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Showing 1 to 4 of 4 for “"Sanfilippo syndrome"”.

  1. Genetic studies in Sanfilippo syndrome, type B

    Vance, Jeffery Marvin1979

    This document only includes an excerpt of the corresponding thesis or dissertation. To request a digital scan of the full text, please contact the Ruth Lilly Medical Library's Interlibrary Loan Department (rlmlill@iu.edu).

    iupui Repository record

  2. Improving CNS Delivery of Genistein for the Treatment of Sanfilippo Syndrome

    Gupte, Manas PravinUniversity of Houston2017

    Statement of the Problem: Sanfilippo syndrome or mucopolysaccharidosis type III (MPS III), a type of lysosomal storage disease, is a rare genetic disorder inherited in an autosomal recessive manner. Individuals affected by this disease lack the ability to produce one of the four enzymes responsible …

    houston Repository record

  3. A Spectrophotometric Assay For Sanfilippo Syndrome, Type D (N-Acetylglucosamine 6-Sulfate Sulfatase Deficiency) With Prenatal Diagnostic Potential.

    Nowakowski, Rodney William

    uab Repository record

  4. Neuropathologic characterization of a canine model of mucopolysaccharidosis IIIB and additional studies in anti-inflammatory therapy and neuroinflammatory kinetics

    Harm, Tyler2021

    … Mucopolysaccharidosis III (MPS III, Sanfilippo Syndrome Type III) is characterized by 4 subtypes in humans (A-D), and fifth subtype in mice (E). MPS IIIB results from a deficiency in ?-N-acetylglucosamindase (Naglu) activity which results in primary accumulation of HS. There is …

    iastate Repository record