Results 161 to 170 of about 12,452,915 (192)
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Newborn screening for mucopolysaccharidosis type II
Molecular Genetics and Metabolism, 2023Barbara K. Burton +10 more
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Protein Aggregation and Autophagy Dysfunction: New Lessons From Mucopolysaccharidoses
Autophagy, 2021Alessandro Fraldi, Antonio Monaco
exaly
[Clinical aspects of mucopolysaccharidosis type II].
Revista de neurologia, 2008To review the clinical and diagnostic aspects of mucopolysaccharidosis type II (Hunter syndrome).The different phenotypes are described and the multisystem clinical symptoms are considered, with special emphasis on skeletal deformities and cardiorespiratory and neurological complications.Paediatricians and certain specialists (in neurology, ORL ...
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Understanding the Early Presentation of Mucopolysaccharidoses Disorders
FIRE Forum for International Research in Education, 2018Hatice Serap Sivri +2 more
exaly
PCR of a VNTR Linked to Mucopolysaccharidosis Type I and Huntington Disease.
Nucleic Acids Research, 1991Charles Phillip Morris +2 more
exaly
Mucopolysaccharidosis type II clinical case
Molecular Genetics and Metabolism, 2013Ludmila Kuzenkova +6 more
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Prevalence Rates of Mucopolysaccharidoses in Poland
Journal of Applied Genetics, 2015Anna Tylki-Szymanska +2 more
exaly
Peripapillary Scleral Deposits in Mucopolysaccharidosis Type II
OphthalmologySamet Gulkas, Ines Fenniri, Anne Fulton
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