Manali V. Chitre

Cambridge, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 17 publications

Pediatric MOG-Ab-Associated Encephalitis: Supporting Early Recognition and Treatment.

Pediatric MOG-Ab-Associated Encephalitis: Supporting Early Recognition and Treatment.

Journal: Neurology(R) neuroimmunology & neuroinflammation
Published: October 11, 2024

Avoiding Premature Diagnostic Closure: Lessons from Two Children with Neurotransmitter Disorders Associated with Dual Pathology.

Avoiding Premature Diagnostic Closure: Lessons from Two Children with Neurotransmitter Disorders Associated with Dual Pathology.

Journal: Movement disorders clinical practice
Published: March 06, 2024

Evolution of brain MRI lesions in paediatric myelin-oligodendrocyte glycoprotein antibody-associated disease (MOGAD) and its relevance to disease course.

Evolution of brain MRI lesions in paediatric myelin-oligodendrocyte glycoprotein antibody-associated disease (MOGAD) and its relevance to disease course.

Journal: Journal of neurology, neurosurgery, and psychiatry
Published: September 01, 2023

Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders.

Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders.

Journal: American journal of human genetics
Published: March 13, 2023

Clinical, neuroradiological, and molecular characterization of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder.

Clinical, neuroradiological, and molecular characterization of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 05, 2023

Biallelic variants in TAMM41 are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease.

Biallelic variants in TAMM41 are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease.

Journal: HGG advances
Published: October 18, 2021

Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease.

Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease.

Journal: Human molecular genetics
Published: June 23, 2021

Use of Disease-Modifying Therapies in Pediatric Relapsing-Remitting Multiple Sclerosis in the United Kingdom.

Use of Disease-Modifying Therapies in Pediatric Relapsing-Remitting Multiple Sclerosis in the United Kingdom.

Journal: Neurology(R) neuroimmunology & neuroinflammation
Published: December 07, 2020

Correlation between the total number of features of paediatric pseudotumour cerebri syndrome and cerebrospinal fluid pressure.

Correlation between the total number of features of paediatric pseudotumour cerebri syndrome and cerebrospinal fluid pressure.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: July 12, 2019

Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome.

Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome.

Journal: The Journal of clinical investigation
Published: July 08, 2019

Sudden onset of lower limb flaccid paralysis.

Sudden onset of lower limb flaccid paralysis.

Journal: Archives of disease in childhood. Education and practice edition
Published: July 25, 2018

PEHO syndrome: the endpoint of different genetic epilepsies.

PEHO syndrome: the endpoint of different genetic epilepsies.

Journal: Journal of medical genetics
Published: February 20, 2018
Showing 1-12 of 17

Last Updated: 09/26/2026