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… syndrome? Wernicke-Korsakoff syndrome is a neurological disorder caused by the lack of thiamine (vitamin B1) . The … abuse Dietary deficiencies Prolonged vomiting Eating disorders Effects of chemotherapy B1 deficiency causes damage … is slow and, usually, incomplete. Without treatment, these disorders can be disabling and life-threatening. file-medical …
… syndrome? Coffin-Lowry syndrome is a rare genetic disorder characterized by craniofacial (head and facial) and … trials are studies that allow us to learn more about disorders and improve care. They can help connect patients … can learn more about the Coffin-Lowry syndrome and related disorders. Clinical research uses human volunteers to help …
… gene, SPG20) belongs to a group of nervous system disorders called hereditary spastic paraplegias. The main feature of these disorders are muscle weakness and spasms in the legs that … proteins. Troyer syndrome is an autosomal recessive disorder, which means that both parents must carry it and …
… Slurred speech (dysarthria) Difficulty swallowing (dysphagia) Drooling Other symptoms may include: Tremor of the …
… Description The mission of the NINDS Division of Clinical Research is to provide oversight for clinical trials to test the safety and efficacy of … by category. View information related to translational research . Policy for Submitting Applications Proposing …
… of new diagnostics and treatments for neurological disorders. However, advancing a therapeutic molecule or … research findings towards patient use for neurological disorders and stroke by providing researchers in academia and … by the private sector, so that anyone with a neurologic disorder may benefit from NINDS-funded research. Here, we …
… Friday, February 28, 2020 Rare diseases often don’t have the same name recognition that … on understanding and treating these prevalent disorders, rare diseases have equally important stories to tell. These … United States as conditions affecting Roughly one-third of rare diseases include neurological components and symptoms, …
… Myotonia congenita is an inherited neuromuscular disorder characterized by the inability of muscles to quickly … trials are studies that allow us to learn more about disorders and improve care. They can help connect patients … can learn more about myotonia congenita and related disorders. Clinical research uses human volunteers to help …
… On this page What is arachnoiditis? Arachnoiditis is a disorder caused by the inflammation of the arachnoid. The … trials are studies that allow us to learn more about disorders and improve care. They can help connect patients … scientists can learn more about arachnoiditis and related disorders. Clinical research uses human volunteers to help …
… scientific progress and reduce the burden of neurological disorders. NINDS Strategic Plan home » Communications Table … scientific progress and reduce the burden of neurological disorders. Achieving NINDS’s mission requires dynamic and … source of credible, timely information on neurological disorders. NINDS strives to rapidly disseminate scientific …