List of works - Joanne Ng

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2

scientific article

Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood

scientific article

Monoamine neurotransmitter disorders--clinical advances and future perspectives.

scientific article published on 22 September 2015

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.

scientific article

De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions

scientific article published on April 2016

Successful treatment of two paediatric cases of anti-NMDA receptor encephalitis with Cyclophosphamide: The need for early aggressive immunotherapy in tumour negative paediatric patients

scientific article published on 09 August 2011

Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy

scientific journal article

Salbutamol benefits children with congenital myasthenic syndrome due to DOK7 mutations

scientific article published on 05 December 2012

What is new for monoamine neurotransmitter disorders?

scientific article published on 03 April 2014

Surgical revascularisation for childhood moyamoya.

scientific article published on 09 May 2012

Delineation of the movement disorders associated withFOXG1mutations: Table 1

scientific article

Clinical features and pharmacotherapy of childhood monoamine neurotransmitter disorders

scientific article

How commonly do children with complex cerebral arteriopathy have renovascular disease?

scientific article published on 18 December 2012

Perinatal systemic gene delivery using adeno-associated viral vectors

scientific article

Skull base osteomyelitis leading to lateral medullary syndrome in a child

scientific article published on 26 January 2007

Laparoscopic antegrade continence enema using a two-port technique.

scientific article published in April 2006

Stroke in a child with neurofibromatosis type 2

scientific article published on 11 April 2008

H-type tracheoesophageal fistula masquerading as achalasia cardia in a 13-year-old child

scientific article published on 01 April 2006

Methods of standing from supine and percentiles for time to stand and to run 10 meters in young children

scientific article published on 09 October 2012

Expert opinion on emerging drugs in childhood arterial ischemic stroke

scientific article published on March 31, 2011

Congenital intestinal fistula with exomphalos minor.

scientific article

ATP1A3-related neurological disorders and cerebellar ataxia in childhood

scientific article published on 16 October 2020

Is intravenous urography necessary in the assessment of renal duplex system in children?

scientific article published on June 2009

List of works by Joanne Ng

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2

Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood

Monoamine neurotransmitter disorders--clinical advances and future perspectives.

Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.

De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions

Successful treatment of two paediatric cases of anti-NMDA receptor encephalitis with Cyclophosphamide: The need for early aggressive immunotherapy in tumour negative paediatric patients

Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in Infancy

Salbutamol benefits children with congenital myasthenic syndrome due to DOK7 mutations

What is new for monoamine neurotransmitter disorders?

Surgical revascularisation for childhood moyamoya.

Delineation of the movement disorders associated withFOXG1mutations: Table 1

Clinical features and pharmacotherapy of childhood monoamine neurotransmitter disorders

How commonly do children with complex cerebral arteriopathy have renovascular disease?

Perinatal systemic gene delivery using adeno-associated viral vectors

Skull base osteomyelitis leading to lateral medullary syndrome in a child

Laparoscopic antegrade continence enema using a two-port technique.

Stroke in a child with neurofibromatosis type 2

H-type tracheoesophageal fistula masquerading as achalasia cardia in a 13-year-old child

Methods of standing from supine and percentiles for time to stand and to run 10 meters in young children

Expert opinion on emerging drugs in childhood arterial ischemic stroke

Congenital intestinal fistula with exomphalos minor.

ATP1A3-related neurological disorders and cerebellar ataxia in childhood

Is intravenous urography necessary in the assessment of renal duplex system in children?