Cherif Beldjord
Paris, France
Last Updated: 09/26/2026
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Found 18 publications
Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome.
Journal: European journal of medical genetics
Published: November 17, 2017
Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 08, 2016
PINK1 and FLNA mutations association: A role for atypical parkinsonism?
Journal: Parkinsonism & related disorders
Published: September 28, 2015
Mosaic parental germline mutations causing recurrent forms of malformations of cortical development.
Mosaic parental germline mutations causing recurrent forms of malformations of cortical development.
Journal: European journal of human genetics : EJHG
Published: May 12, 2015
New NOBOX mutations identified in a large cohort of women with primary ovarian insufficiency decrease KIT-L expression.
Journal: The Journal of clinical endocrinology and metabolism
Published: December 17, 2014
X-chromosome inactivation in female patients with Fabry disease.
Journal: Clinical genetics
Published: November 25, 2014
Abnormal sodium current properties contribute to cardiac electrical and contractile dysfunction in a mouse model of myotonic dystrophy type 1.
Journal: Neuromuscular disorders : NMD
Published: October 21, 2014
Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly.
Journal: Acta neuropathologica communications
Published: June 02, 2014
Bilateral frontoparietal polymicrogyria.
Journal: Indian journal of pediatrics
Published: March 18, 2014
Dental caries and enamelin haplotype.
Journal: Journal of dental research
Published: February 04, 2014
Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1.
Journal: Archives of cardiovascular diseases
Published: July 05, 2013
Last Updated: 09/26/2026