Niemann–Pick Disease Type C
Por um escritor misterioso
Descrição
Niemann-Pick disease type C (NPC) is a disabling, lysosomal-storage disorder that has been diagnosed prenatally, neonatally, during childhood, and even into adulthood.
Miglustat in Niemann-Pick disease type C patients: a review, Orphanet Journal of Rare Diseases
IJMS, Free Full-Text
Frontiers Lysosomal and Mitochondrial Liaisons in Niemann-Pick Disease
Niemann-Pick disease type C-presenting as persistent neonatal jaundice: a rare case report
Oxidative Stress: A Pathogenic Mechanism for Niemann-Pick Type C Disease
Laboratory diagnosis of Niemann-Pick disease type C: the filipin staining test.
Health Tip on New Treatment that Shows Promise in Niemann-Pick Type C Disorder - Health Tips
Frontiers Adult-Onset Niemann–Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult
National Niemann-Pick Disease Foundation, Inc. - October is Global Niemann-Pick Disease Awareness Month! For more information on Niemann-Pick Disease or to make a donation to NNPDF go to www.nnpdf.org
Niemann- Pick Disease Type C (NPC) Market Report 2023-2033 - Wissen Research
Molecular mechanism(s) of neurodegeneration in Niemann-Pick type C disease - Ruđer Bošković Institute
Niemann-Pick disease type C, Orphanet Journal of Rare Diseases
Niemann-Pick disease type C Alzheimer Society of Canada
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