Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jody M.W. Van den Ouweland"'
Autor:
Rob Janssen, Jef Serré, Ianthe Piscaer, Ruben Zaal, Henny van Daal, Carolien Mathyssen, Pieter Zanen, Jody M.W. van den Ouweland, Wim Janssens
Publikováno v:
ERJ Open Research, Vol 6, Iss 4 (2020)
Background Vitamin D supplementation lowers exacerbation frequency in severe vitamin D-deficient patients with COPD. Data regarding the effect of vitamin D on elastin degradation are lacking. Based on the vitamin's anti-inflammatory properties, we hy
Externí odkaz:
https://doaj.org/article/06fa840969df467585c957d226cb09a1
Autor:
Anton S.M. Dofferhoff, Ianthe Piscaer, Leon J. Schurgers, Jona Walk, Jody M.W. van den Ouweland, Tilman M. Hackeng, Pim A. de Jong, Reinoud Gosens, Petra Lux, Henny van Daal, Cecile Maassen, Esther G.A. Maassen, Loes E.M. Kistemaker, Cees Vermeer, Emiel F.M. Wouters, Rob Janssen
Background: A significant proportion of SARS-CoV-2-infected patients develops respiratory failure. Thromboembolism is also prevalent in coronavirus disease 2019 (Covid-19). Vitamin K plays a role in coagulation and possibly also in lung diseases. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98e9213895ff2480df5434c960b834fd
https://doi.org/10.20944/preprints202004.0457.v2
https://doi.org/10.20944/preprints202004.0457.v2
Autor:
Ronald J.E. Pennings, Lambert D. Dikkeschei, Guy Van Camp, Jody M.W. van den Ouweland, Patrick L. M. Huygen, Kim Cryns, Cor W. R. J. Cremers
Publikováno v:
Audiology and Neurotology. 9:51-62
This study examined the audiovestibular profile of 11 Wolfram syndrome patients (4 males, 7 females) from 7 families, with identified WFS1 mutations, and the audiometric profile of 17 related heterozygous carriers of WFS1 mutations. Patients with Wol
Autor:
Theru A. Sivakumaran, Marci M. Lesperance, Terry-Lynn Young, Jody M.W. van den Ouweland, Guy Van Camp, Richard J.H. Smith, Cor W. R. J. Cremers, Kris Flothmann, Ronald J.E. Pennings, Kim Cryns
Publikováno v:
Human Mutation, 22, 275-87
Human Mutation, 22(4), 275-287. Wiley
Human Mutation, 22, 4, pp. 275-87
Human mutation
Human Mutation, 22(4), 275-287. Wiley
Human Mutation, 22, 4, pp. 275-87
Human mutation
WFS1 is a novel gene and encodes an 890 amino-acid glycoprotein (wolframin), predominantly localized in the endoplasmic reticulum. Mutations in WFS1 underlie autosomal recessive Wolfram syndrome and autosomal dominant low frequency sensorineural hear
Autor:
Jody M.W. van den Ouweland, Frits A. J. Muskiet, Jeroen W.P. Römer, Sanne Bruins, Fey P. L. van der Dijs, M. Rebecca Fokkema, Mike J. L. DeJongste
Publikováno v:
Clinical Chemistry, 50(11), 2052-2058. AMER ASSOC CLINICAL CHEMISTRY
Background: Plasma B-type natriuretic peptide (BNP) and N-terminal proBNP (NT-proBNP) are promising markers for heart failure diagnosis, prognosis, and treatment. Insufficient data on the intraindividual biological variation (CVi) of BNP and NT-proBN
Comparison of a New Procalcitonin Assay from Roche with the Established Method on the Brahms Kryptor
Autor:
Jody M.W. van den Ouweland, Holger K. de Wolf, Jacqueline M. T. Klein Gunnewiek, Yvonne Berk, Menno de Metz
Publikováno v:
Clinical Chemistry. 55:1043-1044
Procalcitonin (PCT) is a 13-kDa peptide and a precursor of calcitonin. In a healthy population, PCT concentrations are negligible (1). In systemic bacterial and fungal infections, plasma concentrations are raised, whereas concentrations remain fairly
Autor:
Kim Cryns, Theru A. Sivakumaran, Jody M.W. Van den Ouweland, Ronald J.E. Pennings, Cor W.R.J. Cremers, Kris Flothmann, Terry-Lynn Young, Richard J.H. Smith, Marci M. Lesperance, Guy Van Camp
Publikováno v:
Human Mutation; Oct2003, Vol. 22 Issue 4, p275, 13p