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Articles by Sameer Vyas
South African Journal of Radiology
Case Report Alaipreet Kaur, Sameer Vyas, Atul Jain, Hemlata Jangir South African Journal of Radiology | Vol 30, No 1 | a3542 | DOI: https://doi.org/10.4102/sajr.v30i1.3542 | © 2026 Alaipreet Kaur, Sameer Vyas, Atul Jain, Hemlata Jangir | This work is licensed under CC Attribution 4.0 Submitted: 23 May 2026 | Published: 31 July 2026 About the author(s) Alaipreet Kaur, Department of Radiodiagnosis, Division of Neuroimaging and Interventional Neuroradiology, Post Graduate Institute of Medical...
Is Endoscopic Approach Alone Adequate for the Management of Ureterovaginal Fistulas?
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Utility of Anterior Segment Optical Coherence Tomography in Muscle Aplasia
Short Subjects Abstract Congenital absence of the extraocular muscles is a relatively rare entity that is diagnosed by magnetic resonance imaging and is usually associated with craniofacial syndromes, microcornea, microphthalmos, and coloboma. The authors describe anterior segment optical coherence tomography as a quick and valuable modality in this setting before subjecting the patient to magnetic resonance imaging or computed tomography. [J Pediatr Ophthalmol Strabismus.
FOXG1 variant presenting as unexplained irritability and peculiar crying spells
Ajay Sharma Ajay Sharma Affiliations Pediatric Neurology Unit, Department of Pediatrics, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India Search for articles by this author Priyanka Madaan Priyanka Madaan Correspondence Corresponding author: Priyanka Madaan, Pediatric Neurology Unit, Department of Pediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh, India, Tel.: +917888913994 Affiliations Pediatric Neurology Unit, Department of...
Meier-Gorlin syndrome presenting as early infantile epileptic encephalopathy
Meier-Gorlin syndrome presenting as early infantile epileptic encephalopathy Statistics from Altmetric.com Request Permissions If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways. Copyright information: © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions.
Mystery Case: An infant with developmental delay, epileptic spasms, and acrocyanosis
A 10-month-old girl presented with global developmental delay, epileptic spasms, and easy bruisability. She was fourth-born of third-degree consanguineous parents with 3 healthy siblings. The perinatal period was uneventful. Examination revealed microcephaly, central hypotonia, acrocyanosis, mottled skin, and petechiae over extremities (figure 1). Neuroimaging revealed peculiar findings (figure 2). EEG revealed modified hypsarrhythmia (figure 3).
Teaching NeuroImages: When MRI is a clue in episodic ataxia
A 3-year-old girl presented with episodic ataxia for the past month. It lasted for 1–2 days continuously after a febrile illness. MRI was suggestive of a neurometabolic disorder (figure, A–L). Plasma valine and leucine and urinary branched-chain aminoacids were elevated. Clinical exome revealed a homozygous, missense, pathogenic variation in BCKDHB gene (exon 5, chr6:80878686A>C; p.His191Pro).
Extensive cerebellar necrosis
Extensive cerebellar necrosis Statistics from Altmetric.com Request Permissions If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways. Copyright information: © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.
Acute disseminated encephalomyelitis: complication of a vaccine preventable disease
Acute disseminated encephalomyelitis: complication of a vaccine preventable disease Arundhati Banerjee1, Renu Suthar2, Sameer Vyas3 and Mini P Singh4 1 Pediatric Neurology Unit, Department of Pediatrics, Advanced Pediatric Center, Post Graduate Institute of Medical education and Research, Chandigarh, Chandigarh, India 2 Pediatric Neurology Unit, Department of Pediatrics, Advanced Pediatric Center, Post Graduate Institute of Medical Education and Research, Chandigarh, Chandigarh, India 3...
HIV-Associated Diffuse Intracranial Aneurysmal Arteriopathy
If You Build It, Will They Come? Getting Medical Professionals to Use the Bridge of Evidence for Improved Recognition of Physical Child Abuse
Involvement of bilateral posterior limb of internal capsule in hypernatraemic dehydration
A 3-month-old male infant presented with loose stools and vomiting for the past 2 weeks and altered sensorium for the past 5 days. He was being administered inadequately diluted oral rehydration solution. On examination, he had moderate encephalopathy, depressed anterior fontanel and doughy skin. Laboratory investigations showed serum sodium 200 mEq/L, potassium 6.1 mEq/L, chloride 129 mEq/L, urea 136 mg/dL and creatinine 0.7 mg/dL.
Angiodysplastic Sturge Weber syndrome
A 3-year-old boy presented with global developmental delay, abnormal craniofacial growth and left focal seizures since infancy. He was the first child of a non-consanguineous couple with unremarkable perinatal period. Family history was non-contributory.
INTERNATIONAL JOURNAL OF CIVIL ENGINEERING AND TECHNOLOGY (IJCIET) © IAEME Publication | https://iaeme.com/Home/journal/IJCIET
Articles Archive Subject Area Indexing Aims & Scope Editorial Board For Authors Publication Fees 1 Central Soil and Materials Research Station, Delhi, India. 2 Central Soil and Materials Research Station, Delhi, India. 3 Central Soil and Materials Research Station, Delhi, India. 4 Central Soil and Materials Research Station, Delhi, India. 5 Central Soil and Materials Research Station, Delhi, India. 6 Central Soil and Materials Research Station, Delhi, India.
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