McArdle

Brian, 20th century British neurologist. See M. disease, M.-Schmid-Pearson disease, M. syndrome.

Medical dictionary. 2011.

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  • McArdle — Irish name:MacArdghail Ethnicity Irish/Celtic Information Place of origin County Monaghan, Ireland[1] Notable members …   Wikipedia

  • McArdle — ist der Familienname von: Brian McArdle (1911–2002), britischer Kinderarzt, Erstbeschreiber des Morbus McArdle Kenndal McArdle (* 1987), kanadischer Eishockeyspieler McArdle steht außerdem für: Morbus McArdle, eine Glykogenspeicherkrankheit …   Deutsch Wikipedia

  • McArdle — This famous Irish surname recorded in the spellings of MacArdle, MacCardle, MacArdell, and the short forms of McArdle, McCardle, and McCardell, is an anglicized form of the Gaelic Mac Ardghail. This derives from mac meaning son of, and the… …   Surnames reference

  • McArdle — …   Useful english dictionary

  • McArdle's disease — McArdle s disease, McBurney s point see entries alphabetized as MC Mc·Ar·dle s disease mək ärd əlz n glycogen storage disease that is inherited as an autosomal recessive trait, is marked esp. by muscle weakness and myoglobinuria, and is caused by …   Medical dictionary

  • McArdle disease — McArdle disease. См. гликогеноз V типа. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) …   Молекулярная биология и генетика. Толковый словарь.

  • McArdle Laboratory — The McArdle Laboratory for Cancer Research is a basic cancer research facility located on the University of Wisconsin–Madison campus in Madison, Wisconsin. It is also the Department of Oncology in the University of Wisconsin.[1] The current staff …   Wikipedia

  • McArdle-Krankheit — Klassifikation nach ICD 10 E74.0 Glykogenspeicherkrankheit (Glykogenose) McArdle Krankheit …   Deutsch Wikipedia

  • McArdle-Syndrom — Klassifikation nach ICD 10 E74.0 Glykogenspeicherkrankheit (Glykogenose) McArdle Krankheit …   Deutsch Wikipedia

  • McArdle's disease — ▪ pathology also called  Glycogenosis Type V,         rare hereditary deficiency of the enzyme glycogen phosphorylase in muscle cells. In the absence of this enzyme, muscles cannot break down animal starch (glycogen) to meet the energy… …   Universalium

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