Results 151 to 160 of about 410,791 (266)

Current and emerging management options for patients with Morquio A syndrome

open access: yesTherapeutics and Clinical Risk Management, 2013
Mohamed F Algahim, G Hossein AlmassiDivision of Cardiothoracic Surgery, Medical College of Wisconsin, Milwaukee, WI, USAAbstract: Morquio A syndrome is a lysosomal storage disease associated with mucopolysaccharidosis. It is caused by a deficiency of the
Algahim MF, Almassi GH
doaj  

Keratan sulfate as a marker for medullary bone in fossil vertebrates

open access: green, 2021
Aurore Canoville   +3 more
openalex   +2 more sources

Persistent elevations of alkaline phosphatase as an early indicator of GM1 gangliosidosis

open access: yesMolecular Genetics and Metabolism Reports
GLB1-related disorders are autosomal recessive lysosomal diseases caused by enzymatic deficiency of β-galactosidase. Enzymatic deficiency of β-galactosidase may lead to one of two phenotypes, GM1 gangliosidosis or mucopolysaccharidosis IVB (MPS IVB). GM1
Iskren Menkovic   +6 more
doaj   +1 more source

Primary cell culture of meningothelial cells—a new model to study the arachnoid in glaucomatous optic neuropathy [PDF]

open access: yes, 2018
Background: In a previous report, we found that the occurrence and amount of meningothelial cell nests in the subarachnoid space are significantly increased in glaucomatous optic nerves compared to normals.
Fan, Bin   +5 more
core  

Monoclonal antibodies to keratan sulfate immunolocalize ramified microglia in paraffin and cryostat sections of rat brain. [PDF]

open access: bronze, 1993
Antonio Bertolotto   +4 more
openalex   +1 more source

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