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3. Placental hypoxia-induced alterations in vascular function, morphology, and endothelial barrier integrity

6. Central areolar choroidal dystrophy associated with dominantly inherited drusen. (Clinical Science)

9. The 2588G to C mutation in the ABCR gene is a mild frequent founder mutation in the western European population and allows the classification of ABCR mutations in patients with Stargardt disease

23. A Manifesto: An Invitation from the School of Speculative Documentary

41. De nouveaux défis pour la liturgie

42. Transmission Experiments with a Virus Causing Dermatitis and Ulcerative Stomatitis in Cattle in Ruanda-Urundi

43. CONTRALATERAL EFFECTS IN THE ELECTRO-OCULOGRAM

44. Early findings in central areolar choroidal dystrophy

45. FLAT TYPE ELECTRO-OCULOGRAM (EOG)

46. Congenital sensory neuropathy

47. Pattern reversal visual evoked potentials in eyes with macular holes and their fellow eyes

48. Scotopization and pseudoprotanomaly in blue-yellow colour vision defects

49. Reticular dystrophy of the retinal pigment epithelium and choroidal neovascularization A fluorescein and ICGV study

50. RETINAL FUNCTIONS IN DOMINANT CYSTOID MACULAR DYSTROPHY (DCMD)

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