Jonghe, Vincent Timmerman

Journal:

Neurobiology of Disease

Year:

2006

Language:

english

File:

PDF, 211 KB

english, 2006

46

A Sequence-Ready BAC/PAC Contig and Partial Transcript Map of Approximately 1.5 Mb in Human Chromosome 17q25 Comprising Multiple Disease Genes

Gregor Kuhlenbäumer, , Anja Schirmacher, , Jan Meuleman, Fadel Tissir, Jurgen Del-Favero, Florian Stögbauer, Peter Young, Bernd Ringelstein, Christine Van Broeckhoven, Vincent Timmerman

Journal:

Year:

1999

Language:

english

File:

PDF, 159 KB

english, 1999

47

A Clone Contig of 12q24.3 Encompassing the Distal Hereditary Motor Neuropathy Type II Gene

Joy Irobi, Fadel Tissir, Peter De Jonghe, Els De Vriendt, Christine Van Broeckhoven, Vincent Timmerman, Joke Beuten

Journal:

Year:

2000

Language:

english

File:

PDF, 178 KB

english, 2000

48

Exome Sequencing Identifies a REEP1 Mutation Involved in Distal Hereditary Motor Neuropathy Type V

Christian Beetz, Thomas R. Pieber, Nicole Hertel, Maria Schabhüttl, Carina Fischer, Slave Trajanoski, Elisabeth Graf, Silke Keiner, Ingo Kurth, Thomas Wieland, Rita-Eva Varga, Vincent Timmerman, Mary

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 588 KB

english, 2012

49

Middelheim Fabry Study (MiFaS): A retrospective Belgian study on the prevalence of Fabry disease in young patients with cryptogenic stroke

Raf Brouns, Rishi Sheorajpanday, Ellen Braxel, François Eyskens, Robert Baker, Derralynn Hughes, Atul Mehta, Therese Timmerman, Marie-Françoise Vincent, Peter Paul De Deyn

Journal:

Clinical Neurology and Neurosurgery

Year:

2007

Language:

english

File:

PDF, 245 KB

english, 2007

50

The fate of biogenic iron during a phytoplankton bloom induced by natural fertilisation: Impact of copepod grazing

Géraldine Sarthou, Dorothée Vincent, Urania Christaki, Ingrid Obernosterer, Klaas R. Timmermans, Corina P.D. Brussaard

Journal:

Deep Sea Research Part II: Topical Studies in Oceanography

Year:

2008

Language:

english

File:

PDF, 552 KB

english, 2008

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