Sarit Ravid

Haifa, HA, Israel

Last Updated: 09/26/2026

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Found 29 publications

X-Linked Cerebral Adrenoleukodystrophy Presenting With Acute Encephalitis-Like Illness and Optic Neuropathy in a Child.

X-Linked Cerebral Adrenoleukodystrophy Presenting With Acute Encephalitis-Like Illness and Optic Neuropathy in a Child.

Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society

Published: May 14, 2026

Motor, cognitive, affective, and communication outcomes in patients with sustained remission of opsoclonus-myoclonus-ataxia syndrome.

Motor, cognitive, affective, and communication outcomes in patients with sustained remission of opsoclonus-myoclonus-ataxia syndrome.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: June 11, 2025

Exploring the thalamus L-sign: initial findings and associations with white matter injury in premature infants.

Exploring the thalamus L-sign: initial findings and associations with white matter injury in premature infants.

Journal: Pediatric radiology

Published: April 16, 2024

Rapid exome sequencing for children with severe acute encephalopathy - A case series.

Rapid exome sequencing for children with severe acute encephalopathy - A case series.

Journal: European journal of medical genetics

Published: June 08, 2023

Publicly funded exome sequencing for outpatients with neurodevelopmental disorders demonstrates a high rate of unexpected findings impacting medical management.

Publicly funded exome sequencing for outpatients with neurodevelopmental disorders demonstrates a high rate of unexpected findings impacting medical management.

Journal: Genetics in medicine open

Published: March 25, 2023

SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females.

SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females.

Journal: American journal of human genetics

Published: December 07, 2020

Bariatric Surgery-Associated Myelopathy.

Bariatric Surgery-Associated Myelopathy.

Journal: Obesity facts

Published: September 08, 2020

Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course.

Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course.

Journal: Brain : a journal of neurology

Published: February 22, 2019

Acute ataxia in children: Common causes and yield of diagnostic work-up in the era of varicella vaccination.

Acute ataxia in children: Common causes and yield of diagnostic work-up in the era of varicella vaccination.

Journal: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia

Published: September 15, 2018

Highly Selective Eating in Autism Spectrum Disorder Leading to Scurvy: A Series of Three Patients.

Highly Selective Eating in Autism Spectrum Disorder Leading to Scurvy: A Series of Three Patients.

Journal: Pediatric neurology

Published: August 18, 2018

A new approach for assessing executive functions in everyday life, among adolescents with Genetic Generalised Epilepsies.

A new approach for assessing executive functions in everyday life, among adolescents with Genetic Generalised Epilepsies.

Journal: Neuropsychological rehabilitation

Published: May 02, 2018

Severe infantile epileptic encephalopathy associated with D-glyceric aciduria: report of a novel case and review.

Severe infantile epileptic encephalopathy associated with D-glyceric aciduria: report of a novel case and review.

Journal: Metabolic brain disease

Published: November 04, 2017

Showing 1-12 of 29

Last Updated: 09/26/2026