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Prolonged TcdA and TcdB exposure significantly decreases NHE3 and DRA levels, leading to dysfunctional water and solute absorption, causing osmotic diarrhea
Mutations in the GPIHBP1 gene result in a form of familial chylomicronemia syndrome (FCS) that was originally identified as hyperlipoproteinemia type 1D
[PMC free article: PMC3816061] [PubMed: 24222937] 304
Repigmentation and new growth of hairs after anti-interleukin-17 therapy with secukinumab for psoriasis
ISBN 978-0-87969-571-2
Management of the depressive component of bipolar disorder
