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

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

I whakaputaina 2001

Whiwhi kuputuhi katoa
Artigo

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2

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

I whakaputaina 2002

Whiwhi kuputuhi katoa
Artigo

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3

Monitoring of Epstein-Barr Virus DNA Load in Peripheral Blood by Quantitative Competitive PCR mā 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

I whakaputaina 1999

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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TREATMENT OF POSTTRANSPLANT LYMPHOPROLIFERATIVE DISEASE WITH RITUXIMAB mā 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

I whakaputaina 2002

Whiwhi kuputuhi katoa
Artigo

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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... mā 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

I whakaputaina 2005

Whiwhi kuputuhi katoa
Artigo

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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... mā 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

I whakaputaina 2001

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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7

A Phase I Trial of Epstein-Barr Virus Gp350 Vaccine for Children With Chronic Kidney Disease Awaiting Transplantation mā 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

I whakaputaina 2009

Whiwhi kuputuhi katoa
Artigo

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8

Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro mā 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

I whakaputaina 2014

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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9

Epstein-Barr Virus DNA Load in Nasopharyngeal Brushings and Whole Blood in Nasopharyngeal Carcinoma Patients before and after Treatment mā 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

I whakaputaina 2013

Whiwhi kuputuhi katoa
Artigo

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10

Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders mā 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

I whakaputaina 2016

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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11

Variation in a range of mTOR-related genes associates with intracranial volume and intellectual disability mā 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

I whakaputaina 2017

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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12

Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability mā 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

I whakaputaina 2016

Whiwhi kuputuhi katoa
Revisão

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

I whakaputaina 2020

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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14

Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss mā 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

I whakaputaina 2023

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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15

Noninvasive Prenatal Test Results Indicative of Maternal Malignancies: A Nationwide Genetic and Clinical Follow-Up Study mā 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

I whakaputaina 2022

Whiwhi kuputuhi katoa
Artigo

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The performance of genome sequencing as a first-tier test for neurodevelopmental disorders mā 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

I whakaputaina 2022

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing mā 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

I whakaputaina 2024

Whiwhi kuputuhi katoa
Artigo

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

I whakaputaina 2019

Whiwhi kuputuhi katoa
Artigo

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19

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

I whakaputaina 2022

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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20

A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency mā 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

I whakaputaina 2017

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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