Screening women at increased risk with MRI: Monday 3 October 2005, 08:45–10:45

por Boetes, C, Veltman, J
Publicado 2005

Disease gene discovery in male infertility: past, present and future

por Xavier, M. J., Salas-Huetos, A., Oud, M. S., Aston, K. I., Veltman, J. A.
Publicado 2020

Breast tumor characteristics of BRCA1 and BRCA2 gene mutation carriers on MRI

por Veltman, J., Mann, R., Kok, T., Obdeijn, I. M., Hoogerbrugge, N., Blickman, J. G., Boetes, C.
Publicado 2008

Contrast-enhanced magnetic resonance imaging of the breast: the value of pharmacokinetic parameters derived from fast dynamic imaging during initial enhancement in classifying lesi...

por Veltman, J., Stoutjesdijk, M., Mann, R., Huisman, H. J., Barentsz, J. O., Blickman, J. G., Boetes, C.
Publicado 2008

Diagnostic performance of eNose technology in COVID-19 patients after hospitalization

por van Raaij, B. F.M., Veltman, J. D., Hameete, J. F., Stöger, J. L., Geelhoed, J. J.M.
Publicado 2023

Multisite Evaluation of Cepheid Xpert Carba-R Assay for Detection of Carbapenemase-Producing Organisms in Rectal Swabs

por Tato, M., Ruiz-Garbajosa, P., Traczewski, M., Dodgson, A., McEwan, A., Humphries, R., Hindler, J., Veltman, J., Wang, H., Cantón, R.
Publicado 2016

Understanding the Psychosocial Effects of WES Test Results on Parents of Children with Rare Diseases

por Krabbenborg, Lotte, Vissers, L. E. L. M., Schieving, J., Kleefstra, T., Kamsteeg, E. J., Veltman, J. A., Willemsen, M. A., Van der Burg, S.
Publicado 2016

Imaging breast malignancies with the Twente Photoacoustic Mammoscope 2

por Schoustra, S. M., De Santi, B., op ’t Root, T. J. P. M., Klazen, C. A. H., van der Schaaf, M., Veltman, J., Steenbergen, W., Manohar, S.
Publicado 2023

Zoledronic acid impairs myeloid differentiation to tumour-associated macrophages in mesothelioma

por Veltman, J D, Lambers, M E H, van Nimwegen, M, Hendriks, R W, Hoogsteden, H C, Hegmans, J P J J, Aerts, J G J V
Publicado 2010

Trisomic dose of several chromosome 21 genes perturbs haematopoietic stem and progenitor cell differentiation in Down's syndrome

por De Vita, S, Canzonetta, C, Mulligan, C, Delom, F, Groet, J, Baldo, C, Vanes, L, Dagna-Bricarelli, F, Hoischen, A, Veltman, J, Fisher, E M C, Tybulewicz, V L J, Nizetic, D
Publicado 2010

Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia

por Oud, M S, Okutman, Ö, Hendricks, L A J, de Vries, P F, Houston, B J, Vissers, L E L M, O’Bryan, M K, Ramos, L, Chemes, H E, Viville, S, Veltman, J A
Publicado 2020

Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders

por Oud, M S, Houston, B J, Volozonoka, L, Mastrorosa, F K, Holt, G S, Alobaidi, B K S, deVries, P F, Astuti, G, Ramos, L, Mclachlan, R I, O’Bryan, M K, Veltman, J A, Chemes, H E, Sheth, H
Publicado 2021

Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies

por Vissers, L. E. L. M., Stankiewicz, P., Yatsenko, S. A., Crawford, E., Creswick, H., Proud, V. K., de Vries, B. B. A., Pfundt, R., Marcelis, C. L. M., Zackowski, J., Bi, W., van Kessel, A. Geurts, Lupski, J. R., Veltman, J. A.
Publicado 2007

De novo mutations in children born after medical assisted reproduction

por Smits, R M, Xavier, M J, Oud, M S, Astuti, G D N, Meijerink, A M, de Vries, P F, Holt, G S, Alobaidi, B K S, Batty, L E, Khazeeva, G, Sablauskas, K, Vissers, L E L M, Gilissen, C, Fleischer, K, Braat, D D M, Ramos, L, Veltman, J A
Publicado 2022

Step forward in early recognition of systemic sclerosis: data from the Leiden CCISS cohort

por Liem, Sophie I E, Ciaffi, Jacopo, van Leeuwen, Nina Marijn, Boonstra, Maaike, Ahmed, Saad, Beaart-van de Voorde, Liesbeth J J, Corsel, Anja, Dhondai, Talitha, Ninaber, Maarten K, Geelhoed-Veltman, J J Miranda, Heuvers, Marlies E, Tushuizen, Maarten E, Ajmone Marsan, Nina, Kiès, Philippine, Schouffoer, Anne A, Huizinga, Tom W J, Allaart, Cornelia F, De Vries-Bouwstra, Jeska
Publicado 2023

Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability

por Riazuddin, S, Hussain, M, Razzaq, A, Iqbal, Z, Shahzad, M, Polla, D L, Song, Y, van Beusekom, E, Khan, A A, Tomas-Roca, L, Rashid, M, Zahoor, M Y, Wissink-Lindhout, W M, Basra, M A R, Ansar, M, Agha, Z, van Heeswijk, K, Rasheed, F, Van de Vorst, M, Veltman, J A, Gilissen, C, Akram, J, Kleefstra, T, Assir, M Z, Grozeva, D, Carss, K, Raymond, F L, O'Connor, T D, Riazuddin, S A, Khan, S N, Ahmed, Z M, de Brouwer, A P M, van Bokhoven, H, Riazuddin, S
Publicado 2016

A de novo paradigm for male infertility

por Oud, M. S., Smits, R. M., Smith, H. E., Mastrorosa, F. K., Holt, G. S., Houston, B. J., de Vries, P. F., Alobaidi, B. K. S., Batty, L. E., Ismail, H., Greenwood, J., Sheth, H., Mikulasova, A., Astuti, G. D. N., Gilissen, C., McEleny, K., Turner, H., Coxhead, J., Cockell, S., Braat, D. D. M., Fleischer, K., D’Hauwers, K. W. M., Schaafsma, E., Nagirnaja, L., Conrad, D. F., Friedrich, C., Kliesch, S., Aston, K. I., Riera-Escamilla, A., Krausz, C., Gonzaga-Jauregui, C., Santibanez-Koref, M., Elliott, D. J., Vissers, L. E. L. M., Tüttelmann, F., O’Bryan, M. K., Ramos, L., Xavier, M. J., van der Heijden, G. W., Veltman, J. A.
Publicado 2022