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 *

145 related articles for article (PubMed ID: 9134190)

  • 1. The spectrum of arthrogryposis in 33 chinese children.
    Wong V
    Brain Dev; 1997 Apr; 19(3):187-96. PubMed ID: 9134190
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Congenital muscular dystrophy associated with lethal arthrogryposis multiplex congenita.
    Moerman P; Fryns JP; Van Dijck H; Lauweryns JM
    Virchows Arch A Pathol Anat Histopathol; 1985; 408(1):43-8. PubMed ID: 3933170
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Lethal congenital muscular dystrophy with arthrogryposis multiplex congenita: three new cases and review of the literature.
    Sombekke BH; Molenaar WM; van Essen AJ; Schoots CJ
    Pediatr Pathol; 1994; 14(2):277-85. PubMed ID: 8008690
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Arthrogryposis multiplex congenita: etiology, genetics, classification, diagnostic approach, and general aspects.
    Hall JG
    J Pediatr Orthop B; 1997 Jul; 6(3):159-66. PubMed ID: 9260643
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of a group unrelated patients with arthrogryposis multiplex congenita.
    Valdés-Flores M; Casas-Avila L; Hernández-Zamora E; Kofman S; Hidalgo-Bravo A
    J Pediatr (Rio J); 2016; 92(1):58-64. PubMed ID: 26453511
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tabulation of findings in the muscular dystrophies and in myotonia dystrophica.
    Danowski TS; Wissinger HA; Hohmann TC; Gerneth JA; Folkers K; Vester JW; Fisher ER
    Arch Phys Med Rehabil; 1971 May; 52(5):193-200. PubMed ID: 4931852
    [No Abstract]   [Full Text] [Related]  

  • 7. Neuropathologic aspects of arthrogryposis multiplex congenita.
    Banker BQ
    Clin Orthop Relat Res; 1985 Apr; (194):30-43. PubMed ID: 3978931
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lethal congenital muscular dystrophy in two sibs with arthrogryposis multiplex: new entity or variant of cobblestone lissencephaly syndrome?
    Seidahmed MZ; Sunada Y; Ozo CO; Hamid F; Campbell KP; Salih MA
    Neuropediatrics; 1996 Dec; 27(6):305-10. PubMed ID: 9050048
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Electromyographic characteristics of congenital and early onset motor unit diseases.
    Fowler WM; Taylor RG; Munsat TL
    Arch Phys Med Rehabil; 1971 Aug; 52(8):343-61. PubMed ID: 5284447
    [No Abstract]   [Full Text] [Related]  

  • 10. Arthrogryposis multiplex congenita: spectrum of pathologic changes.
    Banker BQ
    Hum Pathol; 1986 Jul; 17(7):656-72. PubMed ID: 3721492
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Arthrogryposis multiplex congenita, Pena-Shokeir phenotype, with gastroschisis and agenesis of the leg.
    Agapitos M; Georgiou-Theodoropoulou M; Koutselinis A; Papacharalambus N
    Pediatr Pathol; 1988; 8(4):409-13. PubMed ID: 2974953
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Schwartz-Jampel syndrome.
    al Gazali LI
    Clin Dysmorphol; 1993 Jan; 2(1):47-54. PubMed ID: 8298738
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Orthopaedic aspects of the Schwartz syndrome.
    Horan F; Beighton P
    J Bone Joint Surg Am; 1975 Jun; 57(4):542-4. PubMed ID: 1141267
    [No Abstract]   [Full Text] [Related]  

  • 14. The distal arthrogryposes: delineation of new entities--review and nosologic discussion.
    Hall JG; Reed SD; Greene G
    Am J Med Genet; 1982 Feb; 11(2):185-239. PubMed ID: 7039311
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Arthrogryposis multiplex congenita: a report of two cases.
    Brooks JG; Coster DJ
    Aust N Z J Ophthalmol; 1994 May; 22(2):127-32. PubMed ID: 7917267
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Arthrogryposis.
    Hall JG
    Am Fam Physician; 1989 Jan; 39(1):113-9. PubMed ID: 2643273
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Extending the spectrum of distal arthrogryposis.
    Gripp KW; Scott CI; Brockett BC; Nicholson L; Mackenzie WG
    Am J Med Genet; 1996 Nov; 65(4):286-90. PubMed ID: 8923937
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Muscular dystrophies of childhood.
    Slater GE; Swaiman KF
    Pediatr Ann; 1977 Mar; 6(3):170-93. PubMed ID: 322048
    [No Abstract]   [Full Text] [Related]  

  • 19. Neurogenic arthrogryposis multiplex congenita: clinical and muscle biopsy findings.
    Adams C; Becker LE; Murphy EG
    Pediatr Neurosci; 1988; 14(2):97-102. PubMed ID: 3251214
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A family with autosomal dominant distal arthrogryposis multiplex congenita and brown syndrome.
    Lobefalo LT; Mancini AT; Petitti MT; Verrotti AE; Della Loggia GE; Di Muzio AE; Chiarelli FE; Gallenga PE
    Ophthalmic Genet; 1999 Dec; 20(4):233-41. PubMed ID: 10617921
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.