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Publications by Chrystel Leroy

Greater Prevalence of PROKR2 Mutations in Kallmann Syndrome Patients From the Maghreb Than in European Patients

European Journal of Endocrinology

English

Phenotypic Variability in a Family With Acrodysostosis Type 2 Caused by a Novel PDE4D Mutation Affecting the Serine Target of PKA Phosphorylation

JCRPE Journal of Clinical Research in Pediatric Endocrinology

English

Related publications

PROK2/PROKR2 Signaling and Kallmann Syndrome

Frontiers in Endocrinology

English

Nasal Embryonic LHRH Factor (NELF) Mutations in Patients With Normosmic Hypogonadotropic Hypogonadism and Kallmann Syndrome

Fertility and Sterility

Reproductive Medicine

English

OC8 High Prevalence Ofwt1gene Mutations in Patients With Steroid-Resistant Nephrotic Syndrome

English

Prevalence of BRCA1 and BRCA2 Mutations in Breast Cancer Patients From Brazil

Breast Cancer Research and Treatment

Cancer Research

English

Prevalence of Metabolic Syndrome in the Hospitalized Psychiatric Patients

Medicinski Arhiv

English

Prevalence of Metabolic Syndrome in Patients With Psoriasis

The Scientific World Journal

Molecular Biology

Environmental Science

English

Novel GRN Mutations in Patients With Corticobasal Syndrome

Scientific Reports

Multidisciplinary

English

Mutations in the FGFR2 Gene in Mexican Patients With Apert Syndrome

Genetics and Molecular Research

Molecular Biology

English

Congenital Nephrotic Syndrome (NPHS1): Features Resulting From Different Mutations in Finnish Patients

Kidney International

English