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FAMILIAL IDIOPATHIC STEROID-RESISTANT NEPHROTIC SYNDROME WITH FOCAL SEGMENTAL HYALINOSIS Experts

We have collected the completed list of expert related to FAMILIAL IDIOPATHIC STEROID-RESISTANT NEPHROTIC SYNDROME WITH FOCAL SEGMENTAL HYALINOSIS using public data available on different databases.

FAMILIAL IDIOPATHIC STEROID-RESISTANT NEPHROTIC SYNDROME WITH FOCAL SEGMENTAL HYALINOSIS Experts map



If you find this map or researchers for FAMILIAL IDIOPATHIC STEROID-RESISTANT NEPHROTIC SYNDROME WITH FOCAL SEGMENTAL HYALINOSIS useful, maybe you will be also interested in other rare diseases proffesionals like our leber congenital amaurosis expert list ,or our b-cell chronic lymphocytic leukemia expert list

FAMILIAL IDIOPATHIC STEROID-RESISTANT NEPHROTIC SYNDROME WITH FOCAL SEGMENTAL HYALINOSIS Experts list

Pr Corinne ANTIGNAC

 PARIS. FRANCE

  Responsible for diagnostic tests - Investigator of research project - Coordinator of research network

  • Research area/topic:
    GenPod: Genetic components of podocyte differentiation and disease
  • INSERM U983, CHU Paris - Hôpital Necker-Enfants Malades
    CHU Paris - Hôpital Necker-Enfants Malades
  • corinne.********@***p.fr
Complete Info

Dr Pierre-Louis THARAUX

 PARIS. FRANCE

  Investigator of research project

  • Research area/topic:
    Glomerulonephritis and Focal Segmental Glomerulosclerosis as a Model to Investigate the Link between Inflammation and Kidney Disease: From Basic Mechanisms to Clinical Application
  • PARCC - Paris-Centre de recherche Cardiovasculaire (U970)
    PARCC - Paris-Centre de recherche Cardiovasculaire (U970)
  • pierre_lou**********@***erm.fr
Complete Info

Pr Marcus MÖLLER

 AACHEN. GERMANY

  Coordinator of expert centre - Clinical expert - Investigator of research project - Coordinator of research network

  • Research area/topic:
    Rare-G: The Epidermal Growth Factor System in Rare Glomerular Disease: From Molecular Mechanisms to Therapeutics
  • Universitätsklinikum Aachen
    Universitätsklinikum Aachen
  • mmoe****@***achen.de
Complete Info

Dr Anja LEHNHARDT

 HAMBURG. GERMANY

  Investigator of research project - Manager of registry

  • Research area/topic:
    Genotype-phenotype correlation of patients with WT1 gene mutation
  • UKE - Universitätsklinikum Hamburg-Eppendorf
  • A.Leh******@***.de
Complete Info

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All the contact information provided is based on public data available in orpha.net.