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1

Human Organoids: Tools for Understanding Biology and Treating Diseases

Schutgens, Frans, Clevers, Hans

Journal:

Annual Review of Pathology Mechanisms of Disease

Année:

2020

Langue:

english

Fichier:

PDF, 2.00 MB

english, 2020

2

Tubuloids derived from human adult kidney and urine for personalized disease modeling

Schutgens, Frans, Rookmaaker, Maarten B, Margaritis, Thanasis, Rios, Anne, Ammerlaan, Carola, Jansen, Jitske, Gijzen, Linda, Vormann, Marianne, Vonk, Annelotte, Viveen, Marco, Yengej, Fjodor Yousef, D

Journal:

Nature Biotechnology

Année:

2019

Langue:

english

Fichier:

PDF, 3.64 MB

english, 2019

3

Visitors’ willingness to pay for snow leopard Panthera uncia conservation in the Annapurna Conservation Area, Nepal

Schutgens, Maurice G., Hanson, Jonathan H., Baral, Nabin, Ale, Som B.

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 240 KB

english, 2018

4

What explains tourists’ support for snow leopard conservation in the Annapurna Conservation Area, Nepal?

Hanson, Jonathan H., Schutgens, Maurice, Baral, Nabin

Journal:

Human Dimensions of Wildlife

Année:

2018

Langue:

english

Fichier:

PDF, 1.35 MB

english, 2018

5

The influence of adaptogens on ultraweak biophoton emission: a pilot-experiment

F. W. G. Schutgens, P. Neogi, E. P. A. van Wijk, R. van Wijk, G. Wikman, F. A. C. Wiegant

Journal:

Phytotherapy Research

Année:

2009

Langue:

english

Fichier:

PDF, 145 KB

english, 2009

6

Deficiency of plasmalogens in the cerebro-hepato-renal (Zellweger) syndrome

H. S. A. Heymans, H. v. d. Bosch, R. B. H. Schutgens, W. H. H. Tegelaers, J. -U. Walther, J. Müller-Höcker, P. Borst

Journal:

European Journal of Pediatrics

Année:

1984

Langue:

english

Fichier:

PDF, 876 KB

english, 1984

7

L-2-Hydroxyglutaric aciduria and lactic acidosis

P. G. Barth, R. J. A. Wanders, H. R. Scholte, N. Abeling, C. Jakobs, R. B. H. Schutgens, P. Vreken

Journal:

Journal of Inherited Metabolic Disease

Année:

1998

Langue:

english

Fichier:

PDF, 66 KB

english, 1998

8

Biochemistry of Peroxisomes

van den Bosch, H., Schutgens, R. B. H., Wanders, R. J. A., Tager, J. M.

Journal:

Annual Review of Biochemistry

Année:

1992

Langue:

english

Fichier:

PDF, 1.15 MB

english, 1992

9

Ether lipid synthesis and its deficiency in peroxisomal disorders

H. van den Bosch, G. Schrakamp, D. Hardeman, A.W.M. Zomer, R.J.A. Wanders, R.B.H. Schutgens

Journal:

Année:

1993

Langue:

english

Fichier:

PDF, 1007 KB

english, 1993

10

L-Phenylalanine and UVA Irradiation in the Treatment of Vitiligo

Siddiqui, A.H., Stolk, L·M.L., Bhaggoe, R., Hu, R., Schutgens, R.B.H., Westerhof, W.

Journal:

Année:

1994

Fichier:

PDF, 1.74 MB

1994

11

The association of haemophilic arthropathy with Health-Related Quality of Life: a post hoc analysis

Fischer, K., de Kleijn, P., Negrier, C., Mauser-Bunschoten, E. P., van der Valk, P. R., van Galen, K. P. M., Willemze, A., Schutgens, R.

Journal:

Année:

2016

Langue:

english

Fichier:

PDF, 147 KB

english, 2016

12

Should vitamin K be supplemented instead of antagonised in patients with idiopathic pulmonary fibrosis?

de Brouwer, Bart, Piscaer, Ianthe, von der Thusen, Jan H., Grutters, Jan C., Schutgens, Roger EG., Wouters, Emiel FM., Janssen, Rob

Journal:

Expert Review of Respiratory Medicine

Année:

2018

Langue:

english

Fichier:

PDF, 2.19 MB

english, 2018

13

Local attitudes to the proposed translocation of blue sheep Pseudois nayaur to Sagarmatha National Park, Nepal

Hanson, Jonathan H., Schutgens, Maurice, Lama, Rinzin P., Aryal, Achyut, Dhakal, Maheshwar

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 232 KB

english, 2018

14

Movement behaviour patterns in adults with haemophilia

Timmer, Merel A., Veenhof, Cindy, de Kleijn, Piet, de Bie, Rob A., Schutgens, Roger E. G., Pisters, Martijn F.

