Ruud Berger : rechercher sur Z-Library

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1

Political integration by a detour? ethnic communities and social capital of migrants in Berlin

Berger, Maria, Galonska, Christian, Koopmans, Ruud

Journal:

Journal of Ethnic and Migration Studies

Année:

2004

Langue:

english

Fichier:

PDF, 152 KB

english, 2004

2

Fumarylacetoacetase mutations in tyrosinaemia type I

Helge Rootwelt, Kari Høie, Ruud Berger, Eli Anne Kvittingen

Journal:

Année:

1996

Langue:

english

Fichier:

PDF, 467 KB

english, 1996

3

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

Année:

1998

Langue:

english

Fichier:

PDF, 435 KB

english, 1998

4

Water Accounting and Vulnerability Evaluation (WAVE): Considering Atmospheric Evaporation Recycling and the Risk of Freshwater Depletion in Water Footprinting

Berger, Markus, van der Ent, Ruud, Eisner, Stephanie, Bach, Vanessa, Finkbeiner, Matthias

Journal:

Environmental Science & Technology

Année:

2014

Langue:

english

Fichier:

PDF, 3.02 MB

english, 2014

5

Bürgerschaft, ethnische Netzwerke und die politische Integration von Türken in Amsterdam und Berlin

Berger, Maria, Koopmans, Ruud

Journal:

Forschungsjournal Soziale Bewegungen

Année:

2004

Langue:

german

Fichier:

PDF, 513 KB

german, 2004

6

Mutation analysis for prenatal diagnosis of hereditary tyrosinaemia type 1

Aki Mustonen, Hans Kristian Ploos Van Amstel, Ruud Berger, Matti K. Salo, Lasse Viinikka, Kalle O. J. Simola

Journal:

Prenatal Diagnosis

Année:

1997

Langue:

english

Fichier:

PDF, 26 KB

english, 1997

7

Activation of fatty acid oxidation in the Silver–Russell syndrome and the Brachmann–de Lange syndrome

Dr. Patrick J. Willems, Irene Dijkstra, Henk H. Schierbeek, Ruud Berger, G. Peter A. Smit, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Année:

1988

Langue:

english

Fichier:

PDF, 587 KB

english, 1988

8

D-serine in the developing human central nervous system

Sabine A. Fuchs, Lambertus Dorland, Monique G. De Sain-Van Der Velden, Margriet Hendriks, Leo W. J. Klomp, Ruud Berger, Tom J. De Koning

Journal:

Annals of Neurology

Année:

2006

Langue:

english

Fichier:

PDF, 122 KB

english, 2006

9

Yield of additional metabolic studies in neurodevelopmental disorders

Hannelie M. Engbers, Ruud Berger, Peter van Hasselt, Tom de Koning, Monique G. M. de Sain-van der Velden, Hester Y. Kroes, Gepke Visser

Journal:

Annals of Neurology

Année:

2008

Langue:

english

Fichier:

PDF, 177 KB

english, 2008

10

Reply

Hannelie M. Engbers, Ruud Berger, Peter van Hasselt, Tom de Koning, Monique G. M. de Sain-van der Velden, Hester Kroes, Gepke Visser

Journal:

Annals of Neurology

Année:

2009

Langue:

english

Fichier:

PDF, 36 KB

english, 2009

11

Hereditary tyrosinemia type I: A new clinical classification with difference in prognosis on dietary treatment

Francjan J. Van Spronsen, Yolande Thomasse, G. Peter A. Smit, James V. Leonard, Peter T. Clayton, Vaclav Fidler, Ruud Berger, Hugo S. A. Heymans

Journal:

Année:

1994

Langue:

english

Fichier:

PDF, 505 KB

english, 1994

12

Reduced expression of ATP7B affected by Wilson disease–causing mutations is rescued by pharmacological folding chaperones 4-phenylbutyrate and curcumin

Peter V. E. van den Berghe, Janneke M. Stapelbroek, Elmar Krieger, Prim de Bie, Stan F. J. van de Graaf, Reinoud E. A. de Groot, Ellen van Beurden, Ellen Spijker, Roderick H. J. Houwen, Ruud Berger, L

Journal:

Année:

2009

Langue:

english

Fichier:

PDF, 1.86 MB

english, 2009

13

Folding defects in P-type ATP 8B1 associated with hereditary cholestasis are ameliorated by 4-phenylbutyrate

Lieke M. van der Velden, Janneke M. Stapelbroek, Elmar Krieger, Peter V. E. van den Berghe, Ruud Berger, Patricia M. Verhulst, Joost C. M. Holthuis, Roderick H. J. Houwen, Leo W. J. Klomp, Stan F. J.

