Generalized Stiffness in Hereditary Hyperekplexia Responsive to Trihexyphenidyl: A Novel Finding-Reference-Cited by-同舟云学术

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Generalized Stiffness in Hereditary Hyperekplexia Responsive to Trihexyphenidyl: A Novel Finding

Published:2023-10-29 Issue: Volume: Page:
ISSN:0009-9228
Container-title:Clinical Pediatrics
language:en
Short-container-title:Clin Pediatr (Phila)

Author:

Rudrabhatla Pavan Kumar¹,Divya K. P.²,Fasaludeen Alfiya³,Menon Ramshekhar N.³,Cherian Ajith¹,Urulangodi Madhusoodanan⁴,Sundaram Soumya³^ORCID

Affiliation:

1. R Madhavan Nayar Centre for Comprehensive Epilepsy Care, Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, India

2. Comprehensive Care Centre for Movement Disorders, Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, India

3. Pediatric Neurology and Neurodevelopmental Disorders, Department of Neurology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, India

4. Department of Biochemistry, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, India

Publisher

SAGE Publications

Subject

Pediatrics, Perinatology and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.1177/00099228231203300

Reference13 articles.

1. Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay

2. Balint B, Thomas R. Hereditary hyperekplexia overview. 2007 Jul 31 [Updated 2019 Dec 19]. In: Adam MP, Ardinger HH, Pagon RA, eds. GeneReviews® [Internet]. Seattle, WA: University of Washington; 1993-2021. https://www.ncbi.nlm.nih.gov/books/NBK1260/

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