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Publications by Cristiana Picco

Phospholipid Scrambling Activity by TMEM16E/Ano5: Opposite Effects of Mutations Causing Bone Dysplasia and Muscular Dystrophy

Biophysical Journal

English

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New POMT2 Mutations Causing Congenital Muscular Dystrophy: Identification of a Founder Mutation

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Bone Dystrophy Associated With Muscular Dystrophy

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Actininopathy – A New Muscular Dystrophy Caused by ACTN2 Dominant Mutations

Annals of Neurology

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Macular Dystrophy Presenting in One of Two Siblings With Limb-Girdle Muscular Dystrophy Type 2L Due to Mutation of ANO5

Sensory Systems

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Phospholipid Composition of Tissues in Calves Suffering From Nutritional Muscular Dystrophy

British Journal of Nutrition

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A Role of TMEM16E Carrying a Scrambling Domain in Sperm Motility

Molecular and Cellular Biology

Molecular Biology

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Insights Into Bone Health in Duchenne Muscular Dystrophy

BoneKEy Reports

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Myotonic Muscular Dystrophy: Defective Phospholipid Metabolism in the Erythrocyte Plasma Membrane.

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Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy

American Journal of Human Genetics

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