Journal:

Année:

2010

Langue:

english

Fichier:

PDF, 3.90 MB

english, 2010

14

P18 is a tumor suppressor gene involved in human medullary thyroid carcinoma and pheochromocytoma development

Wendy van Veelen, Rob Klompmaker, Martijn Gloerich, Carola J.R. van Gasteren, Eric Kalkhoven, Ruud Berger, Cornelis J.M. Lips, Rene H. Medema, Jo W.M. Höppener, Dennis S. Acton

Journal:

International Journal of Cancer

Année:

2009

Langue:

english

Fichier:

PDF, 356 KB

english, 2009

15

Quantification of free and total sialic acid excretion by LC–MS/MS

Maria van der Ham, Berthil H.C.M.T. Prinsen, Jan G.M. Huijmans, Nicolaas G.G.M. Abeling, Bert Dorland, Ruud Berger, Tom J. de Koning, Monique G.M. de Sain-van der Velden

Journal:

Journal of Chromatography B

Année:

2007

Langue:

english

Fichier:

PDF, 360 KB

english, 2007

16

Idiopathic hypoalbuminemia explained by reduced synthesis rate and an increased catabolic rate

Berthil H.C.M.T Prinsen, George A Kaysen, Leo W.J Klomp, Jose de Boer, P.Hugh R Barrett, Paul J Thornalley, Sinan Battah, Ruud Berger, Ton J Rabelink, Monique G.M.de Sain-van der Velden

Journal:

Clinical Biochemistry

Année:

2002

Langue:

english

Fichier:

PDF, 125 KB

english, 2002

17

Homocysteine and methionine metabolism in ESRD: A stable isotope study

Van Guldener, Coen, Kulik, Wim, Berger, Ruud, Dijkstra, Denise A., Jakobs, Cornelis, Reijngoud, Dirk-Jan, Donker, Ab J.M., Stehouwer, Coen D.A., De Meer, Kees

Journal:

Kidney International

Année:

1999

Langue:

english

Fichier:

PDF, 272 KB

english, 1999

18

Increased albumin and fibrinogen synthesis rate in patients with chronic renal failure

Prinsen, Berthil H.C.M.T., Rabelink, Ton J., Beutler, Jaap J., Kaysen, George A., De Boer, Jose, Boer, Walther H., Hagen, E. Christiaan, Berger, Ruud, De Sain-Van Der Velden, Monique G.M.

Journal:

Kidney International

Année:

2003

Langue:

english

Fichier:

PDF, 124 KB

english, 2003

19

Hypertriglyceridemia in patients with chronic renal failure: Possible mechanisms

Prinsen, Berthil H.C.M.T., De Sain-Van Der Velden, Monique G.M., De Koning, Eelco J.P., Koomans, Hein A., Berger, Ruud, Rabelink, Ton J.

Journal:

Kidney International

Année:

2003

Langue:

english

Fichier:

PDF, 464 KB

english, 2003

20

Two missense mutations causing tyrosinemia type 1 with presence and absence of immunoreactive fumarylacetoacetase

Helge Rootwelt, Janice Chou, William A. Gahl, Ruud Berger, Turgay Coşkun, Else Brodtkorb, Eli Anne Kvittingen

Journal:

Année:

1994

Langue:

english

Fichier:

PDF, 725 KB

english, 1994

21

Tyrosinemia type 1 — complex splicing defects and a missense mutation in the fumarylacetoacetase gene

Helge Rootwelt, Tom Kristensen, Ruud Berger, Kari Høie, Eli Anne Kvittingen

Journal:

Année:

1994

Langue:

english

Fichier:

PDF, 606 KB

english, 1994

22

The copper-transporting capacity of ATP7A mutants associated with Menkes disease is ameliorated by COMMD1 as a result of improved protein expression

Willianne I. M. Vonk, Prim de Bie, Catharina G. K. Wichers, Peter V. E. van den Berghe, Rozemarijn van der Plaats, Ruud Berger, Cisca Wijmenga, Leo W. J. Klomp, Bart van de Sluis

