Hakutulokset - Servi J.C. Stevens

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  1. 1
    Toward Standardization of Epstein-Barr Virus DNA Load Monitoring: Unfractionated Whole Blood as Preferred Clinical Specimen

    Toward Standardization of Epstein-Barr Virus DNA Load Monitoring: Unfractionated Whole Blood as Preferred Clinical Specimen Tekijä Servi J.C. Stevens, Inge Pronk, Jaap M. Middeldorp

    Julkaistu 2001
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  2. 2
    High Epstein–Barr virus (EBV) DNA loads in HIV-infected patients: correlation with antiretroviral therapy and quantitative EBV serology

    High Epstein–Barr virus (EBV) DNA loads in HIV-infected patients: correlation with antiretroviral therapy and quantitative EBV serology Tekijä Servi J.C. Stevens, Brian S. N. Blank, Paul H.M. Smits, Pieter L. Meenhorst, Jaap M. Middeldorp

    Julkaistu 2002
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  3. 3
    Monitoring of Epstein-Barr Virus DNA Load in Peripheral Blood by Quantitative Competitive PCR

    Monitoring of Epstein-Barr Virus DNA Load in Peripheral Blood by Quantitative Competitive PCR Tekijä Servi J.C. Stevens, Marcel B. H. J. Vervoort, Adriaan J. C. van den Brule, Pieter L. Meenhorst, Chris J.L.M. Meijer, Jaap M. Middeldorp

    Julkaistu 1999
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  4. 4
    TREATMENT OF POSTTRANSPLANT LYMPHOPROLIFERATIVE DISEASE WITH RITUXIMAB

    TREATMENT OF POSTTRANSPLANT LYMPHOPROLIFERATIVE DISEASE WITH RITUXIMAB Tekijä Erik A.M. Verschuuren, Servi J.C. Stevens, Gustaaf W. van Imhoff, Jaap M. Middeldorp, Conny de Boer, Gerard H. Koëter, Hauw The, Wim van der Bij

    Julkaistu 2002
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  5. 5
    Diagnostic Value of Measuring Epstein-Barr Virus (EBV) DNA Load and Carcinoma-Specific Viral mRNA in Relation to Anti-EBV Immunoglobulin A (IgA) and IgG Antibody Levels in Blood of Nasopharyngeal Carcinoma Patients from Indonesia

    Diagnostic Value of Measuring Epstein-Barr Virus (EBV) DNA Load and Carcinoma-Specific Viral mRNA in Relation to Anti-EBV Immunoglobulin A (IgA) and IgG Antibody Levels in Blood of... Tekijä Servi J.C. Stevens, Sandra A.W.M. Verkuijlen, Bambang Hariwiyanto, Harijadi Harijadi, Jajah Fachiroh, Dewi Kartikawati Paramita, I. Bing Tan, Sophia M. Haryana, Jaap M. Middeldorp

    Julkaistu 2005
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  6. 6
    Frequent monitoring of Epstein-Barr virus DNA load in unfractionated whole blood is essential for early detection of posttransplant lymphoproliferative disease in high-risk patients

    Frequent monitoring of Epstein-Barr virus DNA load in unfractionated whole blood is essential for early detection of posttransplant lymphoproliferative disease in high-risk patient... Tekijä Servi J.C. Stevens, Erik A.M. Verschuuren, Inge Pronk, Wim van der Bij, Martin C. Harmsen, T H Thé, Chris J.L.M. Meijer, Adriaan J. C. van den Brule, Jaap M. Middeldorp

    Julkaistu 2001
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  7. 7
    A Phase I Trial of Epstein-Barr Virus Gp350 Vaccine for Children With Chronic Kidney Disease Awaiting Transplantation

