BASIC FUNCTIONS OF TELECOMMUNICATION CHANNEL ELEMENTS FOR SUCCESSFUL INFORMATION TRANSMISSION



Outcomes of a Physician Survey on the Type, Progression, Assessment, and Treatment of Neurological Disease in Mucopolysaccharidoses

The mucopolysaccharidosis (MPS) disorders are a group of rare, inherited lysosomal storage disorders.In each of the 11 MPS (sub)types, deficiency in a specific lysosomal enzyme (1 of 11 Outdoor Pub Table w/FP identified enzymes) leads to accumulation of glycosaminoglycans, resulting in cell, tissue, and multi-organ dysfunction.There is great hetero

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