Works matching AU Gulati, Sheffali

Results: 257

Epilepsy in children with Down syndrome.

Published in:

Epileptic Disorders, 2011, v. 13, n. 1, p. 1, doi. 10.1684/epd.2011.0415

By:

Arya, Ravindra;
Kabra, Madhulika;
Gulati, Sheffali

Publication type:

Article

The vaccine–autism connection: No link, still debate, and we are failing to learn the lessons.

Published in:

2025

By:

Gulati, Sheffali;
Sharawat, Indar Kumar;
Panda, Prateek Kumar;
Kothare, Sanjeev V

Publication type:

Editorial

Correlation Between Neuronal Apoptosis Inhibitory Protein (NAIP), SMN2, and SMA Phenotypes: A Tertiary Care Centre Experience From India.

Published in:

American Journal of Medical Genetics. Part A, 2025, v. 197, n. 7, p. 1, doi. 10.1002/ajmg.a.64057

By:

Chakraborty, Soumalya;
Singh, Amita;
Perveen, Shama;
Chowdhury, Madhumita Roy;
Ali, Salman;
Gupta, Neerja;
Gulati, Sheffali;
Kabra, Madhulika

Publication type:

Article

POLR3-Related Leukodystrophy: A Case Series from the Indian Scenario.

Published in:

Neurology India, 2025, v. 73, n. 2, p. 325, doi. 10.4103/neurol-india.Neurol-India-D-24-00198

By:

Meena, Ankit Kumar;
Wander, Arvinder;
Mahesan, Aakash;
Kamila, Gautam;
Kumar, Atin;
Chakrabarty, Biswaroop;
Jauhari, Prashant;
Gulati, Sheffali

Publication type:

Article

Acquired Demyelination Syndrome in Children and Adolescents: 10 Years Experience from a Tertiary Care Centre in North India.

Published in:

Neurology India, 2024, v. 72, n. 5, p. 997, doi. 10.4103/neurol-india.NI_1141_20

By:

Chakrabarty, Biswaroop;
Gulati, Sheffali;
Madaan, Priyanka;
Kumar, Atin;
Sondhi, Vishal;
Dubey, Rachna;
Gupta, Juhi;
Pandey, R M

Publication type:

Article

White Matter Mineralization in an Adolescent Girl with Vanishing White Matter Disease.

Published in:

Neurology India, 2024, v. 72, n. 3, p. 684, doi. 10.4103/neurol-india.Neurol-India-D-24-00070

By:

Choudhary, Puneet K.;
Mahesan, Aakash;
Kamila, Gautam;
Meena, Ankit K.;
Jauhari, Prashant;
Chakrabarty, Biswaroop;
Kumar, Atin;
Gulati, Sheffali

Publication type:

Article

MELAS Syndrome: Rare Early Presentation of a Known Stroke Mimic.

Published in:

Neurology India, 2024, v. 72, n. 3, p. 645, doi. 10.4103/neurol-india.Neurol-India-D-24-00065

By:

Mahesan, Aakash;
Kamila, Gautam;
Sundaram, Mohana;
Kumar, Atin;
Jauhari, Prashant;
Chakrabarty, Biswaroop;
Gulati, Sheffali

Publication type:

Article

A Relook at Cerebral Palsy Beyond Motor Pathology: A Cross-Sectional Study of Sensory Processing Abilities.

Published in:

Neurology India, 2024, v. 72, n. 3, p. 590, doi. 10.4103/ni.ni_1108_22

By:

Mahesan, Aakash;
Jauhari, Prashant;
Singhal, Mita;
Gulati, Sheffali;
Chakrabarty, Biswaroop;
Sirolia, Vivek;
Pandey, Ravindra Mohan

Publication type:

Article

Evaluation of Infantile Brachial Plexopathy Using 3T MRI and High-Resolution Ultrasound: Experience From a Tertiary Care Centre.