    A Phase I Trial of Epstein-Barr Virus Gp350 Vaccine for Children With Chronic Kidney Disease Awaiting Transplantation Tekijä Lesley Rees, E. Jane Tizard, Andrew Morgan, W. D. Cubitt, S. Finerty, T Oyewole-Eletu, Karen Owen, Collin Royed, Servi J.C. Stevens, Rukshana Shroff, Manjit Tanday, A.D. Wilson, Jaap M. Middeldorp, P L Amlot, Neil Steven

    Julkaistu 2009
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  8. 8
    Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro

    Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro Tekijä Senthilkumar A. Natesan, Alex J. Bladon, Serdar Coşkun, Wafa Qubbaj, R. Prates, S. Munné, Edith Coonen, J. Dreesen, Servi J.C. Stevens, Aimée Paulussen, Sharyn Stock‐Myer, L. Wilton, Souraya Jaroudi, Dagan Wells, Anthony P. Brown, Alan H. Handyside

    Julkaistu 2014
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  9. 9
    Epstein-Barr Virus DNA Load in Nasopharyngeal Brushings and Whole Blood in Nasopharyngeal Carcinoma Patients before and after Treatment

    Epstein-Barr Virus DNA Load in Nasopharyngeal Brushings and Whole Blood in Nasopharyngeal Carcinoma Patients before and after Treatment Tekijä Marlinda Adham, Astrid E. Greijer, Sandra A.W.M. Verkuijlen, Hedy Juwana, Sabine Fleig, Lisnawati Rachmadi, Octavia Malik, A. N. Kurniawan, Averdi Roezin, Soehartati Gondhowiardjo, Djumhana Atmakusumah, Servi J.C. Stevens, Bambang Hermani, I. Bing Tan, Jaap M. Middeldorp

    Julkaistu 2013
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  10. 10
    Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders

    Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders Tekijä Rolph Pfundt, Marisol del Rosario, Lisenka E.L.M. Vissers, Michael Kwint, Irene M. Janssen, Nicole de Leeuw, Helger G. Yntema, Marcel Nelen, Dorien Lugtenberg, Erik‐Jan Kamsteeg, Nienke Wieskamp, Alexander P.A. Stegmann, Servi J.C. Stevens, Richard J. Rodenburg, Annet Simons, Arjen R. Mensenkamp, Tuula Rinne, Christian Gilissen, Hans Scheffer, Joris A. Veltman, Jayne Y. Hehir‐Kwa

    Julkaistu 2016
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  11. 11
    Variation in a range of mTOR-related genes associates with intracranial volume and intellectual disability

    Variation in a range of mTOR-related genes associates with intracranial volume and intellectual disability Tekijä Margot R.F. Reijnders, Maria Kousi, Geeske M. van Woerden, Marieke Klein, Janita Bralten, Grazia M.S. Mancini, Ton van Essen, Martina Proietti Onori, Eric Smeets, M. van Gastel, Alexander P.A. Stegmann, Servi J.C. Stevens, Stefan H. Lelieveld, Christian Gilissen, Rolph Pfundt, Perciliz L. Tan, Tjitske Kleefstra, Barbara Franke, Ype Elgersma, Nicholas Katsanis, Han G. Brunner

    Julkaistu 2017
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  12. 12
    Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability

    Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability Tekijä Stefan H. Lelieveld, Margot R.F. Reijnders, Rolph Pfundt, Helger G. Yntema, Erik‐Jan Kamsteeg, Petra de Vries, Bert B.A. de Vries, Marjolein H. Willemsen, Tjitske Kleefstra, Katharina Löhner, Maaike Vreeburg, Servi J.C. Stevens, Ineke van der Burgt, Ernie M.H.F. Bongers, Alexander P.A. Stegmann, Patrick Rump, Tuula Rinne, Marcel Nelen, Joris A. Veltman, Lisenka E.L.M. Vissers, Han G. Brunner, Christian Gilissen

    Julkaistu 2016
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  13. 13
    Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imaging

    Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imaging Tekijä Chantal Deden, Kornelia Neveling, Dimitra Zafeiropopoulou, Christian Gilissen, Rolph Pfundt, Tuula Rinne, Nicole de Leeuw, Brigitte H. W. Faas, Thatjana Gardeitchik, Suzanne C.E.H. Sallevelt, Aimée Paulussen, Servi J.C. Stevens, Esther Sikkel, Mariet W. Elting, Merel C. van Maarle, Karin E. M. Diderich, Nicole Corsten‐Janssen, Klaske D. Lichtenbelt, Guus Lachmeijer, Lisenka E.L.M. Vissers, Helger G. Yntema, Marcel Nelen, Ilse Feenstra, Wendy A.G. van Zelst–Stams

    Julkaistu 2020
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  14. 14
    Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss

    Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss Tekijä Rick Essers, И. Н. Лебедев, Ants Kurg, Е. А. Фонова, Servi J.C. Stevens, Rebekka M. Koeck, Ulrike von Rango, Lloyd Brandts, Spyridon Panagiotis Deligiannis, Nikitina Tv, Е. А. Саженова, Е. Н. Толмачева, А. А. Кашеварова, D. A. Fedotov, Viktoria V. Demeneva, Д. И. Жигалина, Г.В. Дроздов, Salwan Al‐Nasiry, Merryn Macville, Arthur van den Wijngaard, Jos Dreesen, Aimée Paulussen, Alexander Hoischen, Han G. Brunner, Andres Salumets, Masoud Zamani Esteki

    Julkaistu 2023
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  15. 15
    Noninvasive Prenatal Test Results Indicative of Maternal Malignancies: A Nationwide Genetic and Clinical Follow-Up Study

    Noninvasive Prenatal Test Results Indicative of Maternal Malignancies: A Nationwide Genetic and Clinical Follow-Up Study Tekijä Catharina J. Heesterbeek, Sietse Aukema, Robert‐Jan H. Galjaard, Elles M. J. Boon, Malgorzata I. Srebniak, Katelijne Bouman, Brigitte H. W. Faas, Lutgarde Govaerts, Mariëtte J.V. Hoffer, Nicolette S. den Hollander, Klaske D. Lichtenbelt, Merel C. van Maarle, Lisanne van Prooyen Schuurman, Maartje C. van Rij, G. Heleen Schuring‐Blom, Servi J.C. Stevens, Gita Tan-Sindhunata, Masoud Zamani Esteki, Christine de Die‐Smulders, Vivianne C. G. Tjan‐Heijnen, Lidewij Henneman, Erik A. Sistermans, Merryn Macville

    Julkaistu 2022
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  16. 16
    The performance of genome sequencing as a first-tier test for neurodevelopmental disorders

    The performance of genome sequencing as a first-tier test for neurodevelopmental disorders Tekijä Bart van der Sanden, Gaby Schobers, Jordi Corominas Galbany, David A. Koolen, Margje Sinnema, Jeroen van Reeuwijk, Connie T. R. M. Stumpel, Tjitske Kleefstra, Bert B.A. de Vries, Martina Ruiterkamp‐Versteeg, Nico Leijsten, Michael Kwint, Ronny Derks, Hilde Swinkels, Amber den Ouden, Rolph Pfundt, Tuula Rinne, Nicole de Leeuw, Alexander P.A. Stegmann, Servi J.C. Stevens, Arthur van den Wijngaard, Han G. Brunner, Helger G. Yntema, Christian Gilissen, Marcel Nelen, Lisenka E.L.M. Vissers

    Julkaistu 2022
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  17. 17
    Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing

    Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing Tekijä A Janssen, Rebekka M. Koeck, Rick Essers, Ping Cao, Wanwisa van Dijk, Marion Drüsedau, Jeroen Meekels, Burcu Yaldiz, Maartje van de Vorst, Bart de Koning, Debby M.E.I. Hellebrekers, Servi J.C. Stevens, Su Ming Sun, Malou Heijligers, Sonja A. de Munnik, Chris M.J. van Uum, Juul Achten, Lars Hamers, Marjan Naghdi, Lisenka E.L.M. Vissers, Ron J T van Golde, Guido de Wert, Jos Dreesen, Christine de Die‐Smulders, Edith Coonen, Han G. Brunner, Arthur van den Wijngaard, Aimée Paulussen, Masoud Zamani Esteki

