Function of WFS1 and WFS2 in the Central Nervous System: Implications for Wolfram Syndrome and Alzheimer’s disease

February 19, 2021:

Function of WFS1 and WFS2 in the Central Nervous System: Implications for Wolfram Syndrome and Alzheimer’s disease

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A link between new diabetes cases and COVID-19

February 18, 2021:

https://www.gmtoday.com/a-link-between-new-diabetes-cases-and-covid-19/article_245e6f94-708f-11eb-af15-038e0c45313b.html

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Diabetes monitoring without the needle

February  17, 2021:

Diabetes monitoring without the needle

https://www.axios.com/newsletters/axios-future-077b74ab-996c-4bc4-be7f-d65225e28663.html?chunk=1&utm_term=emshare#story1

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A Model of Adolescent Sleep Health and Risk for Type 2 Diabetes

February 16, 2021:

A Model of Adolescent Sleep Health and Risk for Type 2 Diabetes

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LEGO Braille Bricks make their way down under

February 14, 2021:

This new toy normalizes braille and allows sighted kids and those who are blind or have low vision to play together

LEGO Braille Bricks make their way down under

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Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches

February 12, 2021:

Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches

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Metformin use reduces risk of death for patients with COVID-19 and diabetes

Metformin use reduces risk of death for patients with COVID-19 and diabetes

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Estrogen-based Therapy Shows Potential to Protect Vision in Mouse Model

February 7, 2021:

Estrogen-based Therapy Shows Potential to Protect Vision in Mouse Model

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Characterization of a novel variant in the HR1 domain of MFN2 in a patient with ataxia, optic atrophy and sensorineural hearing loss

February 5, 2021:

Characterization of a novel variant in the HR1 domain of MFN2 in a patient with ataxia, optic atrophy and sensorineural hearing loss

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Long-Term Dietary Changes in Subjects with Glucose Galactose Malabsorption Secondary to Biallelic Mutations of SLC5A1

February 2, 2021:

Long-Term Dietary Changes in Subjects with Glucose Galactose Malabsorption Secondary to Biallelic Mutations of SLC5A1

 

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