Infantile gangliosidoses: Mapping a timeline of clinical changes.

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Distinct progression patterns of brain disease in infantile and juvenile gangliosidoses: Volumetric quantitative MRI study.

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Infantile gangliosidoses: Mapping a timeline of clinical changes.

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Infantile gangliosidoses: Mapping a timeline of clinical changes.

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Infantile gangliosidoses: Mapping a timeline of clinical changes.

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Infantile gangliosidoses: Mapping a timeline of clinical changes.

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Infantile gangliosidoses: Mapping a timeline of clinical changes

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Chester B Whitley

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Evelyn S Redtree

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Jeanine R Jarnes Utz

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Kelly King

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Lynn Schema

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Richard Ziegler

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An Overview of the Ketogenic Diet for Pediatric Epilepsy

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Natural history of infantile G(M2) gangliosidosis.

Optimal clinical management of children receiving the ketogenic diet: recommendations of the International Ketogenic Diet Study Group

The natural history of juvenile or subacute GM2 gangliosidosis: 21 new cases and literature review of 134 previously reported.

Pharmacokinetics, safety and tolerability of miglustat in the treatment of pediatric patients with GM2 gangliosidosis.

Gastrointestinal disturbances and their management in miglustat-treated patients.

Glycosphingolipid lysosomal storage diseases: therapy and pathogenesis.

Clinical Findings and Natural History in Ten Unrelated Families with Juvenile and Adult GM1 Gangliosidosis.

The natural history of cognitive dysfunction in late-onset GM2 gangliosidosis.

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170-179

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scholarly article

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10.1016/J.YMGME.2017.04.011

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121

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Sarah Kim

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2017-04-29T00:00:00Z

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Infantile gangliosidoses: Mapping a timeline of clinical changes.

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P2860

P2860

Infantile gangliosidoses: Mapping a timeline of clinical changes.

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