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Difference between revisions of "Mitochondrial Medicine Society"

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== Further information ==
Dear colleagues,
The Mitochondrial Medicine Society is trying to study the state of clinical mitochondrial medicine in the US. This study will involve a series of 5-10 surveys and phone conferences. If you are a US based attending physician that runs a mitochondrial disease clinic or sees a large number of patients with mitochondrial disease and would like to participate, please notify us by writing to [mailto:[email protected] [email protected]]
Please note that if you attended the Clinic Director's workshop at the annual Mitochondrial Disease meeting, you do not have to write back and will automatically be included.
Thank you for your assistance and we look forward to hearing from you.
Sincerely,
Sumit Parikh for the Mitochondrial Medicine Society




>> View the [http://www.mitosoc.org/clinics/ '''mitochondrial global networks map'''], administered by Amy Goldstein.
>> View the [http://www.mitosoc.org/clinics/ '''mitochondrial global networks map'''], administered by Amy Goldstein.

Revision as of 17:06, 21 March 2017


high-resolution terminology - matching measurements at high-resolution


Mitochondrial Medicine Society

Description

The Mitochondrial Medicine Society (MMS) was founded in 2000 and represents an international group of physicians, researchers and clinicians working towards the better diagnosis, management, and treatment of mitochondrial diseases.

Abbreviation: MMS

Reference: MMS



MitoPedia topics: MitoGlobal Organizations 

MitoGlobal

Contact details

President

Amy Goldstein, MD
E-mail: [email protected]



>> View the mitochondrial global networks map, administered by Amy Goldstein.