This paper reviews publications in the literature on performance degradation of and mitigation
strategies for polymer electrolyte membrane (PEM) fuel cells. Durability is one of the …

Frontotemporal dementia (FTD) with ubiquitin-immunoreactive neuronal inclusions (both
cytoplasmic and nuclear) of unknown nature has been linked to a chromosome 17q21 region (…

Several families with an early–onset form of familial Alzheimer's disease have been found to
harbour mutations at a specific codon (717) of the gene for the β–amyloid precursor protein (…

Progressive external ophthalmoplegias (PEO) characterized by accumulation of large-scale
mitochondrial DNA (mtDNA) deletions are rare human diseases. We mapped a new locus …

Background Amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD)
are extremes of a clinically, pathologically, and genetically overlapping disease spectrum…

Male patients with fragile X syndrome lack FMR1 protein due to silencing of the FMR1 gene
by amplification of a CGG repeat and subsequent methylation of the promoter region. The …

Genetic variants in the triggering receptor expressed on myeloid cells 2 (TREM2) have
been linked to Nasu-Hakola disease, Alzheimer’s disease (AD), Parkinson’s disease, …

Hereditary motor and sensory neuropathy type I (HMSN I) or Charcot-Marie-Tooth disease
type 1 (CMT 1) is an autosomal dominant disorder of the peripheral nervous system …

Charcot-Marie-Tooth disease (CMT) is the most common inherited neuromuscular disease
and is characterized by considerable clinical and genetic heterogeneity 1 . We previously …

This paper reviews the compositions, design and methods of fabrication of air cathodes for
alkali zinc–air fuel cells (ZAFCs), one of the few successfully commercialized fuel cells. The …