Chantal Loirat
Loirat, Chantal
VIAF ID: 1146822114907381039 (Personal)
Permalink: http://viaf.org/viaf/1146822114907381039
Preferred Forms
- 100 0 _ ‡a Chantal Loirat
- 100 1 _ ‡a Loirat, Chantal
4xx's: Alternate Name Forms (4)
Works
Title | Sources |
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Alternative complement pathway assessment in patients with atypical HUS. | |
Enteric-coated mycophenolate sodium in de novo pediatric renal transplant patients | |
Hemolytic-uremic syndrome: what is the mechanism? | |
Hereditary hemolytic uremic syndromes and thrombotic thrombocytopenic purpura | |
Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases | |
HNF1beta/TCF2 mutations impair transactivation potential through altered co-regulator recruitment | |
Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome | |
Hypophosphatemia, hyperphosphaturia, and bisphosphonate treatment are associated with survival beyond infancy in generalized arterial calcification of infancy | |
In vivo expression of putative LMX1B targets in nail-patella syndrome kidneys | |
Mutational analysis of CLC-5, cofilin and CLC-4 in patients with Dent's disease | |
Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome | |
Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome | |
Successful pre-transplant management of a patient with anti-factor H autoantibodies-associated haemolytic uraemic syndrome | |
Varicella as a trigger of atypical haemolytic uraemic syndrome associated with complement dysfunction: two cases |