N. Losekoot: search on Z-Library

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1

Barriers and challenges in the application of Six Sigma in the hospitality industry

Kokkranikal, Jithendran, Antony, Jiju, Kosgi, Hasib, Losekoot, Erwin

Journal:

International Journal of Productivity and Performance Management

Year:

2013

Language:

english

File:

PDF, 160 KB

english, 2013

2

Mutation detection by denaturing gradient gel electrophoresis (DGGE)

Riccardo Fodde, Monique Losekoot

Journal:

Year:

1994

Language:

english

File:

PDF, 1.11 MB

english, 1994

3

Analysis of missense variants in thePKHD1-gene in patients with autosomal recessive polycystic kidney disease (ARPKD)

Monique Losekoot, Cathleen Haarloo, Claudia Ruivenkamp, Stefan J. White, Martijn H. Breuning, Dorien J. M. Peters

Journal:

Year:

2005

Language:

english

File:

PDF, 2.39 MB

english, 2005

4

Out for the count: some methodological questions in ‘publications counting’ literature

Erwin Losekoot, Constantinos S. Verginis, Roy C. Wood

Journal:

International Journal of Hospitality Management

Year:

2001

Language:

english

File:

PDF, 114 KB

english, 2001

5

The application of facilities management expertise to the hotel renovation process

Hassanien, Ahmed, Losekoot, Erwin

Journal:

Year:

2002

Language:

english

File:

PDF, 104 KB

english, 2002

6

An Assessment of Key Hotel Guest Contact Personnel in Handling Guest Complaints

Tantawy, Alaa, Losekoot, Erwin

Journal:

Journal of Quality Assurance in Hospitality & Tourism

Year:

2000

Language:

english

File:

PDF, 147 KB

english, 2000

7

[IEEE 2005 IEEE International Geoscience and Remote Sensing Symposium, 2005. IGARSS '05. - Seoul, Korea (25-29 July 2005)] Proceedings. 2005 IEEE International Geoscience and Remote Sensing Symposium, 2005. IGARSS '05. - Operational use of ship detection to combat illegal fishing in the Southern Indian Ocean

Losekoot, M., Schwab, P.

Year:

2005

Language:

english

File:

PDF, 656 KB

english, 2005

8

IGF1, IGF1R and SHOX Mutation Analysis in Short Children Born Small for Gestational Age and Short Children with Normal Birth Size (Idiopathic Short Stature)

Caliebe, Janina, Broekman, Sander, Boogaard, Merel, Bosch, Cathy A.J., Ruivenkamp, Claudia A.L., Oostdijk, Wilma, Kant, S.G., Binder, Gerhard, Ranke, Michael B., Wit, Jan M., Losekoot, Monique

Journal:

Hormone Research in Paediatrics

Year:

2012

Language:

english

File:

PDF, 197 KB

english, 2012

9

Successful Long-Term Growth Hormone Therapy in a Girl with Haploinsufficiency of the Insulin-Like Growth Factor-I Receptor due to a Terminal 15q26.2->qter Deletion Detected by Multiplex Ligation Probe Amplification

Walenkamp, Marie J. E., de Muinck Keizer-Schrama, Sabine M. P. F., de Mos, Marianne, Kalf, Margot E., van Duyvenvoorde, Hermine A., Boot, Annemieke M., Kant, Sarina G., White, Stefan J., Losekoot, Mon

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2008

Language:

english

File:

PDF, 125 KB

english, 2008

10

"The only thing I know is that I know nothing": 5-fluorouracil in human milk

Peccatori, F. A., Giovannetti, E., Pistilli, B., Bellettini, G., Codacci-Pisanelli, G., Losekoot, N., Curigliano, G., Azim, H. A., Goldhirsch, A., Peters, G. J.

Journal:

Annals of Oncology

Year:

2012

Language:

english

File:

PDF, 127 KB

english, 2012

11

Hospitality in hospitals: The importance of caring about the patient

Kelly, Rosalind, Losekoot, Erwin, Wright-StClair, Valerie A.