Published in:

Neurology India, 2024, v. 72, n. 2, p. 326, doi. 10.4103/ni.ni_818_21

By:

Ramachandran, Anupama;
Jana, Manisha;
Kumar, Atin;
Kandasamy, Devasenathipathy;
Naranje, Priyanka;
Gupta, Arun Kumar;
Gulati, Sheffali;
Chakrabarty, Biswaroop;
Singhal, Maneesh

Publication type:

Article

Novel Therapeutic Strategies of Non-Invasive Brain Stimulation and Nanomedicine in Pediatric Cerebral Palsy Patients.

Published in:

Neurology India, 2024, v. 72, n. 2, p. 248, doi. 10.4103/ni.ni_953_22

By:

Mufti, Aliya;
Gulati, Sheffali;
Kochhar, Kanwal P.;
Alam, Iqbal;
Wadhwa, Sanjay;
Sikka, Kapil;
Saxena, Rohit;
Jain, Suman

Publication type:

Article

Congenital Myasthenia Syndrome Due to a Novel DPAGT1 Gene Mutation – An Error of Glycosylation Masquerading as a Congenital Myopathy.

Published in:

Neurology India, 2024, v. 72, n. 1, p. 175, doi. 10.4103/neurol-india.Neurol-India-D-23-00582

By:

Mahesan, Aakash;
Kamila, Gautam;
Tiwari, Richa;
Das, Sumanta;
Sharma, Mehar;
Jauhari, Prashant;
Chakrabarty, Biswaroop;
Gulati, Sheffali

Publication type:

Article

Novel SLC16A2 Gene Mutation: A Rare Case of Delayed Myelination with Dysthyroidism,v Allan–Herndon–Dudley Syndrome.

Published in:

Neurology India, 2023, v. 71, n. 6, p. 1282, doi. 10.4103/0028-3886.391343

By:

Mahesan, Aakash;
Kamila, Gautam;
Choudhary, Puneet;
Jauhari, Prashant;
Chakrabarty, Biswaroop;
Kumar, Atin;
Gulati, Sheffali

Publication type:

Article

Teaching Neuroimage: A Rare Case of Encephalocraniocutaneous Lipomatosis: A Clinico-Radiological Diagnosis.

Published in:

Neurology India, 2023, v. 71, n. 5, p. 1122, doi. 10.4103/0028-3886.388083

By:

Mahesan, Aakash;
Kamila, Gautam;
Jauhari, Prashant;
Chakrabarty, Biswaroop;
Kumar, Atin;
Gulati, Sheffali

Publication type:

Article

Teaching Neuroimage - Aicardi Syndrome: A Triad of Epileptic Spasms, Agenesis of Corpus Callosum, and Chorio-Retinal Lacunae.

Published in:

Neurology India, 2023, v. 71, n. 5, p. 1114, doi. 10.4103/0028-3886.388086

By:

Mahesan, Aakash;
Kamila, Gautam;
Puri, Prabhav;
Kumar, Vinod;
Kumar, Atin;
Jauhari, Prashant;
Chakrabarty, Biswaroop;
Gulati, Sheffali

Publication type:

Article

Teaching Neuroimage: Juvenile Krabbe -- A MRI Pattern Recognition in Leukodystrophy.

Published in:

Neurology India, 2023, v. 71, n. 4, p. 839, doi. 10.4103/0028-3886.383812

By:

Mahesan, Aakash;
Kamila, Gautam;
Choudhary, Puneet;
Jauhari, Prashant;
Chakrabarty, Biswaroop;
Kumar, Atin;
Gulati, Sheffali

Publication type:

Article

A Genetically Confirmed Case of Laminopathy: Clues from the Clinical Picture and Muscle Biopsy.

Published in:

Neurology India, 2023, v. 71, n. 2, p. 390, doi. 10.4103/0028-3886.375391

By:

Badal, Sachendra;
Sharma, Mehar C.;
Chakrabarty, Biswaroop;
Jauhari, Prashant;
Gulati, Sheffali

Publication type:

Article

Solving the Riddle of Developmental Delay with Hair Microscopy: Trichothiodystrophy (MPLKIP Mutation in an Indian Child).

