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1

CFD simulation of outdoor ventilation of generic urban configurations with different urban densities and equal and unequal street widths

Ramponi, Rubina, Blocken, Bert, de Coo, Laura B., Janssen, Wendy D.

Journal:

Building and Environment

Year:

2015

Language:

english

File:

PDF, 1.44 MB

english, 2015

2

A 4–base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome

I. F. M. De Coo, W. O. Renier, W. Ruitenbeek, H. J. Ter Laak, M. Bakker, H. Schägger, B. A. Van Oost, H. J. M. Smeets

Journal:

Annals of Neurology

Year:

1999

Language:

english

File:

PDF, 3.49 MB

english, 1999

3

The unfolding clinical spectrum of POLG mutations

Blok, M J, van den Bosch, B J, Jongen, E, Hendrickx, A, de Die-Smulders, C E, Hoogendijk, J E, Brusse, E, de Visser, M, Poll-The, B T, Bierau, J, de Coo, I F, Smeets, H J

Journal:

Journal of Medical Genetics

Year:

2009

Language:

english

File:

PDF, 300 KB

english, 2009

4

Robert Campin

Journal:

Wiener Jahrbuch für Kunstgeschichte

Year:

1991

Language:

german

File:

PDF, 903 KB

german, 1991

5

A Medieval Look at the Merode Annunciation

Journal:

Zeitschrift für Kunstgeschichte

Year:

1981

Language:

english

File:

PDF, 6.55 MB

english, 1981

6

Differential efficacy of non-invasive vagus nerve stimulation for the acute treatment of episodic and chronic cluster headache: A meta-analysis

de Coo, Ilse F, Marin, Juana CA, Silberstein, Stephen D, Friedman, Deborah I, Gaul, Charly, McClure, Candace K, Tyagi, Alok, Liebler, Eric, Tepper, Stewart J, Ferrari, Michel D, Goadsby, Peter J

Journal:

Year:

2019

Language:

english

File:

PDF, 659 KB

english, 2019

7

Preparation of coated nanoparticles for a new mucosal vaccine delivery system

Olga Borges, Gerrit Borchard, J. Coos Verhoef, Adriano de Sousa, Hans E. Junginger

Journal:

International Journal of Pharmaceutics

Year:

2005

Language:

english

File:

PDF, 405 KB

english, 2005

8

Comparison of the effect of different chitosan salts and N-trimethyl chitosan chloride on the permeability of intestinal epithelial cells (Caco-2)

Awie F Kotzé, Henrik L Lueßen, Bas J de Leeuw, (A)Bert G de Boer, J Coos Verhoef, Hans E Junginger

Journal:

Journal of Controlled Release

Year:

1998

Language:

english

File:

PDF, 311 KB

english, 1998

9

123 Defective Complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome

Irenaeus F.M. de Coo, Mike Gerards, Willem Sluiter, Bianca J.C. van den Bosch, Margrit Frentzen, Kees C. Schoonderwoerd, Hubert J.M. Smeets

Journal:

Year:

2010

Language:

english

File:

PDF, 44 KB

english, 2010

10

Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophy

Mike Gerards, Bianca van den Bosch, Chantal Calis, Kees Schoonderwoerd, Klaartje van Engelen, Marina Tijssen, René de Coo, Anneke van der Kooi, Hubert Smeets

Journal:

Year:

2010

Language:

english

File:

PDF, 564 KB

english, 2010

11

Skeletal muscle mitochondrial dysfunction is secondary to type 2 diabetes and can be improved by prolonged exercise training

F.H.J. van Tienen⁎, S.F.E. Praet, H.M. de Feyter, N.M. van den Broek, P.J. Lindsey, K.G.C. Schoonderwoerd, I.F.M. de Coo, K. Nicolay, J.J. Prompers, H.J.M. Smeets, L.J.C. van Loon

Journal:

Year:

2011

Language:

english

File:

