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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 4213898)

  • 1. The familial association of neurofibromatosis, peroneal muscular atrophy, congenital deafness, partial albinism, and Axenfeld's defect.
    Bradley WG; Richardson J; Frew IJ
    Brain; 1974 Sep; 97(3):521-32. PubMed ID: 4213898
    [No Abstract]   [Full Text] [Related]  

  • 2. Peripheral neurofibromatosis and peroneal muscular atrophy.
    Bosch EP; Murphy MJ; Cancilla PA
    Neurology; 1981 Nov; 31(11):1408-14. PubMed ID: 6796901
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Case of Axenfeld's anomaly with juvenile glaucoma].
    Mielnikowa T; Dalkowska A; KruszyƄska M
    Klin Oczna; 1971; 41(2):247-51. PubMed ID: 5575395
    [No Abstract]   [Full Text] [Related]  

  • 4. Peroneal muscular atrophy with autosomal dominant inheritance.
    McLeod JG; Low PA
    Clin Exp Neurol; 1977; 14():142-53. PubMed ID: 616594
    [TBL] [Abstract][Full Text] [Related]  

  • 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]  

  • 14. Posterior embryotoxin (Axenfeld's syndrome).
    Hamed HH
    Bull Ophthalmol Soc Egypt; 1968; 61(65):147-8. PubMed ID: 5309781
    [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]  

  • 20. [Congenital glaucoma-juvenile glaucoma].
    Weekers R; Prijot E
    Arch Ophtalmol Rev Gen Ophtalmol; 1974 May; 34(5):437-44. PubMed ID: 4280897
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.