86,661 research outputs found
Computerunterstützte Erkennung von Stoffwechselerkrankungen
No full textHofestädt R, Herre H, Trefz F. Computerunterstützte Erkennung von Stoffwechselerkrankungen. Informatik-Berichte. Vol 9. Leipzig: Universität Leipzig; 1996
RAMEDIS: Vernetzte Forschung am Beispiel angeborener Stoffwechselerkrankungen.
No full textTöpel T, Mischke U, Scheible D, Trefz F, Hofestädt R. RAMEDIS: Vernetzte Forschung am Beispiel angeborener Stoffwechselerkrankungen. Informatik, Biometrie und Epidemiologie in Medizin und Biologie. 2002;33(2 - 3):79-80
Supporting genotype-phenotype correlation with the rare metabolic diseases database Ramedis
No full textTöpel T, Scholz U, Mischke U, Scheible D, Hofestädt R, Trefz F. Supporting genotype-phenotype correlation with the rare metabolic diseases database Ramedis. Silico Biology. 2002;2:36
METAGENE and RAMEDIS: databases for metabolic diseases and patients with inborn errors on metabolism
No full textTrefz F, Scheible D, Götz H, Töpel T, Hofestädt R, Frauendienst-Egger G. METAGENE and RAMEDIS: databases for metabolic diseases and patients with inborn errors on metabolism. Journal of Inherited Metabolic Disease. 2008;31:289
Harnstoffzykluserkrankungen und Organoazidämien: Aufnahme in das erweiterte Neugeborenen-Screening?
No full textTrefz FK, Scheible D, Frauendienst-Egger G, et al. Harnstoffzykluserkrankungen und Organoazidämien: Aufnahme in das erweiterte Neugeborenen-Screening? Pädiatrie hautnah,. 2005;17(8):19-20
www.ramedis.de: Database for long term follow up of patients with rare metabolic diseases
No full textTrefz FK, Töpel T, Scheible D, Frauendienst-Egger G, Hofestädt R. www.ramedis.de: Database for long term follow up of patients with rare metabolic diseases. JOURNAL OF INHERITED METABOLIC DISEASE. 2006;29(Suppl. 1):84
Expanded newborn screening: Long-term follow up of 63 patients screened by tandem mass spectrometry
No full textScheible D, Töpel T, Frauendienst-Egger G, Hofestädt R, Wallner S, Trefz FK. Expanded newborn screening: Long-term follow up of 63 patients screened by tandem mass spectrometry. JOURNAL OF INHERITED METABOLIC DISEASE. 2007;30(Suppl. 1):3
Expanded newborn screening: Long term follow up of 25 patients with organic acidemias and urea cycle disorders
No full textTrefz FK, Töpel T, Scheible D, Frauendienst-Egger G, Hofestädt R. Expanded newborn screening: Long term follow up of 25 patients with organic acidemias and urea cycle disorders. JOURNAL OF INHERITED METABOLIC DISEASE. 2006;29(Suppl. 1):84
RAMEDIS - Rare Metabolic Diseases Publishing Tool for Genotype-Phenotype Correlation
No full textHofestädt R, Mischke U, Scholz U, Töpel T, Scheible D, Trefz FK. RAMEDIS - Rare Metabolic Diseases Publishing Tool for Genotype-Phenotype Correlation. In: Patel VL, ed. Proceedings of the 10th World Congress on Medical Informatics. Studies in health technology and informatics. Vol 84. Amsterdam: IOS Press; 2001: 970-974
Variations on the Author
No full text“Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship
- …
