Hendrica Belge
Overview
Explore the profile of Hendrica Belge including associated specialties, affiliations and a list of published articles.
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Articles
18
Citations
346
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0
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Recent Articles
1.
Verploegen M, Vargas-Poussou R, Walsh S, Alpay H, Amouzegar A, Ariceta G, et al.
Nephrol Dial Transplant
. 2022 Feb;
37(12):2474-2486.
PMID: 35137195
Background: Small cohort studies have reported high parathyroid hormone (PTH) levels in patients with Bartter syndrome and lower serum phosphate levels have anecdotally been reported in patients with Gitelman syndrome....
2.
Lopez-Garcia S, Downie M, Kim J, Boyer O, Walsh S, Nijenhuis T, et al.
Nephrol Dial Transplant
. 2020 Dec;
PMID: 33367818
Background: Primary nephrogenic diabetes insipidus (NDI) is a rare disorder and little is known about treatment practices and long-term outcome. Methods: Paediatric and adult nephrologists contacted through European professional organizations...
3.
Olinger E, Hofmann P, Kidd K, Dufour I, Belge H, Schaeffer C, et al.
Kidney Int
. 2020 May;
98(3):717-731.
PMID: 32450155
Autosomal dominant tubulointerstitial kidney disease (ADTKD) is an increasingly recognized cause of end-stage kidney disease, primarily due to mutations in UMOD and MUC1. The lack of clinical recognition and the...
4.
Hureaux M, Ashton E, Dahan K, Houillier P, Blanchard A, Cormier C, et al.
Kidney Int
. 2019 Nov;
96(6):1408-1416.
PMID: 31672324
Hereditary tubulopathies are rare diseases with unknown prevalence in adults. Often diagnosed in childhood, hereditary tubulopathies can nevertheless be evoked in adults. Precise diagnosis can be difficult or delayed due...
5.
van der Wijst J, Belge H, Bindels R, Devuyst O
Physiol Rev
. 2019 Jun;
99(3):1575-1653.
PMID: 31215303
The identification of genes causing inherited kidney diseases yielded crucial insights in the molecular basis of disease and improved our understanding of physiological processes that operate in the kidney. Monogenic...
6.
Henrard C, Belge H, Fastre S, Di Monaco S, Revencu N, Hammer F, et al.
Blood Press
. 2019 Jan;
28(2):139-143.
PMID: 30623691
We report the case of a 42-year-old patient referred for suspicion of fibromuscular dysplasia in the context of a carotid artery dissection occurring after a minor trauma. Initial complaints included...
7.
Corre T, Arjona F, Hayward C, Youhanna S, de Baaij J, Belge H, et al.
J Am Soc Nephrol
. 2017 Nov;
29(1):335-348.
PMID: 29093028
Magnesium (Mg) homeostasis is critical for metabolism. However, the genetic determinants of the renal handling of Mg, which is crucial for Mg homeostasis, and the potential influence on metabolic traits...
8.
Gabriel S, Belge H, Gassama A, Debaix H, Luciani A, Fehr T, et al.
Kidney Int
. 2017 Feb;
91(4):842-855.
PMID: 28143656
Dent disease is a rare X-linked tubulopathy caused by mutations in the endosomal chloride-proton exchanger (ClC-5) resulting in defective receptor-mediated endocytosis and severe proximal tubule dysfunction. Bone marrow transplantation has...
9.
Corre T, Olinger E, Harris S, Traglia M, Ulivi S, Lenarduzzi S, et al.
Pflugers Arch
. 2016 Dec;
469(1):91-103.
PMID: 27915449
The nature and importance of genetic factors regulating the differential handling of Ca and Mg by the renal tubule in the general population are poorly defined. We conducted a genome-wide...
10.
Belge H, Dahan K, Cambier J, Benoit V, Morelle J, Bloch J, et al.
Nephrol Dial Transplant
. 2016 Jul;
32(5):830-837.
PMID: 27387476
Background: Hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome is a rare autosomal dominant disorder, secondary to mutations in the GATA-3 gene. Due to its wide range of penetrance and expressivity,...