BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

68 related articles for article (PubMed ID: 5980428)

  • 1. Clinicopathologic conference.
    Tex Med; 1966 Dec; 62(12):82-90. PubMed ID: 5980428
    [No Abstract]   [Full Text] [Related]  

  • 2. Myotonic dystrophy with no trinucleotide repeat expansion.
    Thornton CA; Griggs RC; Moxley RT
    Ann Neurol; 1994 Mar; 35(3):269-72. PubMed ID: 8122879
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Neonatal form of myotonic dystrophy].
    Romero González J; Barrio Andrés C; Mateos Beato F; Salcedo Posadas A
    An Esp Pediatr; 1985 Mar; 22(4):328-31. PubMed ID: 4003959
    [No Abstract]   [Full Text] [Related]  

  • 4. [Myotonic dystrophy].
    Nesterov LN; Sushcheva GP; Viatkina SIa; Nesterova IM
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1983; 83(11):1636-41. PubMed ID: 6232784
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Anicteric cholestasis: an unusual presentation of myotonic dystrophy.
    Syn WK; Palejwala AA
    Intern Med J; 2009 Mar; 39(3):206-7. PubMed ID: 19383073
    [No Abstract]   [Full Text] [Related]  

  • 6. Myotonia dystrophica (a case report).
    Misra R; Misra NP
    J Assoc Physicians India; 1981 Jul; 29(7):569-72. PubMed ID: 7328082
    [No Abstract]   [Full Text] [Related]  

  • 7. Presentation of myotonic dystrophy.
    Smith DL
    Br J Hosp Med; 1993 Dec 15-1994 Jan 18; 50(11):684. PubMed ID: 8124557
    [No Abstract]   [Full Text] [Related]  

  • 8. Myotonic dystrophy in infancy and childhood.
    Hanson PA
    Pediatr Ann; 1984 Feb; 13(2):123-4, 126. PubMed ID: 6709403
    [No Abstract]   [Full Text] [Related]  

  • 9. Proximal myotonic myopathy syndrome in the absence of trinucleotide repeat expansions.
    Stoll G; von Giesen HJ; Koch MC; Arendt G; Benecke R
    Muscle Nerve; 1995 Jul; 18(7):782-3. PubMed ID: 7783769
    [No Abstract]   [Full Text] [Related]  

  • 10. Batten disease: ocular features, differential diagnosis and diagnosis by enzyme analysis.
    Zeman W
    Birth Defects Orig Artic Ser; 1976; 12(3):441-53. PubMed ID: 782600
    [No Abstract]   [Full Text] [Related]  

  • 11. The cataract pateint with myotonic dystrophy.
    Van Dyk HJ; Swan KC
    Trans Am Acad Ophthalmol Otolaryngol; 1967; 71(5):838-46. PubMed ID: 6066202
    [No Abstract]   [Full Text] [Related]  

  • 12. [XXII. Boeck's disease in the differential diagnosis of degenerative muscular diseases].
    Bock HE; Gayer J; Müller G; Nieth H
    Med Welt; 1966 Apr; 17():984-6. PubMed ID: 5985778
    [No Abstract]   [Full Text] [Related]  

  • 13. [Value of myometric findings in the morphological differential diagnosis of neuromuscular disorders (author's transl)].
    Pongratz D
    Microsc Acta Suppl; 1980; Suppl 4():38-43. PubMed ID: 6931279
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Psychopathology: a primary feature of myotonic dystrophy.
    Ambrosini PG; Nurnberg HG
    Psychosomatics; 1979 Jun; 20(6):393-5, 398-9. PubMed ID: 515321
    [No Abstract]   [Full Text] [Related]  

  • 15. [Global cardiac insufficiency initiating myocardial infarction in Steinert's disease].
    Heraudeau A; Page A; Guyot JC; Monie J; Besson I; Caze MC; Pouget-Abadie JF
    Ann Cardiol Angeiol (Paris); 1983 May; 32(3):187-90. PubMed ID: 6614812
    [No Abstract]   [Full Text] [Related]  

  • 16. Myotonia atrophica.
    Mil Med; 1968 Sep; 133(9):722 passim. PubMed ID: 4977103
    [No Abstract]   [Full Text] [Related]  

  • 17. Proximal myotonic myopathy.
    Moxley RT; Ricker K
    Muscle Nerve; 1995 May; 18(5):557-8. PubMed ID: 7739648
    [No Abstract]   [Full Text] [Related]  

  • 18. [Maxillofacial manifestations of Steinert's myotonic dystrophy. Clinical and therapeutic aspects].
    Mercier J; Bennani F; Ferri J; Piot B
    Rev Stomatol Chir Maxillofac; 1995; 96(2):74-82. PubMed ID: 7732325
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Shank sign in myotonic dystrophy type-1 (DM-1).
    Pradhan S
    J Clin Neurosci; 2007 Jan; 14(1):27-32. PubMed ID: 17092719
    [TBL] [Abstract][Full Text] [Related]  

  • 20. New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2).
    Sallinen R; Vihola A; Bachinski LL; Huoponen K; Haapasalo H; Hackman P; Zhang S; Sirito M; Kalimo H; Meola G; Horelli-Kuitunen N; Wessman M; Krahe R; Udd B
    Neuromuscul Disord; 2004 Apr; 14(4):274-83. PubMed ID: 15019706
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.