Christophe Simian
20 Rue Leblanc
Paris, 75015, France
Paris, 75015, France
Last Updated: 09/26/2026
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Found 9 publications
Validation of a liquid chromatography coupled to tandem mass spectrometry method for simultaneous quantification of tryptophan and 10 key metabolites of the kynurenine pathway in plasma and urine: Application to a cohort of acute kidney injury patients.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: April 08, 2022
Frequency of de novo variants and parental mosaicism in vascular Ehlers-Danlos syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: March 27, 2018
Clinical and Genetic Spectrum of Bartter Syndrome Type 3.
Journal: Journal of the American Society of Nephrology : JASN
Published: October 03, 2016
The MITF, p.E318K Variant, as a Risk Factor for Pheochromocytoma and Paraganglioma.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 30, 2016
Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences.
Journal: The Journal of clinical endocrinology and metabolism
Published: March 11, 2016
Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas.
Journal: Human molecular genetics
Published: December 17, 2013
Mosaicism in HIF2A-related polycythemia-paraganglioma syndrome.
Journal: The Journal of clinical endocrinology and metabolism
Published: November 27, 2013
A decade (2001-2010) of genetic testing for pheochromocytoma and paraganglioma.
Journal: Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
Published: April 21, 2012
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Last Updated: 09/26/2026