Cerebrospinal Fluid Monoamine Metabolite Analysis in Pediatric Movement Disorders

Homovanillic acid in cerebrospinal fluid of 1388 children with neurological disorders

(2013) Marta Molero-Luis et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Status dystonicus: Predictors of outcome and progression patterns of underlying disease

(2012) Alfonso Fasano et al.   MOVEMENT DISORDERS

Sepiapterin reductase deficiency: A Treatable Mimic of Cerebral Palsy

(2011) Jennifer Friedman et al.   ANNALS OF NEUROLOGY

The monoamine neurotransmitter disorders: an expanding range of neurological syndromes

(2011) Manju A Kurian et al.   LANCET NEUROLOGY

Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis

(2010) M. A. Willemsen et al.   BRAIN

Hereditary progressive dystonia with marked diurnal fluctuation

(2010) Masaya Segawa   BRAIN & DEVELOPMENT

Phenotypic variability, neurological outcome and genetics background of 6-pyruvoyl-tetrahydropterin synthase deficiency

(2010) V Leuzzi et al.   CLINICAL GENETICS

Mitochondrial diseases mimicking neurotransmitter defects

(2008) Angels Garcia-Cazorla et al.   MITOCHONDRION