Journal:

Hospitality & Society

Year:

2016

Language:

english

File:

PDF, 823 KB

english, 2016

12

Phenotypic Features and Response to GH Treatment of Patients With a Molecular Defect of the IGF-1 Receptor

Walenkamp, Marie J E, Robers, Jasmijn M L, Wit, Jan M, Zandwijken, Gladys R J, van Duyvenvoorde, Hermine A, Oostdijk, Wilma, Hokken-Koelega, Anita C S, Kant, Sarina G, Losekoot, Monique

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2019

Language:

english

File:

PDF, 741 KB

english, 2019

13

Predictive testing of 25 percent at-risk individuals for Huntington disease (1987-1997)

Maat-Kievit, Anneke, Vegter-van der Vlis, Maria, Zoeteweij, Moniek, Losekoot, Monique, van Haeringen, Arie, Roos, Raymund A.C.

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 130 KB

english, 1999

14

Experience in prenatal testing for Huntington's disease in The Netherlands: procedures, results and guidelines (1987–1997)

Anneke Maat-Kievit, Maria Vegter-van der Vlis, Moniek Zoeteweij, Monique Losekoot, Arie van Haeringen, Humphrey Kanhai, Raymund Roos

Journal:

Prenatal Diagnosis

Year:

1999

Language:

english

File:

PDF, 169 KB

english, 1999

15

First-trimester diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) using PPT enzyme assay and CLN1 mutation analysis

B. B. A. de Vries, W. J. Kleijer, J. L. M. Keulemans, Y. V. Voznyi, P. F. Franken, M. C. M. Eurlings, R. J. Galjaard, M. Losekoot, C. E. Catsman-Berrevoets, M. H. Breuning, P. E. M. Taschner, O. P. va

Journal:

Prenatal Diagnosis

Year:

1999

Language:

english

File:

PDF, 163 KB

english, 1999

16

Rapid detection of point mutations and polymorphisms of the α-globin genes by DGGE and SSCA

Kees L. Harteveld, Angelien J.G.A.M. Heister, Piero C. Giordano, Monique Losekoot, Luigi F. Bernini

Journal:

Year:

1996

Language:

english

File:

PDF, 807 KB

english, 1996

17

First-trimester diagnosis of late-infantile neuronal ceroid lipofuscinosis (LINCL) by tripeptidyl peptidase I assay and CLN2 mutation analysis

W. J. Kleijer, O. P. van Diggelen, J. L. M. Keulemans, M. Losekoot, V. H. Garritsen, H. Stroink, D. Majoor-Krakauer, P. F. Franken, M. C. M. Eurlings, P. E. M. Taschner, F. J. Los, R. J. H. Galjaard

Journal:

Prenatal Diagnosis

Year:

2001

Language:

english

File:

PDF, 53 KB

english, 2001

18

Using a roster and haplotyping is useful in risk assessment for persons with intermediate and reduced penetrance alleles in Huntington disease

Anneke Maat-Kievit, Paula Helderman-van den Enden, Monique Losekoot, Peter de Knijff, René Belfroid, Maria Vegter-van der Vlis, Raymund Roos, Martijn Breuning

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 121 KB

english, 2001

19

RNF135 mutations are not present in patients with Sotos syndrome-like features

Remco Visser, Nynke Koelma, Linda Vijfhuizen, Michiel J.R. van der Wielen, Sarina G. Kant, Martijn H. Breuning, Jan M. Wit, Monique Losekoot

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 80 KB

english, 2009

20

Adult neuronal ceroid lipofuscinosis with palmitoyl-protein thioesterase deficiency: First adult-onset patients of a childhood disease

Otto P. Van Diggelen, Stephane Thobois, Caroline Tilikete, Marie-Thérèse Zabot, Joke L. M. Keulemans, Patrick A. Van Bunderen, Peter E. M. Taschner, Monique Losekoot, Yakov V. Voznyi

Journal:

Annals of Neurology

Year:

2001

Language:

english

File:

PDF, 823 KB

english, 2001

21

Asn540Thr substitution in the fibroblast growth factor receptor 3 tyrosine kinase domain causing hypochondroplasia

