Naureen Akhtar Selected Research

Manz syndrome

1/2011	Mutation in the tight-junction gene claudin 19 (CLDN19) and familial hypomagnesemia, hypercalciuria, nephrocalcinosis (FHHNC) and severe ocular disease.
6/2006	A familial hypomagnesemia--hypercalciuria (Manz syndrome).

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Naureen Akhtar Research Topics

Disease

2	Nephrotic Syndrome (Syndrome, Nephrotic) 04/2022 - 10/2015
2	Nephrocalcinosis 01/2011 - 06/2006
2	Manz syndrome 01/2011 - 06/2006
1	Dehydration (Water Stress) 02/2020
1	Renal Tubular Acidosis (Distal Renal Tubular Acidosis) 02/2020
1	Acidosis 02/2020
1	Vomiting 02/2020
1	Inborn Genetic Diseases (Disease, Hereditary) 02/2020
1	Proteinuria 10/2015
1	Gitelman Syndrome 04/2009
1	Alkalosis 04/2009
1	Tetany (Spasmophilia) 06/2006
1	Hypercalciuria 06/2006
1	Rickets (Rachitis) 06/2006
1	Polyuria 06/2006

Drug/Important Bio-Agent (IBA)

1	SteroidsIBA 04/2022
1	dirhodium tetraacetate (DRTA)IBA 02/2020
1	Pharmaceutical PreparationsIBA 10/2015
1	Immunosuppressive Agents (Immunosuppressants)IBA 10/2015
1	Tacrolimus (Prograf)FDA LinkGeneric 10/2015
1	ClaudinsIBA 01/2011
1	Sodium Chloride SymportersIBA 04/2009
1	MagnesiumIBA 06/2006
1	CalciumIBA 06/2006

Therapy/Procedure

1	Therapeutics 04/2022