Marina Michelson
Tel Aviv, TA, Israel
Last Updated: 09/26/2026
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Found 16 publications
Familial Mediterranean Fever Is Associated with Higher Atopic Morbidity: Evidence from a Country-Wide Case-Control Study.
Journal: The journal of allergy and clinical immunology. In practice
Published: January 25, 2026
Familial Mediterranean fever is associated with higher atopic morbidity: evidence from a countrywide case-control study.
Journal: The journal of allergy and clinical immunology. In practice
Published: January 25, 2026
The Clinical, Histological, and Genetic Spectrum of RYR1 Variants-A Multi-Center Israeli Cohort Study.
Journal: Journal of clinical medicine
Published: December 09, 2025
Elevated iron levels in tears of patients diagnosed with WDR45 X-linked optic atrophy.
Journal: Orphanet journal of rare diseases
Published: November 21, 2024
Clinical profiling and medical management of Israeli individuals with Phelan McDermid syndrome.
Journal: Orphanet journal of rare diseases
Published: August 24, 2024
EEFSEC deficiency: A selenopathy with early-onset neurodegeneration.
Journal: American journal of human genetics
Published: June 07, 2024
Novel phenotype associated with homozygous likely pathogenic variant in the POP1 gene.
Journal: Clinical genetics
Published: October 25, 2023
Variants in the WDR45 Gene Within the OPA-2 Locus Associate With Isolated X-Linked Optic Atrophy.
Journal: Investigative ophthalmology & visual science
Published: October 11, 2023
Juvenile mucopolysaccharidosis plus disease caused by a missense mutation in VPS33A.
Journal: Human mutation
Published: August 23, 2022
Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders.
Journal: Journal of human genetics
Published: June 06, 2021
Microdeletion of 16q24.1-q24.2-A unique etiology of Lymphedema-Distichiasis syndrome and neurodevelopmental disorder.
Journal: American journal of medical genetics. Part A
Published: April 01, 2021
Infantile onset progressive cerebellar atrophy and anterior horn cell Degeneration-A novel phenotype associated with mutations in the PLA2G6 gene.
Journal: European journal of medical genetics
Published: June 13, 2019
Last Updated: 09/26/2026