Jérôme Harambat

Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment

Pierre Cochat, Sally A. Hulton, Cécile Acquaviva et al. · Nephrology Dialysis Transplantation · 2012 · 335 citations · Full text

Medicine, Biochemistry, Nephrology +17

Acute Neurological Involvement in Diarrhea-Associated Hemolytic Uremic Syndrome

Sylvie Nathanson, Thérèsa Kwon, Monique Elmaleh et al. · Clinical Journal of the American Society of Nephrology · 2010 · 226 citations

Medicine, Infectious Diseases, Neurology +15

Characteristics and Outcomes of Children with Primary Oxalosis Requiring Renal Replacement Therapy

Jérôme Harambat, Karlijn J. van Stralen, Laura Espinosa et al. · Clinical Journal of the American Society of Nephrology · 2012 · 156 citations · Full text

Medicine, Nephrology, Pediatrics +11

Genotype–phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome

Jérôme Harambat, Sonia Fargue, Cécile Acquaviva et al. · Kidney International · 2009 · 154 citations · Full text

Life Sciences, Genetics, Molecular Genetics +6

Genotype–phenotype associations in WT1 glomerulopathy

Beata S. Lipska‐Ziętkiewicz, Bruno Ranchin, Paraskevas Iatropoulos et al. · Kidney International · 2014 · 154 citations · Full text

Medicine, Genetics, Nephrology +14