PDF, 57 KB

english, 2011

12

A meta-analysis of the equity premium

van Ewijk, Casper, de Groot, Henri L.F., Santing, A.J. (Coos)

Journal:

Journal of Empirical Finance

Year:

2012

Language:

english

File:

PDF, 603 KB

english, 2012

13

A multicenter study on Leigh syndrome: disease course and predictors of survival

Sofou, Kalliopi, De Coo, Irenaeus F M, Isohanni, Pirjo, Ostergaard, Elsebet, Naess, Karin, De Meirleir, Linda, Tzoulis, Charalampos, Uusimaa, Johanna, De Angst, Isabell B, Lönnqvist, Tuula, Pihko, Hel

Journal:

Orphanet Journal of Rare Diseases

Year:

2014

Language:

english

File:

PDF, 770 KB

english, 2014

14

ACTA2 mutation with childhood cardiovascular, autonomic and brain anomalies and severe outcome

Meuwissen, Marije E.C., Lequin, Maarten H., Bindels-de Heus, Karen, Bruggenwirth, Hennie T., Knapen, Maarten F.C.M., Dalinghaus, Michiel, de Coo, René, van Bever, Yolande, Winkelman, Beerend H.J., Man

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 1.00 MB

english, 2013

15

Leber’s hereditary optic neuropathy with late disease onset: clinical and molecular characteristics of 20 patients

Dimitriadis, Konstantin, Leonhardt, Miriam, Yu-Wai-Man, Patrick, Kirkman, Matthew, Korsten, Alex, De Coo, Irenaeus F, Chinnery, Patrick, Klopstock, Thomas

Journal:

Orphanet Journal of Rare Diseases

Year:

2014

Language:

english

File:

PDF, 196 KB

english, 2014

16

Germline activating AKT3 mutation associated with megalencephaly, polymicrogyria, epilepsy and hypoglycemia

Nellist, Mark, Schot, Rachel, Hoogeveen-Westerveld, Marianne, Neuteboom, Rinze F., van der Louw, Elles J.T.M., Lequin, Maarten H., Bindels-de Heus, Karen, Sibbles, Barbara J., de Coo, René, Brooks, Al

Journal:

Molecular Genetics and Metabolism

Year:

2015

Language:

english

File:

PDF, 1.04 MB

english, 2015

17

PRRT2 mutation causes benign familial infantile convulsions

de Vries, B., Callenbach, P. M. C., Kamphorst, J. T., Weller, C. M., Koelewijn, S. C., Houten, R. t., de Coo, I. F. M., Brouwer, O. F., van den Maagdenberg, A. M. J. M.

Journal:

Year:

2012

Language:

english

File:

PDF, 191 KB

english, 2012

18

Symptomatic Trigeminal Autonomic Cephalalgias

de Coo, Ilse F., Wilbrink, Leopoldine A., Haan, Joost

Journal:

Current Pain and Headache Reports

Year:

2015

Language:

english

File:

PDF, 328 KB

english, 2015

19

RYR1 -related myopathies: a wide spectrum of phenotypes throughout life

Snoeck, M., van Engelen, B. G. M., Küsters, B., Lammens, M., Meijer, R., Molenaar, J. P. F., Raaphorst, J., Verschuuren-Bemelmans, C. C., Straathof, C. S. M., Sie, L. T. L., de Coo, I. F., van der Pol

Journal:

European Journal of Neurology

Year:

2015

Language:

english

File:

PDF, 723 KB

english, 2015

20

Molybdenum cofactor deficiency: Identification of a patient with homozygote mutation in the MOCS3 gene

Huijmans, Jan G. M., Schot, Rachel, de Klerk, Johannis B. C., Williams, Monique, de Coo, René F. M., Duran, Marinus, Verheijen, Frans W., van Slegtenhorst, Marjon, Mancini, Grazia M. S.

