Suchergebnisse - (Person:"Veerapandiyan, Aravindhan")

PubPharm (68)

1

Long-Term Follow-Up Cares and Check Initiative : A Program to Advance Long-Term Follow-Up in Newborns Identified with a Disease through Newborn Screening

enthalten in: International journal of neonatal screening | 2024

von Lietsch, M. | Chan, K. | Taylor, J. | +11

2

Management of Select Adverse Events Following Delandistrogene Moxeparvovec Gene Therapy for Patients With Duchenne Muscular Dystrophy

enthalten in: Journal of neuromuscular diseases | 2024

von Zaidman, C. | Goedeker, N. | Aqul, A. | +11

3

Child Neurology : KMT2B-Related Dystonia in a Young Child With Worsening Gait Abnormality

enthalten in: Neurology | 2023

von Schuberth, K. | Ramani, P. | Beemarajan, E. | +1

4

Epilepsy Characteristics in Duchenne and Becker Muscular Dystrophies

enthalten in: Child neurology open | 2023

von Ramani, P. | Fawcett, K. | Guntrum, D. | +3

5

Estimate of the incidence of PANDAS and PANS in 3 primary care populations

enthalten in: Frontiers in pediatrics | 2023

von Wald, E. | Eickhoff, J. | Flood, G. | +7

6

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

7

An expanded access program of risdiplam for patients with Type 1 or 2 spinal muscular atrophy

enthalten in: Annals of clinical and translational neurology | 2022

von Kwon, J. | Arya, K. | Kuntz, N. | +12

8

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

9

Palliative care in Duchenne muscular dystrophy : Goals of care discussions and beyond

enthalten in: Muscle & nerve | 2022

von Veerapandiyan, A. | Rao, V.

CommentOn: Muscle Nerve. 2022 Jun;65(6):646-651. - PMID 35119694

10

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay due to Novel Mutations in the SACS Gene

enthalten in: Journal of investigative medicine high impact case reports | 2022

von Sharma, R. | Aravindhan, A. | Puente, C. | +1

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