Works matching AU Yoganathan, Sangeetha

Results: 46

EEG lateralization and seizure outcome following peri-insular hemispherotomy for pediatric hemispheric epilepsy.

Published in:

Child's Nervous System, 2019, v. 35, n. 7, p. 1189, doi. 10.1007/s00381-019-04067-6

By:

Abraham, Ananth P.;
Thomas, Maya Mary;
Mathew, Vivek;
Muthusamy, Karthik;
Yoganathan, Sangeetha;
Jonathan, G. Edmond;
Prabhu, Krishna;
Daniel, Roy Thomas;
Chacko, Ari G.

Publication type:

Article

Hypomyelination, Hypodontia, Hypogonadotropic Hypogonadism (4H) Syndrome With Vertebral Anomalies: A Novel Association.

Published in:

Journal of Child Neurology, 2015, v. 30, n. 7, p. 937, doi. 10.1177/0883073814541470

By:

Muthusamy, Karthik;
Sudhakar, Sniya V.;
Yoganathan, Sangeetha;
Thomas, Maya Mary;
Alexander, Mathew

Publication type:

Article

Isolated Cerebellar Involvement in Vitamin B12 Deficiency: A Case Report.

Published in:

Journal of Child Neurology, 2014, v. 29, n. 11, p. NP161, doi. 10.1177/0883073813513498

By:

Chakrabarty, Biswaroop;
Dubey, Rachana;
Yoganathan, Sangeetha;
Kumar, Ajay;
Gulati, Sheffali;
Kumar, Atin

Publication type:

Article

Pediatric Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis: Experience of a Tertiary Care Teaching Center From North India.

Published in:

Journal of Child Neurology, 2014, v. 29, n. 11, p. 1453, doi. 10.1177/0883073813494474

By:

Chakrabarty, Biswaroop;
Tripathi, Manjari;
Yoganathan, Sangeetha;
Pandit, Awadh Kishore;
Sinha, Aditi;
Rathi, Bhim Singh;
Gulati, Sheffali

Publication type:

Article

Congenital Thrombotic Thrombocytopenic Purpura Associated With Moyamoya Syndrome in a 3-Year-Old Girl: A Case Report.

Published in:

2012

By:

Jain, Puneet;
Yoganathan, Sangeetha;
Sharma, Suvasini;
Motwani, Jayashree;
Kumar, Atin;
Kabra, Madhulika;
Gulati, Sheffali

Publication type:

Case Study

A Tale of Treatable Infantile Neuroregression and Diagnostic Dilemma with Glutaric Aciduria Type I.

Published in:

Journal of Pediatric Neurosciences, 2017, v. 12, n. 4, p. 356, doi. 10.4103/jpn.JPN_35_17

By:

Yoganathan, Sangeetha;
Varman, Mugil;
Oommen, Samuel Philip;
Thomas, Maya

Publication type:

Article

A tropical menace of co-infection of Japanese encephalitis and neurocysticercosis in two children.

Published in:

2016

By:

Yoganathan, Sangeetha;
Sudhakar, Sniya Valsa;
Thomas, Maya Mary;
Yadav, Vikas Kapildeo

Publication type:

Case Study

KCTD7‐related progressive myoclonic epilepsy: Report of 42 cases and review of literature.

Published in:

Epilepsia (Series 4), 2024, v. 65, n. 3, p. 709, doi. 10.1111/epi.17880

By:

Yoganathan, Sangeetha;
Whitney, Robyn;
Thomas, Maya;
Danda, Sumita;
Chettali, Akbar Mohamed;
Prasad, Asuri N.;
Farhan, Sali M. K.;
AlSowat, Daad;
Abukhaled, Musaad;
Aldhalaan, Hesham;
Gowda, Vykuntaraju K.;
Kinhal, Uddhava V.;
Bylappa, Arun Y.;
Konanki, Ramesh;
Lingappa, Lokesh;
Parchuri, Bindu Madhavi;
Appendino, Juan P.;
Scantlebury, Morris H.;
Cunningham, Jessie;
Hadjinicolaou, Aristides

Publication type:

Article

KCNT1‐related epilepsy: An international multicenter cohort of 27 pediatric cases.

