Florian Eichler received his M.D. from the University of Vienna Medical School. After graduating from medical school in 1997, he entered residency in Pediatrics and pursued studies on cerebral blood flow and metabolism at the University of Vienna. In 1999 he won a scholarship to study in vivo MR spectroscopy in pediatric patients with metabolic and neurometabolic conditions at Johns Hopkins (Stipendium Metabolicum 1999) and joined the laboratory of Dr. Hugo Moser dedicated to peroxisomal disorders at the Kennedy Krieger Institute. Following his research fellowship at Johns Hopkins he underwent residency training in Child Neurology at the Massachusetts General Hospital (MGH). After completing residency in 2005 he joined the staff at MGH.
Now an Associate Professor of Neurology at Harvard Medical School he is extending his research into animal models of neurodegenerative disorders. His research focus is on the genetics of peroxisomal disorders, lipid metabolism, and spatial aspects of nuclear magnetic resonance spectroscopy. As director of the leukodystrophy clinic at the Massachusetts General Hospital he sees patients with a variety of white matter disorders. He currently holds several NIH awards funding studies to analyze metabolic changes seen in the brain by MR measures and to determine the neurotoxicity of newly discovered atypical sphingolipids.
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Mass General Neurology
55 Fruit St.
Boston, MA 02114
Phone: 855-644-6387
Mass General for Children: Pediatric Neurology
55 Fruit St.
Yawkey Center for Outpatient Care
Suite 6B
Boston, MA 02114
Phone: 617-724-6400
Medical Education
American Board Certifications
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My expertise lies in neurogenetics and translational neuroscience. The topic of my research is unraveling the disease mechanisms of monogenetic disorders affecting the nervous system. This allows my lab to explore the relationship of mutant genes to specific biochemical defects and their contribution to neurodegeneration. As director of the leukodystrophy service at MGH I see patients with a variety of neurogenetic disorders and am actively studying abnormal accumulation of lipids such as very long chain fatty acids and desoxysphingoid bases in both my clinic and my laboratory. My clinical research studies have defined disease progression in adrenoleukodystrophy, metachromatic leukodystrophy and Tay Sachs Disease. Recently we were able to show that levels of desoxysphingoid bases in mice and humans with an inherited form of neuropathy contribute to disease and can be lowered by supplementation with L-serine.
We are so grateful to Dr. Eichler and team. Dr. Eichler has provided our son with truly exceptional care-his deep expertise, compassion, and unwavering commitment have made all the difference in our journey. He takes the time to listen, explain, and guide every decision with both heart and precision. We are endlessly grateful to have him in our ... Read More
Dr. Eichler diagnosed my son and he is the most incredible Dr.
Both Dr. [redacted] and Dr. Eichler were excellent and I think we have a good path forward to determine a diagnosis. They also were very good listeners.
Dr. Eichler is the most knowledgeable and professional doctor that I have ever worked with. He is a blessing to our son and our whole family. His open, warm, and giving personality is beyond description.
HE TRULY CARED AND I TRUST HIM TO FIND OUT WHAT IS WRONG WITH ME. HE WAS GREAT AND SO WAS HIS NURSE
Extreme professionalism
Dr eichler is amazing as well as Dr. [redacted]. They are smart, dynamic, compassionate and supportive.
Made me feel. Very comfortable to speak about my medical issues. Explain everything so I fully understand issues.
Makes me feel hopeful
I have always been treated very well by this provider and his staff. They answer my questions and spend the time needed to address any concerns I have.