Nessuna malattia è così rara
da non meritare attenzione

Didascalia : Accreditato = ;

• • PAESI BASSI
  • Gelderland
  • NIJMEGEN
  • 
  • Molecular diagnosis of Intestinal Hypomagnesemia (TRPM6 gene)
  • UMC St Radboud - Universitair Medisch Centrum St Radboud
  • Ulteriori informazioni
• • PAESI BASSI
  • Gelderland
  • NIJMEGEN
  • 
  • Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
  • UMC St Radboud - Universitair Medisch Centrum St Radboud
  • Ulteriori informazioni
• • GERMANIA
  • Sachsen
  • WEIßWASSER
  • Molecular diagnosis of intestinal hypomagnesemia (TRPM6 gene)
  • Praxis Dr. Mato Nagel
  • Ulteriori informazioni
• • GERMANIA
  • Nordrhein-Westfalen
  • MÜNSTER
  • Molecular diagnosis of intestinal hypomagnesemia (TRPM6 gene)
  • Universitätsklinikum Münster
  • Ulteriori informazioni
• • SPAGNA
  • Andalucía
  • MÁLAGA
  • Molecular diagnosis of hypomagnesemia caused by selective magnesium malabsorption. TRPM6 gene.
  • GENETAQ
  • Ulteriori informazioni
• • FRANCIA
  • ILE-DE-FRANCE
  • PARIS
  • Diagnosis of familial primary hypomagnesemia by exploration of the renal function
  • CHU Paris Ouest - Hôpital Européen Georges Pompidou
  • Ulteriori informazioni
• • GERMANIA
  • Berlin
  • BERLIN
  • Molecular diagnosis of intestinal hypomagnesemia (TRPM6 gene)
  • Max-Delbrück-Centrum für Molekulare Medizin (MDC)
  • Ulteriori informazioni
• • AUSTRIA
  • WIEN
  • WIEN
  • Biochemical diagnosis of inborn errors of metabolism (including Austrian newborn screening program for inborn errors of metabolism)
  • Medizinische Universität Wien
  • Ulteriori informazioni