Ava Garnett, Nail-Patella Syndrome Advocate, Praised on NY State Assembly Floor
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Ava Garnett, Nail-Patella Syndrome Advocate, Praised on NY State Assembly Floor

By Jodee Redmond from In The Cloud Copy Assemblywoman Nicole Malliotakis (R-East Shore/South Brooklyn) introduced Ava Rose Garnett in New York’s Capitol building in Albany recently. Miss Garnett is a…

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La Vacuna Nasal Previene la Pérdida Neuronal en Modelos de Ratones de la Enfermedad de Alzheimer

Según un artículo en The Asahi Shimbun, científicos japoneses han desarrollado una nueva vacuna para mitigar la degeneración neuronal causada por la enfermedad de Alzheimer. La vacuna, administrada por vía…

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Boston Man Tackling Duchenne Muscular Dystrophy Cure After Sibling’s Diagnosis
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Boston Man Tackling Duchenne Muscular Dystrophy Cure After Sibling’s Diagnosis

by Jodee Redmond from In The Cloud Copy Rich Horgan is the founder of the Boston-based biotech non-profit, Cure Rare Diseases. The 28-year-old decided to take action over concerns about…

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Literally One of a Kind: 10-Year-Old Child Only Person with Rare Form of Congenital Disorders of Glycosylation
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Literally One of a Kind: 10-Year-Old Child Only Person with Rare Form of Congenital Disorders of Glycosylation

By Caitlin Seida from In The Cloud Copy If you've never heard of CDG, or congenital disorders of glycosylation, you're not alone. The rare family of diseases, all inheritable, are…

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RDMD Gets $14 Million in Financing, Partners with UCB to Research Progressive Supranuclear Palsy
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RDMD Gets $14 Million in Financing, Partners with UCB to Research Progressive Supranuclear Palsy

  According to BioSpace, healthcare technology company RDMD has raised $14 million in Series A financing, and developed a partnership with UCB. In addition to growing their platform to discuss…

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