Published in:

Neurology India, 2022, v. 70, n. 5, p. 2302, doi. 10.4103/0028-3886.359296

By:

Sachendra, Badal;
Biswaroop, Chakrabarty;
Bhawana, Aggarwal;
Saurabh, Bhatia;
Prashant, Jauhari;
Neerja, Gupta;
Madhulika, Kabra;
Sheffali, Gulati

Publication type:

Article

Classical Clinical and Radiological Findings in Fucosidosis.

Published in:

2022

By:

Badal, Sachendra;
Luhar, Zulfiqar;
Chakrabarty, Biswaroop;
Kumar, Atin;
Jauhari, Prashant;
Gulati, Sheffali

Publication type:

Journal Article

Acute Isolated External Ophthalmoplegia: Think of Anti-GQ1b Antibody Syndrome.

Published in:

Neurology India, 2022, v. 70, n. 5, p. 2159, doi. 10.4103/0028-3886.359274

By:

Badal, Sachendra;
Jauhari, Prashant;
Singh, Sonali;
Kamilla, Gautam;
Chakrabarty, Biswaroop;
Gulati, Sheffali

Publication type:

Article

Diaphragmatic Flutter: An Unusual Sign of Multifarious Etiologic Entities.

Published in:

Neurology India, 2022, v. 70, n. 5, p. 2137, doi. 10.4103/0028-3886.359180

By:

Vaishakh, Anand;
Juhi, Gupta;
Sonali, Singh;
Prashant, Jauhari;
Manisha, Jana;
Biswaroop, Chakrabarty;
Sheffali, Gulati

Publication type:

Article

Serum Trace Elements in Children with Well-Controlled and Drug Refractory Epilepsy Compared to Controls: An Observational Study.

Published in:

Neurology India, 2022, v. 70, n. 5, p. 1846, doi. 10.4103/0028-3886.359205

By:

Chakrabarty, Biswaroop;
Dogra, Ankush Singh;
Toteja, G. S.;
Pandey, R. M.;
Paul, Vinod K.;
Gulati, Sheffali

Publication type:

Article

X-linked Myopathy with Excessive Autophagy - A Rare Cause of Vacuolar Myopathy in Children.

Published in:

Neurology India, 2022, v. 70, n. 4, p. 1643, doi. 10.4103/0028-3886.355110

By:

Rajeshwari, Madhu;
Dhiman, Neena;
Chakrabarty, Biswaroop;
Gulati, Sheffali;
Shamim, Uzma;
Faruq, Mohammed;
Suri, Vaishali;
Sharma, Mehar Chand

Publication type:

Article

Hyperekplexia: A Frequent Near Miss in Infants and Young Children.

Published in:

2022

By:

Gupta, Juhi;
Badal, Sachendra;
Anand, Vaishakh;
Jauhari, Prashant;
Chakrabarty, Biswaroop;
Gulati, Sheffali

Publication type:

journal article

Tuberous Sclerosis Complex: Are We Prepared For The Paradigm Shift?

Published in:

2021

By:

Anand, Vaishakh;
Badal, Sachendra;
Gulati, Sheffali

Publication type:

Letter

Cerebral Venous Sinus Thrombosis in a Child with Lesch-Nyhan Syndrome.

Published in:

2021

By:

Manokaran, Ranjith;
Jauhari, Prashant;
Chakrabarty, Biswaroop;
Gupta, Neerja;
Kumar, Atin;
Gulati, Sheffali;
Manokaran, Ranjith K

Publication type:

Case Study

COVID-19 and Child Neurology Care.

Published in:

2020

By:

Gulati, Sheffali;
Gupta, Juhi;
Madaan, Priyanka

Publication type:

Letter

The Development and Validation of DSM 5-Based AIIMS-Modified INDT ADHD Tool for Diagnosis of ADHD: A Diagnostic Test Evaluation Study.

