Fruit fly study identifies potential therapeutic target for form of ALS, FTD
UF neuroscientists collaborate on international study revealing a potential therapeutic target for ALS, FTD linked to TDP-43.
UF neuroscientists collaborate on international study revealing a potential therapeutic target for ALS, FTD linked to TDP-43.
In The Conversation, Drs. Bhavana Patel and Torge Rempe explain stiff person syndrome, its symptoms, treatment approaches and more.
Dr. Mayra Montalvo provides an insight on the clinical picture and outcomes of patients with seizures and myelin oligodendrocyte glycoprotein antibody disease.
AMX0035 was tested at UF, Mass General and partnering sites and then approved by the FDA to treat ALS.
Researchers explore a case of acute akinetic mutism caused by cerebral fat embolisms from hemoglobin sickle cell disease.
UF neurologists identify a distinct collection of brain fibers to target with deep brain stimulation for tremor suppression in multiple sclerosis.
Trial drug combination shows potential to prolong survival of ALS patients by more than six months.
Trial drug combination shows potential to prolong survival of ALS patients by more than six months.
UF researchers team up with international partners to improve understanding and treatment of two rare hereditary neuromuscular disorders.
UF was the No. 2 enroller of patients for multisite ALS trial.