Resultado da Busca
Há 1 dia · The French neurologist Jean-Martin Charcot photographed his most famous hysterics and hypnotised them on stage in front of 400 weekly spectators. Charcot’s star patient Marie ‘Blanche’ Wittman was known as the ‘Queen of the Hysterics’.
Há 3 dias · ABSTRACT. Jean-Martin Charcot (1825–1893) is known to have possessed interesting works of art, e.g. Jan Steen’s Marriage at Cana.In 1899, his pupil and colleague Henry Meige (1866–1940) wrote that Charcot had been interested in a painting (after a drawing) by Bruegel, named Les Arracheurs de Pierres de Teste.
Há 1 dia · However, the real first descriptions of the concept of ‘spastic paraplegia’ were later credited to Wilhem Erb (1840–1921) who described “spinalen Symptomencomplex” in 1875 (then “spastic spinal paralysis” in 1877) and Jean-Martin Charcot (1825–1893) who reported on “tabès dorsal spasmodique” (“spasmodic dorsal tabes”) in 1876 : so the term “Erb-Charcot paralysis ...
Há 4 dias · Other doctors of the era, like neurologist Jean-Martin Charcot, considered railway spine to be a traditional case of hysteria—at the time essentially defined as the nervous instability of people, mostly women, who were generally associated with some kind of moral failing.
Há 3 dias · In the 1800s, Jean-Martin Charcot coined the term “Amyotrophic Lateral Sclerosis” (ALS), highlighting muscular atrophy and hardening of lateral spinal cord tissues . ALS is a progressive and heterogeneous neurodegenerative disorder associated with degeneration of cortical or “upper” and spinal or “lower” motor neurons.
Há 1 dia · El 30 de mayo se celebra el “Día Mundial contra la Esclerosis Múltiple”, que este año tiene como lema: "Navegando juntos la Esclerosis Múltiple", el objetivo de esta conmemoración es el de concienciar sobre ella y promover la solidaridad con las personas que la padecen. La esclerosis múltiple es una enfermedad crónica, autoinmune ...
Há 10 horas · La ELA fue descrita por primera vez en 1869 por el médico francés Jean-Martin Charcot. Desde entonces, los avances en la comprensión de la enfermedad han sido significativos. En la década de 1990, se identificaron mutaciones en el gen SOD1 como causa de formas hereditarias de ELA, lo que impulsó la investigación sobre los mecanismos subyacentes de la enfermedad.
