Suchergebnisse - (Person:"Veerapandiyan, Aravindhan")

PubPharm (80)

41

A novel intronic homozygous mutation in the AMT gene of a patient with nonketotic hyperglycinemia and hyperammonemia

enthalten in: Metabolic brain disease | 2019

von Silverstein, S. | Veerapandiyan, A. | Hayes-Rosen, C. | +2

42

Electronic health record cue identifies epilepsy patients at risk for obstructive sleep apnea

enthalten in: Neurology. Clinical practice | 2018

von Mulvey, M. | Veerapandiyan, A. | Marks, D. | +1

43

Variable penetrance of Andersen-Tawil syndrome in a family with a rare missense KCNJ2 mutation

enthalten in: Neurology. Genetics | 2018

von Deeb, R. | Veerapandiyan, A. | Tawil, R. | +1

44

A novel intronic homozygous mutation in the AMT gene of a patient with nonketotic hyperglycinemia and hyperammonemia

enthalten in: Metabolic brain disease | 2018

von Silverstein, S. | Veerapandiyan, A. | Hayes-Rosen, C. | +2

45

A novel intronic homozygous mutation in the AMT gene of a patient with nonketotic hyperglycinemia and hyperammonemia

enthalten in: Metabolic brain disease | 2018

von Silverstein, S. | Veerapandiyan, A. | Hayes-Rosen, C. | +2

46

A novel intronic homozygous mutation in the AMT gene of a patient with nonketotic hyperglycinemia and hyperammonemia

enthalten in: Metabolic brain disease | 2018

von Silverstein, S. | Veerapandiyan, A. | Hayes-Rosen, C. | +2

47

Use of Head Computed Tomography (CT) in the Pediatric Emergency Department in Evaluation of Children With New-Onset Afebrile Seizure

enthalten in: Journal of child neurology | 2018

von Veerapandiyan, A. | Aravindhan, A. | Takahashi, J. | +3

48

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

enthalten in: Acta neurologica Belgica | 2018

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

49

Cervical puncture to deliver nusinersen in patients with spinal muscular atrophy

enthalten in: Neurology | 2018

von Veerapandiyan, A. | Pal, R. | D'Ambrosio, S. | +6

50

Early-onset epileptic encephalopathy with myoclonic seizures related to 9q33.3-q34.11 deletion involving STXBP1 and SPTAN1 genes

enthalten in: Epileptic disorders : international epilepsy journal with videotape | 2018

von Aravindhan, A. | Shah, K. | Pak, J. | +1