hepatolenticular disease

  • 31Derek Denny-Brown (doctor) — Derek Ernest Denny Brown OBE (1901 ndash; 20 April 1981) was a neurologist. Working in Oxford, London and Boston, he made major contributions to the field of neurology, such as the development of electromyography, physiology of micturition and… …

    Wikipedia

  • 32penicillamine — A degradation product of penicillin; a chelating agent used in the treatment of lead poisoning, hepatolenticular degeneration, and cystinuria, and in the removal of excess copper in Wilson …

    Medical dictionary

  • 33Samuel Alexander Kinnier Wilson — (December 6, 1878 May 12, 1937) was a British neurologist who was born in Cedarville, New Jersey. A year after Wilson s birth, his father died and his family moved to Edinburgh. In 1902 he graduated with an M.B. from the University of Edinburgh,… …

    Wikipedia

  • 34Hematemesis — Infobox Disease Name = Hematemesis Caption = DiseasesDB = 30745 ICD10 = ICD10|K|92|0|k|92 ICD9 = ICD9|578.0 ICDO = OMIM = MedlinePlus = eMedicineSubj = med eMedicineTopic = 3565 MeshName = Hematemesis MeshNumber = C23.550.414.788.400 Hematemesis… …

    Wikipedia

  • 35Dimercaprol — Dimercaprol …

    Wikipedia

  • 36C5H11NO2S — Penicillamine Pen i*cil lam*ine, n. (Chem., Med.) a substance ({C5H11NO2S}) which is a degradation product of the penicillins. Chemically it is 3 mercapto D valine. It has chelating properties and is used in medicine as an antirheumatic and to… …

    The Collaborative International Dictionary of English

  • 37Penicillamine — Pen i*cil lam*ine, n. (Chem., Med.) a substance ({C5H11NO2S}) which is a degradation product of the penicillins. Chemically it is 3 mercapto D valine. It has chelating properties and is used in medicine as an antirheumatic and to chelate copper… …

    The Collaborative International Dictionary of English

  • 38enfermedad de Wilson — Eng. Wilson s disease Ver degeneración hepatolenticular …

    Diccionario de oftalmología

  • 39БОЛЕЗНЬ ВИЛЬСОНА, БОЛЕЗНЬ ВИЛЬСОНА-КОНОВАЛОВА — (Wilsons disease) врожденное нарушение метаболизма меди, характеризующееся недостаточным содержанием в организме церулоплазмина (в норме образующего нетоксичное соединение с медью). Свободная медь может оседать в клетках печени, вызывая развитие… …

    Толковый словарь по медицине