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Sanfilippo syndrome
Pathophysiology of Mucopolysaccharidosis
Mucopolysaccharidosis Type II: One Hundred Years of Research, Diagnosis, and Treatment
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Sanfilippo Disease Type D: Deficiency of N-Acetylglucosamine-6- Sulfate Sulfatase Required for Heparan Sulfate Degradation
Journal of Inborn Errors of Metabolism & Screening
Anesthetic Considerations and Clinical Manifestations 243
Sanfilippo Type B Syndrome (Mucopolysaccharidosis III B)
Sanfilippo Type C Diagnosis: Assay of Acetyl- Coa: A-Glucosaminide N-Acetyltransferase Using [14C]Glucosamineas Substrate and Leukocytes As Enzyme Source
Mucopolysaccharidosis: Caregiver Quality of Life
RARE Foundation Alliance List RARE Hub 2021-08
Mortality in Patients with Sanfilippo Syndrome Christine Lavery1*, Chris J
Global Genes RARE Foundation Alliance Is Made up of More Than
Autism Spectrum Disorder in a Child with Hunter Syndrome
Sanfilippo Syndrome
A Novel Mutation (P.Met1?) of a Cuban Patient in the NAGLU Gene
Mucopolysaccharidosis Type III (Sanfilippo Syndrome):Developing Drugs for Treatment Guidance for Industry
Cardiac Problems Associated with the Mps Syndromes
Sanfilippo Syndrome Type B, a Lysosomal Storage Disease, Is Also a Tauopathy
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From Hypertransaminasemia to Mucopolysaccharidosis IIIA
Genetically Corrected Ipsc-Derived Neural Stem Cell Grafts Deliver Enzyme Replacement to Affect CNS Disease in Sanfilippo B Mice
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Correction of Cellular Metachromasia in Cultured Fibroblasts in Several Inherited Mucopolysaccharidoses* B
A Review of Pricing and Reimbursement for Abeona Therapuetics' Gene Therpay Products to Treat Sanfilippo Syndrome
Mucopolysaccharidosis Type 3B in an Adult with Pancytopenia: a Rare Case Report Pansitopenisi Olan Erişkin Mukopolisakkaridoz Tip 3B Olgusu: Nadir Bir Olgu Sunumu
Characterization of a Murine Model of Mucopolysaccharidosis Type IIID: a Knockout Model Maryam Jamil Iowa State University
Hearing Loss in Mucopolysaccharidoses: Current Knowledge and Future Directions
Neuronal and Astrocytic Differentiation from Sanfilippo C Syndrome Ipscs
The Morbid Anatomy of the Human Genome: Chromosomal Location of Mutations Causing Disease
A Retrospective Chart Review
A Guide to Understanding Sanfilippo Syndrome
Sanfilippo Syndrome: Current Knowledge and Perspectives For
A Guide to Understanding MPS III
Mucopolysaccharidosis (Mps) Panel