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Search Results to Aravindhan Veerapandiyan

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One or more keywords matched the following items that are connected to Veerapandiyan, Aravindhan

Item TypeName
Concept DiGeorge Syndrome
Concept Syndrome
Concept Isaacs Syndrome
Concept Myasthenic Syndromes, Congenital
Academic Article Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutation.
Academic Article Possible induction of West syndrome by oxcarbazepine therapy in a patient with complex partial seizures.
Academic Article A Case of Brown-Vialetto-Van Laere Syndrome Due To a Novel Mutation in SLC52A3 Gene: Clinical Course and Response to Riboflavin.
Academic Article Two patients with an anti-N-methyl-D-aspartate receptor antibody syndrome-like presentation and negative results of testing for autoantibodies.
Academic Article A Rare Syndrome of GRID2 Deletion in 2 Siblings.
Academic Article Chromosome 22q11.2 deletion syndrome in African-American patients: a diagnostic challenge.
Academic Article Novel mutation in mitochondrial DNA in 2 siblings with Leigh syndrome.
Academic Article The role of cephalometry in assessing velopharyngeal dysfunction in velocardiofacial syndrome.
Academic Article Altered development of the dorsolateral prefrontal cortex in chromosome 22q11.2 deletion syndrome: an in vivo proton spectroscopy study.
Academic Article Variable penetrance of Andersen-Tawil syndrome in a family with a rare missense KCNJ2 mutation.
Academic Article Clinical Reasoning: A 6-Year-Old Boy With Muscle Twitching.
Academic Article Congenital Myasthenic Syndrome due to a Novel Mutation in CHAT Gene.
Academic Article Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome.

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