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974 results
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Glycogenosis type V or McArdle's disease.
Gordon N. Gordon N. Dev Med Child Neurol. 2003 Sep;45(9):640-4. doi: 10.1017/s0012162203001178. Dev Med Child Neurol. 2003. PMID: 12948334 Review. No abstract available.
Hereditary vitamin-E deficiency.
Gordon N. Gordon N. Dev Med Child Neurol. 2001 Feb;43(2):133-5. doi: 10.1017/s001216220100024x. Dev Med Child Neurol. 2001. PMID: 11221903 Review. No abstract available.
Ataxia of parietal lobe origin.
Gordon N. Gordon N. Dev Med Child Neurol. 1999 May;41(5):353-5. doi: 10.1017/s0012162299000778. Dev Med Child Neurol. 1999. PMID: 10378764 No abstract available.
Pyridoxine dependency: an update.
Gordon N. Gordon N. Dev Med Child Neurol. 1997 Jan;39(1):63-5. doi: 10.1111/j.1469-8749.1997.tb08206.x. Dev Med Child Neurol. 1997. PMID: 9003732 Review. No abstract available.
Ophthalmoplegia in childhood.
Gordon N. Gordon N. Dev Med Child Neurol. 1994 Apr;36(4):370-4. doi: 10.1111/j.1469-8749.1994.tb11859.x. Dev Med Child Neurol. 1994. PMID: 8157159 Review. No abstract available.
Alternating hemiplegia of childhood.
Gordon N. Gordon N. Dev Med Child Neurol. 1995 May;37(5):464-8. doi: 10.1111/j.1469-8749.1995.tb12030.x. Dev Med Child Neurol. 1995. PMID: 7768346 No abstract available.
Vitamin E deficiency and illness in childhood.
Gordon N. Gordon N. Dev Med Child Neurol. 1987 Aug;29(4):546-9. doi: 10.1111/j.1469-8749.1987.tb02517.x. Dev Med Child Neurol. 1987. PMID: 3315793 Review. No abstract available.
Myalgic encephalomyelitis.
Gordon N. Gordon N. Dev Med Child Neurol. 1988 Oct;30(5):677-82. doi: 10.1111/j.1469-8749.1988.tb04808.x. Dev Med Child Neurol. 1988. PMID: 3068084 Review. No abstract available.
Childhood moyamoya disease.
Gordon N, Isler W. Gordon N, et al. Dev Med Child Neurol. 1989 Feb;31(1):103-7. doi: 10.1111/j.1469-8749.1989.tb08418.x. Dev Med Child Neurol. 1989. PMID: 2646161 Review. No abstract available.
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