Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Jean-Pierre Van Biervliet"'
Autor:
Judith, Baert, Stephanie, Van Biervliet, Jean-Pierre, Van Biervliet, Johan, Vande Walle, Felicia, Bentin, Liesl, De Graeve, Doris, Vandenbossche, Ann, De Guchtenaere
Publikováno v:
Acta clinica Belgica. 74(4)
Publikováno v:
cclm. 48:1751-1755
Background: In cystic fibrosis (CF), changes in fatty acid (FA) composition of serum phospholipids (PL) and cell membranes can account, in part, for the inflammatory state of the disease. The severity of the genotype is known to correlate with the de
Publikováno v:
Current Pediatric Reviews. 5:184-188
Zinc (Zn) is a multipurpose trace element, sufficiency of which is difficult to assess. However, Zn deficiency could negatively influence this disease in different aspects. The symptoms of Zn deficiency as taste disturbances, decreased appetite and i
Autor:
Eddy Robberecht, Dimitri Declercq, Stephanie Van Biervliet, Armand Christophe, Jean-Pierre Van Biervliet, Griet Vanbillemont
Publikováno v:
Annals of Nutrition and Metabolism. 51:541-549
Objective: To evaluate the relation of clinical parameters and genotype with the serum phospholipid fatty acid (FA) composition in cystic fibrosis (CF) patients. Methods: A blood sample was taken from CF patients with stable pulmonary disease for the
Autor:
Jerzy Konstantynowicz, Rosa M. Lamuela-Raventós, Seok Hyun Nam, Stephanie Van Biervliet, Günther Wolfram, Yeon Ri Lee, Palmi V. Jonsson, R. Lala, Mi Young Kang, Hope Barkoukis, H.S. Lee, Elena Roura, Ramon Estruch, Susanne Hailer, Inga Thorsdottir, Francesco Manara, Mehmet Bastemir, Jakob Linseisen, Eddy Robberecht, H.J. Park, Dimitri Declercq, W.Y. Kim, Jean-Pierre Van Biervliet, Chae Eun Kim, Christine M. Marchetti, Katharina Nimptsch, Bunyamin Kaptanoglu, Andrew L. Waterhouse, E. Castagno, John P. Kirwan, Tamás Decsi, Armand Christophe, Cristina Andres-Lacueva, Brian Nolan, Fulya Akin, Berthold Koletzko, M.H. Kim, Radosław Motkowski, Sakita N. Sistrun, F. Savino, Sigurbjorn Bjornsson, Ge. Monti, Guglielmo Bruno, M. Lourdes Mata-Bilbao, Costantino Caroselli, Maria Izquierdo-Pulido, Kurt Gedrich, Szilvia Bokor, Griet Vanbillemont, Raj K. Krishnan, Alfons Ramel, Sabine Rohrmann
Publikováno v:
Annals of Nutrition and Metabolism. 51:499-510
Publikováno v:
Current Pediatric Reviews. 2:107-113
Once the genetic defect of cystic fibrosis (CF), the most common autosomal recessive disease, was discovered, there was hope for quick positive results with gene-therapy. These did not came true, however. Recent CF mice studies by Freedman et al. dem
Publikováno v:
Biological Trace Element Research. 112:205-212
There is no consensus whether zinc (Zn) supplementation is necessary in cystic fibrosis (CF). For assessment of the Zn status, serum Zn concentration is the only easy available method. It is, however age dependent. We compare the serum Zn levels of C
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 94(6)
Publikováno v:
Biological trace element research. 94(1)
Many reports mention marginal zinc status in childhood. Information on serum zinc (Zn) in Belgian children since the last reports are old and feeding habits are changing. Four hundred fifty-seven healthy children (0-14 yr, 262 boys) had a venipunctur
Autor:
Vic Blaton, Jean-Pierre Van Biervliet, Dirk Bernard, Stephanie Van Biervliet, Marc Matthys, Raf Vercaemst
Publikováno v:
Biological trace element research. 79(2)
Previous studies showed low selenium (Se) concentrations in Belgian children. Serum alpha-tocopherol, retinol, total cholesterol, high-density lipoprotein and low-density lipoprotein cholesterol, selenium (Se), and thiobarbituric acid-reactive substa