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The list of publications is indicative and may not include all publications.
Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutation..
Eur J Paediatr Neurol. 13(2), 191-3.
(2009).
Tyrosine hydroxylase deficiency with severe clinical course..
Mol Genet Metab. 97(1), 18-20.
(2009).
Parental reports of health-related quality of life in greek children with neurofibromatosis type 1..
J Pediatr. 155(3), 453; author reply 454.
(2009).
The serotonergic system: its role in pathogenesis and early developmental treatment of autism..
Curr Neuropharmacol. 7(2), 150-7.
(2009).