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multiple system atrophy

Two New Studies Open for Patients with MSA

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Orthostatic hypotension (OH) can cause dizziness, lightheadedness, and even angina on standing. It occurs when the autonomic reflexes […]

dysautonomialab April 10, 2017 multiple system atrophy, Studies

Low blood pressure standing may hold the key to detecting pre-motor MSA

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Scientists at the Center have brought us a step closer to being able to detect the deadly spread […]

dysautonomialab February 22, 2017 Dr. Lucy Kaufmann, horacio kaufmann, Lab News, palma, research paper, research papers, Studies, team, Uncategorized

MSA NJ organizing a fund-raiser picnic for families in the tristate area

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Dear Friends, Multiple System Atrophy New Jersey (MSA NJ) is a non-profit organization, which provides support for patients […]

dysautonomialab September 1, 2016 Uncategorized

An update from the 5th Congress on MSA

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At the 2016 International Congress on MSA, over 130 experts in the field came together for a 2-day […]

dysautonomialab April 27, 2016 horacio kaufmann, Lab News, team, Uncategorized

Join our team: Nurse Practitioner wanted (Position now filled by the wonderful Erin Barnes, NP )

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Looking for an intellectually challenging work environment that values compassionate medical care? Want to advance the boundaries of […]

dysautonomialab January 26, 2016 Lab News, team, training

Low blood pressure standing may be an early sign of brain disease

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Standing upright is complex business and requires a finely tuned set of reflex responses. If these reflex responses […]

dysautonomialab October 6, 2015 editorial, Lab News, research paper, research papers

Dr. Palma wins MSA research award

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The diagnosis of multiple system atrophy (MSA) is often very difficult. As there is no reliable clinical test, […]

dysautonomialab October 1, 2015 Lab News, team, training

The eye in MSA: A window into disease progression?

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The retina is the light-sensitive layer of tissue at the back of the inner eye that is considered part […]

dysautonomialab September 15, 2015 dr. mendoza, Lab News, research papers, team

How YOU can help dysautonomia research

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The Dysautonomia Foundation has supported the Center for over 40 years. This unwavering support allows us to treat children […]

dysautonomialab September 11, 2015 familial dysautonomia, Lab News, team, training

What it means to study rare diseases

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An orphan disease is disease that affects less than 200,000 Americans.  Orphan diseases (also called rare diseases) are surprisingly […]

dysautonomialab August 29, 2015 about, Studies, training

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