Search Results - "Labatut, Delphine"

MYH9-related disorders display heterogeneous kidney involvement and outcome by Tabibzadeh, Nahid, Fleury, Dominique, Labatut, Delphine, Bridoux, Frank, Lionet, Arnaud, Jourde-Chiche, Noémie, Vrtovsnik, François, Schlegel, Nicole, Vanhille, Philippe

“…MYH9-related diseases (MYH9-RD) are autosomal dominant disorders caused by mutations of the gene encoding the non-muscle myosin heavy chain IIA. They are…”
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MYH9-related disorders display heterogeneous kidney involvement and outcome by Tabibzadeh, Nahid, Fleury, Dominique, Labatut, Delphine, Bridoux, Frank, Lionet, Arnaud, Jourde-Chiche, Noemie, Vrtovsnik, Francois, Schlegel, Nicole, Vanhille, Philippe

“…Background. MYH9-related diseases (MYH9-RD) are autosomal dominant disorders caused by mutations of the MYH9 gene encoding the non-muscle myosin heavy chain…”
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Light chain deposition disease without glomerular proteinuria: a diagnostic challenge for the nephrologist by Sicard, Antoine, Karras, Alexandre, Goujon, Jean-Michel, Sirac, Christophe, Bender, Sébastien, Labatut, Delphine, Callard, Patrice, Sarkozy, Clémentine, Essig, Marie, Vanhille, Philippe, Provot, François, Nony, Alain, Nochy, Dominique, Ronco, Pierre, Bridoux, Frank, Touchard, Guy

“…Renal involvement in light chain (LC) deposition disease (LCDD) is typically characterized by nodular glomerulosclerosis and nephrotic range proteinuria. Rare…”
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