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 *

78 related articles for article (PubMed ID: 5902746)

  • 1. [Neruogenic arthropathies in neural muscular atrophy of Charcotmarietooth].
    Borsari G; Jéquier M
    Rev Med Suisse Romande; 1966 Feb; 86(2):145-55. PubMed ID: 5902746
    [No Abstract]   [Full Text] [Related]  

  • 2. [Late syringomyelic osteoarthropathies and deformities].
    Campailla E
    G Psichiatr Neuropatol; 1967; 95(4):925-43. PubMed ID: 5604263
    [No Abstract]   [Full Text] [Related]  

  • 3. Double Charcot's disease.
    Bruckner FE
    Ann Rheum Dis; 1969 May; 28(3):327. PubMed ID: 5772533
    [No Abstract]   [Full Text] [Related]  

  • 4. [The two siblings of Friedreich's ataxia with proximal neurogenic muscular atrophy (author's transl)].
    Ikeda S; Hanyu N; Oguchi K; Yanagisawa N; Tsukagoshi H
    Rinsho Shinkeigaku; 1980 Apr; 20(4):280-5. PubMed ID: 7408332
    [No Abstract]   [Full Text] [Related]  

  • 5. [Two families of chronic neurogenic proximal muscular atrophy with hyperlipemia (author's transl)].
    Oishi M; Nakajima S; Iwagaki T; Toyoda M; Ebihara S; Gotoh F
    Nervenarzt; 1977 Jul; 48(7):386-90. PubMed ID: 904756
    [No Abstract]   [Full Text] [Related]  

  • 6. Double charcot's disease.
    Bruckner FE
    Br Med J; 1968 Jun; 2(5605):603-4. PubMed ID: 5654630
    [No Abstract]   [Full Text] [Related]  

  • 7. Autosomal dominant late adult spinal muscular atrophy, type Finkel.
    Richieri-Costa A; Rogatko A; Levisky R; Finkel N; Frota-Pessoa O
    Am J Med Genet; 1981; 9(2):119-28. PubMed ID: 7258225
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Rheumatic pelvic spondylitis in a patient with progressive spinal muscular atrophy (Kugelberg-Welander syndrome)].
    Lapadula G; Berlingerio G; Tricarico GC; Amendoni GC
    Minerva Med; 1983 Oct; 74(39):2305-7. PubMed ID: 6606791
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Juvenile spinal muscular atrophy--a new hexosaminidase deficiency phenotype.
    Johnson WG; Wigger HJ; Karp HR; Glaubiger LM; Rowland LP
    Trans Am Neurol Assoc; 1981; 106():215-8. PubMed ID: 7348998
    [No Abstract]   [Full Text] [Related]  

  • 10. [Multiple symmetrical and multistructural arthropathies in a patient with syringomyelia].
    Markiewicz M; Kawiak W; Warpechowska M; Hasiec T
    Wiad Lek; 1984 Mar; 37(6):466-9. PubMed ID: 6485330
    [No Abstract]   [Full Text] [Related]  

  • 11. [HLA system in spinal injury patients with neurogenic para-osteo-arthropathies].
    Minaire P; Betuel H; Pilonchery G
    Nouv Presse Med; 1978 Oct; 7(34):3044. PubMed ID: 364410
    [No Abstract]   [Full Text] [Related]  

  • 12. Heritable spinal muscular atrophies.
    Zellweger H; Schneider HJ; Schuldt DR; Mergner W
    Helv Paediatr Acta; 1969 Feb; 24(1):92-105. PubMed ID: 5801822
    [No Abstract]   [Full Text] [Related]  

  • 13. [Chronic spinal muscular atrophy with predominant affection of distal muscles and muscular hypertrophy (author's transl)].
    Fujimori N; Hanyu N; Oguchi K; Yanagisawa N; Tsukagoshi H
    Rinsho Shinkeigaku; 1980 Jun; 20(6):423-9. PubMed ID: 7408341
    [No Abstract]   [Full Text] [Related]  

  • 14. [Familial male hypogonadism in spinal and bulbar muscular atrophy of late onset (Kennedy's disease). A new cause of hypogonadism].
    Gómez JM; Arbizu T; Santamaría J; Quilez A; Soler J; Peres J
    Arch Esp Urol; 1984; 37(1):49-55. PubMed ID: 6721595
    [No Abstract]   [Full Text] [Related]  

  • 15. [Oculopharyngeal muscular dystrophy with neurogenic muscular atrophy. Syndrome or accidental coincidence? (author's transl)].
    Krause KH; Schmitt HP; Hartmann A
    Nervenarzt; 1981 Feb; 52(2):79-84. PubMed ID: 7219621
    [No Abstract]   [Full Text] [Related]  

  • 16. [A sporadic case of the pareto-amyotrophic form of ulcero-mutilating acropathy].
    Pragier G; Galmiche P
    Rev Rhum Mal Osteoartic; 1966; 33(7):440-4. PubMed ID: 5957358
    [No Abstract]   [Full Text] [Related]  

  • 17. [Chronic progressive external ophthalmoplegia, deafness, neurogenic muscular atrophy and hypergonadotropic hypogonadism (author's transl)].
    Hazama R; Tsujihata M; Mori M; Takamori M; Egami T
    Rinsho Shinkeigaku; 1981 Apr; 21(4):304-10. PubMed ID: 7273535
    [No Abstract]   [Full Text] [Related]  

  • 18. [Swallowing disturbances in Werdning-Hoffman disease].
    Nutman J; Nitzan M; Grünebaum M
    Harefuah; 1981 Dec; 101(11):301-3. PubMed ID: 7341358
    [No Abstract]   [Full Text] [Related]  

  • 19. [Severe oligophrenia with amyotrophia in two brothers one of whom presents poikilodermatomyositis with corneal changes (its place among the neuro-cutaneous dystrophies)].
    Martin L; Hariga J
    J Genet Hum; 1968 Jan; 16(3):71-82. PubMed ID: 5710714
    [No Abstract]   [Full Text] [Related]  

  • 20. Hereditary neurogenic muscular atrophies and allied disorders.
    Dyck PJ; Stillwell GK
    Mod Treat; 1966 Mar; 3(2):254-63. PubMed ID: 5906965
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.