C. Gendrot

发表

Systematic analysis of X-inactivation in 19 XLMR families: extremely skewed profiles in carriers in three families

A. Toutain, C. Moraine, M. Raynaud, 2000, European Journal of Human Genetics.

Total Protein Level in Cerebrospinal Fluid is Stable in Elderly Adults

C. Hommet, K. Mondon, É. Beaufils, 2013, Journal of the American Geriatrics Society.

Iron Metabolism Disturbance in a French Cohort of ALS Patients

D. Devos, C. Moreau, P. Vourc'h, 2014, BioMed research international.

MECP 2 is highly mutated in X-linked mental retardation

H. Ropers, J. Fryns, A. Verloes, 2001 .

A Case of Severe Toxicity During Coadministration of Vincristine and Piperacillin: Are Drug Transporters Involved in Vincristine Hypersensitivity and Drug-Drug Interactions?

C. Andres, A. Jonville-Béra, C. L. Le Guellec, 2012, Journal of pediatric hematology/oncology.

X-linked nonspecific mental retardation (MRX) linkage studies in 25 unrelated families: the European XLMR consortium.

S. Claes, H. Kremer, A. Toutain, 1999, American journal of medical genetics.

A second heterozygous MDR3 nonsense mutation associated with intrahepatic cholestasis of pregnancy

C. Andres, Y. Bacq, C. Andres, 2003, Journal of medical genetics.

ABCB4 gene mutations and single-nucleotide polymorphisms in women with intrahepatic cholestasis of pregnancy

C. Andres, Y. Bacq, F. Perrotin, 2009, Journal of Medical Genetics.

[Acute fatty liver of pregnancy and mitochondrial fatty acid oxidation. Consequences for the offspring].

Y. Bacq, F. Labarthe, C. Gendrot, 2017, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

[Recurrent acute fatty liver of pregnancy].

C. Andres, Y. Bacq, F. Perrotin, 2007, Gastroenterologie clinique et biologique.

MECP2 gene mutations in non‐syndromic X‐linked mental retardation: Phenotype–genotype correlation

A. Toutain, A. Verloes, V. Kalscheuer, 2003, American journal of medical genetics. Part A.

X-linked mental retardation with neonatal hypotonia in a French family (MRX15): gene assignment to Xp11.22-Xp21.1.

A. Toutain, M. Raynaud, L. Villard, 1996, American journal of medical genetics.

MECP2 is highly mutated in X-linked mental retardation.

H. Ropers, J. Fryns, A. Verloes, 2001, Human molecular genetics.

Evidence for a new X-linked mental retardation gene in Xp21-Xp22: clinical and molecular data in one family.

A. Toutain, M. Raynaud, L. Colleaux, 1999, American journal of medical genetics.

X-linked nonspecific mental retardation (MRX16) mapping to distal Xq28: linkage study and neuropsychological data in a large family.

J. Chelly, C. Moraine, M. Raynaud, 1999, American journal of medical genetics.

X‐linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric region

A. Toutain, C. Moraine, M. Raynaud, 1994, Clinical genetics.

Preanalytical conditions of point-of-care testing in the intensive care unit are decisive for analysis reliability

F. Espitalier, C. Andres, A. Guillon, 2016, Annals of Intensive Care.

Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis

P. Vourc'h, C. Andres, W. Camu, 2012, Journal of the Neurological Sciences.

Ursodeoxycholic acid therapy in intrahepatic cholestasis of pregnancy: Results in real-world conditions and factors predictive of response to treatment.

C. Andres, Y. Bacq, J. Potin, 2017, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.