What is new for monoamine neurotransmitter disorders?

Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood

(2014) Joanne Ng et al.   BRAIN

What is the role of dopamine in childhood neurological disorders?

(2013) Manju A Kurian   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Homovanillic acid in cerebrospinal fluid of 1388 children with neurological disorders

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

Levodopa-induced dyskinesias in tyrosine hydroxylase deficiency

(2013) Roser Pons et al.   MOVEMENT DISORDERS

Transdermal rotigotine in the treatment of aromatic L-amino acid decarboxylase deficiency

(2013) Mario Mastrangelo et al.   MOVEMENT DISORDERS

Very early pattern of movement disorders in sepiapterin reductase deficiency

(2013) V. Leuzzi et al.   NEUROLOGY

Brain Dopamine–Serotonin Vesicular Transport Disease and Its Treatment

(2013) Jennifer J. Rilstone et al.   NEW ENGLAND JOURNAL OF MEDICINE

Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiency

(2012) M. Stamelou et al.   NEUROLOGY

Tyrosine Hydroxylase Deficiency in Taiwanese Infants

(2012) Ching-Shiang Chi et al.   PEDIATRIC NEUROLOGY

Sepiapterin reductase deficiency: A Treatable Mimic of Cerebral Palsy

(2011) Jennifer Friedman et al.   ANNALS OF NEUROLOGY

Pseudoexon exclusion by antisense therapy in 6-pyruvoyl-tetrahydropterin synthase deficiency

(2011) Sandra Brasil et al.   HUMAN MUTATION

Bilateral subthalamic nucleus deep brain stimulation for dopa-responsive dystonia in a 6-year-old child

(2011) Matthew J. Tormenti et al.   Journal of Neurosurgery-Pediatrics

The monoamine neurotransmitter disorders: an expanding range of neurological syndromes

(2011) Manju A Kurian et al.   LANCET NEUROLOGY

A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood

(2011) Ebba Lohmann et al.   PARKINSONISM & RELATED DISORDERS

“Stiff Neonate” With Mitochondrial DNA Depletion and Secondary Neurotransmitter Defects

(2011) Margaret M. Moran et al.   PEDIATRIC NEUROLOGY

Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis

(2010) M. A. Willemsen et al.   BRAIN

Expanding Phenotype and Clinical Analysis of Tyrosine Hydroxylase Deficiency

(2010) Wai-lan Yeung et al.   JOURNAL OF CHILD NEUROLOGY

Cerebrospinal fluid alterations of the serotonin product, 5-hydroxyindolacetic acid, in neurological disorders

(2010) Elisa De Grandis et al.   JOURNAL OF INHERITED METABOLIC DISEASE

Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study

(2010) Manju A Kurian et al.   LANCET NEUROLOGY

Infantile parkinsonism-dystonia due to dopamine transporter gene mutations: another genetic twist

(2010) Craig Blackstone   LANCET NEUROLOGY

Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency

(2010) L. Brun et al.   NEUROLOGY

Movement disorders in children: Recent advances in management

(2009) Emilio Fernández-Alvarez   INDIAN JOURNAL OF PEDIATRICS

A new perspective on the treatment of aromatic l-amino acid decarboxylase deficiency

(2009) George F.G. Allen et al.   MOLECULAR GENETICS AND METABOLISM

Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling

(2009) Stuart M Chambers et al.   NATURE BIOTECHNOLOGY

Aromatic l-amino acid decarboxylase deficiency in Taiwan

(2008) Hsiu-Fen Lee et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Mitochondrial diseases mimicking neurotransmitter defects

(2008) Angels Garcia-Cazorla et al.   MITOCHONDRION

Two Greek siblings with sepiapterin reductase deficiency

(2008) Marcel M. Verbeek et al.   MOLECULAR GENETICS AND METABOLISM

Results from a phase I safety trial of hAADC gene therapy for Parkinson disease

(2008) J. L. Eberling et al.   NEUROLOGY