Sanaa Eddiry
Toulouse, France
Last Updated: 09/26/2026
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Found 12 publications
Survey on vitamin D supplementation in children in France: Evaluation of real-life practices following the new 2022 French recommendations.
Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
Published: June 14, 2024
Differential DNA methylation in iPSC-derived dopaminergic neurons: a step forward on the role of SNORD116 microdeletion in the pathophysiology of addictive behavior in Prader-Willi syndrome.
Journal: Molecular psychiatry
Published: April 12, 2023
Diagnostic yield of bone fragility gene panel sequencing in children and young adults referred for idiopathic primary osteoporosis at a single regional reference centre.
Journal: Bone reports
Published: February 18, 2022
X-linked hypophosphatemia, obesity and arterial hypertension: data from the XLH21 study.
Journal: Pediatric nephrology (Berlin, Germany)
Published: November 26, 2021
Patients with PWS and related syndromes display differentially methylated regions involved in neurodevelopmental and nutritional trajectory.
Journal: Clinical epigenetics
Published: February 17, 2021
SNORD116 and growth hormone therapy impact IGFBP7 in Prader-Willi syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: September 25, 2020
What can we learn from PWS and SNORD116 genes about the pathophysiology of addictive disorders?
Journal: Molecular psychiatry
Published: July 15, 2020
Ghrelin uses the GHS-R1a/Gi/cAMP pathway and induces differentiation only in mature osteoblasts. This ghrelin pathway is impaired in AIS patients.
Journal: Biochemistry and biophysics reports
Published: April 24, 2020
Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS.
Journal: Stem cell research
Published: August 09, 2016
Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome.
Journal: The Journal of clinical investigation
Published: May 19, 2016
Highly restricted deletion of the SNORD116 region is implicated in Prader-Willi Syndrome.
Journal: European journal of human genetics : EJHG
Published: September 24, 2013
Impairment of adipose tissue in Prader-Willi syndrome rescued by growth hormone treatment.
Journal: International journal of obesity (2005)
Published: September 17, 2013
Showing 1-12 of 12
Last Updated: 09/26/2026