Justine Lerat
Limoges, France
Last Updated: 09/26/2026
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Found 17 publications
IGH 3'RR recombination uncovers a non-germinal center imprint and c-MYC-dependent IGH rearrangement in unmutated chronic lymphocytic leukemia.
Journal: Haematologica
Published: February 13, 2023
History of tonsillectomy and risk of oropharyngeal cancer.
Journal: Oral oncology
Published: October 22, 2020
A sudden bilateral hearing loss caused by inner ear hemorrhage.
Journal: European annals of otorhinolaryngology, head and neck diseases
Published: June 11, 2019
Guidelines (short version) of the French Society of Otorhinolaryngology (SFORL) on cervical lymphatic malformation in adults and children: Diagnosis.
Journal: European annals of otorhinolaryngology, head and neck diseases
Published: March 02, 2019
New PRPS1 variant p.(Met68Leu) located in the dimerization area identified in a French CMTX5 patient.
Journal: Molecular genetics & genomic medicine
Published: February 07, 2019
Hearing loss in inherited peripheral neuropathies: Molecular diagnosis by NGS in a French series.
Journal: Molecular genetics & genomic medicine
Published: January 29, 2019
Implication of the SH3TC2 gene in Charcot-Marie-Tooth disease associated with deafness and/or scoliosis: Illustration with four new pathogenic variants.
Journal: Journal of the neurological sciences
Published: January 23, 2019
A novel pathogenic variant of NEFL responsible for deafness associated with peripheral neuropathy discovered through next-generation sequencing and review of the literature.
Journal: Journal of the peripheral nervous system : JPNS
Published: November 28, 2018
High prevalence of congenital deafness on Reunion Island is due to a founder variant of LHFPL5.
Journal: Clinical genetics
Published: August 30, 2018
A complex homozygous mutation in ABHD12 responsible for PHARC syndrome discovered with NGS and review of the literature.
Journal: Journal of the peripheral nervous system : JPNS
Published: January 04, 2017
Last Updated: 09/26/2026