Concepedia
Author
Elena Levtchenko
Also Known As
Denis Clément, E Levtchenko, E N Levtchenko, E. Levtchenko, E. N. Levtchenko, E.N. Levtchenko, Elena Levtchenko, Elena N Levtchenko, Elena N. Levtchenko, Elena, Levtchenko
507
Publications
11.1K
Citations
55
H-Index
185
Concepts
All Affiliations
1
34
71
3.6K
2
7
467
3
5
369
4
22
26
×
All Concepts
151
6.8K
46
Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia
Karl P. Schlingmann, Justyna Ruminska, Martin Kaufmann, +25
Journal of the American Society of Nephrology
Autosomal-recessive MutationsMetabolic DisorderGeneticsGenetic EpidemiologyPathology +17
2015
270
Novel conditionally immortalized human proximal tubule cell line expressing functional influx and efflux transporters
Martijn J. Wilmer, Moin A. Saleem, Rosalinde Masereeuw, +7
Cell and Tissue Research
Renal PathologyCytoskeletonPt OriginCellular PhysiologyRenal Function +22
2009
215
OCRL controls trafficking through early endosomes via PtdIns4,5P2‐dependent regulation of endosomal actin
Mariella Vicinanza, Antonella Di Campli, Elena Polishchuk, +9
The EMBO Journal
2011
199
Polyhydramnios, Transient Antenatal Bartter’s Syndrome, and<i>MAGED2</i>Mutations
Kamel Laghmani, Bodo B. Beck, Sung-Sen Yang, +30
New England Journal of Medicine
2016
181
Autophagosome–lysosome fusion triggers a lysosomal response mediated by TLR9 and controlled by OCRL
Maria Giovanna De Leo, Leopoldo Staiano, Mariella Vicinanza, +17
Nature Cell Biology
Cell AutophagyMolecular ImmunologyMitophagySignal TransductionAutophagy +10
162
Genotype–phenotype studies in nail-patella syndrome show that LMX1B mutation location is involved in the risk of developing nephropathy
Ernie M.H.F. Bongers, F.T.M. Huysmans, Elena Levtchenko, +15
European Journal of Human Genetics
Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic Epidemiology +8
2005
158
Long-Term Outcome of Biopsy-Proven, Frequently Relapsing Minimal-Change Nephrotic Syndrome in Children
Henriette A.C. Kyrieleis, Marije M. Löwik, Ilse Pronk, +6
Clinical Journal of the American Society of Nephrology
143
Focal segmental glomerulosclerosis in a patient homozygous for a CD2AP mutation
Marije M. Löwik, Patricia J.T.A. Groenen, Ilse Pronk, +6
Kidney International
Glomerular DiseaseGlomerulonephritisFocal Segmental GlomerulosclerosisOphthalmologyMedicine +5
2007
137
Renal Phenotype in Lowe Syndrome
Detlef Böckenhauer, Arend Bökenkamp, William van’t Hoff, +4
2008
136
Mycophenolate mofetil versus cyclosporine for remission maintenance in nephrotic syndrome
Eiske M. Dorresteijn, Joana E. Kist‐van Holthe, Elena Levtchenko, +3
Pediatric Nephrology
124
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