SIR GORDON HOLMES
نویسندگان
چکیده
منابع مشابه
Sir Gordon Holmes.
FORTY MILES from Dublin at Castlebellingham on the coast of Co. Louth, Gordon Morgan Holmes was born in Dillon House on 22 February 1876. A scholar at Trinity College Dublin, he graduated B.A. in 1897, being senior moderator and gold medallist, and qualified in medicine the following year. After serving as a resident medical officer in the Richmond Asylum (now St. Brendan's Hospital), he studie...
متن کاملGordon Holmes Lecture: Gordon Holmes and the neurological heritage.
Sir Gordon Holmes is one of the great figures in the history of twentienth century neurology. In him, there came together the traditions of German and British neurology which moulded a physiological approach to normal and disordered function of the nervous system with a commitment to interpreting clinical phenomena in the light of meticulous pathological examination. He, more than any other ind...
متن کاملSelected papers of Gordon Holmes
the subjective perception of neurological deficit; and with the disorders of vision. Thus, one essay examines sociological aspects of aphasia, another the detection of minimal dysphasia, and others the evolution and possible future of language. His exploration of the relationship between the language of schizophrenics and that of aphasics is particularly fascinating. Other essays deal with miso...
متن کاملSir Gordon Arthur Ransome--a profile of the man.
Professor Ransome was born in Salop, England, on 6th May, 1910, the son of the Rector of Pulverbatch. He attended school at Dauntsey’s and after happy childhood days and still in his youth, he began to show an interest in doctoring. It was not surprising therefore, that in 1933, he obtained a licence to practise medicine from the Royal College of Surgeons and Physicians of London. . . Foremostl...
متن کاملPNPLA6 mutations cause Boucher-Neuhauser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum.
Boucher-Neuhäuser and Gordon Holmes syndromes are clinical syndromes defined by early-onset ataxia and hypogonadism plus chorioretinal dystrophy (Boucher-Neuhäuser syndrome) or brisk reflexes (Gordon Holmes syndrome). Here we uncover the genetic basis of these two syndromes, demonstrating that both clinically distinct entities are allelic for recessive mutations in the gene PNPLA6. In five of s...
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ژورنال
عنوان ژورنال: Medical History
سال: 1975
ISSN: 0025-7273,2048-8343
DOI: 10.1017/s0025727300020147