description of fragile X syndrome, sometimes called the Martin-Bell syndrome;[1][2] introduction of a general classification of negative symptoms[3] of basal ganglia disease[4]
James Purdon MartinFRCP (1893–1984) was a British neurologist.[5][6]
^Martin, J. P. & Bell, J. (1943). "A pedigree of mental defect showing sex-linkage". J. Neurol. Psychiatry. 6 (3–4): 154–157. doi:10.1136/jnnp.6.3-4.154. PMC 1090429. PMID 21611430.
^Kinnell, H. G. (5 September 1987). "Fragile X syndrome: an important preventable cause of mental handicap". Br Med J (Clin Res Ed). 295 (6598): 564–565. doi:10.1136/bmj.295.6598.564. PMC 1248738. PMID 3117231.
^Geary, Elizabeth K.; Seidenberg, Michael; Hermann, Bruce (2009). "Atrophy of Basal Ganglia Nuclei and Negative Symptoms in Temporal Lobe Epilepsy". J Neuropsychiatry Clin Neurosci. 21 (2): 152–159. doi:10.1176/appi.neuropsych.21.2.152. PMC 2714910. PMID 19622686.
^Donaldson, Ivan; Marsden, C. David; Schneider, Susanne (2012). Marsden's book of movement disorders. Oxford University Press. p. 106. ISBN 9780192619112.
^"James Purdon Martin". Munk's Roll, Volume VIII, Lives of the Fellows, Royal College of Physicians.
^"Obituary. J P Martin, MD, DSc, MD, FRCP". BMJ (Clin Res Ed). 228 (6431): 1698. 2 June 1984. doi:10.1136/bmj.288.6431.1698. S2CID 220196085.
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