Sangeetha A. Yoganathan

Vellore, TN, India

Last Updated: 09/26/2026

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Found 115 publications

Response to letter to the editor: Investigating the impact of RapidPlan on Ethos automated planning.

Response to letter to the editor: Investigating the impact of RapidPlan on Ethos automated planning.

Journal: Medical dosimetry : official journal of the American Association of Medical Dosimetrists
Published: April 13, 2026

Serine Biosynthesis Defect: A Treatable Neurometabolic Disorder.

Serine Biosynthesis Defect: A Treatable Neurometabolic Disorder.

Journal: Indian journal of pediatrics
Published: March 24, 2026

A treatable cause of developmental and epileptic encephalopathy: Cerebral folate deficiency in a young child.

A treatable cause of developmental and epileptic encephalopathy: Cerebral folate deficiency in a young child.

Journal: Seizure
Published: March 17, 2026

SEMA6B-Related Progressive Myoclonic Epilepsy Mimicking Angelman Syndrome.

SEMA6B-Related Progressive Myoclonic Epilepsy Mimicking Angelman Syndrome.

Journal: Movement disorders clinical practice
Published: February 12, 2026

Broadening the phenotypic and molecular spectrum of PRS deficiency in females.

Broadening the phenotypic and molecular spectrum of PRS deficiency in females.

Journal: HGG advances
Published: December 10, 2025

Broadening the phenotypic and molecular spectrum of PRS deficiency in females.

Broadening the phenotypic and molecular spectrum of PRS deficiency in females.

Journal: HGG advances
Published: December 10, 2025

GLUT1 Deficiency Syndrome with Coexistent Movement Disorder and Anemia.

GLUT1 Deficiency Syndrome with Coexistent Movement Disorder and Anemia.

Journal: Movement disorders clinical practice
Published: December 09, 2025

Phenotypic Clues in Infantile-Onset Parkinsonism-Dystonia-2: A Treatable Neurotransmitter Disorder.

Phenotypic Clues in Infantile-Onset Parkinsonism-Dystonia-2: A Treatable Neurotransmitter Disorder.

Journal: Movement disorders clinical practice
Published: December 04, 2025

FTH1-Related Neuroferritinopathy: A Rare Form of Neurodegeneration with Brain Iron Accumulation Mimicking Pontocerebellar Hypoplasia.

FTH1-Related Neuroferritinopathy: A Rare Form of Neurodegeneration with Brain Iron Accumulation Mimicking Pontocerebellar Hypoplasia.

Journal: Movement disorders clinical practice
Published: October 23, 2025

Reply: "Leigh Syndrome Due to the Variant c.1019T>C in COX15".

Reply: "Leigh Syndrome Due to the Variant c.1019T>C in COX15".

Journal: Movement disorders clinical practice
Published: September 15, 2025

Child Neurology: Clinical and Imaging Findings in a Child With DHX37 Gene Variant: A Ribosomopathy Masquerading as Cerebral Palsy.

Child Neurology: Clinical and Imaging Findings in a Child With DHX37 Gene Variant: A Ribosomopathy Masquerading as Cerebral Palsy.

Journal: Neurology
Published: September 11, 2025

Feasibility of using geometry-based synthetic dose distributions for Knowledge-based planning model training.

Feasibility of using geometry-based synthetic dose distributions for Knowledge-based planning model training.

Journal: Physica medica : PM : an international journal devoted to the applications of physics to medicine and biology : official journal of the Italian Association of Biomedical Physics (AIFB)
Published: August 29, 2025
Showing 1-12 of 115

Last Updated: 09/26/2026