Published in:

Epilepsia (Series 4), 2020, v. 61, n. 4, p. 679, doi. 10.1111/epi.16480

By:

Borlot, Felippe;
Abushama, Ahmed;
Morrison‐Levy, Nadine;
Jain, Puneet;
Puthenveettil Vinayan, Kollencheri;
Abukhalid, Musaad;
Aldhalaan, Hesham M.;
Almuzaini, Hanin S.;
Gulati, Sheffali;
Hershkovitz, Tova;
Konanki, Ramesh;
Lingappa, Lokesh;
Luat, Aimee F.;
Shafi, Shatha;
Tabarki, Brahim;
Thomas, Maya;
Yoganathan, Sangeetha;
Alfadhel, Majid;
Arya, Ravindra;
Donner, Elizabeth J.

Publication type:

Article

Biotin thiamine responsive basal ganglia disease-A potentially treatable inborn error of metabolism.

Published in:

2016

By:

Muthusamy, Karthik;
Ekbote, Alka V.;
Thomas, Maya M.;
Aaron, Sanjith;
Mathew, Vivek;
Patil, Anil B.;
Sivadasan, Ajith;
Prabhakar, A. T.;
Yoganathan, Sangeetha;
Alexander, Mathew

Publication type:

Letter

Recurrent Painful Ophthalmoplegic Neuropathy: A Cause of Headache.

Published in:

Indian Journal of Pediatrics, 2022, v. 89, n. 4, p. 407, doi. 10.1007/s12098-021-03886-3

By:

Yoganathan, Sangeetha;
Kumar, Madhan;
Sudhakar, SniyaValsa;
Malhotra, Mukul;
Thomas, Maya

Publication type:

Article

An Inherited Cause of Stroke Mimic in a Toddler.

Published in:

2022

By:

Yoganathan, Sangeetha;
Kumar, Madhan;
Sushma, Lenka;
Danda, Sumita;
Thomas, Maya

Publication type:

Letter

Never Miss Sleep Disorder in Children with Drop Attacks.

Published in:

2022

By:

Kumar, Madhan;
Yoganathan, Sangeetha;
P, Murugan T.;
Thomas, Maya Mary

Publication type:

Letter

Unusual Presentation of Adrenal Hypoplasia Congenita.

Published in:

2020

By:

Srinivasaraghavan, Rangan;
Jagadeesh, Anbazhagan;
Yoganathan, Sangeetha;
Mathai, Sarah;
Oommen, Samuel Philip

Publication type:

Letter

A Treatable Cause of Intellectual Disability and Autism in a Young Child.

Published in:

2020

By:

Yoganathan, Sangeetha;
Sharma, Suvasini;
Varman, Mugil;
Malhotra, Mukul;
Chandran, Mahalakshmi;
Arunachal, Gautham;
Thomas, Maya

Publication type:

Letter

Epilepsy, Cognition and Behavior.

Published in:

Indian Journal of Pediatrics, 2014, v. 81, n. 10, p. 1056, doi. 10.1007/s12098-014-1530-4

By:

Gulati, Sheffali;
Yoganathan, Sangeetha;
Chakrabarty, Biswaroop

Publication type:

Article

Eye signs in a child with gene mutation.

Published in:

2022

By:

Yoganathan, Sangeetha;
Kumar, Madhan;
Malhotra, Mukul;
Joy, Praisy;
Danda, Sumita;
Thomas, Maya;
David, Kenny;
Jasper, Anitha;
Selvin, Satheesh;
David, Kenny S;
Selvin, Satheesh Solomon T

Publication type:

journal article

Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian Children.

Published in:

Movement Disorders Clinical Practice, 2022, v. 9, n. 7, p. 886, doi. 10.1002/mdc3.13516

By:

Garg, Divyani;
Yoganathan, Sangeetha;
Shamim, Uzma;
Mankad, Kshitij;
Gulati, Parveen;
Bonifati, Vincenzo;
Botre, Abhijeet;
Kalane, Umesh;
Saini, Arushi Gahlot;
Sankhyan, Naveen;
Srivastava, Kavita;
Gowda, Vykuntaraju K.;
Juneja, Monica;
Kamate, Mahesh;
Padmanabha, Hansashree;
Panigrahi, Debasis;
Pachapure, Shaila;
Udani, Vrajesh;
Kumar, Atin;
Pandey, Sanjay

Publication type:

Article

Acute Encephalitis Syndrome in Children and Adolescents: A Five-Year Descriptive Study From South India.