Journal:

Therapeutic Advances in Hematology

Année:

2020

Langue:

english

Fichier:

PDF, 422 KB

english, 2020

15

Oxygen gradient ektacytometry derivedâbiomarkers are associated with vasoâocclusive crises and correlate with treatment response in sickle cell disease

Rab, Minke A.E., Kanne, Celeste K., Bos, Jennifer, van Oirschot, Brigitte A., Boisson, Camille, Houwing, Maite E., Gerritsma, Jorn, Teske, Erik, Renoux, Celine, Riedl, Jurgen, Schutgens, Roger E.G., B

Journal:

American Journal of Hematology

Année:

2020

Fichier:

PDF, 1.37 MB

2020

16

Variant rhizomelic chondrodysplasia punctata (RCDP) with normal plasma phytanic acid: Clinico-biochemical delineation of a subtype and complementation studies

Barth, Peter G., Wanders, Ronald J. A., Schutgens, Ruud B. H., Staalman, Chris R.

Journal:

American Journal of Medical Genetics

Année:

1996

Langue:

english

Fichier:

PDF, 514 KB

english, 1996

17

Smith-Lemli-Opitz syndrome diagnosed in a 130-year-old anatomical specimen

Oostra, Roelof-Jan, Baljet, Bob, Schutgens, Ruud B. H., Hennekam, Raoul C. M.

Journal:

American Journal of Medical Genetics

Année:

1997

Langue:

english

Fichier:

PDF, 357 KB

english, 1997

18

An age-adapted approach for the use of D-dimers in the exclusion of deep venous thrombosis

Fred J.L.M. Haas, Roger E.G. Schutgens, Douwe H. Biesma

Journal:

American Journal of Hematology

Année:

2009

Langue:

english

Fichier:

PDF, 118 KB

english, 2009

19

A prognostic model for short term adverse events in normotensive patients with pulmonary embolism

Mariette J. Agterof, Roger E.G. Schutgens, Noureddine Moumli, M.J.C. Eijkemans, René van der Griend, Ellen A.M. Tromp, Douwe H. Biesma

Journal:

American Journal of Hematology

Année:

2011

Langue:

english

Fichier:

PDF, 111 KB

english, 2011

20

VACTERL and hydrocephalus

Frits A. Beemer, Ronald J. A. Wanders, Ruud B. J. Schutgens

Journal:

American Journal of Medical Genetics Part A

Année:

1990

Langue:

english

Fichier:

PDF, 98 KB

english, 1990

21

Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter

Marjo S. van der Knaap, Peter A. J. Leegwater, Andrea A.M. Könst, Allerdien Visser, Sakkubai Naidu, Cees B.M. Oudejans, Ruud B.H. Schutgens, Jan C. Pronk

Journal:

Annals of Neurology

Année:

2002

Langue:

english

Fichier:

PDF, 977 KB

english, 2002

22

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

Année:

1992

Langue:

english

Fichier:

PDF, 577 KB

english, 1992

23

The identification of (E)-2-methylglutaconic acid, a new isoleucine metabolite, in the urine of patients with β-ketothiolase deficiency, propionic acidaemia and methylmalonic acidaemia

M. Duran, L. Bruinvis, D. Ketting, J. P. Kamerling, S. K. Wadman, R. B. H. Schutgens

Journal:

Biological Mass Spectrometry = Journal of Mass Spectrometry (Wiley)

Année:

1982

Langue:

english

Fichier:

PDF, 456 KB

english, 1982

24

Composition of LDL as determinant of its susceptibility to in vitro oxidation in patients with well-controlled type 2 diabetes

P. G. Scheffer, S. J. L. Bakker, C. Popp-Snijders, R. J. Heine, R. B. H. Schutgens, T. Teerlink

Journal:

Diabetes/Metabolism Research and Reviews

Année:

2001

Langue:

english

Fichier:

PDF, 108 KB

english, 2001

25

Peroxisome mosaicism in the livers of peroxisomal deficiency patients

Marc Espeel, Hanna Mandel, Florence Poggi, Jan A. M. Smeitink, Ronald J. A. Wanders, Ingrid Kerckaert, Rudolf B. H. Schutgens, Jean-Marie Saudubray, Bwee-Tien Poll-The, Frank Roels

Journal:

Année:

1995

Langue:

english

Fichier:

PDF, 1.22 MB

english, 1995

26

Effect of peroxisome proliferation on ether phospholipid biosynthesizing enzymes in rat liver

Derk Hardeman, Hanneke W.M. Zomer, Ruud B.H. Schutgens, Joseph M. tager, Henk van den Bosch

