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The Impact of the Dardanelles Campaign on British Policy Towards the Arabs: How Gallipoli Shaped the Hussein-McMahon Correspondence

Autor: David J. Charlwood

Publikováno v: British Journal of Middle Eastern Studies. 42:241-252

In 1915, Britain negotiated a deal to persuade the Arabs to join the Allies in the fight against the Ottomans. The Hussein-McMahon correspondence between the British High Commissioner in Egypt, Sir Arthur Henry McMahon, and Sharif Hussein of Mecca wa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fa1fd80b0c46c34cc2458d0ab78ee6bd
https://doi.org/10.1080/13530194.2014.936113

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Genotypes and phenotypes of patients in the UK with carbohydrate-deficient glycoprotein syndrome type 1

Autor: Faiqa Imtiaz, Geoffrey Keir, Viki C. Worthington, Clare E. Beesley, J. Charlwood, N. Mian, M. Champion, Bryan Winchester, Peter E. Clayton

Publikováno v: Journal of Inherited Metabolic Disease. 23:162-174

18 UK patients (14 families) have been diagnosed with the carbohydrate-deficient glycoprotein syndrome (CDGS), type 1, on the basis of their clinical symptoms and/or abnormal electrophoretic patterns of serum transferrin. Eleven out of the 16 infants

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46b3ecb06e6e721e383bb00f241da9e2
https://doi.org/10.1023/a:1005669900330

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Prenatal diagnosis of the carbohydrate-deficient glycoprotein syndrome type 1A (CDG1A) by a combination of enzymology and genetic linkage analysis after amniocentesis or chorionic villus sampling

Autor: Geoffrey Keir, Nasi Mian, Peter E. Clayton, J. Charlwood, Bryan Winchester, Elisabeth Young

Publikováno v: Prenatal Diagnosis. 18:693-699

Two pregnancies at risk for the carbohydrate-deficient glycoprotein syndrome Type 1A (CDG1A, phosphomannomutase deficient) were monitored by enzyme and genetic linkage analyses. The index case in both families had a proven deficiency of phosphomannom

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b75f4cc7391a7318927bef6b4522853
https://doi.org/10.1002/(sici)1097-0223(199807)18:7<693::aid-pd335>3.0.co

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A case of the carbohydrate-deficient glycoprotein syndrome type 1 (CDGS type 1) with normal phosphomannomutase activity

Autor: Nasi Mian, Geoffrey Keir, Andrew W. Johnson, J. Charlwood, Peter E. Clayton, Bryan Winchester

Publikováno v: Journal of Inherited Metabolic Disease. 20:817-827

The carbohydrate-deficient glycoprotein syndrome (CDGS) is a group of disorders characterized biochemically by abnormal glycosylation of serum and cellular glycoproteins. It has been classified into four forms on the basis of the isoelectric focusing

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e505392e1da964dfa3658a0d16599890
https://doi.org/10.1023/a:1005380003902

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