Published in:

Indian Pediatrics, 2024, v. 61, n. 5, p. 413, doi. 10.1007/s13312-024-3126-z

By:

Rebecca, Betsy;
Thomas, Maya;
Abraham, Asha Mary;
Yoganathan, Sangeetha;
Jacob, Ebor;
Kumar, Sathish;
Simon, Anna;
Jasper, Anitha;
Rose, Winsley

Publication type:

Article

Diverse Phenotypes of Mitochondrial Disease With Varying Levels of Heteroplasmy.

Published in:

2025

By:

John, Rebecca;
Chapla, Aaron;
Chacko, Geeta;
Yoganathan, Sangeetha;
Thomas, Maya Mary;
Thomas, Nihal

Publication type:

Case Study

Landscape of genetic infantile epileptic spasms syndrome—A multicenter cohort of 124 children from India.

Published in:

Epilepsia Open, 2023, v. 8, n. 4, p. 1383, doi. 10.1002/epi4.12811

By:

Nagarajan, Balamurugan;
Gowda, Vykuntaraju K.;
Yoganathan, Sangeetha;
Sharawat, Indar Kumar;
Srivastava, Kavita;
Vora, Nitish;
Badheka, Rahul;
Danda, Sumita;
Kalane, Umesh;
Kaur, Anupriya;
Madaan, Priyanka;
Mehta, Sanjiv;
Negi, Sandeep;
Panda, Prateek Kumar;
Rajadhyaksha, Surekha;
Saini, Arushi Gahlot;
Saini, Lokesh;
Shah, Siddharth;
Srinivasan, Varunvenkat M.;
Suthar, Renu

Publication type:

Article

Prevalence and predictors of peripheral neuropathy in nondiabetic children with chronic kidney disease.

Published in:

2018

By:

Yoganathan, Sangeetha;
Bagga, Arvind;
Gulati, Sheffali;
Toteja, G. S.;
Hari, Pankaj;
Sinha, Aditi;
Pandey, Ravindra Mohan;
Irshad, Mohammad

Publication type:

journal article

Novel Imaging Finding and Novel Mutation in an Infant with Molybdenum Cofactor Deficiency, a Mimicker of Hypoxic-Ischaemic Encephalopathy.

Published in:

Iranian Journal of Child Neurology, 2018, v. 12, n. 2, p. 107

By:

YOGANATHAN, Sangeetha;
VALSA SUDHAKAR, Sniya;
THOMAS, Maya;
KUMAR DUTTA, Atanu;
DANDA, Sumita;
CHANDRAN, Mahalakshmi

Publication type:

Article

Utility of Chromosomal Microarray in Children with Unexplained Developmental Delay/Intellectual Disability.

Published in:

Fetal & Pediatric Pathology, 2022, v. 41, n. 2, p. 208, doi. 10.1080/15513815.2020.1791292

By:

Kamath, Vandana;
Yoganathan, Sangeetha;
Thomas, Maya Mary;
Gowri, Mahasampath;
Chacko, Mary Purna

Publication type:

Article

The diagnostic value of congenital and nevoid cutaneous lesions associated with autism spectrum disorders in indian children-A case-control study.

Published in:

Indian Dermatology Online Journal, 2021, v. 12, n. 1, p. 84, doi. 10.4103/idoj.IDOJ_275_20

By:

Varala, Sirisha;
George, Renu;
Mathew, Lydia;
Russell, Paul;
Koshy, Beena;
Oommen, Samuel;
Thomas, Maya;
Muthusamy, Karthik;
Yoganathan, Sangeetha;
Jeyaseelan, L;
Muliyil, Jayaprakash

Publication type:

Article

Ghosal hematodiaphyseal dysplasia and response to corticosteroid therapy.

Published in:

American Journal of Medical Genetics. Part A, 2021, v. 185, n. 2, p. 596, doi. 10.1002/ajmg.a.61961

By:

Joy, Praisy;
Yoganathan, Sangeetha;
Korula, Sophy;
Abraham, Suneetha Susan C;
Barney, Anitha M;
Walter, Vrisha Madhuri;
Gibikote, Sridhar;
Danda, Sumita

Publication type:

Article

Methyl-CpG-binding protein 2 gene mutations and its association with epilepsy: a single centre study from the Indian subcontinent.