Published in:

2020

By:

Gulati, Sheffali;
Saini, Lokesh;
Kaushik, Jaya;
Chakrabarty, Biswaroop;
Arora, N;
Pandey, Ravindra;
Sagar, Rajesh;
Sapra, Savita;
Sharma, Shobha;
Paul, Vinod;
Kaushik, Jaya Shankar;
Arora, N K;
Pandey, Ravindra M;
Paul, Vinod K

Publication type:

journal article

Chronic meningitis with persistent hypoglycorrhachia: An unusual presentation of Lyme's disease.

Published in:

2019

By:

Farmania, Rajni;
Jauhari, Prashant;
Chakrabarty, Biswaroop;
Gulati, Sheffali

Publication type:

Case Study

Isolated striatal lesions: A rare imaging finding of neurofibromatosis type I.

Published in:

2018

By:

Saini, Lokesh;
Jauhari, Prashant;
Chakrabarty, Biswaroop;
Kumar, Atin;
Gulati, Sheffali

Publication type:

journal article

Assessment of cell-free levels of iron and copper in patients with Friedreich's ataxia.

Published in:

BioMetals, 2019, v. 32, n. 2, p. 307, doi. 10.1007/s10534-019-00186-4

By:

Pathak, Deepti;
Srivastava, Achal Kumar;
Gulati, Sheffali;
Rajeswari, Moganty R.

Publication type:

Article

Symptomatic Neurocutaneous Melanosis in a Child.

Published in:

JAMA Neurology, 2013, v. 70, n. 4, p. 516, doi. 10.1001/jamaneurol.2013.2230

By:

Jain, Puneet;
Kannan, Lakshminarayanan;
Kumar, Atin;
Sigamani, Elanthenral;
Suri, Vaishali;
Basheer, Noufal;
Suri, Ashish;
Gulati, Sheffali

Publication type:

Article

Bilateral Thalamic Lesions in a Child.

Published in:

European Neurology, 2013, v. 70, n. 1/2, p. 33, doi. 10.1159/000347221

By:

Jain, Puneet;
Mohamed, akbar;
Sigamani, Elanthenral;
Suri, Vaishali;
Mahapatra, a.K.;
Kumar, atin;
Gulati, Sheffali

Publication type:

Article

Development and validation of DSM-5 based diagnostic tool for children with Autism Spectrum Disorder.

Published in:

PLoS ONE, 2019, v. 14, n. 3, p. 1, doi. 10.1371/journal.pone.0213242

By:

Gulati, Sheffali;
Kaushik, Jaya Shankar;
Saini, Lokesh;
Sondhi, Vishal;
Madaan, Priyanka;
Arora, N. K.;
Pandey, R. M.;
Jauhari, Prashant;
Manokaran, Ranjith K.;
Sapra, Savita;
Sharma, Shobha;
Paul, Vinod K.;
Sagar, Rajesh

Publication type:

Article

Neurodevelopmental outcomes in children with cyanotic congenital heart disease following open heart surgery.

Published in:

Annals of Pediatric Cardiology, 2022, v. 15, n. 1, p. 4, doi. 10.4103/apc.apc_149_21

By:

Shakya, Samir;
Saxena, Anita;
Gulati, Sheffali;
Kothari, Shyam Sunder;
Ramakrishnan, Sivasubramanian;
Gupta, Saurabh Kumar;
Devagourou, Velayoudam;
Talwar, Sachin;
Rajashekar, Palleti;
Sharma, Shobha

Publication type:

Article

Development of a cost of illness inventory questionnaire for children with autism spectrum disorder in South Asia.

