Brysōn. Oikonomikos Logos : Economy, family, and society from Rome to Islam : a critical edition, English translation, and study of Bryson's Management of the estate / Simon Swain
Here are entered works on the Celtic people living in Great Britain from the Iron Age through the Early Middle Ages. Works on citizens of the United Kingdom, the Isle of Man, the Channel Islands, or the British overseas territories not currently residing within those jurisdictions are entered under British
Brzeziński, Andrzej Maciej -- Bibliography : Politycy, dyplomaci i żołnierze : studia i szkice z dziejów stosunków międzynarodowych w XX i XXI wieku ofiarowane Profesorowi Andrzejowi Maciejowi Brzezińskiemu w 70. rocznicę urodzin / pod redakcją Dariusza Jeziornego, Sławomira M. Nowinowskiego, Radosława Pawła Żurawskiego vel Grajewskiego
A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008)
A transmissible spongiform encephalopathy of cattle associated with abnormal prion proteins in the brain. Affected animals develop excitability and salivation followed by ATAXIA. This disorder has been associated with consumption of SCRAPIE infected ruminant derived protein. This condition may be transmitted to humans, where it is referred to as variant or new variant CREUTZFELDT-JAKOB SYNDROME. (Vet Rec 1998 Jul 25;143(41):101-5)