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

Semaphorin-Plexin Signaling : From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome

enthalten in: Pediatric neurology | 2022

von Steele, J. | Morrow, M. | Sarnat, H. | +24

3

Two patients with an anti-N-methyl-D-aspartate receptor antibody syndrome-like presentation and negative results of testing for autoantibodies

enthalten in: Pediatric neurology | 2011

von Shah, R. | Veerapandiyan, A. | Winchester, S. | +2

4

Two Patients With an Anti-N-Methyl-d-Aspartate Receptor Antibody Syndrome-Like Presentation and Negative Results of Testing for Autoantibodies

enthalten in: Pediatric neurology | 2011

von Shah, R. | Veerapandiyan, A. | Winchester, S. | +2

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