about
Clinical features and pharmacotherapy of childhood monoamine neurotransmitter disordersPerinatal systemic gene delivery using adeno-associated viral vectorsDelineation of the movement disorders associated withFOXG1mutations: Table 1Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in InfancyTreatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood.Congenital intestinal fistula with exomphalos minor.De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal LesionsIs intravenous urography necessary in the assessment of renal duplex system in children?Surgical revascularisation for childhood moyamoya.How commonly do children with complex cerebral arteriopathy have renovascular disease?What is new for monoamine neurotransmitter disorders?Monoamine neurotransmitter disorders--clinical advances and future perspectives.Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.Laparoscopic antegrade continence enema using a two-port technique.H-type tracheoesophageal fistula masquerading as achalasia cardia in a 13-year-old childSkull base osteomyelitis leading to lateral medullary syndrome in a childStroke in a child with neurofibromatosis type 2Salbutamol benefits children with congenital myasthenic syndrome due to DOK7 mutationsMethods of standing from supine and percentiles for time to stand and to run 10 meters in young children
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description
hulumtuese
@sq
onderzoeker
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researcher
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հետազոտող
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name
Joanne Ng
@ast
Joanne Ng
@en
Joanne Ng
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Joanne Ng
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Joanne Ng
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Joanne Ng
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Joanne Ng
@en
Joanne Ng
@es
Joanne Ng
@nl
Joanne Ng
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Joanne Ng
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Joanne Ng
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Joanne Ng
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Joanne Ng
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Joanne Ng
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P21
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P496
0000-0002-7946-9965