    Julkaistu 2024
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  18. 18
    Deleterious de novo variants of X‐linked <i>ZC4H2</i> in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita

    Deleterious de novo variants of X‐linked <i>ZC4H2</i> in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita Tekijä Suzanna G.M. Frints, Friederike Hennig, Roberto Colombo, Sébastien Jacquemont, Paulien A. Terhal, Holly H. Zimmerman, David Hunt, Bryce A. Mendelsohn, Ulrike Kordaß, Richard Webster, Margje Sinnema, Omar Abdul‐Rahman, Vanessa Suckow, Alberto Fernández‐Jaén, Kees van Roozendaal, Servi J.C. Stevens, Merryn Macville, Salwan Al‐Nasiry, Koen L.I. van Gassen, N Utzig, Suzanne M. Koudijs, Lesley McGregor, Saskia M. Maas, Diana Baralle, Abhijit Dixit, Peter Wieacker, Marcus Lee, Arthur S. Lee, Elizabeth C. Engle, Gunnar Houge, Gyri Aasland Gradek, Andrew G. L. Douglas, Cheryl Longman, Shelagh Joss, Danita Velasco, Raoul C. M. Hennekam, Hiromi Hirata, Vera M. Kalscheuer

    Julkaistu 2019
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  19. 19
    Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study

    Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study Tekijä Lisanne van Prooyen Schuurman, Erik A. Sistermans, Diane Van Opstal, Lidewij Henneman, Mireille N. Bekker, Caroline J. Bax, Mijntje J. Pieters, Katelijne Bouman, Sonja de Munnik, Nicolette S. den Hollander, Karin E. M. Diderich, Brigitte H. W. Faas, Ilse Feenstra, Attie T. J. I. Go, Mariëtte J.V. Hoffer, Marieke Joosten, Fenne L. Komdeur, Klaske D. Lichtenbelt, Maria Lombardi, Marike Polak, Fernanda Sarquis Jehee, Heleen Schuring‐Blom, Servi J.C. Stevens, Malgorzata I. Srebniak, Ron F. Suijkerbuijk, Gita Tan-Sindhunata, Karuna R. M. van der Meij, Merel C. van Maarle, Vivian Vernimmen, Shama L. van Zelderen‐Bhola, Nicolien T. van Ravesteyn, Maarten F. C. M. Knapen, Merryn Macville, Robert‐Jan H. Galjaard

    Julkaistu 2022
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  20. 20
    A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency

    A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency Tekijä Sandra Jansen, Alexander Hoischen, Bradley P. Coe, Gemma L. Carvill, Hilde Van Esch, Daniëlle G.M. Bosch, Ulla A. Andersen, Carl Baker, Marijke Bauters, Raphael Bernier, Bregje W.M. van Bon, Hedi L. Claahsen‐van der Grinten, Jozef Gécz, Christian Gilissen, Lucia Grillo, Anna Hackett, Tjitske Kleefstra, David A. Koolen, Malin Kvarnung, Martin J. Larsen, Carlo Marcelis, F. Ellis McKenzie, Marie-Lorraine Monin, Caroline Nava, Janneke Schuurs-Hoeijmakers, Rolph Pfundt, Marloes Steehouwer, Servi J.C. Stevens, Connie T. R. M. Stumpel, Fleur Vansenne, Mirella Vinci, Maartje van de Vorst, Petra de Vries, Kali Witherspoon, Joris A. Veltman, Han G. Brunner, Heather C. Mefford, Corrado Romano, Lisenka E.L.M. Vissers, Evan E. Eichler, Bert B.A. de Vries

    Julkaistu 2017
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