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Journal Abstract Search
92 related items for PubMed ID: 1290871
21. Color vison deficiency among medical students: an unnoticed problem. Pramanik T, Sherpa MT, Shrestha R. Nepal Med Coll J; 2010 Jun; 12(2):81-3. PubMed ID: 21222402 [Abstract] [Full Text] [Related]
22. Colour vision, ophthalmological and linkage studies in a pedigree with a tritan defect. Went LN, Völker-Dieben H, de Vries-de Mol EC. Mod Probl Ophthalmol; 1974 Jun; 13(0):272-6. PubMed ID: 4548144 [No Abstract] [Full Text] [Related]
23. Color vision screening for individuals with intellectual disabilities: a comparison between the Neitz Test of Color Vision and Color Vision Testing Made Easy. Barnhardt C, Block SS, Deemer B, Calder AJ, DeLand P. Optometry; 2006 May; 77(5):211-6. PubMed ID: 16651210 [Abstract] [Full Text] [Related]
24. Comparative colour vision and other ophthalmological studies in three families with dominant inherited juvenile optic atrophy. Völker-Dieben HJ, Went LN, de Vries-de Mol EC. Mod Probl Ophthalmol; 1974 May; 13(0):277-81. PubMed ID: 4548145 [No Abstract] [Full Text] [Related]
25. Colour blindness. Gordon N. Public Health; 1998 Mar; 112(2):81-4. PubMed ID: 9581449 [Abstract] [Full Text] [Related]
26. An informative large pedigree with four compound hemizygotes of three combinations of deutan and protan genes. Arias S, Rodríguez A. Acta Cient Venez; 1973 Mar; 24(2):44-52. PubMed ID: 4549004 [No Abstract] [Full Text] [Related]
27. Genealogical studies on interesting families of defective colour vision discovered by a mass examination in Japan and Formosa. Ichikawa H, Majima A. Mod Probl Ophthalmol; 1974 Mar; 13(0):265-71. PubMed ID: 4548143 [No Abstract] [Full Text] [Related]
32. Frequency of colour vision deficiencies in melanoma patients: results of a prospective comparative screening study with the Farnsworth panel D 15 test including 300 melanoma patients and 100 healthy controls. Pföhler C, Tschöp S, König J, Rass K, Tilgen W. Melanoma Res; 2006 Oct; 16(5):413-21. PubMed ID: 17013090 [Abstract] [Full Text] [Related]
33. Genetics of colour vision. Went LN, de Vries-de Mol EC. Mod Probl Ophthalmol; 1976 Oct; 17():96-107. PubMed ID: 1085897 [No Abstract] [Full Text] [Related]
34. A novel mutation in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defect. Gunther KL, Neitz J, Neitz M. Vis Neurosci; 2006 Oct; 23(3-4):403-9. PubMed ID: 16961973 [Abstract] [Full Text] [Related]
35. [Dominant transmitted optic atrophy combined with red-green-blindness in the sense of an acquired deutero disorder]. Früh D, Lauer HJ. Ber Zusammenkunft Dtsch Ophthalmol Ges; 1972 Oct; 71():517-22. PubMed ID: 4542560 [No Abstract] [Full Text] [Related]
36. The at-risk student: a study of visits to the school nurse. Moeckly E, Hansen MC. J Sch Nurs; 1994 Dec; 10(4):15-8. PubMed ID: 7873906 [Abstract] [Full Text] [Related]
37. [Early detection of color blindness from the viewpoint of occupational medicine with various references to internistic and human genetic symptom complexes]. Ebéné RT. Fortschr Med; 1983 Jan 20; 101(3):51-4. PubMed ID: 6600702 [Abstract] [Full Text] [Related]
38. Colour blindness--a rural prevalence survey. Natu M. Indian J Ophthalmol; 1987 Jan 20; 35(2):71-3. PubMed ID: 3502467 [No Abstract] [Full Text] [Related]
39. [Color vision defects in alcoholic women and their relatives]. Cruz-Coke R, Rivera L, Kattan L, Mardones J. Rev Med Chil; 1971 Feb 20; 99(2):118-24. PubMed ID: 5314541 [No Abstract] [Full Text] [Related]
40. Vision screening of school age children in Missouri. Waigandt A, Brown J, Waigandt M, McDougall J, Brand R. J Am Optom Assoc; 1989 Aug 20; 60(8):596-600. PubMed ID: 2794329 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]