Piette P. Deutz-Terlouw, Monique Losekoot, Cora M. Aalfs, Raoul C.M. Hennekam, Egbert Bakker

Journal:

Year:

1998

Language:

english

File:

PDF, 509 KB

english, 1998

22

Hb Utrecht [α2 129(H12)Leu → Pro], a new unstable α2-chain variant associated with a mild α-thalassaemic phenotype

C. L. Harteveld, P. C. Giordano, M. Losekoot, J. G. A. M. Heister, D. Batelaan, P. Van Delft, M. C. A. Bruin, L. F. Bernini

Journal:

British Journal of Haematology

Year:

1996

Language:

english

File:

PDF, 1.59 MB

english, 1996

23

An IVS1–116 (A→G) acceptor splice site mutation in the α2 globin gene causing α+ thalassaemia in two Dutch families

C. L. Harteveld, J. G. A. M. Heister, P. C. Giordano, D. Batelaan, P. v. Delft, H. L. Haak, P. W. Wijermans, M. Losekoot, L. F. Bernini

Journal:

British Journal of Haematology

Year:

1996

Language:

english

File:

PDF, 552 KB

english, 1996

24

Atypical HbH disease in a Surinamese patient resulting from a combination of the −SEA and −α3.7 deletions with HbC heterozygosity

P. C. GIORDANO, C. L. HARTEVELD, J. J. MICHIELS, W. TERPSTRA, D. BATELAAN, P. VAN DELFT, R. J. PLUG, M. J. R. VAN DER WIELEN, M. LOSEKOOT, L. F. BERNINI

Journal:

British Journal of Haematology

Year:

1997

Language:

english

File:

PDF, 446 KB

english, 1997

25

A novel 7·9 kb deletion causing α+-thalassaemia in two independent families of Indian origin

Cornelis L. Harteveld, Peter Van Delft, Pierre W. Wijermans, Mies C. Kappers-Klunne, Jitske Weegenaar, Monique Losekoot, Piero C. Giordano

Journal:

British Journal of Haematology

Year:

2003

Language:

english

File:

PDF, 178 KB

english, 2003

26

A novel δ° arising from a frameshift insertion, detected by direct sequencing of enzymatically amplified DNA

Monique Losekoot, Riccardo Fodde, Piero C. Giordano, Luigi F. Bernini

Journal:

Year:

1989

Language:

english

File:

PDF, 570 KB

english, 1989

27

Partial abnormal pulmonary venous return in Turner syndrome

A. G. Wassenaer, L. J. Lubbers, G. Losekoot

Journal:

European Journal of Pediatrics

Year:

1988

Language:

english

File:

PDF, 663 KB

english, 1988

28

Prevalence and molecular heterogeneity of alfa+thalassemia in two tribal populations from Andhra Pradesh, India

R. Fodde, M. Losekoot, M. H. Broek, M. Oldenburg, N. Rashida, A. Schreuder, J. T. Wijnen, P. C. Giordano, N. V. S. Nayudu, P. Meera Khan, L. F. Bernini

Journal:

Year:

1988

Language:

english

File:

PDF, 447 KB

english, 1988

29

The involvement of Alu repeats in recombination events at the α-globin gene cluster: characterization of two α°-thalassaemia deletion breakpoints

K. L. Harteveld, Monique Losekoot, Riccardo Fodde, Piero C. Giordano, Luigi F. Bernini

Journal:

Year:

1997

Language:

english

File:

PDF, 135 KB

english, 1997

30

α-Thalassemia in The Netherlands: a heterogeneous spectrum of both deletions and point mutations

K. L. Harteveld, Monique Losekoot, Angelien J. G. A. M. Heister, Michiel van der Wielen, Piero C. Giordano, Luigi F. Bernini

Journal:

Year:

1997

Language:

english

File:

PDF, 79 KB

english, 1997

31

Cellular pharmacology of multi- and duplex drugsconsisting of ethynylcytidine and 5-fluoro-2′-deoxyuridine

