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Publications by Max A Spycher

Prenatal Mucopolysaccharidosis II (Hunter): A Pathogenetic Study

Pediatric Research

English

Related publications

Treatment of Mucopolysaccharidosis Type II (Hunter Syndrome): Results From a Systematic Evidence Review

Genetics in Medicine

English

Immunogenicity of Idursulfase and Clinical Outcomes in Very Young Patients (16 Months to 7.5 Years) With Mucopolysaccharidosis II (Hunter Syndrome)

Orphanet Journal of Rare Diseases

English

Mucopolysaccharidosis Type II: Enzyme Replacement Therapy Efficiency

Voprosy Sovremennoi Pediatrii - Current Pediatrics

English

Mucopolysaccharidosis Type II—An Unexpected “3 in 1” Family

Pediatrics and Neonatology

English

Diagnosis of Prenatal-Onset Achondrogenesis Type II by a Multidisciplinary Assessment: A Retrospective Study of 2 Cases

Case Reports in Obstetrics and Gynecology

English

Pharmacoeconomic Evaluation of Drugs Used in Enzyme Replacement Therapy Mucopolysaccharidosis Type II

Pharmacoeconomics: theory and practice

English

Report of a Large Brazilian Family With a Very Attenuated Form of Hunter Syndrome (MPS II)

Internal Medicine

Molecular Biology

English

Tagum Study II: Follow-Up Study at Two Years of Age After Prenatal Exposure to Mercury

English

Biomarkers of Bone Remodeling in Children With Mucopolysaccharidosis Types I, II, and VI

Journal of Pediatric Rehabilitation Medicine

Physical Therapy

English