Journal:

Cellular and Molecular Life Sciences

Année:

2012

Langue:

english

Fichier:

PDF, 980 KB

english, 2012

23

Structural organization of the human short-chainL-3-hydroxyacyl-CoA dehydrogenase gene

Patrick J.C.M. Vredendaal, Inge E.T. van den Berg, An K. Stroobants, Daphne L. van der A, Helga E.M. Malingré, Ruud Berger

Journal:

Mammalian Genome

Année:

1998

Langue:

english

Fichier:

PDF, 161 KB

english, 1998

24

Massage to prevent pressure ulcers: knowledge, beliefs and practice. A cross-sectional study among nurses in the Netherlands in 1991 and 2003

Inge GP Duimel-Peeters, Mirjam A Hulsenboom, Martijn PF Berger, Luc HEH Snoeckx, Ruud JG Halfens

Journal:

Journal of Clinical Nursing

Année:

2006

Langue:

english

Fichier:

PDF, 77 KB

english, 2006

25

A broad-based metabolic approach to study VLDL apoB100 metabolism in patients with ESRD and patients treated with peritoneal dialysis

Prinsen, Berthil H.C.M.T., Rabelink, Ton J., Romijn, Johannes A., Bisschop, Peter H., de Barse, Martina M.J., de Boer, Jose, van Haeften, Timon W., Barrett, P. Hugh R., Berger, Ruud, de Sain-van der V

Journal:

Kidney International

Année:

2004

Langue:

english

Fichier:

PDF, 143 KB

english, 2004

26

Renal proximal tubular cells acquire resistance to cell death stimuli in mice with hereditary tyrosinemia type 1

Luijerink, Marjanka C., van Beurden, Ellen A.C.M., Malingre, Helga E.M., Jacobs, Saskia M.M., Grompe, Markus, Klomp, Leo W.J., Berger, Ruud, van den Berg, Inge E.T.

Journal:

Kidney International

Année:

2004

Langue:

english

Fichier:

PDF, 386 KB

english, 2004

27

A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis

Bull, Laura N., van Eijk, Michiel J.T., Pawlikowska, Ludmila, DeYoung, Joseph A., Juijn, Jenneke A., Liao, Mira, Klomp, Leo W.J., Lomri, Noureddine, Berger, Ruud, Scharschmidt, Bruce R.

Journal:

Nature Genetics

Année:

1998

Fichier:

PDF, 799 KB

1998

28

A missense mutation in FIC1 is associated with greenland familial cholestasis

Leo W.J. Klomp, Laura N. Bull, Alexander S. Knisely, Marjolein A.M. van der Doelen, Jenneke A. Juijn, Ruud Berger, Sylviane Forget, Inge-Merete Nielsen, Hans Eiberg, Roderick H.J. Houwen

Journal:

Année:

2000

Langue:

english

Fichier:

PDF, 437 KB

english, 2000

29

Neurotransmitters in 3-phosphoglycerate dehydrogenase deficiency

Duran, Marinus, Dorland, Lambertus, Jakobs, Cornelis, Wevers, Ron A, Berger, Ruud, Poll-The, Bwee-Tien, de Koning, Tom J

Journal:

European Journal of Pediatrics

Année:

2000

Langue:

english

Fichier:

PDF, 70 KB

english, 2000

30

Increased concentrations of both NMDA receptor co-agonistsd-serine and glycine in global ischemia: a potential novel treatment target for perinatal asphyxia

Fuchs, Sabine A., Peeters-Scholte, Cacha M. P. C. D., Barse, Martina M. J., Roeleveld, Martin W., Klomp, Leo W. J., Berger, Ruud, Koning, Tom J.

Journal:

Année:

2012

Langue:

english

Fichier:

PDF, 312 KB

english, 2012

31

d-Serine: The right or wrong isoform?

