Stephane Decramer
Overview
Explore the profile of Stephane Decramer including associated specialties, affiliations and a list of published articles.
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119
Citations
2460
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Recent Articles
1.
Geraud N, Casemayou A, Alves M, Breuil B, Tkaczyk M, Stanczyk M, et al.
Pediatr Nephrol
. 2024 Nov;
40(4):1023-1032.
PMID: 39614902
Background: There are proposed roles for inflammation in the development of congenital obstructive uropathy in the setting of posterior urethral valves (PUV). However, the value of inflammatory proteins as predictive...
2.
Roquigny J, Meuleman M, El Sissy C, Cailliez M, Servais A, Roussey G, et al.
J Am Soc Nephrol
. 2024 Sep;
36(2):264-273.
PMID: 39325562
No abstract available.
3.
Buffin-Meyer B, Richard J, Guigonis V, Weber S, Konig J, Heidet L, et al.
Kidney Int Rep
. 2024 Aug;
9(8):2514-2526.
PMID: 39156164
Introduction: Hepatocyte nuclear factor 1-beta () gene variants or the chromosome 17q12 deletion (17q12del) represent the most common monogenic cause of developmental kidney disease. Although neurodevelopmental disorders have been associated...
4.
Rohner K, Marlais M, Ali A, Decramer S, Didsbury M, Forbes T, et al.
Arch Dis Child
. 2024 Aug;
109(11):958-960.
PMID: 39142824
No abstract available.
5.
Buffin-Meyer B, Klein J, Aziza J, Fernandez M, Feuillet G, Seye M, et al.
Nephrol Dial Transplant
. 2024 Jun;
40(2):341-351.
PMID: 38908913
Background: Congenital anomalies of the kidney and urinary tract (CAKUT), often discovered in utero, cover a wide spectrum of outcomes ranging from normal postnatal kidney function to foetal death. The...
6.
Kachmar J, Boyer O, Lipska-Zietkiewicz B, Moriniere V, Gribouval O, Heidet L, et al.
Kidney Int Rep
. 2024 May;
9(4):973-981.
PMID: 38765578
Introduction: Unlike idiopathic nephrotic syndrome (NS), hereditary podocytopathies are not expected to recur after kidney transplantation. However, some reports of posttransplant recurrence of NS in patients carrying variants in the...
7.
Schanstra J, Decramer S, Buffin-Meyer B, Klein J, Fossum M, Wu H
J Pediatr Urol
. 2024 Jan;
20(3):492-496.
PMID: 38280830
Today, prenatal diagnosis of congenital urogenital malformations is mostly dependent on anatomical variations found on imaging. However, these findings can mislead us in telling us when to intervene, and about...
8.
Belot A, Rice G, Omarjee S, Rouchon Q, Smith E, Moreews M, et al.
Lancet Rheumatol
. 2024 Jan;
2(2):e99-e109.
PMID: 38263665
Background: Systemic lupus erythematosus (SLE) is a rare immunological disorder and genetic factors are considered important in its causation. Monogenic lupus has been associated with around 30 genotypes in humans...
9.
Percheron L, LeBlanc C, Ulinski T, Fila M, Malvy D, Bacchetta J, et al.
Pediatr Nephrol
. 2024 Jan;
39(6):1893-1900.
PMID: 38212419
Background: Schistosomiasis affects approximately 230 million people worldwide. There is an increased incidence of schistosomiasis cases in France acquired from outside the country. This increases the risk of schistosomiasis outbreaks...
10.
Rohner K, Marlais M, Ahn Y, Ali A, Alsharief A, Blejc Novak A, et al.
Nephrol Dial Transplant
. 2024 Jan;
39(8):1299-1309.
PMID: 38211969
Background: Immunoglobulin A vasculitis with nephritis (IgAVN) is the most common vasculitis in children. Due to a lack of evidence, treatment recommendations are based on expert opinion, resulting in variation....