Daniel Landau
Researcher Next ID · RN-042097
Researcher · Biochemistry, Genetics and Molecular Biology
Tel Aviv, Israel
- Works count
- 567
- Citation count
- 7,090
- H-index
- 42
- i10-index
- 93
Research interests
Publications
An international consensus approach to the management of atypical hemolytic uremic syndrome in children
Pediatric Nephrology · 2015 · https://doi.org/10.1007/s00467-015-3076-8
Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome
Pediatric Nephrology · 2008 · https://doi.org/10.1007/s00467-008-0964-1
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
Nature Genetics · 2003 · https://doi.org/10.1038/ng1217
Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia
Nature Genetics · 2002 · https://doi.org/10.1038/ng901
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
Nature Genetics · 2001 · https://doi.org/10.1038/ng752
Current projects
No projects listed.