de Jonghe, Peter: search on Z-Library

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1

The evaluation of bacterial biosensors for screening of water pollutants

François M. van Hoof, Els G. de Jonghe, Michael G. Briers, Peter D. Hansen, Hans J. Pluta, David M. Rawson, Allison J. Wilmer

Journal:

Environmental Toxicology

Year:

1992

Language:

english

File:

PDF, 574 KB

english, 1992

2

Recent Developments in the Synthesis of Supported Catalysts

Munnik, Peter, de Jongh, Petra E., de Jong, Krijn P.

Journal:

Chemical Reviews

Year:

2015

Language:

english

File:

PDF, 29.61 MB

english, 2015

3

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

4

Reversible ammonia-based and liquid organic hydrogen carriers for high-density hydrogen storage: Recent progress

Makepeace, Joshua W., He, Teng, Weidenthaler, Claudia, Jensen, Torben R., Chang, Fei, Vegge, Tejs, Ngene, Peter, Kojima, Yoshitsugu, de Jongh, Petra E., Chen, Ping, David, William I.F.

Journal:

International Journal of Hydrogen Energy

Year:

2019

File:

PDF, 2.25 MB

2019

5

One-session cognitive treatment of dental phobia: preparing dental phobics for treatment by restructuring negative cognitions

Ad De Jongh, Peter Muris, Guusje Ter Horst, Florence Van Zuuren, Nelleke Schoenmakers, Peter Makkes

Journal:

Behaviour Research and Therapy

Year:

1995

Language:

english

File:

PDF, 726 KB

english, 1995

6

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

7

Molecular consequences of dominant Bethlem myopathy collagen VI mutations

Naomi L. Baker, Matthias Mörgelin, Rishika A. Pace, Rachel A. Peat, Naomi E. Adams, R. J. McKinlay Gardner, Lewis P. Rowland, Geoffrey Miller, Peter De Jonghe, Berten Ceulemans, Mark C. Hannibal, Matt

Journal:

Annals of Neurology

Year:

2007

Language:

english

File:

PDF, 479 KB

english, 2007

8

The adsorption and unfolding kinetics determines the folding state of proteins at the air–water interface and thereby the equation of state

Peter A. Wierenga, Maarten R. Egmond, Alphons G.J. Voragen, Harmen H.J. de Jongh

Journal:

Journal of Colloid and Interface Science

Year:

2006

Language:

english

File:

PDF, 278 KB

english, 2006

9

The genetics of Dravet syndrome

Carla Marini, Ingrid E. Scheffer, Rima Nabbout, Arvid Suls, Peter De Jonghe, Federico Zara, Renzo Guerrini

Journal:

Year:

2011

Language:

english

File:

PDF, 75 KB

english, 2011

10

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

Hayer, Stefanie Nicole, Deconinck, Tine, Bender, Benjamin, Smets, Katrien, Züchner, Stephan, Reich, Selina, Schöls, Ludger, Schüle, Rebecca, De Jonghe, Peter, Baets, Jonathan, Synofzik, Matthis

Journal:

Orphanet Journal of Rare Diseases

Year:

2017

Language:

english

File:

PDF, 1.45 MB

english, 2017

11

Disgust sensitivity, blood–injection–injury fear, and dental anxiety

Harald Merckelbach, Peter Muris, Peter J. de Jong, Ad de Jongh

Journal:

Clinical Psychology & Psychotherapy

Year:

1999

Language:

english

File:

PDF, 88 KB

english, 1999

12

A Role of SCN9A in Human Epilepsies, As a Cause of Febrile Seizures and As a Potential Modifier of Dravet Syndrome

Singh, Nanda A., Pappas, Chris, Dahle, E. Jill, Claes, Lieve R. F., Pruess, Timothy H., De Jonghe, Peter, Thompson, Joel, Dixon, Missy, Gurnett, Christina, Peiffer, Andy, White, H. Steve, Filloux, Fra

Journal:

Year:

2009

Language:

english

File:

PDF, 2.62 MB

english, 2009

13

Geen zin meer in seks? Denk aan psychisch trauma!

Jacqueline van Groot,prof.dr. Ad de Jongh,Peter Leusink

Journal:

Huisarts en wetenschap

Year:

2013

Language:

dutch

File:

PDF, 3.65 MB

dutch, 2013

14

Right-handers can be made to think like lefties

Van Langenhove, Tim, Engelborghs, Sebastiaan, Vandenberghe, Rik, Santens, Patrick, Cras, Patrick, Nuytten, Dirk, De Jonghe, Peter, De Deyn, Peter P., Cruts, Marc, Van Broeckhoven, Christine, van der Z

Journal:

Year:

2011

Language:

english

File:

PDF, 410 KB

english, 2011

15

Control and Impact of the Nanoscale Distribution of Supported Cobalt Particles Used in Fischer–Tropsch Catalysis

Munnik, Peter, de Jongh, Petra E., de Jong, Krijn P.

