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Scheie syndrome
Diversity of Mutations and Distribution of Single Nucleotide Polymorphic Alleles in the Human -L-Iduronidase (IDUA) Gene
Mucopolysaccharidosis Type I
MPS1) (Hurler / Scheie Syndrome
Illinois Department of Public Health
Anesthetic Considerations and Clinical Manifestations 243
Hurler Syndrome
Ocular Features of Treatable Lysosomal Storage Disorders— Fabry Disease, Mucopolysaccharidoses I, II, and VI, and Gaucher Disease
Mucopolysaccharidosis I
Ocular Manifestations of Inherited Diseases Maya Eibschitz-Tsimhoni
Lysosomal Storage Disorders Medical Drug Program Summary
(Pseudo- Hurler Polydystrophy). a Case Report
Mucopolysaccharidosis, Type I (MPSI)
Mucopolysaccharidosis 1 (MPS1) (Hurler / Scheie Syndrome)
Diagnosis and Management of Ophthalmologic Features in Patients
Cardiac Problems Associated with the Mps Syndromes
Enzyme Replacement Therapy for Lysosomal Storage Disorders (MPS I, VI) [Aldurazyme, Naglazyme]
A Case Report of a Girl with Polyarticular Disease Refractory
Retinal Changes in Mucopolysaccharidosis I- a Case Report
Top View
Mucopolysaccharidosis (MPS) I Has Family of Diseases Called the Lysosomal Storage Diseases (Lsds)
Clinical and Radiologic Diagnosis of a Patient with Maroteaux-Lamy
Guidelines for the Investigation and Management of Mucopolysaccharidosis Type I
Mucopolysaccharidosis VI
Constitutional Disorders of the Skeleton in Dogs and Cats
Effect of Ocular Biomechanics on Intraocular Pressure Measurement
The Morbid Anatomy of the Human Genome: Chromosomal Location of Mutations Causing Disease
Clinical and Genetic Characteristics of Romanian Patients
The Mucopolysaccharidoses: a Clinical Review and Guide to Management
Mucopolysaccharidosis Type I
Mucopolysaccharidosis Type I (MPS I) (Hurler, Hurler-Scheie and Scheie Syndromes)
Ocular Changes in Patients with Mucopolysaccharidosis I Receiving Enzyme Replacement Therapy a 4-Year Experience
Newborn Screening for Mucopolysaccharidosis Type I
Alpha-Iduronidase Enzyme Activity (Mucopolysaccharidosis Type I)
Alpha-L-Iduronidase Deficiency in a Cat: a Model of Mucopolysaccharidosis I
Recessive Gene List V2.0