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Hurler syndrome
Epidemiology of Mucopolysaccharidoses Update
Long-Term Outcomes of Systemic Therapies for Hurler Syndrome: an International Multicenter Comparison
Pathophysiology of Mucopolysaccharidosis
Mucopolysaccharidosis Type II: One Hundred Years of Research, Diagnosis, and Treatment
MECHANISMS in ENDOCRINOLOGY: Novel Genetic Causes of Short Stature
Hurler Syndrome (Mucopolysaccharidosis Type 1) in a Young Female Patient [Version 1; Peer Review: 3 Approved with Reservations]
Illinois Department of Public Health
Mucopolysaccharidosis I Diagnosing MPS I
Early Disease Progression of Hurler Syndrome Bridget T
Hurler Syndrome (Mucopolysaccharidosis Type I) Reuben Grech, Leo Galvin, Alan O’Hare, Seamus Looby
Anesthetic Considerations and Clinical Manifestations 243
Phenotypic Expression in Mucopolysaccharidosis VII
Hurler Syndrome
Mucopolysaccharidosis Types I and III): Potential Causes and Implications Gé-Ann Kuiper†, Olga L
Keratan and Heparan Sulfaturia: Glucosamine-6-Sulfate Sulfatase Deficiency REUBEN MATALON, M.D., Ph .D.,* REBECCA WAPPNER, M.D.,T MINERVA DEANCHING, M.S.,* IRA K
Genetics and Metabolics Abbreviations and Diagnosis
Mucopolysaccharidosis, Type I (MPSI)
Mucopolysaccharidosis 1 (MPS1) (Hurler / Scheie Syndrome)
Top View
Cardiac Problems Associated with the Mps Syndromes
Dysostosis Multiplex: Pfaundler-Hurler Syndrome Report of Two Cases
Hunter's Syndrome and Oral Manifestations
What's New in Newborn Screening?
Gastrointestinal Symptoms in Lysosmal Disease
Hurler Syndrome: a Mini Review
Mucopolysaccharidosis (MPS) I Has Family of Diseases Called the Lysosomal Storage Diseases (Lsds)
Correction of Cellular Metachromasia in Cultured Fibroblasts in Several Inherited Mucopolysaccharidoses* B
(MPS I): a Systematic Review of Evidence Report of Final Findings Final Version 1.1
Characterization of a Murine Model of Mucopolysaccharidosis Type IIID: a Knockout Model Maryam Jamil Iowa State University
Molecular Therapy and Gene Therapy for Hurler Syndrome a THESIS
Hearing Loss in Mucopolysaccharidoses: Current Knowledge and Future Directions
Hurler Syndrome: A-L- Iduronidase Activity in Leukocytes As a Method for Heterozygote Detection
The Mucopolysaccharidoses: a Clinical Review and Guide to Management
Mucopolysaccharidosis Type I
Genetic Testing of Mucopolysaccharidoses Disease Using Multiplex PCR- Based Panels of STR Markers: in Silico Analysis of Novel Mutations
Mucopolysaccharidosis Type I (MPS I) (Hurler, Hurler-Scheie and Scheie Syndromes)
Alpha-Iduronidase Enzyme Activity (Mucopolysaccharidosis Type I)
(Sanfilippo Disease): a Case Study with Ultrastructural, Biochemical, and Radiological Findings
Identification of Four Recurrent IDUA Sequence Changes That Significantly Reduce Enzyme Activity
Alpha-L-Iduronidase Deficiency in a Cat: a Model of Mucopolysaccharidosis I
A Guide to Understanding Mucopolysaccharidosis (MPS) I Table of Contents Founded in 1984, the Canadian Society for Mucopolysaccharide and Related Diseases Inc
Sanfilippo Syndrome: Current Knowledge and Perspectives For
Mucopolysaccharidosis (Mps) Panel
Differences in MPS I and MPS II Disease Manifestations
Mucopolysaccharidosis Type I: Current Treatments, Limitations, and Prospects for Improvement