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- этимология
Что (кто) такое Krabbe"s leukodystrophy - определение
KRABBE DISEASE IS A LYSOSOMAL DISORDER THAT AFFECTS THE WHITE MATTER OF THE CENTRAL AND PERIPHERAL NERVOUS SYSTEMS. IT INCLUDES INFANTILE, LATE-INFANTILE/JUVENILE AND ADULT FORMS.
Krabbes disease; Krabbe's disease; Globoid Cell Leukodystrophy; Krabbé disease; Leukodystrophy, globoid cell; Krabbe leukodystrophy; Diffuse Globoid Body Sclerosis; Globoid cell leukodystrophy; Gfalactosyl ceramide lipidosis; Galactosyl ceramide lipidosis; Krabbe Disease; Galactosylceramide lipidosis
Frederik Michael Krabbe
DANISH AUTOBIOGRAPHER
Friderich Michael Krabbe
Frederik Michael Krabbe (1725–1796)Topsøe-Jensen, Vol 2, pp 25–27. was a Danish naval officer and master shipbuilder (fabrikmester)
Metachromatic leukodystrophy
HUMAN DISEASE
Metachromatic Leukodystrophy; Leukodystrophy, metachromatic; Arylsulfatase A deficiency; Leukodystrophy, psuedometachromatic; Psuedometachromatic leukodystrophy; Arylsulphatase A deficiency; Sulphatide lipidosis; Sulphatidosis; Sulfatide lipisodid; Sulfatide lipidoris; Metachromatic-type leukodystrophy
Metachromatic leukodystrophy (MLD) is a lysosomal storage disease which is commonly listed in the family of leukodystrophies as well as among the sphingolipidoses as it affects the metabolism of sphingolipids. Leukodystrophies affect the growth and/or development of myelin, the fatty covering which acts as an insulator around nerve fibers throughout the central and peripheral nervous systems.
Jörgen Krabbe
DANISH–SWEDISH LAWYER AND NOBLEMAN
User:Sanninav/sandbox; Draft:Jörgen Krabbe
Baron Jörgen Iversen Krabbe of Krogholm Castle (now Krageholm) (1633–1678) was a Danish jurist and later a Swedish nobleman, who was one of the most influential men in the province of Scania and played an important role during the Scanian War of 1676–1679. He was executed by the Swedes for high treason.
Википедия
Krabbe disease
Krabbe disease (KD) (also known as globoid cell leukodystrophy or galactosylceramide lipidosis) is a rare and often fatal lysosomal storage disease that results in progressive damage to the nervous system. KD involves dysfunctional metabolism of sphingolipids and is inherited in an autosomal recessive pattern. The disease is named after the Danish neurologist Knud Krabbe (1885–1961).
