D Telio, J Shepherd, D Forrest, L Zypchen… - Bone Marrow …, 2011 - nature.com Light chain and light and heavy chain deposition disease (LCDD and LHCDD) are plasma cell dyscrasias in which aggregation and deposition of Ig components leads to organ dysfunction. Although similar in principle to light chain (AL) amyloidosis, there are a ... All 3 versions
[HTML] from ascopubs.orgSAJ Rule, S Poplar, PAS Evans… - Journal of Clinical …, 2011 - jco.ascopubs.org We report on a 60-year-old man who presented as an emergency with an acute abdomen in 2003. He had been completely well until shortly before this presentation with no symptoms of note; specifically, he described no weight loss, no night sweats, no fevers, and no change ... Related articles - All 4 versions
J Kuhle, D Leppert, A Petzold, A Regeniter… - Neurology, 2011 - AAN Enterprises ... Abstract. Objective: Neurodegeneration is now accepted as a pathologic hallmark of multiple sclerosis (MS). We sought to discover whether CSF levels of neurofilament heavychain protein (NfH SMI35 ) correlate with disability, disease activity, or specific stages of MS. ... Cited by 3 - Related articles - All 4 versions
T Terada - Pathology & Oncology Research, 2011 - Springer ... Plasma cell neoplasms may produce various immunoglobulins- related proteins, and produces several associated disorders such as amyloidosis, M-proteinemia, urine Bence-Jones protein, heavychaindisease, and light chaindisease [1]. In the present case, the author ... Related articles - All 3 versions
MN Weedon, R Hastings, R Caswell, W Xie… - The American Journal of …, 2011 - Elsevier ... we have identified a mutation in DYNC1H1 that causes Charcot-Marie-Tooth disease by using exome sequencing in a large dominant pedigree. The mouse models also harboring mutations in the homodimerization domain of cytoplasmic dynein heavychain 1 support the ...
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