Published in:

Journal of Genetics, 2020, v. 99, n. 1, p. 1, doi. 10.1007/s12041-020-01244-4

By:

Kamdar, Payal;
Thomas, Maya;
Yoganathan, Sangeetha;
Muthusamy, Karthik;
Koshy, Beena;
Oommen, Samuel Philip;
Aaron, Rekha;
Barney, Anitha;
Abraham, Suneetha Susan C.;
Danda, Sumita

Publication type:

Article

Hereditary Folate Malabsorption: A Rare Treatable Disorder with Hematological and Neurological Manifestations.

Published in:

2022

By:

Kumar, Madhan;
Yoganathan, Sangeetha;
Todari, Siddarth;
Suresh, Parvathy;
Chandran, Mahalakshmi;
Danda, Sumita;
Mathew, Leni Grace;
Koshy, Beena;
Thomas, Maya

Publication type:

Case Study

Phenotypic Pleiotropy in Arginase Deficiency: A Single Center Cohort.

Published in:

Annals of Indian Academy of Neurology, 2022, v. 25, n. 6, p. 1104, doi. 10.4103/aian.aian_612_22

By:

Bharathi, Narmadham K.;
Thomas, Maya Mary;
Yoganathan, Sangeetha;
Chandran, Mahalakshmi;
Aaron, Rekha;
Danda, Sumita

Publication type:

Article

Late onset multiple Acyl-CoA dehydrogenase deficiency: A rare treatable neurometabolic disorder.

Published in:

2022

By:

Korula, Sophy;
Yoganathan, Sangeetha;
Peter, Jeyanthi;
Chandran, Mahalakshmi;
Christudass, Chrithunesa;
Danda, Sumita

Publication type:

Letter to the Editor

Fumaric aciduria: A rare cause of refractory epilepsy.

Published in:

2022

By:

Yoganathan, Sangeetha;
Srinivasaraghavan, Rangan;
Kumar, Madhan;
Kratz, Lisa;
Mular, Shraddha;
Sudhakar, Sniya;
Malik, Prateek;
Chandran, Mahalakshmi;
Thomas, Maya;
Danda, Sumita

Publication type:

Case Study

Management of children and adolescents with Wilson Disease and neurological worsening following D–Penicillamine therapy: A single centre experience.

Published in:

Annals of Indian Academy of Neurology, 2022, v. 25, n. 4, p. 698, doi. 10.4103/aian.aian_519_21

By:

Kumar, Madhan;
Murugan, T;
Lionel, Arul;
Thomas, Maya;
Mannam, Pavithra;
Yoganathan, Sangeetha

Publication type:

Article

Oculodigital Sign: A Clinical Clue for Diagnosis.

Published in:

2022

By:

Yoganathan, Sangeetha;
Kumar, Madhan;
John, Deepa;
Danda, Sumita;
Oommen, Samuel P.;
Umakant, Sayli B.;
Thomas, Maya

Publication type:

Letter to the Editor

Child with D-2-Hydroxyglutaric Aciduria Type II: A Rare Neurometabolic Disorder.

Published in:

2021

By:

Srinivasaraghavan, Rangan;
Sharma, Suvasini;
Kratz, Lisa;
Malik, Prateek;
Yoganathan, Sangeetha;
Danda, Sumita;
Oommen, Samuel Philip

Publication type:

Case Study

Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental Disorder.

Published in:

2021

By:

Yoganathan, Sangeetha;
Srinivasaraghavan, Rangan;
Chandran, Mahalakshmi;
Kratz, Lisa;
Koshy, Beena;
Sudhakar, Sniya Valsa;
Arunachal, Gautham;
Thomas, Maya;
Danda, Sumita

Publication type:

Letter to the Editor

Metabolic Or Ischemic Stroke in Succinic Semi-Aldehyde Dehydrogenase Deficiency Due to the Homozygous Variant c. 1343 + 1_1343 + 3delGTAinsTT in ALDH5A1.

Published in:

2021

By:

Yoganathan, Sangeetha;
Arunachal, Gautham;
Kratz, Lisa;
Varman, Mugil;
Thomas, Maya;
Sudhakar, Sniya V.;
Oommen, Samuel P.;
Danda, Sumita

Publication type:

Letter to the Editor

Imaging Findings in TRPM6-Related Hypomagnesemia with Secondary Hypocalcemia.

