TY  - JOUR
A1  - Henk, Lars Thorben
T1  - Édouard Louis’ «J’accuse». Ein spätmoderner Adept Zolas?
JF  - promptus - Würzburger Beiträge zur Romanistik
N2  - French history of literature is undoubtedly characterized by a tradition of social criticism portraying the working class’ misery that can be traced back at least to the 19th century. Among these depictions, Zola’s novels have a prominent position. This is, among other aspects, due to their pretended scientific foundation and their pretentious claims to be scientific studies. The contemporary author Édouard Louis situates himself in this tradition of Zola’s naturalism. This invites us to examine the interrelation between Zola and Louis more closely. Based on the common ground of scientific foundation, scientific ambition and social commitment pursued in their novels, it will be demonstrated that Louis is a late-modern Zola whose milieu and character descriptions follow in detail Zola’s constructions.
KW  - Zola
KW  - misery
KW  - literature
KW  - scientific novel
KW  - Louis
Y1  - 2022
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-329777
SN  - 2364-6705
VL  - 8
ER  - 
TY  - THES
A1  - Zink, Jürgen
T1  - Rotpeter als Bororo? - Drei Erzählungen Franz Kafkas vor dem Hintergrund eines "literarischen Primitivismus" um 1900
T1  - -
N2  - No abstract available
KW  - Kafka
KW  - Franz
KW  - Primitivismus
KW  - Mythos
KW  - kafka
KW  - primitivismus
KW  - literatur
KW  - 1900
KW  - kafka
KW  - primitivism
KW  - literature
KW  - 1900
Y1  - 2005
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-17500
ER  - 
TY  - THES
A1  - Linsenmann, Thomas
T1  - Das neonatale Kraniopharyngeom - Ein kasuistischer Beitrag und Literaturübersicht
T1  - Neonatal Craniopharyngioma - A case report and review of the literature
N2  - Das Kraniopharyngeom ist eine dysontogenetische Mittellinienfehlbildung mit raumforderndem Charakter. Die Ätiopathogenese ist noch ungeklärt. Bildgebende Verfahren (Sonographie, MRT) ermöglichen bereits pränatal eine Diagnostik. Das neonatale Kraniopharyngeom ist sehr selten. Bisher finden sich in der Literatur nur wenige Fallberichte von denen operative Verläufe sowie klinische Langzeitverläufe bekannt sind. Es bleibt eine Kontroverse hinsichtlich Radikalität und Zeitpunkt der Operation, nicht aber dahingehend, dass die operationsmikroskopische Versorgung die Therapie der Wahl des neonatalen Kraniopharyngeoms darstellt. Die Nähe zur hypophysären-hypothalamischen Achse bedingt eine hohe Komorbidität der Kinder prä- und postoperativ.
N2  - Craniopharyngioma are embryogenic malformations of the sellar area. With an overall incidence of 0.5–2 new cases per million population per year, 30–50% of all cases occur in childhood.As the survival rate after craniopharyngioma diagnosed during childhood and adolescence is high, prognosis and quality of life in survivors mainly depend on adverse late effects such as hypopituitarism and obesity. Appropriate laboratory diagnostics of endocrine deficiencies and sufficient hormonal substitution have significant impact on prognosis. A review of the literature reveal only some few cases of neonatal craniopharyngioma. Modern picture-giving proceeds such as MRI enable a early diagnosis. On the one hand there is a controversy concerning the radicalness and the time of operation on the other hand the microsurgical resection is meant to be the goldstandard in the therapy of neonatal craniopharyngiomas.
KW  - Neurochirurgie
KW  - Neugeborenes
KW  - NMR-Tomographie
KW  - Hypophyse
KW  - Hypophysenhormon
KW  - pränatal
KW  - Kraniopharyngeom
KW  - pterionaler Zugang
KW  - mikrochirurgische Resektion
KW  - Literatur
KW  - neonatal
KW  - craniopharyngioma
KW  - mri
KW  - ct-scan
KW  - literature
Y1  - 2010
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-49757
ER  -