Published in:

2022

By:

Chaudhary, Divya;
Bhat, Bhargav;
Shields, Gemma E.;
Davies, Linda M.;
Green, Jonathan;
Verghis, Tara;
Roy, Reetabrata;
Kumar, Divya;
Kakra, Minal;
Vajaratkar, Vivek;
Lall, Gitanjali;
Pandey, Sonakshi;
Johri, Sanchita;
Shakeel, Saani;
Patel, Vikram;
Juneja, Monica;
Gulati, Sheffali;
Divan, Gauri

Publication type:

journal article

Adverse effects & drug load of antiepileptic drugs in patients with epilepsy: Monotherapy versus polytherapy.

Published in:

Indian Journal of Medical Research, 2017, v. 145, n. 3, p. 317, doi. 10.4103/ijmr.IJMR_710_15

By:

Joshi, Rupa;
Tripathi, Manjari;
Gupta, Pooja;
Gulati, Sheffali;
Gupta, Yogendra Kumar

Publication type:

Article

Ophthalmic examination as a means to diagnose Subacute Sclerosing Panencephalitis: an optical coherence tomography and ultrawide field imaging evaluation.

Published in:

Eye & Vision, 2017, v. 4, p. 1, doi. 10.1186/s40662-016-0066-2

By:

Tripathy, Koushik;
Chawla, Rohan;
Mittal, Kanhaiya;
Farmania, Rajni;
Venkatesh, Pradeep;
Gulati, Sheffali

Publication type:

Article

Blood Heavy Metal Levels in Children with Autism Spectrum Disorder: A Cross- Sectional Study From Northern India.

Published in:

Journal of Nepal Paediatric Society, 2019, v. 39, n. 1, p. 6, doi. 10.3126/jnps.v39i1.19905

By:

Sehgal, Rachna;
Gulati, Sheffali;
Gupta, Yogendra Kumar;
Sapra, Savita;
Mehta, Manju;
Pandey, Ravindra Mohan;
Kumar, Gajendra;
Srivastava, Amita;
Kabra, Madhulika

Publication type:

Article

Detection of Mycobacterium tuberculosis GlcB or HspX Antigens or devRDNA Impacts the Rapid Diagnosis of Tuberculous Meningitis in Children.

Published in:

PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0044630

By:

Haldar, Sagarika;
Sankhyan, Naveen;
Sharma, Neera;
Bansal, Anjali;
Jain, Vitul;
Gupta, V. K.;
Juneja, Monica;
Mishra, Devendra;
Kapil, Arti;
Singh, Urvashi B.;
Gulati, Sheffali;
Kalra, Veena;
Tyagi, Jaya Sivaswami

Publication type:

Article

Acute onset flaccid quadriparesis in pediatric non-Hodgkin lymphoma: Vincristine induced or Guillain-Barré syndrome?

Published in:

Pediatric Blood & Cancer, 2010, v. 55, n. 6, p. 1234, doi. 10.1002/pbc.22684

By:

Bahl, Ankur;
Chakrabarty, Biswaroop;
Gulati, Sheffali;
Raju, K.N. Vykunta;
Raja, Ali;
Bakhshi, Sameer

Publication type:

Article

Socio-cultural Adaptation and Validation of Ages and Stages Questionnaire (ASQ 3) in Indian Children Aged 2 to 24 Months.

Published in:

Indian Pediatrics, 2023, v. 60, n. 11, p. 908, doi. 10.1007/s13312-023-3034-7

By:

Gulati, Sheffali;
Israni, Anil;
Squires, Jane;
Singh, Ajay;
Madaan, Priyanka;
Kamila, Gautam;
Pandey, R. M.

Publication type:

Article

Postnatal Maturation of Amplitude Integrated Electroencephalography (aEEG) in Preterm Small for Gestational Age Neonates.

Published in:

Indian Pediatrics, 2018, v. 55, n. 10, p. 865, doi. 10.1007/s13312-018-1396-z

By:

ARORA, KAMALDEEP;
THUKRAL, ANU;
SANKAR, M. JEEVA;
GULATI, SHEFFALI;
DEORARI, ASHOK K.;
PAUL, VINOD K.;
AGARWAL, RAMESH

Publication type:

Article

A novel homozygous mutation in POLR3A gene causing 4H syndrome: a case report.

