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1. Perspective on Schistosomiasis Drug Discovery: Highlights from a Schistosomiasis Drug Discovery Workshop at Wellcome Collection, London, September 2022

3. Chemotherapy of filariasis – established strategies and new developments

5. Filarial nematode phenotypic screening cascade to identify compounds with anti-parasitic activity for drug discovery optimization

8. Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial

10. Childhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis

13. Estimating the number of breeders from helminth larvae with genomic data

14. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

15. Filariasis research – from basic research to drug development and novel diagnostics, over a decade of research at the Institute for Medical Microbiology, Immunology and Parasitology, Bonn, Germany

16. Correction: A systematic review and an individual patient data meta-analysis of ivermectin use in children weighing less than fifteen kilograms: Is it time to reconsider the current contraindication?

17. Erratum:Correction: A systematic review and an individual patient data meta-analysis of ivermectin use in children weighing less than fifteen kilograms: Is it time to reconsider the current contraindication? (PLoS neglected tropical diseases (2021) 15 3 (e0009144))

18. Erratum: Correction: A systematic review and an individual patient data meta-analysis of ivermectin use in children weighing less than fifteen kilograms: Is it time to reconsider the current contraindication? (PLoS neglected tropical diseases (2021) 15 3 (e0009144))

26. Solving unsolved rare neurological diseases-a Solve-RD viewpoint

27. Doxycycline Leads to Sterility and Enhanced Killing of Female Onchocerca volvulus Worms in an Area With Persistent Microfilaridermia After Repeated Ivermectin Treatment: A Randomized, Placebo-Controlled, Double-Blind Trial

30. Discovery of Substituted Di(pyridin-2-yl)-1,2,4-thiadiazol-5-amines as Novel Macrofilaricidal Compounds for the Treatment of Human Filarial Infections

31. FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum

32. Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

38. Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial

40. Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

41. Correction: Solving unsolved rare neurological diseases : A Solve-RD viewpoint

42. Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

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