Journal:

Journal of the American Chemical Society

Year:

2014

Language:

english

File:

PDF, 9.30 MB

english, 2014

16

The effect of calcium dobesilate on vascular endothelial function, blood pressure, and markers of oxidation in obese male smokers: a placebo-controlled randomised clinical trial

Miranda T. Schram, Frank Stam, Renate T. de Jongh, Greetje de Vries, Rob A.J.M. van Dijk, Erik H. Serné, Deva Lampe, Prabath W.B. Nanayakkara, Maarten E. Tushuizen, Peter G. Scheffer, Casper G. Schalk

Journal:

Atherosclerosis

Year:

2003

Language:

english

File:

PDF, 339 KB

english, 2003

17

Reversible ammonia-based and liquid organic hydrogen carriers for high-density hydrogen storage: Recent progress

Makepeace, Joshua W., He, Teng, Weidenthaler, Claudia, Jensen, Torben R., Chang, Fei, Vegge, Tejs, Ngene, Peter, Kojima, Yoshitsugu, de Jongh, Petra E., Chen, Ping, David, William I.F.

Journal:

International Journal of Hydrogen Energy

Year:

2019

Language:

english

File:

PDF, 2.25 MB

english, 2019

18

Hereditary neuralgic amyotrophy

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

Journal:

Year:

2001

Language:

english

File:

PDF, 30 KB

english, 2001

19

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

20

Unusual Aß amyloid deposition in Alzheimer's disease due to an APP T7141 mutation at the γ42-secretase site

Chris De Jonghe, Samir Kumar-Singh, Marc Cruts, Reinhold Kleinert, Hugo Vanderstichele, Eugeen J.M. Vanmechelen, Peter Kroisel, Christine Van Broeckhoven

Journal:

Neurobiology of Aging

Year:

2000

Language:

english

File:

PDF, 194 KB

english, 2000

21

Deciphering the genetic basis of Moraxella catarrhalis complement resistance: a critical role for the disulphide bond formation system

de Vries, Stefan P. W., Rademakers, Rob J. A., van der Gaast-de Jongh, Christa E., Eleveld, Marc J., Hermans, Peter W. M., Bootsma, Hester J.

Journal:

Molecular Microbiology

Year:

2014

Language:

english

File:

PDF, 504 KB

english, 2014

22

Obese But Not Normal-Weight Women With Polycystic Ovary Syndrome Are Characterized by Metabolic and Microvascular Insulin Resistance

Ketel, Iris J. G., Stehouwer, Coen D. A., Serné, Erik H., Korsen, Ted J. M., Hompes, Peter G. A., Smulders, Yvo M., de Jongh, Renate T., Homburg, Roy, Lambalk, Cornelis B.

Journal:

Obstetric and Gynecologic Survey

Year:

2009

Language:

english

File:

PDF, 621 KB

english, 2009

23

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

24

Epilepsy as part of the phenotype associated with ATP1A2 mutations

Liesbet Deprez, Sarah Weckhuysen, Katelijne Peeters, Tine Deconinck, Kristl G. Claeys, Lieve R.F. Claes, Arvid Suls, Tine Van Dyck, André Palmini, Gert Matthijs, Wim Van Paesschen, Peter De Jonghe

Journal:

Year:

2008

Language:

english

File:

PDF, 244 KB

english, 2008

25

Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation

Lubov Blumkin, Arvid Suls, Tine Deconinck, Peter De Jonghe, Ilan Linder, Sara Kivity, Ron Dabby, Esther Leshinsky-Silver, Dorit Lev, Tally Lerman-Sagie

Journal:

European Journal of Paediatric Neurology

Year:

2012

Language:

english

File:

PDF, 629 KB

english, 2012

26

Toxicokinetics of an environmentally relevant mixture of dioxin-like PHAHs with or without a non-dioxin-like PCB in a semi-chronic exposure study in female sprague Dawley rats

Simone A. van der Plas, Joost de Jongh, Maria Faassen-Peters, Gunilla Scheu, Martin van den Berg, Abraham Brouwer

Journal:

Year:

1998

Language:

english

File:

