strumpell marie disease
1Bechterew-Strümpell-Marie-Krankheit — Klassifikation nach ICD 10 M45 Spondylitis ankylosans …
2Disease — Illness or sickness often characterized by typical patient problems (symptoms) and physical findings (signs). Disruption sequence: The events that occur when a fetus that is developing normally is subjected to a destructive agent such as the… …
3Marie — Pierre, French neurologist, 1853–1940. See M. ataxia, Charcot M. Tooth disease, Bamberger M. disease, Bamberger M. syndrome, M. Strümpell disease, Strümpell M. disease, Brissaud M. syndrome, Foix Cavany M. syndrome …
4Strümpell — Ernst Adolf von, German physician, 1853–1925. See S. disease, S. phenomenon, S. reflex, Fleischer S. ring, S. Marie disease, Marie S. disease …
5Marie-Strumpell disease — Ma·rie Strüm·pell disease also Ma·rie Strüm·pell s disease mä rē stru̇m pəl(z) n ANKYLOSING SPONDYLITIS Ma·rie mȧ rē Pierre (1853 1940) French neurologist. Marie began his career in neurology under the tutelage of the celebrated neurologist Jean …
6Marie-Strumpell disease — noun a chronic form of spondylitis primarily in males and marked by impaired mobility of the spine; sometimes leads to ankylosis • Syn: ↑ankylosing spondylitis, ↑rheumatoid spondylitis • Hypernyms: ↑spondylitis, ↑autoimmune disease, ↑autoimmune… …
7Adolph Strümpell — Infobox Scientist name = Adolph Strümpell image width = caption = birth date = birth date|1853|6|29|mf=y birth place = death date = 1925 death place = residence = citizenship = nationality = ethnicity = field = Neurology work institution = alma… …
8Morbus Bechterew-Marie-Strümpell — Klassifikation nach ICD 10 M45 Spondylitis ankylosans …
9Pierre Marie — Infobox Scientist name = Pierre Marie box width = image width =150px caption = Pierre Marie birth date = September 9, 1853 birth place = death date = April 13. 1940 death place = residence = citizenship = nationality = ethnicity = field =… …
10Charcot-Marie-Tooth disease — A neuromuscular disease, the most common inherited disorder of peripheral nerves, characterized by progressively debilitating weakness. The disease is also called peroneal muscular atrophy and hereditary motor and sensory neuropathy. The foremost …