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5. Nettleship-Falls X-linked ocular albinism with Axenfeld's anomaly. A case report. Hayakawa M; Kato K; Nakajima A; Yoshiike T; Ogawa H Ophthalmic Paediatr Genet; 1986 Aug; 7(2):109-14. PubMed ID: 3785879 [TBL] [Abstract][Full Text] [Related]
6. Oculocutaneous albinism and corneal mesodermal dysgenesis. Ricci B; Lacerra F Am J Ophthalmol; 1981 Oct; 92(4):587. PubMed ID: 7294125 [No Abstract] [Full Text] [Related]
7. [Axenfeld's syndrome with retarded ocular hypertonia]. Arneodo J; Martin GA; Agostini M; Saracco JB Bull Soc Ophtalmol Fr; 1973 Jan; 73(1):165-9. PubMed ID: 4787575 [No Abstract] [Full Text] [Related]
8. Motor nerve conduction velocity in peroneal muscular atrophy: evidence for genetic heterogeneity. Thomas PK; Calne DB J Neurol Neurosurg Psychiatry; 1974 Jan; 37(1):68-75. PubMed ID: 4813428 [TBL] [Abstract][Full Text] [Related]
9. [Histological changes in peripheral nerves in spinal Werdnig-Hoffmann muscular atrophy]. Drac H Neuropatol Pol; 1977; 15(1):1-16. PubMed ID: 840382 [No Abstract] [Full Text] [Related]
10. [Motor nerve conduction velocity in early forms of infantile spinal amyotrophy. Diagnostic problems]. Echenne B; Georgesco M; Dapres G Rev Electroencephalogr Neurophysiol Clin; 1984 Apr; 13(4):329-35. PubMed ID: 6463301 [TBL] [Abstract][Full Text] [Related]
11. [Conduction velocity in peripheral nerves in healthy and sick children]. Ryniewicz B Neurol Neurochir Pol; 1975; 9(6):701-4. PubMed ID: 1202397 [TBL] [Abstract][Full Text] [Related]
12. JUVENILE GLAUCOMA WITH AXENFELD'S SYNDROME: A HISTOLOGIC REPORT. SUGAR HS Am J Ophthalmol; 1965 Jun; 59():1012-9. PubMed ID: 14292709 [No Abstract] [Full Text] [Related]
13. Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography. Buchthal F; Behse F Brain; 1977 Mar; 100 Pt 1():41-66. PubMed ID: 861715 [No Abstract] [Full Text] [Related]
15. [Familial neurogenic amyotrophy, similar to Charcot-Marie-Tooth disease. Clinical and ultrastructural study]. Vital C; Julien J; Vallat JM; Le Blanc M Rev Neurol (Paris); 1970 Jan; 122(1):15-28. PubMed ID: 5433253 [No Abstract] [Full Text] [Related]
16. Axenfeld-Rieger syndrome: a theory of mechanism and distinctions from the iridocorneal endothelial syndrome. Shields MB Trans Am Ophthalmol Soc; 1983; 81():736-84. PubMed ID: 6676983 [TBL] [Abstract][Full Text] [Related]
17. A case of scapulo-tibio-peroneal syndrome. Electromyographic and histoenzymologic considerations. Negri S; Caraceni T; Cornelio F Eur Neurol; 1973; 10(1):31-40. PubMed ID: 4269485 [No Abstract] [Full Text] [Related]
18. Anterior segment and retinal pigmentary abnormalities in arteriohepatic dysplasia. Puklin JE; Riely CA; Simon RM; Cotlier E Ophthalmology; 1981 Apr; 88(4):337-47. PubMed ID: 7254780 [TBL] [Abstract][Full Text] [Related]
19. [Myotonic dystrophy and peroneal muscular atrophy in 2 siblings]. Goldsztajn M; Korohoda J; Stefanko S Neurol Neurochir Pol; 1971; 5(4):575-8. PubMed ID: 5122061 [No Abstract] [Full Text] [Related]