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 *

87 related articles for article (PubMed ID: 9677061)

  • 1. King syndrome: further clinical variability and review of the literature.
    Graham GE; Silver K; Arlet V; Der Kaloustian VM
    Am J Med Genet; 1998 Jul; 78(3):254-9. PubMed ID: 9677061
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The King syndrome: malignant hyperthermia, myopathy, and multiple anomalies.
    McPherson EW; Taylor CA
    Am J Med Genet; 1981; 8(2):159-65. PubMed ID: 7282770
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new autosomal recessive syndrome with Noonan-like phenotype, myopathy with congenital contractures and malignant hyperthermia.
    Kousseff BG; Nichols P
    Birth Defects Orig Artic Ser; 1985; 21(2):111-7. PubMed ID: 4041573
    [No Abstract]   [Full Text] [Related]  

  • 4. RYR1-Related Myopathies: Clinical, Histopathologic and Genetic Heterogeneity Among 17 Patients from a Portuguese Tertiary Centre.
    Samões R; Oliveira J; Taipa R; Coelho T; Cardoso M; Gonçalves A; Santos R; Melo Pires M; Santos M
    J Neuromuscul Dis; 2017; 4(1):67-76. PubMed ID: 28269792
    [TBL] [Abstract][Full Text] [Related]  

  • 5. King syndrome: a genetically heterogenous phenotype due to congenital myopathies.
    Chitayat D; Hodgkinson KA; Ginsburg O; Dimmick J; Watters GV
    Am J Med Genet; 1992 Aug; 43(6):954-6. PubMed ID: 1415346
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene.
    Jungbluth H; Zhou H; Hartley L; Halliger-Keller B; Messina S; Longman C; Brockington M; Robb SA; Straub V; Voit T; Swash M; Ferreiro A; Bydder G; Sewry CA; Müller C; Muntoni F
    Neurology; 2005 Dec; 65(12):1930-5. PubMed ID: 16380615
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Congenital myopathies: clinical and immunohistochemical study.
    Thaha F; Gayathri N; Nalini A
    Neurol India; 2011; 59(6):879-83. PubMed ID: 22234203
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Anesthetic management of the King-Denborough syndrome].
    Iwatsubo T; Yoshikawa M; Karashima Y; Kurita N; Shimoda T; Takahashi H; Horiuchi T; Kitaguchi K; Furuya H
    Masui; 2001 Apr; 50(4):390-3. PubMed ID: 11345752
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dominantly inherited malignant hyperthermia (MH) in the King-Denborough syndrome.
    Isaacs H; Badenhorst ME
    Muscle Nerve; 1992 Jun; 15(6):740-2. PubMed ID: 1508238
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptor.
    Monnier N; Romero NB; Lerale J; Nivoche Y; Qi D; MacLennan DH; Fardeau M; Lunardi J
    Hum Mol Genet; 2000 Nov; 9(18):2599-608. PubMed ID: 11063719
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Noonan syndrome: a review.
    Mendez HM; Opitz JM
    Am J Med Genet; 1985 Jul; 21(3):493-506. PubMed ID: 3895929
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Isoenzymes of creatine phosphokinase in serum of families with malignant hyperpyrexia.
    Meltzer HY; Hassan SZ; Russo P; Cho HW
    Anesth Analg; 1976; 55(6):797-9. PubMed ID: 1033694
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Tel Hashomer camptodactyly syndrome: report of a case with myopathic features.
    Patton MA; McDermot KD; Lake BD; Baraitser M
    J Med Genet; 1986 Jun; 23(3):268-71. PubMed ID: 3723560
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Noonan syndrome: the changing phenotype.
    Allanson JE; Hall JG; Hughes HE; Preus M; Witt RD
    Am J Med Genet; 1985 Jul; 21(3):507-14. PubMed ID: 4025385
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neurofibromatosis with fully expressed Noonan syndrome.
    Abuelo DN; Meryash DL
    Am J Med Genet; 1988 Apr; 29(4):937-41. PubMed ID: 3135755
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Myotonic chondrodystrophy (or Schwartz-Jampel syndrome). Study of siblings and review of the literature].
    Desbois JC; Guyou JM; Grenet P; Herrault A
    Ann Pediatr (Paris); 1977 Sep; 24(8-9):563-74. PubMed ID: 16211910
    [No Abstract]   [Full Text] [Related]  

  • 17. Myopathy in a patient with chromosome 22q11 deletion.
    Mongini T; Doriguzzi C; Arduino C; Brusco A; Bortolotto S; Mutani R; Palmucci L
    Neuropediatrics; 2001 Apr; 32(2):107-9. PubMed ID: 11414642
    [No Abstract]   [Full Text] [Related]  

  • 18. Myopathy with trabecular muscle fibers.
    Weller B; Carpenter S; Lochmüller H; Karpati G
    Neuromuscul Disord; 1999 Jun; 9(4):208-14. PubMed ID: 10399746
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prevention of malignant hyperpyrexia.
    Lancet; 1973 Jun; 1(7814):1225. PubMed ID: 4122568
    [No Abstract]   [Full Text] [Related]  

  • 20. King syndrome in pregnancy.
    Abel DE; Grotegut CA
    Obstet Gynecol; 2003 May; 101(5 Pt 2):1146-9. PubMed ID: 12738133
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.