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Insect Science|May 12, 2025
Functional validation of a white pupae minimal gene construct in Ceratitis capitata (Diptera: Tephritidae)Lucas Henrique Figueiredo Prates, Roswitha A Aumann, Inga Sievers, et al.
Laryngo- Rhino- Otologie|April 9, 2020
[Cervical lymphadenitis caused by non-tuberculous mycobacteria in children with different residence]Efstathios Papatsoutsos, Volker Aumann, Peter Vorwerk, et al.
European Journal of Pediatrics|April 1, 1997
Final height and puberty in 40 patients after antileukaemic treatment during childhoodK Mohnike, W Dörffel, J Timme, et al.
Cancer Medicine|November 24, 2021
Dose-adjusted EPOCH-R is not superior to sequential R-CHOP/R-ICE as a frontline treatment for newly diagnosed primary mediastinal B-cell lymphoma: Results of a bi-center retrospective studyYael Morgenstern, Shlomzion Aumann, Neta Goldschmidt, et al.
Infection|October 14, 2003
Influenza B pneumonia with Staphylococcus aureus superinfection associated with parvovirus B19 and concomitant agranulocytosisS Krell, I Adams, U Arnold, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1990
Prospective study on the influence of radiochemotherapy on pituitary function in children with acute leukaemia and NHLU Kluba, U Mittler, K Mohnike, et al.
BMC Biotechnology|February 2, 2024
Deep orange gene editing triggers temperature-sensitive lethal phenotypes in Ceratitis capitataGermano Sollazzo, Katerina Nikolouli, Georgia Gouvi, et al.
The Canadian Veterinary Journal = La Revue Veterinaire Canadienne|January 26, 2026
Identification of botulism C/D in 2 dogs <i>via</i> polymerase chain reactionAlexandre Dubois, Antoine Chamagne, Caroline Le Maréchal, et al.
Sleep|June 5, 2013
Differential effects on fast and slow spindle activity, and the sleep slow oscillation in humans with carbamazepine and flunarizine to antagonize voltage-dependent Na+ and Ca2+ channel activityAmr Ayoub, Dominic Aumann, Anne Hörschelmann, et al.
The Journal of Clinical Endocrinology and Metabolism|January 15, 2002
Congenital secondary hypothyroidism caused by exon skipping due to a homozygous donor splice site mutation in the TSHbeta-subunit geneJoachim Pohlenz, Alexandra Dumitrescu, Ulrich Aumann, et al.
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