Archana Varghese

Bengaluru, KA, India

Last Updated: 09/26/2026

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Found 10 publications

Adolescent onset of susceptibility to acute infection-induced encephalopathy-9 mimicking immune-mediated encephalitis.

Adolescent onset of susceptibility to acute infection-induced encephalopathy-9 mimicking immune-mediated encephalitis.

Journal: BMJ case reports
Published: August 10, 2026

Developmental delay, white matter changes, and multiple endocrine hormone deficiencies in MADD-related disorders: a new case and phenotypic expansion.

Developmental delay, white matter changes, and multiple endocrine hormone deficiencies in MADD-related disorders: a new case and phenotypic expansion.

Journal: Clinical dysmorphology
Published: January 19, 2026

Paediatric myelin oligodendrocyte glycoprotein antibody-associated disease with NMDA receptor encephalitis: overlap syndrome and challenges in the antibody testing.

Paediatric myelin oligodendrocyte glycoprotein antibody-associated disease with NMDA receptor encephalitis: overlap syndrome and challenges in the antibody testing.

Journal: BMJ case reports
Published: December 18, 2025

Acute leukoencephalopathy with restricted diffusion (ALERD) in a toddler: A diagnostic challenge unmasking hereditary sensory autonomic neuropathy type 4.

Acute leukoencephalopathy with restricted diffusion (ALERD) in a toddler: A diagnostic challenge unmasking hereditary sensory autonomic neuropathy type 4.

Journal: BMJ case reports
Published: December 12, 2025

Hypoglycorrhachia: From Glucose Transporter Type 1 Deficiency Syndrome (GLUT1DS) to Pyridox(am)ine-5'-Phosphate Oxidase (PNPO) Deficiency: A Fifteen-Year Diagnostic Journey Redefined by Genomic Insights.

Hypoglycorrhachia: From Glucose Transporter Type 1 Deficiency Syndrome (GLUT1DS) to Pyridox(am)ine-5'-Phosphate Oxidase (PNPO) Deficiency: A Fifteen-Year Diagnostic Journey Redefined by Genomic Insights.

Journal: Indian journal of pediatrics
Published: November 12, 2025

A decade of diagnostic uncertainty: from neurodevelopmental disorders to the discovery of autoimmune encephalitis.

A decade of diagnostic uncertainty: from neurodevelopmental disorders to the discovery of autoimmune encephalitis.

Journal: BMJ case reports
Published: September 15, 2025

Familial recurrent febrile encephalopathy: an atypical presentation of acute necrotising encephalopathy type 1 with unusual neuroimaging findings.

Familial recurrent febrile encephalopathy: an atypical presentation of acute necrotising encephalopathy type 1 with unusual neuroimaging findings.

Journal: BMJ case reports
Published: August 27, 2025

Megalencephalic Leukoencephalopathy Type 2B.

Megalencephalic Leukoencephalopathy Type 2B.

Journal: Indian journal of pediatrics
Published: August 15, 2025

From acute flaccid paralysis (AFP)-Guillain-Barre Syndrome (GBS) and myelitis to progressive encephalopathy : acute disseminated encephalomyelitis (ADEM) atypical presentation of rabies following dog bite.

From acute flaccid paralysis (AFP)-Guillain-Barre Syndrome (GBS) and myelitis to progressive encephalopathy : acute disseminated encephalomyelitis (ADEM) atypical presentation of rabies following dog bite.

Journal: BMJ case reports
Published: June 25, 2025

USP18 gene mutation associated with recurrent encephalopathy, intracranial calcification, and microcephaly: case report, long-term follow-up, and literature review.

USP18 gene mutation associated with recurrent encephalopathy, intracranial calcification, and microcephaly: case report, long-term follow-up, and literature review.

Journal: Clinical dysmorphology
Published: April 28, 2025
Showing 1-10 of 10

Last Updated: 09/26/2026