What Is Niemann-Pick Disease?
Por um escritor misterioso
Descrição
Niemann-Pick disease symptoms vary. The disease includes a group of conditions characterized by accumulation of sphingomyelin in cells of the body.
Morbidity and mortality in type B Niemann–Pick disease
Niemann-Pick disease type C-presenting as persistent neonatal jaundice: a rare case report
Niemann-Pick Disease - A Bibliography by Parker, Philip M.
Diagnostic workup and management of patients with suspected Niemann-Pick type C disease - Apostolos Papandreou, Paul Gissen, 2016
Miglustat for treatment of Niemann-Pick C disease: a randomised controlled study - The Lancet Neurology
Niemann-Pick Disease - Western New York Urology Associates
Niemann-Pick Disease, A Pipeline Analysis Report 2018, Technavio
MedRewind - #132 Niemann-Pick disease (Types A and B) : caused by the inability to degrade sphingomyelin due to a deficiency of sphingomyelinase, a type of phospholipase C. In the severe infantile
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 #NiemannPickC
Niemann-Pick disease type C, Orphanet Journal of Rare Diseases
Niemann Pick Disease - Rivin
Frontiers Adult-Onset Niemann–Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult
Niemann-Pick Diseases - The Medical Biochemistry Page
IJMS, Free Full-Text
Niemann Pick Disease Type C - Symptoms, Causes, Treatment
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