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25. [Intrinsic unilateral paralysis of the third pair; regressive evolution with secondary Argyll Robertson pupil sign]. POURSINES Y; ALLIEZ J Rev Otoneuroophtalmol; 1954; 26(2):85-6. PubMed ID: 13225290 [No Abstract] [Full Text] [Related]
26. [Argyll-Robertson and other pupillary abnormalities in neurosyphilis--with special reference to the detection of peripheral lesions]. Okada F Hokkaido Igaku Zasshi; 1983 May; 58(3):265-70. PubMed ID: 6137444 [TBL] [Abstract][Full Text] [Related]
27. [The man behind the syndrome: Douglas Argyll Robertson. He started the debate on the Argyll Robertson pupil--a peculiar ocular condition, not yet completely clarified]. Hörnsten G Lakartidningen; 1986 Jul; 83(30-31):2566-7. PubMed ID: 3528716 [No Abstract] [Full Text] [Related]
30. Argyll Robertson: 'twas better to be his pupil than to have his pupil. Ravin JG Ophthalmology; 1998 May; 105(5):867-70. PubMed ID: 9593389 [TBL] [Abstract][Full Text] [Related]
31. Denial of blindness and Argyll Robertson pupils without syphilis; report of case. LUTT CJ Bull Los Angel Neuro Soc; 1947 Dec; 12(4):189-91. PubMed ID: 20273041 [No Abstract] [Full Text] [Related]
32. [The sign of Argyll-Robertson in the multiple sclé rose]. ROUQUES L; VOISIN J; PAUTRAT J Bull Mem Soc Med Hop Paris; 1948 May 7-; 64(16-17):474-8. PubMed ID: 18107825 [No Abstract] [Full Text] [Related]
33. [Unilateral Argyll-Robertson sign, a sequel of paralysis of the common oculomotor nerve]. THIEBAUT F; MATAVULJ N Rev Otoneuroophtalmol; 1957; 29(4):253-4. PubMed ID: 13518925 [No Abstract] [Full Text] [Related]
34. [Clinical, histologic and genealogic aspects of Déjerine-Sottas disease]. CREUTZFELDT HG; CURTIUS F; KRUGER KH Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr; 1951; 186(4):341-60. PubMed ID: 14857718 [No Abstract] [Full Text] [Related]
35. Argyll-Robertson-like pupils in the neural type of Charcot-Marie-Tooth disease. Salisachs P; Lapresle J Eur Neurol; 1977; 16(1-6):172-5. PubMed ID: 615709 [TBL] [Abstract][Full Text] [Related]
36. [Two cases for diagnosis: Charcot-Maris amyotrophia or interstitial hypertrophic neuritis?]. THEVENARD A; BERDET H Rev Neurol (Paris); 1958 May; 98(5):416-9. PubMed ID: 13579821 [No Abstract] [Full Text] [Related]
37. [SIGN OF ARGYLL-ROBERTSON OF NON-SPECIFIC ETIOLOGY IN THE COURSE OF DIABETIC NEUROPATHY]. LINQUETTE M; FOSSATI P; LUEZ G; DECOULX M; WOILLEZ M Diabete; 1964; 12():269-74. PubMed ID: 14238766 [No Abstract] [Full Text] [Related]
38. [Tumors of the mesencephalon and ocular symptomatology; considerations on the etiological value of the Argyll Robertson sign]. LASIERRA PA; SANCHEZ ARROYO J Hisp Med; 1955 Apr; 12(130):147-54. PubMed ID: 13242039 [No Abstract] [Full Text] [Related]
39. [Formation of "onion bulbs" in Charcot-Marie-Tooth and Dejerine-Sottas hypertrophic neuropathies]. Jedrzejowska H; Drac H; Sawicka E Neuropatol Pol; 1975; 13(1):93-106. PubMed ID: 1118064 [No Abstract] [Full Text] [Related]
40. Monocular elevator paresis, Argyll Robertson pupils and sarcoidosis. Kirkham TH; Kline LB Can J Ophthalmol; 1976 Oct; 11(4):330-5. PubMed ID: 974857 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]