Irene V. Bijnsdorp, Reto A. Schwendener, Herbert Schott, Iduna Fichtner, Kees Smid, Adrie C. Laan, Sarah Schott, Nienke Losekoot, Richard J. Honeywell, Godefridus J. Peters

Journal:

Investigational New Drugs

Year:

2011

Language:

english

File:

PDF, 204 KB

english, 2011

32

Simple and selective method for the determination of various tyrosine kinase inhibitors used in the clinical setting by liquid chromatography tandem mass spectrometry

R. Honeywell, K. Yarzadah, E. Giovannetti, N. Losekoot, E.F. Smit, M. Walraven, J.S.W. Lind, C. Tibaldi, H.M. Verheul, G.J. Peters

Journal:

Journal of Chromatography B

Year:

2010

Language:

english

File:

PDF, 591 KB

english, 2010

33

Hepatocyte nuclear factor (HNF)1A and HNF4A substitution occurring simultaneously in a family with maturity-onset diabetes of the young

H. J. B. H. Beijers, M. Losekoot, R. J. Odink, B. Bravenboer

Journal:

Diabetic Medicine

Year:

2009

Language:

english

File:

PDF, 80 KB

english, 2009

34

Juvenile-onset neuronal ceroid lipofuscinosis with infantile CLN1 mutation and palmitoyl-protein thioesterase deficiency

R. Kälviäinen, K. Eriksson, M. Losekoot, I. Sorri, I. Harvima, P. Santavuori, I. Järvelä, T. Autti, R. Vanninen, T. Salmenperä, O. P. Van Diggelen

Journal:

European Journal of Neurology

Year:

2007

Language:

english

File:

PDF, 506 KB

english, 2007

35

Neuronal Intranuclear and Neuropil Inclusions for Pathological Assessment of Huntington’s Disease

Marion Maat-Schieman, Raymund Roos, Monique Losekoot, Josephine Dorsman, Corrie Welling-Graafland, Ingrid Hegeman-Kleinn, Freerk Broeyer, Martijn Breuning, Sjoerd Van Duinen

Journal:

Brain Pathology

Year:

2007

Language:

english

File:

PDF, 310 KB

english, 2007

36

Thymidine phosphorylase in cancer cells stimulates human endothelial cell migration and invasion by the secretion of angiogenic factors

Bijnsdorp, I V, Capriotti, F, Kruyt, F A E, Losekoot, N, Fukushima, M, Griffioen, A W, Thijssen, V L, Peters, G J

Journal:

British Journal of Cancer

Year:

2011

Language:

english

File:

PDF, 480 KB

english, 2011

37

A European pilot quality assessment scheme for molecular diagnosis of Huntington's disease

Losekoot, Monique, Bakker, Bert, Laccone, Franco, Stenhouse, Su, Elles, Rob

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 78 KB

english, 1999

38

Trifluorothymidine Resistance Is Associated with Decreased Thymidine Kinase and Equilibrative Nucleoside Transporter Expression or Increased Secretory Phospholipase A2

Temmink, O. H., Bijnsdorp, I. V., Prins, H. J., Losekoot, N., Adema, A. D., Smid, K., Honeywell, R. J., Ylstra, B., Eijk, P. P., Fukushima, M.

Journal:

Molecular Cancer Therapeutics

Year:

2010

Language:

english

File:

PDF, 430 KB

english, 2010

39

Separation of his-purkinje potentials from coinciding atrium signals: Removal of the P-wave from the electrocardiogram

A. Peper, R. Jonges, T. G. Losekoot, C. Grimbergen

Journal:

Medical and Biological Engineering and Computing

Year:

1982

Language:

english

File:

PDF, 480 KB

english, 1982

40

Recording of surface His-Purkinje potentials

A. Peper, R. Jonges, T. G. Losekoot, C. A. Grimbergen

Journal:

Medical and Biological Engineering and Computing

Year:

1985

Language:

english

File:

PDF, 1.97 MB

english, 1985

41

Method for the computation of an accurate zero reference for ECG signals

A. Peper, R. Jonges, C. A. Grimbergen, T. G. Losekoot, J. Strackee

Journal:

Medical and Biological Engineering and Computing

Year:

1990

Language:

english

File:

PDF, 1.31 MB

english, 1990

42

Oxaliplatin activity in selected and unselected human ovarian and colorectal cancer cell lines

Paul Noordhuis, Adri C. Laan, Kasper van de Born, Nienke Losekoot, Ietje Kathmann, Godefridus J. Peters

Journal:

Biochemical Pharmacology

Year:

2008

Language:

english

File:

PDF, 535 KB

english, 2008

43

Detection of fetal erythroblasts in maternal blood by onestep gradient enrichment and immunocytochemical recognition

J.C. Oosterwijk, W.E. Mesker, M.C.M. Ouwerkerk, C.F.H.M. Knepflé, M.J.M. van der Burg, C.C. Wiesmeijer, G.C. Beverstock, M. Losekoot, L.F. Bernini, G.J.B. van Ommen, J.J.P. van de Kamp, H.H.H. Kanhai,

Journal:

Early Human Development

Year:

1996

Language:

english

File:

PDF, 157 KB

english, 1996

44

Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: a rapid and reliable diagnostic approach to beta thalassaemia

M. Losekoot, R. Fodde, C. L. Harteveld, H. van Heeren, P. C. Giordano, L. F. Bernini

Journal:

British Journal of Haematology

Year:

1990

Language:

english

File:

PDF, 905 KB

english, 1990

45

Rapid identification by denaturing gradient gel electrophoresis of mutations in the γ-globin gene promoters in non-deletion type HPFH

E. Gottardi, M. Losekoot, R. Fodde, G. Saglio, C. Camaschella, L. F. Bernini

Journal:

British Journal of Haematology

Year:

1992

Language:

english

File:

PDF, 841 KB

english, 1992

46

A novel polyadenylation signal mutation in the α2-globin gene causing α thalassaemia

C. L. Harteveld, M. Losekoot, H. Haak, J. G. A. M. Heister, P. C. Giordano, L. F. Bernini

Journal:

British Journal of Haematology

Year:

1994

Language:

english

File:

PDF, 404 KB

english, 1994

47

Multiple recombination events are responsible for the heterogeneity of α+-thalassemia haplotypes among the forest tribes of Andhra Pradesh, India

R. FODDE, C. L. HARTEVELD, M. LOSEKOOT, P. C. GIORDANO, P. MEERA KHAN, N. V. S. NAYUDU, L. F. BERNINI

Journal:

Annals of Human Genetics

Year:

1991

Language:

english

File:

PDF, 531 KB

english, 1991

48

Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation

E.K. Bijlsma, A. Collins, F.T. Papa, M.I. Tejada, P. Wheeler, E.A.J. Peeters, A.C.J. Gijsbers, J.M. van de Kamp, M. Kriek, M. Losekoot, A.J. Broekma, J.A. Crolla, M. Pollazzon, M. Mucciolo, E. Katzaki

Journal:

European Journal of Medical Genetics

Year:

2012

Language:

english

File:

PDF, 1.28 MB

english, 2012

49

The severe short stature in two siblings with a heterozygous IGF1 mutation is not caused by a dominant negative effect of the putative truncated protein

H.A. van Duyvenvoorde, J. van Doorn, J. Koenig, L. Gauguin, W. Oostdijk, J.D. Wade, M. Karperien, C.A.L. Ruivenkamp, M. Losekoot, P.A. van Setten, M.J.E. Walenkamp, C. Noordam, P. De Meyts, J.M. Wit

Journal:

Growth Hormone & IGF Research

Year:

2011

Language:

english

File:

PDF, 570 KB

english, 2011

50

Prevalence and clinical phenotype of the p.Val226Met glucokinase gene mutation in French Canadians in Quebec, Canada

Mélanie Henderson, Emile Levy, Edgard Delvin, Monique Losekoot, Marie Lambert

Journal:

Molecular Genetics and Metabolism

Year:

2007

Language:

english

File:

PDF, 224 KB

english, 2007

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