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7. Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis

12. Non-invasive intracranial pressure monitoring for high-grade gliomas patients treated with radiotherapy: results of the GMaPIC trial.

23. Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome

24. CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival

25. Preserved Auditory Steady State Response and Envelope-Following Response in Severe Brainstem Dysfunction Highlight the Need for Cross-Checking.

26. Les auteurs

30. NOS1 mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits: reversal with NO therapy in infantile mice

31. NOS1 mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile mice

35. Nitric Oxide deficiency linking a defective minipuberty to the appearance of comorbidities: new therapeutic possibilities

36. Recherche sur les impacts du bruit des éoliennes sur l'Humain : son, perception, santé (RIBEolH)

37. Programming cochlear implants with artificial intelligence

38. Collaborateurs

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