Niemann–Pick disease

Niemann–Pick disease is a form of sphingolipidosis, a lysosomal storage diseases. In patients with this disorder, the sphinogolipid is stored is smal

Rare Diseases India on X: Niemann-Pick is a rare, inherited disease that affects the body's ability to metabolize fat within cells. However, with timely diagnosis and treatment, patients can lead a near-normal

Elevation of plasma lysosphingomyelin-509 and urinary bile acid metabolite in Niemann-Pick disease type C-affected individuals - Top Articles selected by the Editor - Molecular Genetics and Metabolism Reports - Journal - Elsevier

Niemann-Pick disease Information

Lipid trafficking defects in Niemann-Pick type C disease

Niemann Pick Disease - Rivin

Niemann-Pick Disease - A Bibliography by Parker, Philip M.

Niemann-Pick Disease, Types C1 (D)

NNPDF on X: October is Global Niemann-Pick Disease Awareness Month! For more information on Niemann-Pick Disease or to make a donation to NNPDF go to #niemannpick #ASMD #NPC #raredisease #NNPDF /

Niemann-Pick disease types A and B (NORD): Video

JCM, Free Full-Text

A new regulatory mechanism of STARD1 in Niemann-Pick disease type C (NPC), discovered

Frontiers Lysosomal and Mitochondrial Liaisons in Niemann-Pick Disease

Niemann-Pick disease A or B in four pediatric patients and SMPD1 mutation carrier frequency in the Mexican population