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Your search keyword '"Gulati, Sheffali"' showing total 24 results
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24 results on '"Gulati, Sheffali"'

1. Bilateral facial palsy in lymphomatous meningitis

Author

Madaan, Priyanka, Jauhari, Prashant, Chakrabarty, Biswaroop, Kumar, Atin, Tripathy, Sarthak, Damle, Nishikant, and Gulati, Sheffali

Subjects
Arachnoiditis -- Case studies -- Diagnosis, Paralysis, Facial -- Case studies -- Diagnosis, Pediatric research, Health
Abstract

Byline: Priyanka. Madaan, Prashant. Jauhari, Biswaroop. Chakrabarty, Atin. Kumar, Sarthak. Tripathy, Nishikant. Damle, Sheffali. Gulati A 9-year-old boy presented with bilateral lower-motor-neuron facial-palsy, progressive hearing-loss, and radiating-pains in legs for [...]

Published
2021

2. Stroke as an initial manifestation of thiamine-responsive megaloblastic anemia

Author

Madaan, Priyanka, Jauhari, Prashant, Michael, Shruthi, Sinha, Aditi, Chakrabarty, Biswaroop, and Gulati, Sheffali

Subjects
Pyrimidines, Medical research, Cardiovascular diseases -- Risk factors, Sickle cell anemia -- Risk factors, Stroke -- Risk factors, Childhood, Ischemia, Pediatrics, Anemia, Health
Abstract

Byline: Priyanka. Madaan, Prashant. Jauhari, Shruthi. Michael, Aditi. Sinha, Biswaroop. Chakrabarty, Sheffali. Gulati Sir, Pediatric arterial ischemic stroke (AIS) is relatively uncommon and often under-recognized. It comprises 5%-10% of all [...]

Published
2020

3. Intravenous immunoglobulin for severe protracted pediatric Guillain-Barre syndrome: Is single dose adequate?

Author

Madaan, Priyanka, Jauhari, Prashant, Shruthi, N., Chakrabarty, Biswaroop, and Gulati, Sheffali

Subjects
Guillain-Barre syndrome -- Development and progression -- Care and treatment, Immunoglobulins -- Health aspects, Dose-response relationship, Health
Abstract

Byline: Priyanka. Madaan, Prashant. Jauhari, N. Shruthi, Biswaroop. Chakrabarty, Sheffali. GulatiSir,Guillain-Barre syndrome (GBS) is an acute immune-mediated polyradiculoneuropathy which may be demyelinating (acute inflammatory demyelinating polyradiculoneuropathy) or axonal (acute motor [...]

Published
2019

6. A genetically proven case of Pelizaeus-Merzbacher disease: Clinicoradiological clues

Author

Saini, Lokesh, Chakrabarty, Biswaroop, Kumar, Atin, and Gulati, Sheffali

Subjects
Health
Abstract

Byline: Lokesh. Saini, Biswaroop. Chakrabarty, Atin. Kumar, Sheffali. Gulati Sir, A 5-month-old boy presented with global developmental delay, generalized looseness of the body, and jerky, chaotic eye movements. There was [...]

Published
2016

7. The spectrum of leukodystrophies in children: Experience at a tertiary care centre from North India

Author

Gulati, Sheffali, Jain, Puneet, Chakrabarty, Biswaroop, Kumar, Atin, Gupta, Neerja, and Kabra, Madhulika

Subjects
Pediatric research, Globoid cell leukodystrophy -- Diagnosis -- Care and treatment -- Research, Health
Abstract

Byline: Sheffali. Gulati, Puneet. Jain, Biswaroop. Chakrabarty, Atin. Kumar, Neerja. Gupta, Madhulika. Kabra Objective: The objective of this study is to retrospectively collect and then describe the clinico-radiographical profile of [...]

Published
2016

8. How I treat a first single seizure in a child

Author

Gulati, Sheffali and Kaushik, Jaya

Subjects
Anticonvulsants -- Dosage and administration -- Research, Epilepsy -- Care and treatment -- Research, Health
Abstract

Byline: Sheffali. Gulati, Jaya. Kaushik An epileptic seizure is defined as transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in brain. There are diverse [...]

Published
2016

9. Recurrent headache in a five year old boy

Author

Saini, Lokesh, Kumar, Ranjith, Chakrabarty, Biswaroop, and Gulati, Sheffali

Subjects
Recurrence (Disease) -- Causes of -- Research, Migraine -- Diagnosis -- Causes of -- Care and treatment -- Case studies, Health
Abstract

Byline: Lokesh. Saini, Ranjith. Kumar, Biswaroop. Chakrabarty, Sheffali. Gulati Headache is infrequent in early childhood. Headache and neurological deficits associated with cerebrospinal fluid (CSF) lymphocytosis (HaNDL), a variant of migraine, [...]

Published
2016

10. Acquired demyelinating disorders of central nervous system: A pediatric cohort

Author

Gulati, Sheffali, Chakrabarty, Biswaroop, Kumar, Atin, Jain, Puneet, Patel, Harsh, and Saini, Lokesh

Subjects
Demyelinating diseases -- Diagnosis -- Care and treatment -- Research, Pediatric neurology -- Research, Health
Abstract

Byline: Sheffali. Gulati, Biswaroop. Chakrabarty, Atin. Kumar, Puneet. Jain, Harsh. Patel, Lokesh. Saini Objective : This is a retrospective chart review of consecutive children with acquired demyelinating disorders presenting to [...]

