Citation de gavarneur
Cantatrix sopranica
Démonstration expérimentale d'une organisation tomatotopique chez la Cantatrice.
L'auteur étude les fois que le lancement de la tomate il provoquit la réaction yellante chez la Chantatrice et demonstre que divers plusieures aires de la cervelle elles etait implicatées dans le response, en particular, le trajet légumier, les nuclei thalameux et le fiçure musicien de l'hémisphère nord.
As observed at the turn of the century by Marks & Spencer (1899), who first named the ``yelling reaction'' (YR), the striking effects of tomato throwing on Sopranoes have been extensively described. Although numerous behavioral (Zeeg & Puss, 1931; Roux & Combaluzier, 1932; Sinon et al., 1948), pathological (Hun & Deu, 1960), comparative (Karybb & Szyla, 1973) and follow-up (Else & Vire, 1974) studies have permitted a valuable description of these typical responses, neuroanatomical, as well as neurophysiological data, are, in spite of their number, surprisingly confusing. In their henceforth late twenties' classical demonstrations, Chou & Lai (1927 a, b, c, 1928 a, b, 1929 a, 1930) have ruled out the hypothesis of a pure facio-facial nociceptive reflex that has been advanced for many years by a number of authors (Mace & Doyne, 1912; Payre & Tairnelle, 1916; Sornette & Billevayzé, 1925). Since that time, numerous observations have been made that have tried to decipher the tangling puzzle as well as the puzzling tangle of the afferent and/or efferent sides of the YR and led to the rather chaotic involvement of numberless structures and paths: trigeminal (Loewenstein et al., 1930), bitrigeminal (Von Aitick, 1940), quadritrigeminal (Van der Deder, 1950), supra-, infra-, and inter-trigeminal (Mason & Ragoun, 1960) afferents have been likely pointed out as well as macular (Zakouski, 1954), saccular (Bortsch, 1955), utricular (Malosol, 1956), ventricular (Tarama, 1957), monocular (Zubrowska, 1958), binocular (Chachlik, 1959-1960), triocular (Strogonoff, 1960), auditive (Balalaika, 1515) and digestive (Alka-Seltzer, 1815) inputs. Spinothalamic (Attou & Ratathou, 1974), rubrospinal (Maotz & Toung, 1973), nigro-suiatal (Szentagothai, 1972), reticular (Pompeiano et al., 1971), hypothalamic (Hubel & Wiesel, 1970), mesolimbic (Kuffler, 1969) and cerebellar (High & Low, 1968) pathways have been vainly searched out for a tentative explanation of the YR organization and almost every part of the somesthesic (Pericoloso & Sporgersi, 1973), motor (Ford, 1930), commissural (Gordon & Bogen, 1974) and associative (Einstein et al., 1974) cortices have been found responsible for the progressive building-up of the response although, up-to-now, no decisive demonstration of both the input and output of the YR programming has been convincely advanced.
Démonstration expérimentale d'une organisation tomatotopique chez la Cantatrice.
L'auteur étude les fois que le lancement de la tomate il provoquit la réaction yellante chez la Chantatrice et demonstre que divers plusieures aires de la cervelle elles etait implicatées dans le response, en particular, le trajet légumier, les nuclei thalameux et le fiçure musicien de l'hémisphère nord.
As observed at the turn of the century by Marks & Spencer (1899), who first named the ``yelling reaction'' (YR), the striking effects of tomato throwing on Sopranoes have been extensively described. Although numerous behavioral (Zeeg & Puss, 1931; Roux & Combaluzier, 1932; Sinon et al., 1948), pathological (Hun & Deu, 1960), comparative (Karybb & Szyla, 1973) and follow-up (Else & Vire, 1974) studies have permitted a valuable description of these typical responses, neuroanatomical, as well as neurophysiological data, are, in spite of their number, surprisingly confusing. In their henceforth late twenties' classical demonstrations, Chou & Lai (1927 a, b, c, 1928 a, b, 1929 a, 1930) have ruled out the hypothesis of a pure facio-facial nociceptive reflex that has been advanced for many years by a number of authors (Mace & Doyne, 1912; Payre & Tairnelle, 1916; Sornette & Billevayzé, 1925). Since that time, numerous observations have been made that have tried to decipher the tangling puzzle as well as the puzzling tangle of the afferent and/or efferent sides of the YR and led to the rather chaotic involvement of numberless structures and paths: trigeminal (Loewenstein et al., 1930), bitrigeminal (Von Aitick, 1940), quadritrigeminal (Van der Deder, 1950), supra-, infra-, and inter-trigeminal (Mason & Ragoun, 1960) afferents have been likely pointed out as well as macular (Zakouski, 1954), saccular (Bortsch, 1955), utricular (Malosol, 1956), ventricular (Tarama, 1957), monocular (Zubrowska, 1958), binocular (Chachlik, 1959-1960), triocular (Strogonoff, 1960), auditive (Balalaika, 1515) and digestive (Alka-Seltzer, 1815) inputs. Spinothalamic (Attou & Ratathou, 1974), rubrospinal (Maotz & Toung, 1973), nigro-suiatal (Szentagothai, 1972), reticular (Pompeiano et al., 1971), hypothalamic (Hubel & Wiesel, 1970), mesolimbic (Kuffler, 1969) and cerebellar (High & Low, 1968) pathways have been vainly searched out for a tentative explanation of the YR organization and almost every part of the somesthesic (Pericoloso & Sporgersi, 1973), motor (Ford, 1930), commissural (Gordon & Bogen, 1974) and associative (Einstein et al., 1974) cortices have been found responsible for the progressive building-up of the response although, up-to-now, no decisive demonstration of both the input and output of the YR programming has been convincely advanced.
