Francoise Janssen
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Explore the profile of Francoise Janssen including associated specialties, affiliations and a list of published articles.
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16
Citations
567
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Recent Articles
1.
Duong H, Piepsz A, Khelif K, Collier F, De Man K, Damry N, et al.
Eur J Nucl Med Mol Imaging
. 2014 Dec;
42(6):940-6.
PMID: 25504023
Purpose: The main criteria used for deciding on surgery in children with presumed antenatally detected pelviureteric junction obstruction (PPUJO) are the level of hydronephrosis (ultrasonography), the level of differential renal...
2.
Dang L, Doan T, Doan N, Pham T, Smets F, Thi M, et al.
BMC Pediatr
. 2013 Nov;
13:183.
PMID: 24206763
Background: Recent studies on Vietnamese children have shown that kidney diseases are not detected early enough to prevent chronic renal failure. The dipstick test is a simple and useful tool...
3.
Duong H, Piepsz A, Collier F, Khelif K, Christophe C, Cassart M, et al.
Urology
. 2013 Jun;
82(3):691-6.
PMID: 23726167
Objective: To determine, in children with antenatally detected pelviureteric junction (PUJ) stenosis, what factors may be predictive for deterioration of differential renal function (DRF) in case of conservative treatment or...
4.
Avni E, Vandenhoute K, Devriendt A, Ismaili K, Hackx M, Janssen F, et al.
Pediatr Radiol
. 2010 Aug;
41(1):76-81.
PMID: 20714714
The clinical classification of nephrotic syndrome (NS) is based on age at presentation. However, this classification is arbitrary because the majority of early onset NS has a genetic origin and...
5.
Matejas V, Hinkes B, Alkandari F, Al-Gazali L, Annexstad E, Aytac M, et al.
Hum Mutat
. 2010 Jun;
31(9):992-1002.
PMID: 20556798
Mutations of LAMB2 typically cause autosomal recessive Pierson syndrome, a disorder characterized by congenital nephrotic syndrome, ocular and neurologic abnormalities, but may occasionally be associated with milder or oligosymptomatic disease...
6.
van Zelm M, Smet J, Adams B, Mascart F, Schandene L, Janssen F, et al.
J Clin Invest
. 2010 Mar;
120(4):1265-74.
PMID: 20237408
Antibody deficiencies constitute the largest group of symptomatic primary immunodeficiency diseases. In several patients, mutations in CD19 have been found to underlie disease, demonstrating the critical role for the protein...
7.
Hiep T, Ismaili K, Collart F, van Damme-Lombaerts R, Godefroid N, Ghuysen M, et al.
Pediatr Nephrol
. 2010 Feb;
25(5):935-40.
PMID: 20148340
The aim of this study was to report on the clinical characteristics and outcomes of Belgian children with chronic kidney disease (CKD). Between 2001 and 2005, we followed 143 new...
8.
Harambat J, Fargue S, Acquaviva C, Gagnadoux M, Janssen F, Liutkus A, et al.
Kidney Int
. 2009 Dec;
77(5):443-9.
PMID: 20016466
We sought to ascertain the long-term outcome and genotype-phenotype correlations available for primary hyperoxaluria type 1 in a large retrospective cohort study. We examined the clinical history of 155 patients...
9.
Fargue S, Harambat J, Gagnadoux M, Tsimaratos M, Janssen F, Llanas B, et al.
Kidney Int
. 2009 Jul;
76(7):767-73.
PMID: 19571789
Primary hyperoxaluria type 1 results from alanine:glyoxylate aminotransferase deficiency. Due to genotype/phenotype heterogeneity in this autosomal recessive disorder, the renal outcome is difficult to predict in these patients and the...
10.
Ismaili K, Pawtowski A, Boyer O, Wissing K, Janssen F, Hall M
Pediatr Nephrol
. 2008 Aug;
24(2):287-94.
PMID: 18709391
The aim of the study was to present our experience in treating children with genetic forms of nephrotic syndrome and diagnosing these diseases. We retrospectively reviewed the clinical data, mutational...