Remi Salomon
Overview
Explore the profile of Remi Salomon including associated specialties, affiliations and a list of published articles.
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Articles
128
Citations
3943
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Recent Articles
1.
Dubois S, Duneton C, Salomon R, Salomon R, Ulinski T, Boizeau P, et al.
Horm Res Paediatr
. 2025 Jan;
:1-9.
PMID: 39820089
Introduction: Growth retardation is common in children with chronic kidney disease (CKD) and reflects CKD severity. Recombinant human growth hormone (rhGH) treatment was approved for CKD in 1995. We describe...
2.
Garnier A, Brochard K, Kwon T, Sellier-Leclerc A, Lahoche A, Launay E, et al.
J Am Soc Nephrol
. 2023 Jun;
34(9):1561-1573.
PMID: 37303085
Significance Statement: Shiga toxin-related hemolytic uremic syndrome (STEC-HUS) is a serious condition, characterized by multiorgan thrombotic microangiopathy, mainly affecting children. Renal involvement is severe, with approximately half of patients requiring...
3.
Petzold F, Billot K, Chen X, Henry C, Filhol E, Martin Y, et al.
Kidney Int
. 2023 May;
104(2):378-387.
PMID: 37230223
Nephronophthisis (NPH) is an autosomal-recessive ciliopathy representing one of the most frequent causes of kidney failure in childhood characterized by a broad clinical and genetic heterogeneity. Applied to one of...
4.
Chbihi M, Eveillard L, Riller Q, Brousse R, Berthaud R, Quartier P, et al.
J Nephrol
. 2022 Oct;
36(3):829-839.
PMID: 36208405
Objectives: Class IV lupus nephritis (LN) is one of the most frequent and severe types of involvement in pediatric systemic lupus erythematosus. Gold standard treatment consists of intravenous (i.v.) Cyclophosphamide...
5.
Sobrino S, Abdo C, Neven B, Denis A, Gouge-Biebuyck N, Clave E, et al.
Kidney Int
. 2022 Sep;
103(1):70-76.
PMID: 36108807
Long-term multilineage hematopoietic donor chimerism occurs sporadically in patients who receive a transplanted solid organ enriched in lymphoid tissues such as the intestine or liver. There is currently no evidence...
6.
Garcia H, Serafin A, Silbermann F, Poree E, Viau A, Mahaut C, et al.
Proc Natl Acad Sci U S A
. 2022 Apr;
119(18):e2115960119.
PMID: 35482924
Nephronophthisis (NPH) is an autosomal recessive tubulointerstitial nephropathy belonging to the ciliopathy disorders and known as the most common cause of hereditary end-stage renal disease in children. Yet, no curative...
7.
Quatredeniers M, Bienaime F, Ferri G, Isnard P, Poree E, Billot K, et al.
Hum Mol Genet
. 2022 Jan;
31(13):2121-2136.
PMID: 35043953
Renal ciliopathies are the leading cause of inherited kidney failure. In autosomal dominant polycystic kidney disease (ADPKD), mutations in the ciliary gene PKD1 lead to the induction of CCL2, which...
8.
Dorval G, Balducci E, Kaltenbach S, Chomton M, Krid S, Rabant M, et al.
Kidney Int
. 2021 Sep;
100(4):948-950.
PMID: 34556303
No abstract available.
9.
Diana J, Manceau S, Rabeony T, Elie C, Jolaine V, Zamora S, et al.
J Clin Apher
. 2021 Sep;
36(6):823-830.
PMID: 34469617
Introduction: Therapeutic plasma exchange (TPE) is acknowledged to be an effective treatment in life-threatening pediatric disorders. Apheresis for pediatric diseases has been poorly investigated, and most studies to date featured...
10.
Colin E, Courtois G, Brouzes C, Pulman J, Rabant M, Rotig A, et al.
Haematologica
. 2021 Aug;
106(12):3202-3205.
PMID: 34407605
No abstract available.