1,009 results on '"Pinckers, A."'
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2. Placental hypoxia-induced alterations in vascular function, morphology, and endothelial barrier integrity
3. Placental hypoxia-induced alterations in vascular function, morphology, and endothelial barrier integrity
4. Colour vision in macular gliosis, cysts, holes and oedema: an approach to depth localization
5. Speculative documentary photography
6. Central areolar choroidal dystrophy associated with dominantly inherited drusen. (Clinical Science)
7. Predictive value of pattern VEP, pattern ERG and hole size in macular hole surgery
8. Refined mapping of the gene for autosomal dominant retinitis pigmentosa (RP17) on chromosome 17q22
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
10. Anomaloscope examination in macular gliosis, macular holes and central serous choroidopathy
11. Prognostic value of pattern reversal visual-evoked potentials in idiopathic epiretinal membrane
12. Genetic fine mapping of the gene for recessive Stargardt disease
13. Discriminative power of visual evoked potential characteristics in multiple sclerosis
14. Linkage analysis in a Dutch family with X-linked recessive congenital stationary night blindness (XL-CSNB)
15. Pathologic scotopization: A shortened Nagel-II anomaloscopic micro-screw method
16. Colour vision in retinitis pigmentosa: Influence of cystoid macular edema
17. Influence of pathologic scotopization on the extended Rayleigh Match
18. An analysis of colour vision in 10,000 patients
19. Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type
20. Scotopization and the Nagel-II anomaloscope
21. The electro-oculogram in uveal melanoma: A prospective study
22. Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR gene
23. A Manifesto: An Invitation from the School of Speculative Documentary
24. A Manifesto: An Invitation from the School of Speculative Documentary
25. Two sibs with chorioretinal dystrophy, hypogonadotrophic hypogonadism, and cerebellar ataxia: Boucher-Neuhauser syndrome
26. Stable and Progressive Hearing Loss in Type 2A Usherʼs Syndrome
27. Variable hearing loss in Usher's syndrome type 2a
28. Gyrate Atrophy and Choroidal Neovascularization
29. Juvenile atrophy of pigment epithelium and choriocapillaris
30. Pattern-reversal visual evoked potentials in patients with epiretinal membrane
31. Effect of Steady Hypothermia and Normothermia on Multimodality Evoked Potentials in Human Poikilothermia
32. Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS gene
33. Ocular and systemic manifestations of cerebrotendinous xanthomatosis
34. Null mutation in the human 11- cis retinol dehydrogenase gene associated with fundus albipunctatus
35. Absent Cone Function (a Survey of Clinical Cases)
36. Contralateral Effect in the Electro-Oculogram: Experimental Verification and Clinical Implications
37. The Light-Sensitive Negative Component in Clinical Electrooculography
38. Clinical Color Vision Examination
39. Results of a Shortened Lightness Discrimination Test
40. Colour Vision in Patients Suspected of Intoxication
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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