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 824 KB

english, 2017

21

SAE Technical Paper Series [SAE International International Congress & Exposition - (FEB. 24, 1992)] SAE Technical Paper Series - Airbag Simulations with the Madymo Fem Module

Bruijs, W.E.M., de Coo, P.J.A., Ashmore, R.J., Giles, A.R.

Year:

1992

Language:

english

File:

PDF, 486 KB

english, 1992

22

SAE Technical Paper Series [SAE International Stapp Car Crash Conference - (NOV. 05, 1990)] SAE Technical Paper Series - Airbag Modelling Techniques

Nieboer, J.J., Wismans, J., de Coo, P.J.A.

Year:

1990

Language:

english

File:

PDF, 1.31 MB

english, 1990

23

SAE Technical Paper Series [SAE International International Congress & Exposition - (FEB. 25, 1991)] SAE Technical Paper Series - Advances in MADYMO Crash Simulations

Lupker, H. A., de Coo, P. J. A., Nieboer, J. J., Wismans, J.

Year:

1991

Language:

english

File:

PDF, 708 KB

english, 1991

24

Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosis

Vandervore, Laura V., Schot, Rachel, Hoogeboom, A. Jeannette M., Lincke, Carsten, de Coo, Irenaeus F., Lequin, Maarten H., Dremmen, Marjolein, van Unen, Leontine M.A., Saris, Jasper J., Jansen, Anna C

Journal:

European Journal of Medical Genetics

Year:

2018

Language:

english

File:

PDF, 3.75 MB

english, 2018

25

Autosomal recessive limb‐girdle and Miyoshi muscular dystrophies in the Netherlands: the clinical and molecular spectrum of 244 patients.

ten Dam, L., Frankhuizen, W.S., Linssen, W.H.J.P., Straathof, C.S., Niks, E.H., Faber, C.G., Fock, J.M., Kuks, J.B., Brusse, E., de Coo, I.F., Voermans, N., Verrips, A., Hoogendijk, J.E., van der Pol,

Journal:

Clinical Genetics

Year:

2019

Language:

english

File:

PDF, 956 KB

english, 2019

26

A Clinical Diagnostic Algorithm for Early Onset Cerebellar Ataxia

Brandsma, R., Verschuuren-Bemelmans, C.C., Amrom, D., Barisic, N., Baxter, P., Bertini, E., Blumkin, L., Brankovic-Sreckovic, V., Brouwer, O.F., Bürk, K., Catsman-Berrevoets, C.E., Craiu, D., de Coo,

Journal:

European Journal of Paediatric Neurology

Year:

2019

Language:

english

File:

PDF, 912 KB

english, 2019

27

Within-person pain variability and physical activity in older adults with osteoarthritis from six European countries

Timmermans, Erik J., de Koning, Elisa J., van Schoor, Natasja M., van der Pas, Suzan, Denkinger, Michael D., Dennison, Elaine M., Maggi, Stefania, Pedersen, Nancy L., Otero, Ángel, Peter, Richard, Coo

Journal:

BMC Musculoskeletal Disorders

Year:

2019

File:

PDF, 598 KB

2019

28

An out-of-frame cytochrome b gene deletion from a patient with parkinsonism is associated with impaired complex III assembly and an increase in free radical production

Michele Rana, Irenaeus De Coo, Francisca Diaz, Hubert Smeets, Carlos T. Moraes

Journal:

Annals of Neurology

Year:

2000

Language:

english

File:

PDF, 974 KB

english, 2000

29

Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch families

G.M.S. Mancini, C.E. Catsman-Berrevoets, I.F.M. de Coo, F.K. Aarsen, J.H.J. Kamphoven, J.G. Huijmans, M. Duran, M.S. van der Knaap, C. Jakobs, G.S. Salomons

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 356 KB

english, 2005

30

Re: Polymicrogyria versus pachygyria in 22q11 microdeletion

Marie Claire Y. de Wit, Maarten H. Lequin, René F.M. de Coo, Grazia M.S. Mancini

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 28 KB

english, 2005

31

Additional mitochondrial DNA mutations may explain extra-ocular involvement in LHON

