Neil S. Gordon
Huntlywood
Wilmslow
UK
Name/email consistency: high
- Guanidinoacetate methyltransferase deficiency (GAMT). Gordon, N. Brain Dev. (2010)
- Cerebral folate deficiency. Gordon, N. Dev. Med. Child. Neurol (2009)
- Sydenham's chorea, and its complications affecting the nervous system. Gordon, N. Brain Dev. (2009)
- Spontaneous intracranial hypotension. Gordon, N. Dev. Med. Child. Neurol (2009)
- Segawa's disease: dopa-responsive dystonia. Gordon, N. Int. J. Clin. Pract. (2008)
- Wiring of the brain. Gordon, N. Eur. J. Paediatr. Neurol. (2008)
- Sjögren-Larsson syndrome. Gordon, N. Dev. Med. Child. Neurol (2007)
- Glutaric aciduria types I and II. Gordon, N. Brain Dev. (2006)
- Idiopathic intracranial hypertension. Gordon, N.S. Eur. J. Paediatr. Neurol. (2006)
- Alpers syndrome: progressive neuronal degeneration of children with liver disease. Gordon, N. Dev. Med. Child. Neurol (2006)
- Acyl-CoA dehydrogenase deficiency: varieties with neurological involvement. Gordon, N. Dev. Med. Child. Neurol (2005)
- Focal dystonia, with special reference to writer's cramp. Gordon, N.S. Int. J. Clin. Pract. (2005)
- Unexpected development of artistic talents. Gordon, N. Postgrad. Med. J (2005)
- The neurology of sign language. Gordon, N. Brain Dev. (2004)
- Succinic semialdehyde dehydrogenase deficiency (SSADH) (4-hydroxybutyric aciduria, gamma-hydroxybutyric aciduria). Gordon, N. Eur. J. Paediatr. Neurol. (2004)
- Giant axonal neuropathy. Gordon, N. Dev. Med. Child. Neurol (2004)
- Ornithine transcarbamylase deficiency: a urea cycle defect. Gordon, N. Eur. J. Paediatr. Neurol. (2003)
- Glycogenosis type V or McArdle's disease. Gordon, N. Dev. Med. Child. Neurol (2003)
- Glucose transporter type1 (GLUT-1) deficiency. Gordon, N., Newton, R.W. Brain Dev. (2003)
- Alexander disease. Gordon, N. Eur. J. Paediatr. Neurol. (2003)
- Sleep apnoea in infancy and childhood. Considering two possible causes: obstruction and neuromuscular disorders. Gordon, N. Brain Dev. (2002)
- Stuttering: incidence and causes. Gordon, N. Dev. Med. Child. Neurol (2002)
- Worster-drought and congenital bilateral perisylvian syndromes. Gordon, N. Dev. Med. Child. Neurol (2002)
- Pantothenate kinase-associated neurodegeneration (Hallervorden-Spatz syndrome). Gordon, N. Eur. J. Paediatr. Neurol. (2002)
- Infantile neuroaxonal dystrophy (Seitelberger's disease). Gordon, N. Dev. Med. Child. Neurol (2002)
- Sudden unexpected death in epilepsy. Gordon, N. Dev. Med. Child. Neurol (2001)