Basal Ganglia Disease Mimicking Acute Encephalitis Syndrome Among Infants of Bodo Tribe, Assam

Author:

Webster Jemin J.,Beryl Shafini,George Koshy,Wungram Athin G.,Karuppusami Reka

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference4 articles.

1. Jaiswal RK, Dhariwal AC, Sen PK, et al. National programme for prevention and control of Japanese encephalitis (JE)/acute encephalitis syndrome (AES) — An update. J Commun Dis. 2014;46:119–27.

2. Deðerliyurt A, Gündüz M, Ceylaner S, et al. Neonatal form of biotin-thiamine-responsive basal ganglia disease. Clues to diagnosis. Turkish J Pediatr. 2019;61: 261–66.

3. Colledge N. Molecular and Genetic Factors in Disease; Functional Anatomy and Physiology; Mitochondria and Energy Production. Davidson’s Principles and Practices of Medicine, Churchill Livingstone/Elsevier; 2010. P. 44.

4. Dhir S, Tarasenko M, Napoli E, et al. Neurological, psychiatric, and biochemical aspects of thiamine deficiency in children and adults. Front Psych. 2019;10:207.

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