Einat Lahav
Ramat Gan, TA, Israel
Last Updated: 09/26/2026
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Found 13 publications
A Case of Pediatric Atypical Pseudoxanthoma Elasticum.
Journal: International journal of dermatology
Published: April 07, 2025
Endocrine Abnormalities and Growth Pattern in Single Large-Scale Mitochondrial DNA Deletion Syndromes.
Journal: Acta paediatrica (Oslo, Norway : 1992)
Published: December 10, 2024
Long-term hematopoietic dysfunction in patients with large-scale mitochondrial DNA deletion syndromes.
Journal: Pediatric blood & cancer
Published: January 17, 2024
Mitochondrial augmentation of hematopoietic stem cells in children with single large-scale mitochondrial DNA deletion syndromes.
Journal: Science translational medicine
Published: December 21, 2022
White epidermal nevus as an early sign of tuberous sclerosis complex-A case series.
Journal: Pediatric dermatology
Published: October 29, 2022
A multidisciplinary nephrogenetic referral clinic for children and adults-diagnostic achievements and insights.
Journal: Pediatric nephrology (Berlin, Germany)
Published: August 23, 2021
An Israeli tuberous sclerosis cohort: the efficacy of different anti-epileptic strategies.
Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: April 10, 2021
Kidney and urinary tract findings among patients with Kabuki (make-up) syndrome.
Journal: Pediatric nephrology (Berlin, Germany)
Published: March 24, 2021
Whole exome sequencing in childhood-onset lupus frequently detects single gene etiologies.
Journal: Pediatric rheumatology online journal
Published: June 09, 2019
A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism.
Journal: Human genetics
Published: December 20, 2016
Crossed ectopic kidney: prenatal diagnosis and postnatal follow-up.
Journal: Prenatal diagnosis
Published: December 17, 2016
Last Updated: 09/26/2026