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Kennedy Krieger awards research endowments to 2 pediatric specialists - Vimarsana News

Kennedy Krieger awards research endowments to 2 pediatric specialists

Dr. Ali Fatemi and Dr. Miya Asato, internationally known pediatric specialists at Kennedy Krieger Institute, have been named as recipients of endowed chairs, the institute announced Wednesday. Fatemi, the institute’s chief medical officer and director of the Moser Center for Leukodystrophies, was named the Blum-Moser Chair for Pediatric Neurology and Asato, who serves as the ...

Power Moves: Under Armour has a new CEO, and Greater Baltimore Committee has its first public safety data officer - Vimarsana News

Power Moves: Under Armour has a new CEO, and Greater Baltimore Committee has its first public safety data officer

Plus, Pothik Chatterjee leaves LifeBridge Health and more end-of-year leadership changes in Baltimore tech and business.

Leaders & Legacies: Harold and Margaret Moser, - Vimarsana News

Leaders & Legacies: Harold and Margaret Moser,

Harold and Margaret Moser, "Mr. & Mrs. Naperville," are featured in the next "Leaders and Legacies: Stories of Local Impact," an ongoing series brought to you in partnership with DuPage Foundation and the Daily Herald.

Poxel SA: Poxel Announces the Formation of its Scientific Advisory Board for Rare Metabolic Diseases - Vimarsana News

Poxel SA: Poxel Announces the Formation of its Scientific Advisory Board for Rare Metabolic Diseases

POXEL SA (Euronext POXEL FR0012432516), a clinical stage biopharmaceutical company developing innovative treatments for chronic diseases with metabolic pathophysiology, including non-alcoholic steatohepatitis

Arlington Family Raises $400K to Research Cure for Daughter's Disease - Vimarsana News

Arlington Family Raises $400K to Research Cure for Daughter's Disease

March 8, 2021 at 2:30pm Arlington’s Ellie McGinn and her family recently raised nearly half a million dollars to fund research into Ellie’s rare degenerative brain and spinal cord disease. Ellie, 12, has lived with LBSL (leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation) for the last 10 years. It affects fewer than 100 people worldwide and currently has no cure. Her family has been actively fundraising for a cure since 2013. This year’s all-virtual efforts in honor of Rare Disease Day on Feb. 28 drew a total of $400,000 in donations from around the w...

Source: arlnow.com