L. Spruijt, J.E. Hoogendijk, A.T.M. Hendrickx, I.F. de Coo, P.A. Doevendans, P.T.V.M. de Jong, W.G.M. Spliet, H. Kroes, H.J. Smeets

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 151 KB

english, 2006

32

Phenotypic consequences of a novel SCO2 gene mutation

Rob M. Verdijk, Ronald de Krijger, Kees Schoonderwoerd, Valeria Tiranti, Hubert Smeets, Lutgarde C.P. Govaerts, René de Coo

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 160 KB

english, 2008

33

Periventricular nodular heterotopia and distal limb deficiency: A recurrent association

Marie Claire Y. de Wit, Irenaeus F.M. de Coo, Rachel Schot, A. Jeannette M. Hoogeboom, Maarten H. Lequin, Annemieke J.M.H. Verkerk, Grazia M.S. Mancini

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 155 KB

english, 2010

34

Unbalanced der(5)t(5;20) translocation associated with megalencephaly, perisylvian polymicrogyria, polydactyly and hydrocephalus

Annemieke J.M.H. Verkerk, Rachel Schot, Laura van Waterschoot, Hannie Douben, Pino J. Poddighe, Maarten H. Lequin, Linda S. de Vries, Paulien Terhal, Johanne M.D. Hahnemann, Irenaeus F.M. de Coo, Mari

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 369 KB

english, 2010

35

Early onset neuropathy in a compound form of Charcot–Marie–Tooth disease

Farid Meggouh, Marianne de Visser, Willem F. M. Arts, Rene I. F. M. De Coo, Ivo N. van Schaik, Frank Baas

Journal:

Annals of Neurology

Year:

2005

Language:

english

File:

PDF, 65 KB

english, 2005

36

Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities

M. S. van der Knaap, L. M. E. Smit, P. G. Barth, C. E. Catsman-Berrevoets, O. F. Brouwer, J. H. Begeer, I. F. M. de Coo, J. Valk

Journal:

Annals of Neurology

Year:

1997

Language:

english

File:

PDF, 2.23 MB

english, 1997

37

P086 Pediatric myelodysplastic syndrome in a family with mitochondrial DNA mutations

A. De Vries, C. Zwaan, I. de Coo, D. Hellebrekers, A. Hendrickx, H. Smeets, H. Beverloo, M. van den Heuvel-Eibrink

Journal:

Leukemia Research

Year:

2009

Language:

english

File:

PDF, 41 KB

english, 2009

38

234 Role of mitochondrial DNA mutations in childhood MDS

A. de Vries, M. Zwaan, B. Beverloo, I. de Coo, G. Schoonderwoerd, A. Hendrickx, D. Hellebrekers, H. Smeets, H. Hasle, S. Polychronopoulou, R. Pieters, M. van den Heuvel-Eibrink

Journal:

Leukemia Research

Year:

2011

Language:

english

File:

PDF, 55 KB

english, 2011

39

Familial Partial Epilepsy with Variable Foci in a Dutch Family: Clinical Characteristics and Confirmation of Linkage to Chromosome 22q

Petra M. C. Callenbach, Arn M. J. M. Van Den Maagdenberg, Jouke J. Hottenga, Eelke H. Van Den Boogerd, René F. M. De Coo, Dick Lindhout, Rune R. Frants, Lodewijk A. Sandkuijl, Oebele F. Brouwer

Journal:

Year:

2003

Language:

english

File:

PDF, 109 KB

english, 2003

40

Tijdige diagnostiek en behandeling van de ziekte van Pompe kan irreversibele orgaanschade voorkomen

C.M. van Gelder, M.L.C. Hagemans, J.M.P. van den Hout, J.A.M. Smeitink, I.F.M. de Coo, A.T. van der Ploeg

Journal:

Tijdschrift voor Kindergeneeskunde

Year:

2011

Language:

dutch

File:

PDF, 110 KB

dutch, 2011

41

Human NDUFS3 gene coding for the 30-kDa subunit of mitochondrial Complex I: genomic organization and expression

Vincent Procaccio, Pierre Lescuyer, Ingrid Bourges, Réjane Beugnot, Hervé Duborjal, Danielle Depetris, Bénédicte Mousson, Marie-France Montfort, Hubert Smeets, René De Coo, Jean-Paul Issartel

Journal:

Mammalian Genome

Year:

2000

Language:

english

File:

PDF, 239 KB

english, 2000

42

The structure of the human NDUFV1 gene encoding the 51-kDa subunit of mitochondrial complex I

René F.M. de Coo, Paul A.L. Buddiger, Hubert J.M. Smeets, Bernard A. van Oost

Journal:

Mammalian Genome

Year:

1999

Language:

english

File:

PDF, 761 KB

english, 1999

43

Combined cardiological and neurological abnormalities due tofilamin Agene mutation

Marie Claire Y. de Wit, Irenaeus F. M. de Coo, Maarten H. Lequin, Dicky J. J. Halley, Jolien W. Roos-Hesselink, Grazia M. S. Mancini

Journal:

Clinical Research in Cardiology

Year:

2011

Language:

english

File:

PDF, 222 KB

english, 2011

44

Muscle weakness as presenting symptom of osteogenesis imperfecta

Annemieke M. Boot, Rene F. M. de Coo, Gerard Pals, Sabine M. P. F. de Muinck Keizer-Schrama

Journal:

European Journal of Pediatrics

Year:

2006

Language:

english

File:

PDF, 164 KB

english, 2006

45

Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitus

M. C. Y. de Wit, I. F. M. de Coo, C. Julier, M. Delépine, M. H. Lequin, I. van de Laar, B. J. Sibbles, G. J. Bruining, G. M. S. Mancini

Journal:

Year:

2006

Language:

english

File:

PDF, 201 KB

english, 2006

46

Movement disorder and neuronal migration disorder due toARFGEF2mutation

M. C. Y. de Wit, I. F. M. de Coo, D. J. J. Halley, M. H. Lequin, G. M. S. Mancini

Journal:

Year:

2009

Language:

english

File:

PDF, 226 KB

english, 2009

47

Long-term follow-up and treatment in nine boys with X-linked creatine transporter defect

Jiddeke M. van de Kamp, Petra J. W. Pouwels, Femke K. Aarsen, Leontine W. ten Hoopen, Dirk L. Knol, Johannes B. de Klerk, Ireneus F. de Coo, Jan G. M. Huijmans, Cornelis Jakobs, Marjo S. van der Knaap

Journal:

Journal of Inherited Metabolic Disease

Year:

2012

Language:

english

File:

PDF, 329 KB

english, 2012

48

Experimental analysis of floored interstices in clastic carbonate sediments

John C. Deelman, Jan C.M. de Coo

Journal:

Sedimentary Geology

Year:

1976

Language:

english

File:

PDF, 2.04 MB

english, 1976

49

Labelling and evaluation of (99mTc-atropine)

ConsueloArteaga De Murphy, N. Alexis Vidal, L. Juan Jose Coo, J. Aida Ruiz, Ma.DeLosAngeles Contreras

Journal:

International Journal of Radiation Applications and Instrumentation. Part C. Radiation Physics and Chemistry

Year:

1989

Language:

english

File:

PDF, 55 KB

english, 1989

50

Refinement of the chromosome 16 locus for benign familial infantile convulsions

PMC Callenbach, EH Van Den Boogerd, RFM De Coo, R Ten Houten, JC Oosterwijk, G Hageman, RR Frants, OF Brouwer, AMJM Van Den Maagdenberg

Journal:

Clinical Genetics

Year:

2005

Language:

english

File:

PDF, 145 KB

english, 2005

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