Published
2015

11. Moyamoya disease; suspecting on conventional MRI brain without angiography

Author

Israni, Anil, Chakrabarty, Biswaroop, Gulati, Sheffali, and Kumar, Atin

Subjects
Angiography -- Methods, Moyamoya disease -- Diagnosis -- Care and treatment, Magnetic resonance imaging -- Methods, Health
Abstract

Byline: Anil. Israni, Biswaroop. Chakrabarty, Sheffali. Gulati, Atin. Kumar Clinical Description A 10 year old, premorbidly normal girl presented with history of weakness of right half of the body, right [...]

Published
2015

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

Author

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

Subjects
Brain -- Abscess, Infants (Newborn) -- Diseases, Candida -- Health aspects, Health
Abstract

Byline: Sangeetha. Yoganathan, Biswaroop. Chakrabarty, Sheffali. Gulati, Ajay. Kumar, Atin. Kumar, Manmohan. Singh, Immaculata. Xess Fungi are a relatively uncommon cause of brain abscess in neonates and early infancy. They [...]

Published
2014

13. A case of congenital myopathy masquerading as paroxysmal dyskinesia

Author

Patel, Harsh, Chakrabarty, Biswaroop, Gulati, Sheffali, Sharma, Mehar, and Saini, Lokesh

Subjects
Genetic disorders -- Case studies -- Diagnosis, Movement disorders -- Case studies -- Diagnosis, Muscle diseases -- Case studies -- Diagnosis, Health
Abstract

Byline: Harsh. Patel, Biswaroop. Chakrabarty, Sheffali. Gulati, Mehar. Sharma, Lokesh. Saini Gastroesophageal reflux (GER) disease is a significant comorbidity of neuromuscular disorders. It may present as paroxysmal dyskinesia, an entity [...]

Published
2014

16. Autoimmune encephalitis: A potentially reversible cause of status epilepticus, epilepsy, and cognitive decline

Author

Pandit, Awadh, Ihtisham, Kavish, Garg, Ajay, Gulati, Sheffali, Padma, Madakasira, and Tripathi, Manjari

Subjects
Encephalitis -- Complications and side effects -- Care and treatment, Status epilepticus -- Causes of, Cognition disorders -- Causes of -- Care and treatment, Autoimmune diseases -- Complications and side effects -- Care and treatment, Health
Abstract

Byline: Awadh. Pandit, Kavish. Ihtisham, Ajay. Garg, Sheffali. Gulati, Madakasira. Padma, Manjari. Tripathi Objectives: To review clinical characteristics and response to immunomodulation therapy in autoimmune encephalitis presenting with status epilepticus [...]

Published
2013

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

Author

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

Subjects
BRAIN abscess, CROSS infection, CANDIDEMIA
Abstract

Fungi are a relatively uncommon cause of brain abscess in neonates and early infancy. They are usually associated with predisposing factors like prematurity, low birth weight, use of broad-spectrum antibiotics, and prolonged stay in the intensive care unit. Candida tropicalis (C. tropicalis) is rapidly emerging as a nosocomial threat in the neonatal intensive care settings. This case report describes a neonate with C. tropicalis brain abscess who was diagnosed early and managed aggressively with a favorable outcome. Inadvertent use of intravenous antibiotics can have serious complications such as invasive fungal infection. Correct microbiological diagnosis is the key to successful treatment of deep-seated pyogenic infection. Fungal etiology should always be studied in relevant clinical settings. [ABSTRACT FROM AUTHOR]

Published
2014
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24. Case Report. A case of congenital myopathy masquerading as paroxysmal dyskinesia.

Author

Patel, Harsh, Chakrabarty, Biswaroop, Gulati, Sheffali, Sharma, Mehar C., and Saini, Lokesh

Subjects
GASTROESOPHAGEAL reflux diagnosis, SYNDROMES, HUMAN abnormalities, MOVEMENT disorders, MUSCLE diseases, TREATMENT effectiveness, SYMPTOMS, DIAGNOSIS, GENETICS
Abstract

Gastroesophageal reflux (GER) disease is a significant comorbidity of neuromuscular disorders. It may present as paroxysmal dyskinesia, an entity known as Sandifer syndrome. A 6-week-old neonate presented with very frequent paroxysms of generalized stiffening and opisthotonic posture since day 22 of life. These were initially diagnosed as seizures and he was started on multiple antiepileptics which did not show any response. After a normal video electroencephalogram (VEEG) was documented, possibility of dyskinesia was kept. However, when he did not respond to symptomatic therapy, Sandifer syndrome was thought of and GER scan was done, which revealed severe GER. After his symptoms got reduced to some extent, a detailed clinical examination revealed abnormal facies with flaccid quadriparesis. Muscle biopsy confirmed the diagnosis of a specific congenital myopathy. On antireflux measures, those episodic paroxysms reduced to some extent. Partial response to therapy in GER should prompt search for an underlying secondary etiology. [ABSTRACT FROM AUTHOR]

Published
2014
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