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 *

276 related articles for article (PubMed ID: 13312732)

  • 21. Muscular dystrophy in Northern Ireland. III. Linkage data with particular reference to autosomal limb girdle muscular dystrophy.
    STEVENSON AC; CHEESEMAN EA
    Ann Hum Genet; 1955 Feb; 19(3):165-73. PubMed ID: 14350450
    [No Abstract]   [Full Text] [Related]  

  • 22. [Heart involvement in progressive spinal muscular atrophy. A review of the literature and case histories in childhood].
    Distefano G; Sciacca P; Parisi MG; Parano E; Smilari P; Marletta M; Fiumara A
    Pediatr Med Chir; 1994; 16(2):125-8. PubMed ID: 8078785
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Statistical considerations in the study of spinal muscular atrophy. Dallas-Cincinnati-Newington Spinal Muscular Atrophy (DCN-SMA) Study Group.
    Buncher CR; Samaha F; Iannaccone ST; Russman BS; Cook JD; White M; McLaughlin C
    Muscle Nerve; 1990; 13 Suppl():S45-8. PubMed ID: 2233886
    [No Abstract]   [Full Text] [Related]  

  • 24. Discrimination between neuropathy and myopathy by use of magnetic resonance imaging.
    Suput D; Zupan A; Sepe A; Demsar F
    Acta Neurol Scand; 1993 Feb; 87(2):118-23. PubMed ID: 8442395
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Type III spinal muscular atrophy mimicking muscular dystrophies.
    Alsaman AS; Alshaikh NM
    Pediatr Neurol; 2013 May; 48(5):363-6. PubMed ID: 23583053
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Spinal muscular atrophy with respiratory distress type 1 (SMARD1).
    Kaindl AM; Guenther UP; Rudnik-Schöneborn S; Varon R; Zerres K; Schuelke M; Hübner C; von Au K
    J Child Neurol; 2008 Feb; 23(2):199-204. PubMed ID: 18263757
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Congenital segmental spinal muscular atrophy: a case report.
    Savaş T; Erol I; Özkale Y; Saygi S
    J Child Neurol; 2015 Mar; 30(4):509-12. PubMed ID: 25300987
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Muscular dystrophy in childhood; the genetic aspect; a field study in the Leeds region of clinical types and their inheritance.
    BLYTH H; PUGH RJ
    Ann Hum Genet; 1959 Apr; 23(2):127-63. PubMed ID: 13637556
    [No Abstract]   [Full Text] [Related]  

  • 29. [Contribution to the study of heredity in progressive muscular dystrophy].
    PESCETTO G; FABIANI D
    Sist Nerv; 1959; 11():383-9. PubMed ID: 14432114
    [No Abstract]   [Full Text] [Related]  

  • 30. Benign progressive muscular dystrophy; description of a curious family.
    KRAFT TB
    Folia Psychiatr Neurol Neurochir Neerl; 1955 Jun; 58(3):175-86. PubMed ID: 13262229
    [No Abstract]   [Full Text] [Related]  

  • 31. Xp21 DNA probe in diagnosis of muscular dystrophy and spinal muscular atrophy.
    Clarke A; Davies KE; Gardner-Medwin D; Burn J; Hudgson P
    Lancet; 1989 Feb; 1(8635):443. PubMed ID: 2563824
    [No Abstract]   [Full Text] [Related]  

  • 32. [Combined transmission of three different hereditary diseases in the same family (deforming juvenile osteochondrosis of the hip, hypoplasia of the femur, progressive muscular dystrophy)].
    PFANDLER U
    J Genet Hum; 1952 May; 1(1):56-82. PubMed ID: 12981241
    [No Abstract]   [Full Text] [Related]  

  • 33. [Catamnestic inquiries in conditions of hypertonia in early childhood. With a critical contribution to the differential diagnosis of infantile spinal progressive muscular atrophy (Werdnig-Hoffman disease--myatonia congenital Oppenheilm)].
    HORSTMANN W
    Z Kinderheilkd; 1959; 82():649-67. PubMed ID: 13848453
    [No Abstract]   [Full Text] [Related]  

  • 34. [Progressive muscular dystrophy].
    FRIEDERICHS HF; KIRNBERGER EJ
    Munch Med Wochenschr; 1958 Sep; 100(38):1444-6. PubMed ID: 13590029
    [No Abstract]   [Full Text] [Related]  

  • 35. [Progressive muscular dystrophy].
    SCHADE H
    Munch Med Wochenschr; 1958 Apr; 100(15):595-7. PubMed ID: 13552675
    [No Abstract]   [Full Text] [Related]  

  • 36. [Apropos of heredofamilial juvenile muscular atrophy].
    HAUSMANOWA-PETRUSEWICZ I; SOBKOWICZ H; ZIELINSKA S; DOBOSZ I
    Schweiz Arch Neurol Neurochir Psychiatr; 1962; 90():255-67. PubMed ID: 13961045
    [No Abstract]   [Full Text] [Related]  

  • 37. [Estimation of mutation rate in muscular dystrophy].
    BECKER PE; LENZ F
    Z Mensch Vererb Konstitutionsl; 1955; 33(1):42-56. PubMed ID: 13248061
    [No Abstract]   [Full Text] [Related]  

  • 38. Duchenne muscular dystrophy and spinal muscular atrophy type I segregating in the same family.
    Oldfors A; Martinsson T; Tessin I; Wahlström J; Wang S
    Clin Genet; 1994 Feb; 45(2):97-103. PubMed ID: 8004806
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [A new x-chromosomal muscular dystrophy].
    BECKER PE; KIENER F
    Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr; 1955; 193(4):427-48. PubMed ID: 13249581
    [No Abstract]   [Full Text] [Related]  

  • 40. Muscular dystrophy in Northern Ireland. II. An account of nine additional families.
    STEVENSON AC
    Ann Hum Genet; 1955 Feb; 19(3):159-64. PubMed ID: 14350449
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.