PDF, 999 KB

english, 1998

27

2nd Workshop of the European CMT Consortium: 53rd ENMC International Workshop on Classification and Diagnostic Guidelines for Charcot-Marie-Tooth Type 2 (CMT2–HMSN II) and Distal Hereditary Motor Neuropathy (Distal HMN–Spinal CMT): 26–28 September 1997, Naarden, The Netherlands

Peter De Jonghe, Vincent Timmerman, Christine Van Broeckhoven

Journal:

Neuromuscular Disorders

Year:

1998

Language:

english

File:

PDF, 51 KB

english, 1998

28

Localization of the Gene for the Intermediate Form of Charcot-Marie-Tooth to Chromosome 10q24.1-q25.1

Kristien Verhoeven, Marcello Villanova, Alessandro Rossi, Alessandro Malandrini, Peter De Jonghe, Vincent Timmerman

Journal:

The American Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 725 KB

english, 2001

29

Autosomal Dominant Inherited Neuropathies With Prominent Sensory Loss and Mutilations

Auer-Grumbach, Michaela, De Jonghe, Peter, Verhoeven, Kristien, Timmerman, Vincent, Wagner, Klaus, Hartung, Hans-Peter, Nicholson, Garth A.

Journal:

Archives of Neurology

Year:

2003

Language:

english

File:

PDF, 90 KB

english, 2003

30

Caspr1/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies

Venken, Koen, Meuleman, Jan, Irobi, Joy, Ceuterick, Chantal, Martini, Rudolf, De Jonghe, Peter, Timmerman, Vincent

Journal:

Year:

2001

Language:

english

File:

PDF, 437 KB

english, 2001

31

Recent advances in hereditary sensory and autonomic neuropathies

Verhoeven, Kristien, Timmerman, Vincent, Mauko, Barbara, Pieber, Thomas R, De Jonghe, Peter, Auer-Grumbach, Michaela

Journal:

Current Opinion in Neurology

Year:

2006

Language:

english

File:

PDF, 126 KB

english, 2006

32

A Novel Type of Hereditary Motor and Sensory Neuropathy Characterized by a Mild Phenotype

De Jonghe, Peter, Timmerman, Vincent, Nelis, Eva, De Vriendt, Els, Löfgren, Ann, Ceuterick, Chantal, Martin, Jean-Jacques, Van Broeckhoven, Christine

Journal:

Archives of Neurology

Year:

1999

Language:

english

File:

PDF, 304 KB

english, 1999

33

Confinement Effects for Lithium Borohydride: Comparing Silica and Carbon Scaffolds

Suwarno,, Ngene, Peter, Nale, Angeloclaudio, Eggenhuisen, Tamara M., Oschatz, Martin, Embs, Jan Peter, Remhof, Arndt, de Jongh, Petra E.

Journal:

The Journal of Physical Chemistry C

Year:

2017

Language:

english

File:

PDF, 1.42 MB

english, 2017

34

Uniparental disomy determined by whole-exome sequencing in a spectrum of rare motoneuron diseases and ataxias

Bis, Dana M., Schüle, Rebecca, Reichbauer, Jennifer, Synofzik, Matthis, Rattay, Tim W., Soehn, Anne, de Jonghe, Peter, Schöls, Ludger, Züchner, Stephan

Journal:

Molecular Genetics & Genomic Medicine

Year:

2017

Language:

english

File:

PDF, 712 KB

english, 2017

35

Multisystem proteinopathy due to a homozygous p.Arg159His VCP mutation

De Ridder, Willem, Azmi, Abdelkrim, Clemen, Christoph S., Eichinger, Ludwig, Hofmann, Andreas, Schröder, Rolf, Johnson, Katherine, Töpf, Ana, Straub, Volker, De Jonghe, Peter, Maudsley, Stuart, De Ble

Journal:

Year:

2019

Language:

english

File:

PDF, 786 KB

english, 2019

36

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

37

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

38

Genotype–phenotype analysis in patients with giant axonal neuropathy (GAN)

Olga Koop, Anja Schirmacher, Eva Nelis, Vincent Timmerman, Peter De Jonghe, Bernd Ringelstein, Vedrana Milic Rasic, Philippe Evrard, Jutta Gärtner, Kristl G. Claeys, Silke Appenzeller, Bernd Rautenstr

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 200 KB

english, 2007

39

Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection

Gregor Kuhlenbäumer, Florian Stögbauer, Vincent Timmerman, Peter De Jonghe

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 44 KB

english, 2000

40

The clinical presentation of C9orf72-associated frontotemporal lobar degeneration in an extended Flanders-Belgian cohort

