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 *

103 related articles for article (PubMed ID: 5417642)

  • 1. Optic atrophy, neural deafness, and distal neurogenic amyotrophy; report of a family with two affected siblings.
    Iwashita H; Inoue N; Araki S; Kuroiwa Y
    Arch Neurol; 1970 Apr; 22(4):357-64. PubMed ID: 5417642
    [No Abstract]   [Full Text] [Related]  

  • 2. Optico-acoustic atrophy in distal spinal muscular atrophy.
    Chalmers N; Mitchell JD
    J Neurol Neurosurg Psychiatry; 1987 Feb; 50(2):238-9. PubMed ID: 3572444
    [No Abstract]   [Full Text] [Related]  

  • 3. Familial opticoacoustic nerve degeneration and polyneuropathy.
    Rosenberg RN; Chutorian A
    Neurology; 1967 Sep; 17(9):827-32. PubMed ID: 6069085
    [No Abstract]   [Full Text] [Related]  

  • 4. Familial optic and acoustic nerve degeneration with distal amyotrophy.
    Iwashita H; Inoue N; Kuroiwa Y
    Lancet; 1969 Jul; 2(7613):219-20. PubMed ID: 4183781
    [No Abstract]   [Full Text] [Related]  

  • 5. Charcot-Marie-Tooth disease with Leber optic atrophy.
    McLeod JG; Low PA; Morgan JA
    Neurology; 1978 Feb; 28(2):179-84. PubMed ID: 563998
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Charcot-Marie amyotrophy associated with bilateral optic atrophy and diabetes].
    Giordano C; Bertrand E; Barabe P; Bizouard P
    Med Trop (Mars); 1969; 29(6):720-4. PubMed ID: 5403110
    [No Abstract]   [Full Text] [Related]  

  • 7. Monomelic amyotrophy in siblings.
    Gücüyener K; Aysun S; Topaloglu H; Inan L; Varli K
    Pediatr Neurol; 1991; 7(3):220-2. PubMed ID: 1878104
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Spinocerebellar ataxia associated with localized amyotrophy of the hands, sensorineural deafness and spastic paraparesis in two brothers.
    Gemignani F
    J Neurogenet; 1986 Mar; 3(2):125-33. PubMed ID: 3958822
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A family with Charcot-Marie-Tooth disease and Leber's optic atrophy.
    McLeod JG; Low PA; Morgan JA
    Proc Aust Assoc Neurol; 1975; 12():23-5. PubMed ID: 1215391
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The autosomal dominant syndrome of progressive optic atrophy and congenital deafness.
    Kollarits CR; Pinheiro ML; Swann ER; Marcus DF; Corrie WS
    Am J Ophthalmol; 1979 Jun; 87(6):789-92. PubMed ID: 453309
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Familial ataxia with peroneal muscular atrophy and optic atrophy].
    Bernabo' Brea G; Rathschüler R; Rasore-Quartino A
    Riv Otoneurooftalmol; 1966; 41(4):273-90. PubMed ID: 5991731
    [No Abstract]   [Full Text] [Related]  

  • 12. [Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD syndrome) in 2 siblings].
    Rybakowa M; Wisłocka E; Sołtysik-Wilk E; Pleti M; Bedkowska A
    Endokrynol Pol; 1983; 34(5):337-42. PubMed ID: 6671470
    [No Abstract]   [Full Text] [Related]  

  • 13. [Juvenile diabetes mellitus associated with optic nerve atrophy and neurogenic deafness. Description of 2 cases].
    Della Porta G; De Ritis L
    Minerva Pediatr; 1977 Sep; 29(29):1799-801. PubMed ID: 927400
    [No Abstract]   [Full Text] [Related]  

  • 14. Autosomal dominant cerebellar ataxia with deafness, myoclonus and amyotrophy.
    Melo TP; Ferro JM
    J Neurol Neurosurg Psychiatry; 1989 Dec; 52(12):1448-9. PubMed ID: 2614456
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. [Familial syndrome of diabetes mellitus, primary optic nerve atrophy and inner-ear deafness].
    Sauer H; Chüden H; Gottesbüren H; Schmitz-Valckenberg P; Seitz D
    Dtsch Med Wochenschr; 1973 Feb; 98(6):243-55. PubMed ID: 4684648
    [No Abstract]   [Full Text] [Related]  

  • 17. Behr's syndrome: familial optic atrophy, spastic diplegia and ataxia.
    Landrigan PJ; Berenberg W; Bresnan M
    Dev Med Child Neurol; 1973 Feb; 15(1):41-7. PubMed ID: 4354046
    [No Abstract]   [Full Text] [Related]  

  • 18. HLA type and islet cell antibody status in family with (diabetes insipidus and mellitus, optic atrophy, and deafness) DIDMOAD syndrome.
    Monson JP; Boucher BJ
    Lancet; 1983 Jun; 1(8336):1286-7. PubMed ID: 6134087
    [No Abstract]   [Full Text] [Related]  

  • 19. [CHARCOT-MARIE AMYOTROPHY ASSOCIATED WITH A BILATERAL OPTIC ATROPHY].
    SERRATRICE G; TATOSSIAN A; POINSO Y
    Presse Med (1893); 1964 Oct; 72():2535-6. PubMed ID: 14191631
    [No Abstract]   [Full Text] [Related]  

  • 20. A family with neurogenic atrophy of the distal muscles of the upper limbs: clinical and electrophysiological studies.
    Vignaendra V; Ghee T
    Med J Aust; 1976 Oct; 2(17):639-41. PubMed ID: 994976
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.