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Science at Sanofi

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Advancing Therapy with iGlarLixi: Differentiation from other complex regimens

Advancing Therapy with iGlarLixi: Differentiation from other complex regimens

Insulin advancement in Type 2 diabetes: Unmet needs with commonly-used options

Insulin advancement in Type 2 diabetes: Unmet needs with commonly-used options

EVOLUTION: RWE from Saudi Arabia

EVOLUTION: RWE from Saudi Arabia

Challenges associated with commonly-used insulin advancement options

Challenges associated with commonly-used insulin advancement options

Advancing Therapy with iGlarLixi: Differentiation from complex insulin regimens

Advancing Therapy with iGlarLixi: Differentiation from complex insulin regimens

Chronic Spontaneous Urticaria is an Immune-Mediated Inflammatory Skin Disease

Chronic Spontaneous Urticaria is an Immune-Mediated Inflammatory Skin Disease

Gaucher disease awareness month video

Gaucher disease awareness month video

Pompe don’t lose time video

Pompe don’t lose time video

Gaucher

Gaucher

How To Diagnose LSDs?

How To Diagnose LSDs?

Learn more about early diagnosis of lysosomal storage disorders: Fabry disease, Pompe Disease, Gaucher disease, Acid Sphingomyelinase Deficiency (ASMD, also known as Niemann-Pick Type A/B), mucopolysaccharidoses (MPSs).

Better care for Fabry

Better care for Fabry

Every Moment Matters on the Fabry Journey

Pompe Care Podcast Series

Pompe Care Podcast Series

Welcome to Pompe Care podcast series, today’s episodes we speak to Dr. Amal Al Teneiji, Metabolic Genetics Consultant at Sheikh Khalifa Medical City Abu Dhabi, about Pompe disease. We talk about typical diagnosis of patient journey, challenges facing, new diagnostic technologies, effective ways to support patients and families and social stigma.