Sabine A. Fuchs, Ruud Berger, Tom J. de Koning

Journal:

Année:

2011

Langue:

english

Fichier:

PDF, 447 KB

english, 2011

32

A sensitive and simple ultra-high-performance-liquid chromatography–tandem mass spectrometry based method for the quantification of d-amino acids in body fluids

Wouter F. Visser, Nanda M. Verhoeven-Duif, Roel Ophoff, Steven Bakker, Leo W. Klomp, Ruud Berger, Tom J. de Koning

Journal:

Journal of Chromatography A

Année:

2011

Langue:

english

Fichier:

PDF, 394 KB

english, 2011

33

The effectiveness of massage with and without dimethyl sulfoxide in preventing pressure ulcers: A randomized, double-blind cross-over trial in patients prone to pressure ulcers

Inge G.P. Duimel-Peeters, Ruud J.G. Halfens, Anton W. Ambergen, Ronald H. Houwing, Martijn P.F. Berger, Luc H.E.H. Snoeckx

Journal:

International Journal of Nursing Studies

Année:

2007

Langue:

english

Fichier:

PDF, 186 KB

english, 2007

34

Human Short-Chain L-3-Hydroxyacyl-CoA Dehydrogenase: Cloning and Characterization of the Coding Sequence

Patrick J.C.M. Vredendaal, Inge E.T. van den Berg, Helga E.M. Malingré, An K. Stroobants, Danielle E.M. OldeWeghuis, Ruud Berger

Journal:

Biochemical and Biophysical Research Communications

Année:

1996

Langue:

english

Fichier:

PDF, 362 KB

english, 1996

35

Autosomal Recessive Liver Phosphorylase Kinase Deficiency Caused by a Novel Splice-Site Mutation in the Gene Encoding the Liver Gamma Subunit (PHKG2)

Ellen A.C.M. van Beurden, Michelle de Graaf, Udo Wendel, Richard Gitzelmann, Ruud Berger, Inge E.T. van den Berg

Journal:

Biochemical and Biophysical Research Communications

Année:

1997

Langue:

english

Fichier:

PDF, 168 KB

english, 1997

36

Localization of a New Type of X-Linked Liver Glycogenosis to the Chromosomal Region Xp22 Containing the Liver α-Subunit of Phosphorylase Kinase (PHKA2)

Jan Hendrickx, Paul Coucke, Marie-Claude Hors-Cayla, G.Peter A. Smit, Yoon S. Shin, Johann Deutsch, Jan Smeitink, Ruud Berger, Philip Lee, John Fernandes, Patrick J. Willems

Journal:

Année:

1994

Fichier:

PDF, 301 KB

1994

37

Capillary gas chromatographic profiling of urinary, plasma and erythrocyte sugars and polyols as their trimethylsilyl derivatives, preceded by a simple and rapid prepurification method

Geert Jansen, Frits A.J. Muskiet, Henk Schierbeek, Ruud Berger, Wim van der Slik

Journal:

Clinica Chimica Acta

Année:

1986

Langue:

english

Fichier:

PDF, 1.26 MB

english, 1986

38

Determination of succinylacetone and succinylacetoacetate in physiological samples as the common product 5(3)-methyl-3(5)-isoxazole propionic acid using an isotope dilution method and mass spectrometry

Henk Schierbeek, Ruud Berger

Journal:

Clinica Chimica Acta

Année:

1989

Langue:

english

Fichier:

PDF, 425 KB

english, 1989

39

Hyperinsulinism of infancy associated with a novel splice site mutation in the SCHAD gene

Khalid Hussain, Peter T. Clayton, Steve Krywawych, Ilenia Chatziandreou, Phillipa Mills, D.W. Ginbey, Ans J.J.M. Geboers, Ruud Berger, Inge E.T. van den Berg, Simon Eaton

Journal:

The Journal of Pediatrics

Année:

2005

Langue:

english

Fichier:

PDF, 108 KB

english, 2005

40

d-Amino acids in the central nervous system in health and disease

Sabine A. Fuchs, Ruud Berger, Leo W.J. Klomp, Tom J. de Koning

Journal:

Molecular Genetics and Metabolism

Année:

2005

Langue:

english

Fichier:

PDF, 549 KB

english, 2005

41

Extensive changes in liver gene expression induced by Hereditary Tyrosinemia type I are not normalized by treatment with 2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione (NTBC)

Marjanka C Luijerink, Saskia M.M Jacobs, Ellen A.C.M van Beurden, Leander P Koornneef, Leo W.J Klomp, Ruud Berger, Inge E.T van den Berg

Journal:

Journal of Hepatology

Année:

2003

Langue:

english

Fichier:

PDF, 338 KB

english, 2003

42

Nephrotic proteinuria has no net effect on total body protein synthesis: Measurements with 13C valine

Monique G.M. de Sain-van der Velden, Kees de Meer, Wim Kulik, Christian F. Melissant, Ton J. Rabelink, Ruud Berger, George A. Kaysen

Journal:

American Journal of Kidney Diseases

Année:

2000

Langue:

english

Fichier:

PDF, 42 KB

english, 2000

43

Autosomal Recessive Phosphorylase Kinase Deficiency in Liver, Caused by Mutations in the Gene Encoding the β Subunit (PHKB)

Inge E.T. van den Berg, Ellen A.C.M. van Beurden, Johannis B.C. de Klerk, Otto P. van Diggelen, Helga E.M. Malingré, Marijke M. Boer, Ruud Berger

Journal:

The American Journal of Human Genetics

Année:

1997

Langue:

english

Fichier:

PDF, 784 KB

english, 1997

44

Cerebrospinal fluid d-serine and glycine concentrations are unaltered and unaffected by olanzapine therapy in male schizophrenic patients

Sabine A. Fuchs, Martina M.J. De Barse, Floor E. Scheepers, Wiepke Cahn, Lambertus Dorland, Monique G. de Sain-van der Velden, Leo W.J. Klomp, Ruud Berger, René S. Kahn, Tom J. de Koning

Journal:

European Neuropsychopharmacology

Année:

2008

Langue:

english

Fichier:

PDF, 198 KB

english, 2008

45

Dietary supplementation with multiple micronutrients: No beneficial effects in pediatric cystic fibrosis patients

Johanna H. Oudshoorn, Peter H.C. Klijn, Zandrie Hofman, Hieronymus A.M. Voorbij, Cors K. van der Ent, Ruud Berger, Roderick H.J. Houwen

Journal:

Journal of Cystic Fibrosis

Année:

2007

Langue:

english

Fichier:

PDF, 197 KB

english, 2007

46

Successful treatment of severe OTC deficiency

Ann-Mari Brubakk, Leine L. Teijema, Wim Blom, Ruud Berger

Journal:

The Journal of Pediatrics

Année:

1982

Langue:

english

Fichier:

PDF, 283 KB

english, 1982

47

FIC1, the protein affected in two forms of hereditary cholestasis, is localized in the cholangiocyte and the canalicular membrane of the hepatocyte

Elaine F. Eppens, Saskia W.C. van Mil, J.Marleen L. de Vree, Kam S. Mok, Jenneke A. Juijn, Ronald P.J. Oude Elferink, Ruud Berger, Roderick H.J. Houwen, Leo W.J. Klomp

Journal:

Journal of Hepatology

Année:

2001

Langue:

english

Fichier:

PDF, 491 KB

english, 2001

48

Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11

Saskia W.C. van Mil, Wendy L. van der Woerd, Gerda van der Brugge, Ekkehard Sturm, Peter L.M. Jansen, Laura N. Bull, Inge E.T. van den Berg, Ruud Berger, Roderick H.J. Houwen, Leo W.J. Klomp

Journal:

Gastroenterology

Année:

2004

Langue:

english

Fichier:

PDF, 123 KB

english, 2004

49

Distinct Wilson’s Disease Mutations in ATP7B Are Associated With Enhanced Binding to COMMD1 and Reduced Stability of ATP7B

Prim de Bie, Bart van de Sluis, Ezra Burstein, Peter V.E. van de Berghe, Patricia Muller, Ruud Berger, Jonathan D. Gitlin, Cisca Wijmenga, Leo W.J. Klomp

Journal:

Gastroenterology

Année:

2007

Langue:

english

Fichier:

PDF, 3.76 MB

english, 2007

50

The serine/threonine phosphatase PPM1B (PP2Cβ) selectively modulates PPARγ activity

Tasdelen, Ismayil, van Beekum, Olivier, Gorbenko, Olena, Fleskens, Veerle, van den Broek, Niels J. F., Koppen, Arjen, Hamers, Nicole, Berger, Ruud, Coffer, Paul J., Brenkman, Arjan B., Kalkhoven, Eric

Journal:

Biochemical Journal

Année:

2013

Langue:

english

Fichier:

PDF, 1.26 MB

english, 2013