Suchergebnisse - (Person:"Veerapandiyan, Aravindhan")

PubPharm (4)

1

Infantile-Onset Complex Hereditary Spastic Paraplegia Due to a Novel Mutation in SPAST Gene

enthalten in: Pediatric neurology | 2022

von ElSheikh, R. | Aravindhan, A. | Boysen, S. | +1

CommentOn: Pediatr Neurol. 2022 May;130:7-13. - PMID 35303589

2

Epilepsy in hereditary spastic paraplegia associated with NIPA1 gene

enthalten in: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia | 2022

von Boysen, S. | Elumalai, V. | ElSheikh, R. | +2

CommentOn: J Clin Neurosci. 2021 Dec;94:281-285. - PMID 34863451

3

Pseudometabolic Presentation of Dystrophinopathy in a Family Due to a Rare Nonsense Mutation

enthalten in: Journal of clinical neuromuscular disease | 2020

von Saylam, E. | Aravindhan, A. | Stefans, V. | +1

4

Distal 1q21.1 and proximal 1q21.2 microduplication in a child with attention-deficit hyperactivity disorder

enthalten in: Acta neurologica Belgica | 2019

von Veerapandiyan, A. | Oh, D. | Kornitzer, J.

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