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Lysosomal Leukodystrophies Lysosomal Storage Diseases Associated With White Matter Abnormalities

Maegawa, Gustavo H. B.

Journal of child neurology. Volume 34:Number 6 (2019); pp 339-358 -- [Sage]

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Lysosomal Leukodystrophies Lysosomal Storage Diseases Associated With White Matter Abnormalities

Maegawa, Gustavo H.B.

Journal of child neurology. Volume 34:Number 6 (2019, June); pp 339-358 -- Sage Publications

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Effects of psychosine-reducing agents in the twitcher murine model for Krabbe disease

Katabuchi, Asaka et al.

Molecular genetics and metabolism. Volume 123:Number 2 (2018, February); pp S75-S76

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Generation of neurologically relevant disease-cell models for lysosomal diseases

Katabuchi, Asaka et al.

Molecular genetics and metabolism. Volume 123:Number 2 (2018, February); pp S76-

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Premature Identical Twin Neonates With Sleep Apnea

Ramesh, Anirudh et al.

Clinical pediatrics. Volume 56:Number 11 (2017); pp 1075-1078 -- Sage Publications

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Premature Identical Twin Neonates With Sleep Apnea

Ramesh, Anirudh et al.

Clinical pediatrics -- Sage -- Volume: 56 11; (pages 1075-1078) -- 2017

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Identification of psychosine-reducing small molecule agents for Krabbe disease

Jang, Dae Song et al.

Molecular genetics and metabolism. Volume 120:Issue 1/2 (2017); pp S90-

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Long-term Outcome of 4 Patients With Transcobalamin Deficiency Caused by 2 Novel TCN2 Mutations

Nashabat, Marwan et al.

Journal of pediatric hematology/oncology. Volume 39:Issue 8 (2017); pp e430-e436 -- Lippincott Williams & Wilkins

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Long-term Outcome of 4 Patients With Transcobalamin Deficiency Caused by 2 Novel TCN2 Mutations

Nashabat, Marwan et al.

Journal of pediatric hematology/oncology. Volume 39:Issue 8 (2017, November) -- Lippincott Williams & Wilkins

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Pegunigalsidase alfa, a novel PEGylated ERT for Fabry disease: Two-year safety and efficacy follow up

Hughes, Derralynn et al.

Molecular genetics and metabolism. Volume 123:Number 2 (2018, February); pp S67-S68

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