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1

Helpers' Self-Assessment Biases Before and after Helping Skills Training

Jaeken, Marine, Zech, Emmanuelle, Brison, Céline, Verhofstadt, Lesley L., Van Broeck, Nady, Mikolajczak, Moïra

Journal:

Frontiers in Psychology

Year:

2017

Language:

english

File:

PDF, 794 KB

english, 2017

2

The coherence of life: A new physiology challenging (neo)Darwinism

Journal:

Chaos, Solitons & Fractals

Year:

2009

Language:

english

File:

PDF, 242 KB

english, 2009

3

Overview of on-farm bioremediation systems to reduce the occurrence of point source contamination

Tineke De Wilde, Pieter Spanoghe, Christof Debaer, Jaak Ryckeboer, Dirk Springael, Peter Jaeken

Journal:

Pest Management Science

Year:

2007

Language:

english

File:

PDF, 268 KB

english, 2007

4

Marden-Walker syndrome: case report, literature review and nosologic discussion

Constance Schrander-Stumpel, Christine de Die-Smulders, Marc de Krom, Suzanne Schyns-Fleuren, Ben Hamel, Deni Jaeken, Jean-Pierre Fryns

Journal:

Clinical Genetics

Year:

1993

Language:

english

File:

PDF, 1.28 MB

english, 1993

5

Encounter groups: do they foster psychology students’ psychological development and therapeutic attitudes?

Brison, Céline, Zech, Emmanuelle, Jaeken, Marine, Priels, Jean-Marc, Verhofstadt, Lesley, Van Broeck, Nady, Mikolajczak, Moïra

Journal:

Person-Centered & Experiential Psychotherapies

Year:

2015

Language:

english

File:

PDF, 206 KB

english, 2015

6

Beneficial effects of L-serine and glycine in the management of seizures in 3-phosphoglycerate dehydrogenase deficiency

Dr. Tom J. de Koning, Marinus Duran, Lambertus Dorland, Rob Gooskens, Emile van Schaftingen, Jaak Jaeken, Nenad Blau, Ruud Berger, Bwee Tien Poll-The

Journal:

Annals of Neurology

Year:

1998

Language:

english

File:

PDF, 435 KB

english, 1998

7

Psychological symptoms and sleep disturbances in neuronal ceroid-lipofuscinoses (NCL)

P. Santavuori, T. Linnankivi, J. Jaeken, S. -L. Vanhanen, T. Telakivi, H. Heiskala

Journal:

Journal of Inherited Metabolic Disease

Year:

1993

Language:

english

File:

PDF, 258 KB

english, 1993

8

Improvement of pesticide mineralization in on-farm biopurification systems by bioaugmentation with pesticide-primed soil

Kristel Sniegowski, Karolien Bers, Kris Van Goetem, Jaak Ryckeboer, Peter Jaeken, Pieter Spanoghe, Dirk Springael

Journal:

FEMS Microbiology Ecology

Year:

2011

Language:

english

File:

PDF, 309 KB

english, 2011

9

Characterizing pesticide sorption and degradation in microscale biopurification systems using column displacement experiments

Tineke De Wilde, Jan Mertens, Jirka Šimunek, Kristel Sniegowksi, Jaak Ryckeboer, Peter Jaeken, Dirk Springael, Pieter Spanoghe

Journal:

Environmental Pollution

Year:

2009

Language:

english

File:

PDF, 1.08 MB

english, 2009

10

D,L-3-hydroxybutyrate treatment of multiple acyl-CoA dehydrogenase deficiency (MADD)

Johan LK Van Hove, Stephanie Grünewald, Jaak Jaeken, Philippe Demaerel, Peter E Declercq, Pierre Bourdoux, Klary Niezen-Koning, John E Deanfeld, James V Leonard

Journal:

Year:

2003

Language:

english

File:

PDF, 467 KB

english, 2003

11

CFD prototyping of an air-assisted orchard sprayer aimed at drift reduction

M.A. Delele, P. Jaeken, C. Debaer, K. Baetens, A. Melese Endalew, H. Ramon, B.M Nicolaï, P. Verboven

Journal:

Computers and Electronics in Agriculture

Year:

2007

Language:

english

File:

PDF, 612 KB

english, 2007

12

A novel mutation and first report of dilated cardiomyopathy in ALG6-CDG (CDG-Ic): a case report

Mohammed Al-Owain, Sarar Mohamed, Namik Kaya, Ahmad Zagal, Gert Matthijs, Jaak Jaeken

Journal:

Orphanet Journal of Rare Diseases

Year:

2010

Language:

english

File:

PDF, 540 KB

english, 2010

13

A novel mutation causing mild, atypical fumarylacetoacetase deficiency (Tyrosinemia type I): a case report

David Cassiman, Renate Zeevaert, Elisabeth Holme, Eli-Anne Kvittingen, Jaak Jaeken

Journal:

Orphanet Journal of Rare Diseases

Year:

2009

Language:

english

File:

PDF, 1.36 MB

english, 2009

14

Comparison of the Optical Image Quality in the Periphery of Phakic and Pseudophakic Eyes

Jaeken, Bart, Mirabet, Sandra, Marín, José María, Artal, Pablo

Journal:

Investigative Ophthalmology & Visual Science

Year:

2013

Language:

english

File:

PDF, 675 KB

english, 2013

15

Glycosylation abnormalities in Gdt1p/TMEM165 deficient cells result from a defect in Golgi manganese homeostasis

Potelle, Sven, Morelle, Willy, Dulary, Eudoxie, Duvet, Sandrine, Vicogne, Dorothée, Spriet, Corentin, Krzewinski-Recchi, Marie-Ange, Morsomme, Pierre, Jaeken, Jaak, Matthijs, Gert, De Bettignies, Geof

Journal:

Human Molecular Genetics

Year:

2016

Language:

english

File:

PDF, 1.11 MB

english, 2016

16

Childhood Pompe disease: clinical spectrum and genotype in 31 patients

van Capelle, C. I., van der Meijden, J. C., van den Hout, J. M. P., Jaeken, J., Baethmann, M., Voit, T., Kroos, M. A., Derks, T. G. J., Rubio-Gozalbo, M. E., Willemsen, M. A., Lachmann, R. H., Mengel,

Journal:

Orphanet Journal of Rare Diseases

Year:

2016

Language:

english

File:

PDF, 1.71 MB

english, 2016

17

PIGO deficiency: palmoplantar keratoderma and novel mutations

Marie-Anne Morren,Jaak Jaeken,Gepke Visser…

Journal:

Orphanet Journal of Rare Diseases

Year:

2017

Language:

english

File:

PDF, 5.32 MB

english, 2017

18

Keeping an eye on congenital disorders of O-glycosylation: a systematic literature review

Francisco, R., Pascoal, C., Marques-da-Silva, D., Morava, E., Gole, G. A., Coman, D., Jaeken, J., dos Reis Ferreira, Vanessa

Journal:

Journal of Inherited Metabolic Disease

Year:

2018

Language:

english

File:

PDF, 1.06 MB

english, 2018

19

Reference Module in Biomedical Sciences || Glycosylation and its Disorders: General Overview☆

Year:

2016

Language:

english

File:

PDF, 1.07 MB

english, 2016

20

Patient and observer reported outcome measures to evaluate health-related quality of life in inherited metabolic diseases: a scoping review

Pascoal, Carlota, Brasil, Sandra, Francisco, Rita, Marques-da-Silva, Dorinda, Rafalko, Agnes, Jaeken, Jaak, Videira, Paula A., Barros, Luísa, dos Reis Ferreira, Vanessa

Journal:

Orphanet Journal of Rare Diseases

Year:

2018

File:

PDF, 759 KB

2018

21

Hardikar syndrome: A new syndrome with cleft lip/palate, pigmentary retinopathy and cholestasis

Cools, F., Jaeken, J.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 74 KB

english, 1997

22

Carbohydrate-deficient glycoprotein syndrome due to phosphomannomutase deficiency: The first reported cases from Latin America

de Michelena, Maria Isabel, Franchi, Luis Miguel, Summers, Percy G., De La Fuente, Carlos, Campos, Patricia J., Jaeken, Jaak

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 198 KB

english, 1999

23

Mutation analysis in adenylosuccinate lyase deficiency: Eight novel mutations in the re-evaluated full ADSL coding sequence

Sandrine Marie, Harry Cuppens, Michel Heuterspreute, Martine Jaspers, Eduardo Zambrano Tola, Xiao Xiao Gu, Eric Legius, M.-Françoise Vincent, Jaak Jaeken, Jean-Jacques Cassiman, Georges Van den Berghe

Journal:

Year:

1999

Language:

english

File:

PDF, 282 KB

english, 1999

24

Detection of two novel large deletions in SLC3A1 by semi-quantitative fluorescent multiplex PCR

Jesús Purroy, Luigi Bisceglia, Jaak Jaeken, Paolo Gasparini, Manuel Palacín, Virginia Nunes

Journal:

Year:

2000

Language:

english

File:

PDF, 265 KB

english, 2000

25

Isolated central form of tetrahydrobiopterin deficiency associated with hemizygosity on chromosome 11q and a mutant allele of PTPS

Nenad Blau, Tanja Scherer-Oppliger, Alessandra Baumer, Mariluce Riegel, Ana Matasovic, Albert Schinzel, Jaak Jaeken, Beat Thöny

Journal:

Year:

2000

Language:

english

File:

PDF, 261 KB

english, 2000

26

Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesis

S. Grünewald, T. Imbach, K. Huijben, M. E. Rubio-Gozalbo, A. Verrips, J. B. C. De Klerk, H. Stroink, J. F. De Rijk-Van Andel, J. L. K. Van Hove, U. Wendel, G. Matthijs, T. Hennet, J. Jaeken, R. A. Wev

Journal:

Annals of Neurology

Year:

2000

Language:

english

File:

PDF, 1.26 MB

english, 2000

27

Band 3 glycoprotein and glycophorin A from erythrocytes of children with congenital disorder of glycosylation type-Ia are underglycosylated

Ewa Zdebska, Małlgorzata Musielak, Jaak Jaeken, Jerzy Kościelak

Journal:

Year:

2001

Language:

english

File:

PDF, 105 KB

english, 2001

28

Restrictive dermopathy with distinct morphological abnormalities

Marie-Rose van Hoestenberghe, Eric Legius, Wim Vandevoorde, Albert Eykens, Jaak Jaeken, Ephrem Eggermont, Rita Devos, Chris De Wolf-Peeters, Jean-Pierre Fryns

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 618 KB

english, 1990

29

Clericuzio type poikiloderma with neutropenia is distinct from Rothmund–Thomson syndrome

Johan L.K. Van Hove, Jaak Jaeken, Marijke Proesmans, Kris De Boeck, Kristin Minner, Gert Matthijs, Eric Verbeken, Anouk Demunter, Marc Boogaerts

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 319 KB

english, 2005

30

A previously undescribed form of congenital disorder of glycosylation with variable presentation in siblings: Early fetal loss with hydrops fetalis, and infant death with hypoproteinemia

F.A. McKenzie, M. Fietz, J. Fletcher, R.L.L. Smith, I.M.R. Wright, J. Jaeken

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 160 KB

english, 2007

31

Primary skeletal dysplasia as a major manifesting feature in an infant with congenital disorder of glycosylation type Ia

D. Coman, D. Bostock, M. Hunter, P. Kannu, M. Irving, V. Mayne, M. Fietz, J. Jaeken, R. Savarirayan

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 179 KB

english, 2008

32

Geroderma osteodysplasticum hereditaria and wrinkly skin syndrome in 22 patients from Oman

Anna Rajab, U. Kornak, B. S. Budde, K. Hoffmann, J. Jaeken, P. Nürnberg, S. Mundlos

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 300 KB

english, 2008

33

Hardikar syndrome: Long term outcome of a rare genetic disorder

Andreas Nydegger, Maria Van Dyck, Robert A. Fisher, Jaak Jaeken, Winita Hardikar

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 58 KB

english, 2008

34

Mutations in PEX10 are a cause of autosomal recessive ataxia

Luc Régal, Merel S. Ebberink, Nathalie Goemans, Ronald J. A. Wanders, Linda De Meirleir, Jacques Jaeken, Maarten Schrooten, Rudy Van Coster, Hans R. Waterham

Journal:

Annals of Neurology

Year:

2010

Language:

english

File:

PDF, 173 KB

english, 2010

35

L-2-hydroxyglutaric acidemia: A novel inherited neurometabolic disease

Dr. Peter G. Barth, Georg F. Hoffmann, Jaak Jaeken, Willy Lehnert, Folker Hanefeld, Albert H. Van Gennip, Marinus Duran, Jaap Valk, Ruud B. H. Schutgens, Friedrich K. Trefz, Gabriele Reimann, Hans-Pet

Journal:

Annals of Neurology

Year:

1992

Language:

english

File:

PDF, 577 KB

english, 1992

36

Inborn errors of GABA metabolism

Kenneth M. Gibson, William L. Nyhan, Jaak Jaeken

Journal:

Year:

1986

Language:

english

File:

PDF, 528 KB

english, 1986

37

Dérivés β-anilinovinyliques de bases hétérocycliques I Dérivés Substitués Dans La Fonction Anilino

A. van Dormael, J. Jaeken, J. Nys

Journal:

Bulletin des Sociétés Chimiques Belges

Year:

1949

File:

PDF, 345 KB

1949

38

RFT1 deficiency in three novel CDG patients

Wendy Vleugels, Micha A. Haeuptle, Bobby G. Ng, Jean-Claude Michalski, Roberta Battini, Carlo Dionisi-Vici, Mark D. Ludman, Jaak Jaeken, François Foulquier, Hudson H. Freeze, Gert Matthijs, Thierry He

Journal:

Year:

2009

Language:

english

File:

PDF, 322 KB

english, 2009

39

Fragmentation of negative ions from N-linked carbohydrates, Part 4. Fragmentation of complex glycans lacking substitution on the 6-antenna

David J. Harvey, Jaak Jaeken, Mike Butler, Alison J. Armitage, Pauline M. Rudd, Raymond A. Dwek

Journal:

Journal of Mass Spectrometry

Year:

2010

Language:

english

File:

PDF, 343 KB

english, 2010

40

Localized brain proton NMR spectroscopy in young adult phenylketonuria patients

K. Johannik, P. van Hecke, B. François, G. Marchal, M-H. Smet, J. Jaeken, L. Breysem, G. Wilms, A. L. Baert

Journal:

Magnetic Resonance in Medicine

Year:

1994

Language:

english

File:

PDF, 458 KB

english, 1994

41

Radiochemical assay of adenylosuccinase: Demonstration of parallel loss of activity toward both adenylosuccinate and succinylaminoimidazole car☐amide ribotide in liver of patients with the enzyme defect

Françoise Van den Bergh, M. Françoise^Vincent, Jaak Jaeken, Georges Van den Berghe

Journal:

Analytical Biochemistry

Year:

1991

Language:

english

File:

PDF, 569 KB

english, 1991

42

Effect of glycosylation on the protein pattern in 2-D-gel electrophoresis

Peter Kleinert, Thomas Kuster, Daniel Arnold, Jaak Jaeken, Claus W. Heizmann, Heinz Troxler

Journal:

Year:

2007

Language:

english

File:

PDF, 363 KB

english, 2007

43

Multiplexed glycoproteomic analysis of glycosylation disorders by sequential yolk immunoglobulins immunoseparation and MALDI-TOF MS

Luisa Sturiale, Rita Barone, Angelo Palmigiano, Célestin Nsibu Ndosimao, Paz Briones, Maciej Adamowicz, Jaak Jaeken, Domenico Garozzo

Journal:

Year:

2008

Language:

english

File:

PDF, 472 KB

english, 2008

44

Centromeric instability of chromosomes 1, 9, and 16 associated with combined immunodeficiency

J. P. Fryns, M. Azou, J. Jaeken, E. Eggermont, J. C. Pedersen, H. Berghe

Journal:

Year:

1981

Language:

english

File:

PDF, 260 KB

english, 1981

45

Malformative syndrome associated with a ring 10 chromosome and a translocated 10q/19 chromosome

J. P. Fryns, K. Boeck, J. Jaeken, H. Berghe

Journal:

Year:

1978

Language:

english

File:

PDF, 280 KB

english, 1978

46

Partial monosomy of the long arm of chromosome 16 in a malformed newborn: Karyotype 46,XX,del(16)(q21)

J. P. Fryns, S. Melchoir, J. Jaeken, H. Berghe

Journal:

Year:

1977

Language:

english

File:

PDF, 214 KB

english, 1977

47

Cerebral gigantism syndrome

J. Jaeken, M. Schueren-Lodeweyckx, R. Eeckels

Journal:

European Journal of Pediatrics

Year:

1972

Language:

english

File:

PDF, 851 KB

english, 1972

48

Liver necrosis in the new-born infant: Analysis of some precipitating factors in neonatal care

H. Devlieger, R. Snoeys, L. Wyndaele, J. Jaeken, P. Goddeeris, Ph. Moerman, J. Lauweryns, E. Eggermont

Journal:

European Journal of Pediatrics

Year:

1982

Language:

english

File:

PDF, 1.92 MB

english, 1982

49

Carbamyl phosphate synthetase deficiency with lethal neonatal outcome

J. Jaeken, H. Devlieger, C. Bachmann, J. Aerde, L. Corbeel, E. Eggermont

Journal:

European Journal of Pediatrics

Year:

1982

Language:

english

File:

PDF, 451 KB

english, 1982

50

Congenital folate malabsorption

L. Corbeel, G. Berghe, J. Jaeken, J. Tornout, R. Eeckels

Journal:

European Journal of Pediatrics

Year:

1985

Language:

english

File:

PDF, 775 KB

english, 1985