Journal:

International Journal of Biochemistry

Année:

1990

Langue:

english

Fichier:

PDF, 673 KB

english, 1990

27

Peroxisomes are enlarged in two patients with peroxisomal diseases: Novel cases

D. De Craemer, MJ Zweens, S Lyonnet, RJA Wanders, BT Poll-The, JJJ Waelkens, RBH Schutgens, JM Saudubray, F. Roels

Journal:

Micron and Microscopica Acta

Année:

1991

Langue:

english

Fichier:

PDF, 233 KB

english, 1991

28

Parametrisation of Earth's polarisation spectrum in the ultra-violet

N.A.J Schutgens, P Stammes

Journal:

Journal of Quantitative Spectroscopy and Radiative Transfer

Année:

2002

Langue:

english

Fichier:

PDF, 334 KB

english, 2002

29

Iatrogenic isolated isoleucine deficiency as the cause of an acrodermatitis enteropathica-like syndrome

Bosch, Sillevis Smitt, Van Gennip, Abeling, Schutgens, Bakker, Wijburg

Journal:

British Journal of Dermatology

Année:

1998

Langue:

english

Fichier:

PDF, 421 KB

english, 1998

30

The usefulness of five d-dimer assays in the exclusion of deep venous thrombosis

R. E. G. Schutgens, F. J. L. M. Haas, W. B. M. Gerritsen, F. Van Der Horst, H. K. Nieuwenhuis, D. H. Biesma

Journal:

Journal of Thrombosis and Haemostasis

Année:

2003

Langue:

english

Fichier:

PDF, 129 KB

english, 2003

31

The cerebro-hepato-renal (Zellweger) syndrome: Prenatal detection based on impaired biosynthesis of plasmalogens

R. B. H. Schutgens, G. Schrakamp, R. J. A. Wanders, H. S. A. Heymans, H. W. Moser, A. E. Moser, J. M. Tagers, H. V. D. Bosch, P. Aubourm

Journal:

Prenatal Diagnosis

Année:

1985

Langue:

english

Fichier:

PDF, 490 KB

english, 1985

32

Prenatal diagnosis of inborn errors in peroxisomal β-oxidation

Dr. R. J. A. Wanders, R. B. H. Schutgens, H. van den Bosch, J. M. Tager, W. J. Kleijer

Journal:

Prenatal Diagnosis

Année:

1991

Langue:

english

Fichier:

PDF, 484 KB

english, 1991

33

A misdiagnosis of X-linked adrenoleucodystrophy in cultured chorionic villus cells by the measurement of very long chain fatty acids

R. G. F. Gray, A. Green, T. Cole, V. Davidson, M. Giles, R. B. H. Schutgens, R. J. A. Wanders

Journal:

Prenatal Diagnosis

Année:

1995

Langue:

english

Fichier:

PDF, 370 KB

english, 1995

34

Genetic and biochemical heterogeneity in patients with the rhizomelic form of chondrodysplasia punctata — a complementation study

Judith C. Heikoop, Ronald J. A. Wanders, Anneke Strijland, Rally Purvis, Ruud B. H. Schutgens, Joseph M. Tager

Journal:

Année:

1992

Langue:

english

Fichier:

PDF, 1.25 MB

english, 1992

35

Phenylalanine and UVA light for the treatment of vitiligo

R. H. Cormane, A. H. Siddiqui, W. Westerhof, R. B. H. Schutgens

Journal:

Archives of Dermatological Research

Année:

1985

Langue:

english

Fichier:

PDF, 785 KB

english, 1985

36

Very long chain fatty acids in amniotic fluid from a fetus affected with Zellweger syndrome

C. Jakobs, H. Brink, R. M. Kok, F. Stellaard, W. J. Kleijer, R. J. A. Wanders, R. B. H. Schutgens

Journal:

European Journal of Pediatrics

Année:

1989

Langue:

english

Fichier:

PDF, 106 KB

english, 1989

37

Infantile Refsum disease: an inherited peroxisomal disorder

B. T. Poll-The, J. M. Saudubray, H. A. M. Ogier, M. Odièvre, J. M. Scotto, L. Monnens, L. C. P. Govaerts, F. Roels, A. Cornelis, R. B. H. Schutgens, R. J. A. Wanders, A. W. Schram, J. M. Tager

Journal:

European Journal of Pediatrics

Année:

1987

Langue:

english

Fichier:

PDF, 943 KB

english, 1987

38

Peroxisomal disorders: A newly recognised group of genetic diseases

R. B. H. Schutgens, H. S. A. Heymans, R. J. A. Wanders, H. v. d. Bosch, J. M. Tager

Journal:

European Journal of Pediatrics

Année:

1986

Langue:

english

Fichier:

PDF, 1.18 MB

english, 1986

39

A milder variant of Zellweger syndrome

P. G. Barth, R. B. H. Schutgens, J. A. J. M. Bakkeren, K. P. Dingemans, H. S. A. Heymans, A. C. Douwes, J. M. Moorsel

Journal:

European Journal of Pediatrics

Année:

1985

Langue:

english

Fichier:

PDF, 786 KB

english, 1985

40

Impaired plasmalogen metabolism in infantile Refsum's disease

B. T. Poll-Thé, H. Ogier, J. M. Saudubray, R. B. H. Schutgens, R. J. A. Wanders, H. Bosch, G. Schrakamp

Journal:

European Journal of Pediatrics

Année:

1986

Langue:

english

Fichier:

PDF, 211 KB

english, 1986

41

A prenatal test for the cerebro-hepato-renal (Zellweger) syndrome by demonstration of the absence of catalase-containing particles (peroxisomes) in cultured amniotic fluid cells

R. J. A. Wanders, G. Schrakamp, H. Bosch, J. M. Tager, R. B. H. Schutgens

Journal:

European Journal of Pediatrics

Année:

1986

Langue:

english

Fichier:

PDF, 365 KB

english, 1986

42

Beta-ketothiolase deficiency in a family confirmed by in vitro enzymatic assays in fibroblasts

R. B. H. Schutgens, B. Middleton, J. F. v. d. Blij, J. W. E. Oorthuys, H. A. Veder, T. Vulsma, W. H. H. Tegelaers

Journal:

European Journal of Pediatrics

Année:

1982

Langue:

english

Fichier:

PDF, 479 KB

english, 1982

43

Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductase

A. W. Behbehani, H. Goebel, G. Osse, M. Gabriel, U. Langenbeck, J. Berden, R. Berger, R. B. H. Schutgens

Journal:

European Journal of Pediatrics

Année:

1984

Langue:

english

Fichier:

PDF, 2.09 MB

english, 1984

44

Prenatal diagnosis of Zellweger syndrome by determination of trihydroxycoprostanic acid in amniotic fluid

F. Stellaard, S. A. Langelaar, R. M. Kok, W. J. Kleijer, R. B. H. Schutgens, C. Jakobs

Journal:

European Journal of Pediatrics

Année:

1988

Langue:

english

Fichier:

PDF, 225 KB

english, 1988

45

Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal β-oxidation enzyme proteins

R. J. A. Wanders, R. B. H. Schutgens, G. Schrakamp, H. Bosch, J. M. Tager, A. W. Schram, T. Hashimoto, B. T. Poll-Thé, J. M. Saudubrau

Journal:

European Journal of Pediatrics

Année:

1986

Langue:

english

Fichier:

PDF, 492 KB

english, 1986

46

Immunoblot analysis of peroxisomal proteins in liver and fibroblasts from patients

R. J. A. Wanders, C. Dekker, R. Ofman, R. B. H. Schutgens, P. Mooijer

Journal:

Journal of Inherited Metabolic Disease

Année:

1995

Langue:

english

Fichier:

PDF, 818 KB

english, 1995

47

Measurement of peroxisomal fatty acid β-oxidation in cultured human skin fibroblasts

R. J. A. Wanders, S. Denis, J. P. N. Ruiter, R. B. H. Schutgens, C. W. T. van Roermund, B. S. Jacobs

Journal:

Journal of Inherited Metabolic Disease

Année:

1995

Langue:

english

Fichier:

PDF, 711 KB

english, 1995

48

Acknowledgements

Frank Roels, Sylvia De Bie, Ruud B. H. Schutgens, Guy T. N. Besley

Journal:

Journal of Inherited Metabolic Disease

Année:

1995

Langue:

english

Fichier:

PDF, 84 KB

english, 1995

49

Measurement of dihydroxyacetone-phosphate acyltransferase (DHAPAT) in chorionic villous samples, blood cells and cultured cells

R. J. A. Wanders, R. Ofman, G. J. Romeijn, R. B. H. Schutgens, P. A. W. Mooijer, C. Dekker, H. van den Bosch

Journal:

Journal of Inherited Metabolic Disease

Année:

1995

Langue:

english

Fichier:

PDF, 643 KB

english, 1995

50

3-Hydroxy-3-methylglutaryl-CoA lyase deficiency: absence of clinical symptoms due to a self-imposed dietary fat and protein restriction

H. D. Bakker, R. J. A. Wanders, R. B. H. Schutgens, N. G. G. M. Abeling, A. H. Gennip

Journal:

Journal of Inherited Metabolic Disease

Année:

1993

Langue:

english

Fichier:

PDF, 132 KB

english, 1993