Tim Van Langenhove, Julie van der Zee, Ilse Gijselinck, Sebastiaan Engelborghs, Rik Vandenberghe, Anne Sieben, Patrick Santens, Peter De Jonghe, Patrick Cras, Peter P. De Deyn, Marc Cruts, Christine V

Journal:

Alzheimer's & Dementia

Year:

2012

Language:

english

File:

PDF, 55 KB

english, 2012

41

Nanoconfined LiBH 4 and Enhanced Mobility of Li + and BH 4– Studied by Solid-State NMR

Verkuijlen, Margriet H. W., Ngene, Peter, de Kort, Daan W., Barré, Charlotte, Nale, Angeloclaudio, van Eck, Ernst R. H., van Bentum, P. Jan M., de Jongh, Petra E., Kentgens, Arno P. M.

Journal:

The Journal of Physical Chemistry C

Year:

2012

Language:

english

File:

PDF, 1.53 MB

english, 2012

42

Genetic epileptic encephalopathies: Is all written into the DNA?

Striano, Pasquale, de Jonghe, Peter, Zara, Federico

Journal:

Year:

2013

Language:

english

File:

PDF, 66 KB

english, 2013

43

Exome sequencing reveals HINT1 mutations as a cause of distal hereditary motor neuropathy

Zhao, Hui, Race, Valérie, Matthijs, Gert, De Jonghe, Peter, Robberecht, Wim, Lambrechts, Diether, Van Damme, Philip

Journal:

European Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 398 KB

english, 2014

44

Novel Mutations in the DYNC1H1 Tail Domain Refine the Genetic and Clinical Spectrum of Dyneinopathies

Peeters, Kristien, Bervoets, Sven, Chamova, Teodora, Litvinenko, Ivan, De Vriendt, Els, Bichev, Stoyan, Kancheva, Dahlia, Mitev, Vanyo, Kennerson, Marina, Timmerman, Vincent, De Jonghe, Peter, Tournev

Journal:

Year:

2015

Language:

english

File:

PDF, 555 KB

english, 2015

45

Obese But Not Normal-Weight Women with Polycystic Ovary Syndrome Are Characterized by Metabolic and Microvascular Insulin Resistance

Ketel, Iris J. G., Stehouwer, Coen D. A., Serné, Erik H., Korsen, Ted J. M., Hompes, Peter G. A., Smulders, Yvo M., de Jongh, Renate T., Homburg, Roy, Lambalk, Cornelis B.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2008

Language:

english

File:

PDF, 199 KB

english, 2008

46

Charcot-Marie-Tooth disease type 2G redefined by a novel mutation in LRSAM1

Peeters, Kristien, Palaima, Paulius, Pelayo-Negro, Ana L., García, Antonio, Gallardo, Elena, García-Barredo, Rosario, Mateiu, Ligia, Baets, Jonathan, Menten, Björn, De Vriendt, Els, De Jonghe, Peter,

Journal:

Annals of Neurology

Year:

2016

Language:

english

File:

PDF, 510 KB

english, 2016

47

Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders

Lal, Dennis, May, Patrick, Perez-Palma, Eduardo, Samocha, Kaitlin E., Kosmicki, Jack A., Robinson, Elise B., MÃ¸ller, Rikke S., Krause, Roland, NÃ¼rnberg, Peter, Weckhuysen, Sarah, De Jonghe, Peter, G

Journal:

Genome Medicine

Year:

2020

Language:

english

File:

PDF, 1.61 MB

english, 2020

48

Prognostic factors for medical and productivity costs, and return to work after trauma

de Munter, Leonie, Geraerds, A. J. L. M., de Jongh, Mariska A. C., van der Vlegel, Marjolein, Steyerberg, Ewout W., Haagsma, Juanita A., Polinder, Suzanne, Simmen, Hans-Peter

Journal:

Year:

2020

Language:

english

File:

PDF, 913 KB

english, 2020

49

SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve

Craig L. Bennett, Andrew J. Shirk, Huy M. Huynh, Valerie A. Street, Eva Nelis, Lionel Van Maldergem, Peter De Jonghe, Albena Jordanova, Velina Guergueltcheva, Ivailo Tournev, Peter Van den Bergh, Pave

Journal:

Annals of Neurology

Year:

2004

Language:

english

File:

PDF, 985 KB

english, 2004

50

Reply

Saul A. Mullen, Arvid Suls, Peter De Jonghe, Samuel F. Berkovic, Ingrid E. Scheffer

Journal:

Annals of Neurology

Year:

2010

Language:

english

File:

PDF, 51 KB

english, 2010

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