Published in:

2021

By:

Malik, Prateek;
Bidkar, Sayli Umakant;
Yoganathan, Sangeetha;
Mathai, Sarah;
Danda, Sumita;
Koshy, Beena

Publication type:

Case Study

Guanidinoacetate methyltransferase (GAMT) deficiency, a cerebral creatine deficiency syndrome: A rare treatable metabolic disorder.

Published in:

2020

By:

Yoganathan, Sangeetha;
Arunachal, Gautham;
Kratz, Lisa;
Varman, Mugil;
Sudhakar, Sniya;
Oommen, Samuel;
Jain, Shikha;
Thomas, Maya;
Babuji, Manimegalai

Publication type:

Case Study

Metabolic Stroke: A Novel Presentation in a Child with Succinic Semialdehyde Dehydrogenase Deficiency.

Published in:

Annals of Indian Academy of Neurology, 2020, v. 23, n. 1, p. 113, doi. 10.4103/aian.AIAN_213_18

By:

Yoganathan, Sangeetha;
Arunachal, Gautham;
Kratz, Lisa;
Varman, Mugil;
Thomas, Maya;
Sudhakar, Sniya Valsa;
Oommen, Samuel Philip;
Danda, Sumita

Publication type:

Article

Clinical Profile, Prognostic Indicators, and Therapeutic Outcomes of Pediatric Opsoclonus-Myoclonus-Ataxia Syndrome: A Single-Center Experience from South India.

Published in:

Annals of Indian Academy of Neurology, 2019, v. 22, n. 3, p. 295, doi. 10.4103/aian.AIAN_101_18

By:

Muthusamy, Karthik;
Thomas, Maya;
Yoganathan, Sangeetha;
Sudhakar, Sniya Valsa

Publication type:

Article

Stroke in a Child with Dengue Encephalopathy.

Published in:

2017

By:

Yoganathan, Sangeetha;
Sudhakar, Sniya Valsa;
Priyambada, Leena;
Thomas, Maya

Publication type:

Case Study

Predictors of Outcome in Children with Status Epilepticus during Resuscitation in Pediatric Emergency Department: A Retrospective Observational Study.

Published in:

Annals of Indian Academy of Neurology, 2017, v. 20, n. 2, p. 142, doi. 10.4103/aian.AIAN_369_16

By:

Santhanam, Indumathy;
Yoganathan, Sangeetha;
Sivakumar, V. Akila;
Ramakrishnamurugan, Rubini;
Sathish, Sharada;
Thandavarayan, Murali

Publication type:

Article

Study of Refractory Status Epilepticus from a Tertiary Care Center.

Published in:

Annals of Indian Academy of Neurology, 2017, v. 20, n. 2, p. 116, doi. 10.4103/aian.AIAN_385_16

By:

Kohli, Sahil;
Pasangulapati, Suresh Babu;
Yoganathan, Sangeetha;
Rynjah, Gideon Lyngsyun;
Prabhakar, A. T.;
Aaron, Sanjith;
Alexander, Mathew;
Mathew, Vivek

Publication type:

Article

Menkes disease and response to copper histidine: An Indian case series.

Published in:

Annals of Indian Academy of Neurology, 2017, v. 20, n. 1, p. 62, doi. 10.4103/0972-2327.199907

By:

Yoganathan, Sangeetha;
Thomas, Maya;
Sudhakar, Sniya Valsa;
Arunachal, Gautham;
Danda, Sumita;
Subramanian, Annadurai;
George, Renu

Publication type:

Article

Subacute sclerosing panencephalitis in a child with human immunodeficiency virus (HIV) infection on antiretroviral therapy.

Published in:

Annals of Indian Academy of Neurology, 2015, v. 18, n. 1, p. 96, doi. 10.4103/0972-2327.144299

By:

Muthusamy, Karthik;
Yoganathan, Sangeetha;
Thomas, Maya Mary;
Alexander, Mathew;
Verghese, Valsan Philip

Publication type:

Article

Case Report. Candida tropicalis brain abscess in a neonate: An emerging nosocomial menace.

Published in:

Annals of Indian Academy of Neurology, 2014, v. 17, n. 4, p. 448, doi. 10.4103/0972-2327.144036

By:

Yoganathan, Sangeetha;
Chakrabarty, Biswaroop;
Gulati, Sheffali;
Kumar, Ajay;
Kumar, Atin;
Singh, Manmohan;
Xess, Immaculata

Publication type:

Article