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Wat (wie) is Niemann Pick - definitie
SEVERE METABOLIC DISORDERS IN WHICH SPHINGOMYELIN ACCUMULATES IN LYSOSOMES IN CELLS
Niemann-Pick's disease; Niemann Pick's disease; Niemann Pick disease; Niemann-Pick Disease; Niemann-Pick C1 disease; Niemann-Pick C2 disease; Niemann-pick diseases; Niemann-pick disease, type c; Niemann-pick's; Niemann-Pick; Niemann-Pick Type C; Niemann-Pick disease; Pshingolyelim lipidosis; Sphingomyelin lipidosis; Niemann pick; Niemann Pick; Niemann–Pick Disease; Neimann-Pick Disease; Niemann–Pick diseases; Niemann-Pick diseases
Niemann–Pick disease, type C
AUTOSOMAL RECESSIVE LIPID STORAGE DISORDER THAT IS CHARACTERIZED BY ACCUMULATION OF CHOLESTEROL AND SPHINGOMYELINS IN CELLS OF THE VISCERA AND THE CENTRAL NERVOUS SYSTEM
Niemann-Pick disease type C; Niemann-Pick disease type D; Niemann-Pick disease, Nova Scotian; Niemann-Pick disease, type C; Niemann–Pick C1 disease; Niemann–Pick C2 disease; Niemann-Pick disease, type D; Niemann-Pick's disease type C; Childhood alzheimer's
Niemann–Pick type C (NPC) (colloquially, "Childhood Alzheimer's") is a lysosomal storage disease associated with mutations in NPC1 and NPC2 genes. Niemann–Pick type C affects an estimated 1:150,000 people.
George Niemann
GERMAN ARCHITECT, ART HISTORIAN, ARCHAEOLOGIST AND ARCHITECTURAL HISTORIAN (1841-1912)
Niemann, George
George Niemann (12 July 1841, Hannover – 19 February 1912, Vienna) was a German-Austrian architect and archaeologist.
Hans Niemann
AMERICAN CHESS PLAYER AND GRANDMASTER
User:Jonas1015119/Hans Niemann; Draft:Hans Niemann; Hans Moke Niemann
Hans Moke Niemann (born 2003) is an American chess grandmaster and Twitch streamer. He was awarded the Grandmaster title by FIDE on January 22, 2021.
Wikipedia
Niemann–Pick disease
Niemann–Pick disease is a group of severe inherited metabolic disorders, in which sphingomyelin accumulates in lysosomes in cells (the lysosomes normally degrade material that comes from out of cells).
These disorders involve the dysfunctional metabolism of sphingolipids, which are fats found in cell membranes. They can be considered as a kind of sphingolipidosis, which is included in the larger family of lysosomal storage diseases.
Voorbeelden uit tekstcorpus voor Niemann Pick
1. These mutations are also responsible for four genetic diseases characteristic of Ashkenazi Jews, including Tay–Sachs and the Niemann–Pick and Gaucher syndromes, the study says.