These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
82 related articles for article (PubMed ID: 5622648)
1. [Skin biopsy and study of urinary amino acids in crystalline ectopies]. Bessière E; Verin P; Le Rebeller MJ Bull Soc Ophtalmol Fr; 1967 Nov; 67(11):1028-31. PubMed ID: 5622648 [No Abstract] [Full Text] [Related]
2. Ocular pathology in homocystinuria. Henkind P; Ashton N Trans Ophthalmol Soc U K (1962); 1965; 85():21-38. PubMed ID: 5227183 [No Abstract] [Full Text] [Related]
3. [Cutaneous biopsy and study of urinary amino acids in crystalline lens ectopia]. Bessière E; Vérin P; Broustet A; Le Rebeller MJ Bull Mem Soc Fr Ophtalmol; 1968; 81():327-34. PubMed ID: 5759755 [No Abstract] [Full Text] [Related]
5. Genetic principles for the ophthalmologist. Jackson LG Trans Pa Acad Ophthalmol Otolaryngol; 1974; 27(1):20-8. PubMed ID: 4826418 [No Abstract] [Full Text] [Related]
7. Plasma cell myeloma and associated amino acid disorder. Case with crystalline deposition in the cornea and lens. Handley GJ; Arney GK Arch Intern Med; 1967 Sep; 120(3):353-5. PubMed ID: 6038294 [No Abstract] [Full Text] [Related]
8. Inborn metabolic disorders with associated ocular lesions in Northern Ireland. Martin VA; Carson NA Trans Ophthalmol Soc U K (1962); 1967; 87():847-70. PubMed ID: 5255262 [No Abstract] [Full Text] [Related]
9. Homocystinuria simulating the Marfan syndrome. Schimke RN; McKusick VA; Pollack AD Trans Assoc Am Physicians; 1965; 78():60-72. PubMed ID: 5864983 [No Abstract] [Full Text] [Related]
10. [Attempted clinical orientation in the diagnosis of amino acid metabolism disorders. I. Urinary symptoms, neuropsychic symptoms and ocular symtpoms]. Boisse J Presse Med (1893); 1968 Apr; 76(19):903-6. PubMed ID: 5645352 [No Abstract] [Full Text] [Related]
11. Ocular manifestations of familial hyperlysinemia. Smith TH; Holland MG; Woody NC Trans Am Acad Ophthalmol Otolaryngol; 1971; 75(2):355-60. PubMed ID: 5557172 [No Abstract] [Full Text] [Related]
12. HOMOCYSTINURIA. STUDIES OF 20 FAMILIES WITH 38 AFFECTED MEMBERS. SCHIMKE RN; MCKUSICK VA; HUANG T; POLLACK AD JAMA; 1965 Aug; 193():711-9. PubMed ID: 14328469 [No Abstract] [Full Text] [Related]
14. [Gene pleiotropism in Marfan's syndrome--analysis of 53 cases]. Mai CK Zhonghua Yan Ke Za Zhi; 1983 Jul; 19(4):231-2. PubMed ID: 6416784 [No Abstract] [Full Text] [Related]
15. Disorders of nitrogen absorption. Silk DB Clin Gastroenterol; 1982 Jan; 11(1):47-72. PubMed ID: 7037240 [No Abstract] [Full Text] [Related]
16. [Metabolism inborn errors and eye manifestations]. François J; Sole P; Rigal D; Rouher F Ann Ocul (Paris); 1972 Mar; 205(3):263-81. PubMed ID: 5053180 [No Abstract] [Full Text] [Related]
17. A new polygenic disturbance: cystinuria, leucinuria and spinal muscular atrophy. Radu H; Tanase-Mogoş I; Roşu AM; Killyen I; Ionescu V J Neurol; 1974; 207(1):73-83. PubMed ID: 4142888 [No Abstract] [Full Text] [Related]
18. [Physiopathology of the crystalline lens]. Skubiszewska T Pol Tyg Lek; 1981 Apr; 36(14):509-11. PubMed ID: 7267425 [No Abstract] [Full Text] [Related]
19. [Type II oculo-cutaneous tyrosinosis]. Gounod N; Ogier H; Dufier JL; Larrègue M; Saudubray JM; de Prost Y Ann Dermatol Venereol; 1984; 111(8):697-8. PubMed ID: 6152137 [No Abstract] [Full Text] [Related]