Mucopolysaccharidosis (MPS) Physical Symptom Score: Development, Reliability, and Validity

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Association of somatic burden of disease with age and neuropsychological measures in attenuated mucopolysaccharidosis types I, II and VI.Beneath the floor: re-analysis of neurodevelopmental outcomes in untreated Hurler syndrome.

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P2860

Mucopolysaccharidosis (MPS) Physical Symptom Score: Development, Reliability, and Validity

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2015 nî lūn-bûn

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Mucopolysaccharidosis (MPS) Ph ...... ent, Reliability, and Validity

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Mucopolysaccharidosis (MPS) Ph ...... ent, Reliability, and Validity

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Mucopolysaccharidosis (MPS) Ph ...... ent, Reliability, and Validity

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Mucopolysaccharidosis (MPS) Ph ...... ent, Reliability, and Validity

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P2860

Diagnosis and treatment trends in mucopolysaccharidosis I: findings from the MPS I Registry.

Cord-blood transplants from unrelated donors in patients with Hurler's syndrome.

Prevalence of lysosomal storage disorders.

The prevalence of and survival in Mucopolysaccharidosis I: Hurler, Hurler-Scheie and Scheie syndromes in the UK

Cognitive, medical, and neuroimaging characteristics of attenuated mucopolysaccharidosis type II.

Can mucopolysaccharidosis type I disease severity be predicted based on a patient's genotype? A comprehensive review of the literature.

Mucopolysaccharidosis I: management and treatment guidelines.

Neurocognitive and neuropsychiatric phenotypes associated with the mutation L238Q of the α-L-iduronidase gene in Hurler-Scheie syndrome.

The mucopolysaccharidoses. Diagnosis, molecular genetics and treatment.

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61-68

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scholarly article

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10.1007/8904_2015_485

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Mucopolysaccharidosis (MPS) Physical Symptom Score: Development, Reliability, and Validity

about

P2860

P2860

Mucopolysaccharidosis (MPS) Physical Symptom Score: Development, Reliability, and Validity

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P2093

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P478

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P5875

P698

P932