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 *

131 related articles for article (PubMed ID: 3799921)

  • 61. [Nemaline myopathy. General review apropos of 3 cases].
    Pagès M; Ramos J; Pagès AM; Echenne B
    Ann Pathol; 1987; 7(3):216-22. PubMed ID: 3325069
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Fiber density in congenital muscle fiber type disproportion. I. Congenital myopathies.
    Rowińska-Marcińska K; Strugalska MH; Hausmanowa-Petrusewicz I
    Electromyogr Clin Neurophysiol; 1990 Dec; 30(8):475-81. PubMed ID: 2286172
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Muscle histochemistry in congenital muscular dystrophy with central nervous system involvement.
    Nonaka I; Sugita H; Takada K; Kumagai K
    Muscle Nerve; 1982 Feb; 5(2):102-6. PubMed ID: 6461828
    [TBL] [Abstract][Full Text] [Related]  

  • 64. [A case of severe infantile form of congenital nemaline myopathy with extensive fatty replacement of the skeletal muscles].
    Shimizu J; Matsumura K; Noguchi H
    Rinsho Shinkeigaku; 1990 Oct; 30(10):1123-7. PubMed ID: 2177691
    [TBL] [Abstract][Full Text] [Related]  

  • 65. [A case of adult-onset nemaline myopathy (adult-onset rod disease) with distal muscular hypertrophy].
    Mitsui T; Miyata K; Kira J; Kobayashi T; Goto I
    Rinsho Shinkeigaku; 1991 May; 31(5):546-9. PubMed ID: 1657478
    [TBL] [Abstract][Full Text] [Related]  

  • 66. [Congenital muscle fiber disproportion (congenital muscle fiber type 1 fiber atrophy)].
    Szokol M; György I; Soltész M
    Orv Hetil; 1980 Aug; 121(31):1895-8. PubMed ID: 7454302
    [No Abstract]   [Full Text] [Related]  

  • 67. Slow myosin heavy chain isozyme in nemaline myopathy.
    Biral D; Damiani E; Margreth A; Scarpini E; Scarlato G
    Neurology; 1985 Sep; 35(9):1360-3. PubMed ID: 4022386
    [TBL] [Abstract][Full Text] [Related]  

  • 68. [An unusual myopathy: the so-called congenital fiber-type disproportion].
    Lössner J; Ziegan J; Oertel G
    Z Gesamte Inn Med; 1979 Nov; 34(22):685-7. PubMed ID: 549303
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Nemaline (rod) myopathy: the need for histochemical evaluation of affected families.
    Bender AN; Willner JP
    Ann Neurol; 1978 Jul; 4(1):37-42. PubMed ID: 697323
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Congenital myopathy with uniform type 1 fiber predominance and type 2 fiber hypoplasia: report of one case.
    Huang ML; Tsai CH; Lee CC
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1998; 39(1):62-4. PubMed ID: 9553297
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Progressive unilateral hypertrophic myopathy: a case study.
    Pihko H; Lehtinen I; Tikkanen H; Härkönen M; Rapola J; Lamminen A; Sahlman A; Somer H
    Muscle Nerve; 1993 Jan; 16(1):63-8. PubMed ID: 8423834
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Congenital nemaline myopathy with dilated cardiomyopathy: an autopsy study.
    Ishibashi-Ueda H; Imakita M; Yutani C; Takahashi S; Yazawa K; Kamiya T; Nonaka I
    Hum Pathol; 1990 Jan; 21(1):77-82. PubMed ID: 2295510
    [TBL] [Abstract][Full Text] [Related]  

  • 73. [Myopathy of congenital fiber type disproportion. Description of a clinical case].
    Millefiorini E; Paolella P; Antonini G; Millefiorini M
    Riv Neurol; 1984; 54(6):383-9. PubMed ID: 6528207
    [TBL] [Abstract][Full Text] [Related]  

  • 74. [A case of nemaline myopathy studied over a period of nine years (author's transl)].
    Pou-Serradell A; Navarro C
    Rev Neurol (Paris); 1978 Apr; 134(4):295-302. PubMed ID: 725401
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large family.
    Sobrido MJ; Fernández JM; Fontoira E; Pérez-Sousa C; Cabello A; Castro M; Teijeira S; Alvarez S; Mederer S; Rivas E; Seijo-Martínez M; Navarro C
    Brain; 2005 Jul; 128(Pt 7):1716-27. PubMed ID: 15857933
    [TBL] [Abstract][Full Text] [Related]  

  • 76. [Congenital fiber type disproportion associated with aortic coarctation complex: a case report].
    Noda Y; Aoki Y; Ishikita T; Tada H; Morooka K; Saji T; Matsuo N
    No To Hattatsu; 1990 Jan; 22(1):88-90. PubMed ID: 2294956
    [No Abstract]   [Full Text] [Related]  

  • 77. Congenital myopathy with mosaic fibers and interlacing sarcomeres: a new structural myopathy.
    Marbini A; Gemignani F; Badiali L; Bellanova MF; Margarito F
    Acta Neuropathol; 1998 Dec; 96(6):643-50. PubMed ID: 9845295
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Clinical course correlates poorly with muscle pathology in nemaline myopathy.
    Ryan MM; Ilkovski B; Strickland CD; Schnell C; Sanoudou D; Midgett C; Houston R; Muirhead D; Dennett X; Shield LK; De Girolami U; Iannaccone ST; Laing NG; North KN; Beggs AH
    Neurology; 2003 Feb; 60(4):665-73. PubMed ID: 12601110
    [TBL] [Abstract][Full Text] [Related]  

  • 79. [Nemaline myopathy (congenital rod disease) - clinical picture, histology, and histochemistry].
    Voncina D; Tivadar I; Dekleva A
    Neurologija; 1978; 26(1-4):169-74. PubMed ID: 754016
    [No Abstract]   [Full Text] [Related]  

  • 80. [Neonatal hypotonias with congenital disproportion of various types of muscular fiber, especially type I fibers. Demonstration of the familial character of this new entity].
    Fardeau M; Harpey JP; Caille B; Lafourcade J
    Arch Fr Pediatr; 1975 Dec; 32(10):901-13. PubMed ID: 1231675
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.