Published in:

2018

By:

Tewari, Vishal V.;
Mehta, Ritu;
Sreedhar, C. M.;
Tewari, Kunal;
Mohammad, Akbar;
Gupta, Neerja;
Gulati, Sheffali;
Kabra, Madhulika

Publication type:

journal article

Manual of Pediatric EEG.

Published in:

Current Medicine Research & Practice, 2024, v. 14, n. 5, p. 233, doi. 10.4103/cmrp.cmrp_148_24

By:

Gulati, Sheffali

Publication type:

Article

Pompe disease: An Indian series diagnosed on muscle biopsy by ultrastructural characterization.

Published in:

Ultrastructural Pathology, 2018, v. 42, n. 3, p. 211, doi. 10.1080/01913123.2018.1447624

By:

Kakkar, Aanchal;
Sharma, Mehar C.;
Nambirajan, Aruna;
Gulati, Sheffali;
Bhatia, Rohit;
Suri, Vaishali;
Sarkar, Chitra

Publication type:

Article

Glycogen Storage Disorder due to Glycogen Branching Enzyme (GBE) Deficiency: A Diagnostic Dilemma.

Published in:

Ultrastructural Pathology, 2015, v. 39, n. 4, p. 293, doi. 10.3109/01913123.2015.1014612

By:

Kakkar, Aanchal;
Sharma, Mehar Chand;
Nambirajan, Aruna;
Sarkar, Chitra;
Suri, Vaishali;
Gulati, Sheffali

Publication type:

Article

The spectrum of neurological manifestations and genotype–phenotype correlation in Indian children with Gaucher disease.

Published in:

American Journal of Medical Genetics. Part A, 2023, v. 191, n. 4, p. 1038, doi. 10.1002/ajmg.a.63115

By:

Venkatachari, Mahesh;
Chakraborty, Soumalya;
Correa, Alec Reginald Errol;
Mishra, Puneeta;
Kocchar, Kanwal Preet;
Kabra, Madhulika;
Chakrabarty, Biswaroop;
Kalaivani, Mani;
Sapra, Savita;
Mishra, Pallavi;
Gulati, Sheffali;
Gupta, Neerja

Publication type:

Article

Bilateral pallidotomy for acquired or heredodegenerative generalized dystonia in children.

Published in:

Neurosurgical Focus, 2022, v. 53, n. 4, p. 1, doi. 10.3171/2022.7.FOCUS22332

By:

Garg, Kanwaljeet;
Singh, Manmohan;
Samala, Raghu;
Rajan, Roopa;
Gulati, Sheffali;
Goyal, Vinay

Publication type:

Article

Decoding of novel missense TSC2 gene variants using in-silico methods.

Published in:

BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0891-y

By:

Sudarshan, Shruthi;
Kumar, Manoj;
Kaur, Punit;
Kumar, Atin;
G., Sethuraman;
Sapra, Savita;
Gulati, Sheffali;
Gupta, Neerja;
Kabra, Madhulika;
Roy Chowdhury, Madhumita

Publication type:

Article

Neurodevelopmental disorders in children aged 2-9 years: Population-based burden estimates across five regions in India.

Published in:

2018

By:

Arora, Narendra K.;
Nair, M. K. C.;
Gulati, Sheffali;
Deshmukh, Vaishali;
Mohapatra, Archisman;
Mishra, Devendra;
Patel, Vikram;
Pandey, Ravindra M.;
Das, Bhagabati C.;
Divan, Gauri;
Murthy, G. V. S.;
Sharma, Thakur D.;
Sapra, Savita;
Aneja, Satinder;
Juneja, Monica;
Reddy, Sunanda K.;
Suman, Praveen;
Mukherjee, Sharmila B.;
Dasgupta, Rajib;
Tudu, Poma

Publication type:

journal article