E. Wesby-van Swaay

发表

Infection rates in patients from five rheumatoid arthritis (RA) registries: contextualising an RA clinical trial programme

K. Michaud, J. Greenberg, D. Pappas, 2017, RMD Open.

Can rheumatoid arthritis (RA) registries provide contextual safety data for modern RA clinical trials? The case for mortality and cardiovascular disease

K. Michaud, J. Greenberg, D. Pappas, 2016, Annals of the rheumatic diseases.

Uniparental disomy with and without confined placental mosaicism: a model for trisomic zygote rescue

S. Verhoef, A. V. D. van den Ouweland, D. Halley, 1998, Prenatal diagnosis.

Nephrology Dialysis Transplantation Analysis of a large family with the second type of autosomal dominant polycystic kidney disease

B. Veldhuisen, M. Breuning, D. Peters, 2005 .

Using epidemiological registry data to provide background rates as context for adverse events in a rheumatoid arthritis drug development program: a coordinated approach

Trung Nghia Tran, K. Michaud, J. Greenberg, 2015, Pharmacoepidemiology and drug safety.

How comparable are rates of malignancies in patients with rheumatoid arthritis across the world? A comparison of cancer rates, and means to optimise their comparability, in five RA registries.

K. Michaud, J. Greenberg, D. Pappas, 2016, Annals of the rheumatic diseases.

Molecular analysis of SALL1 mutations in Townes-Brocks syndrome.

W. Reardon, K. Devriendt, O. Gabrielli, 1999, American journal of human genetics.

Restrictive dermopathy. Report of 12 cases. Dutch Task Force on Genodermatology.

C. V. van Asperen, F. Beemer, P. Steijlen, 1998, Archives of dermatology.

Molecular detection of a translocation (Y;11)(q11.2;q24) in a 45,X male with signs of Jacobsen syndrome

B. Oostra, B. Eussen, E. Wesby-van Swaay, 1992, Human Genetics.

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.

B. D. de Vries, B. Oostra, J. Fryns, 1993, Journal of medical genetics.

Bilateral hereditary micro-epiphyseal dysplasia: Further delineation of the phenotype with 40 years follow-up

P. Heutink, D. Lindhout, B. Jansen, 2002, International Orthopaedics.

A gene for nonspecific X-linked mental retardation (MRX41) is located in the distal segment of Xq28.

E. Mariman, H. Kremer, B. Hamel, 1996, American journal of medical genetics.

Uniparental disomy with and without confined placental mosaicism: a model for trisomic zygote rescue

S. Verhoef, A. V. D. van den Ouweland, D. Halley, 1998, Prenatal diagnosis.