BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

195 related articles for article (PubMed ID: 26984661)

  • 21. Targeted disruption of Shp2 in chondrocytes leads to metachondromatosis with multiple cartilaginous protrusions.
    Kim HK; Feng GS; Chen D; King PD; Kamiya N
    J Bone Miner Res; 2014 Mar; 29(3):761-9. PubMed ID: 23929766
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Differential diagnosis of multiple hereditary exostosis: presentation of a clinical case with secondary chondrosarcoma and literature review].
    Sansón-RíoFrío JA; Santiesteban N; Bahena RI; Villavicencio VV; Martínez-Said H; Padilla RA; Cuellar HM
    Acta Ortop Mex; 2009; 23(6):376-82. PubMed ID: 20377004
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Metachondromatosis: report of a family with facial features mildly resembling trichorhinophalangeal syndromePediatr Radiol 1997 Nov;27(11):864.
    Herman TE; Chines A; McAlister WH; Gottesman GS; Eddy MC; Whyte MP
    Pediatr Radiol; 1997 May; 27(5):436-41. PubMed ID: 9133359
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Clinical and radiographic analysis of osteochondromas and growth disturbance in hereditary multiple exostoses.
    Porter DE; Emerton ME; Villanueva-Lopez F; Simpson AH
    J Pediatr Orthop; 2000; 20(2):246-50. PubMed ID: 10739291
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Hereditary multiple exostoses: case report.
    Yinusa W; Owoola AM; Esin IA
    Niger J Clin Pract; 2010 Jun; 13(2):218-22. PubMed ID: 20499760
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Metachondromatosis: a report of two cases in a family.
    Ikegawa S; Nagano A; Matsushita T; Nakamura K
    Nihon Seikeigeka Gakkai Zasshi; 1992 May; 66(5):460-6. PubMed ID: 1506743
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Postzygotic mosaicism of a novel PTPN11 mutation in monozygotic twins discordant for metachondromatosis.
    Rydzanicz M; Glinkowski W; Walczak A; Koppolu A; Kostrzewa G; Gasperowicz P; Pollak A; Stawiński P; Płoski R
    Am J Med Genet A; 2022 May; 188(5):1482-1487. PubMed ID: 35112464
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A mutant PTH/PTHrP type I receptor in enchondromatosis.
    Hopyan S; Gokgoz N; Poon R; Gensure RC; Yu C; Cole WG; Bell RS; Jüppner H; Andrulis IL; Wunder JS; Alman BA
    Nat Genet; 2002 Mar; 30(3):306-10. PubMed ID: 11850620
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Subungueal exostosis of fingers in hereditary multiple exostosis. 3 cases].
    Schmitt AM; Bories A; Baran R
    Ann Dermatol Venereol; 1997; 124(3):233-6. PubMed ID: 9686054
    [TBL] [Abstract][Full Text] [Related]  

  • 30. EXT2-positive multiple hereditary osteochondromas with some features suggestive of metachondromatosis.
    Vining NC; Done S; Glass IA; Parnell SE; Sternen DL; Leppig KA; Mosca VS; Goldberg MJ
    Skeletal Radiol; 2012 May; 41(5):607-10. PubMed ID: 21892728
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Avascular necrosis of the capital femoral epiphysis in metachondromatosis.
    Keret D; Bassett GS
    J Pediatr Orthop; 1990; 10(5):658-61. PubMed ID: 2394820
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Canine multiple cartilaginous exostoses: unusual manifestations and a review of the literature.
    Jacobson LS; Kirberger RM
    J Am Anim Hosp Assoc; 1996; 32(1):45-51. PubMed ID: 8963735
    [TBL] [Abstract][Full Text] [Related]  

  • 33. An unusual example of hereditary multiple exostoses: a case report and review of the literature.
    Chilvers R; Gallagher JA; Jeffery N; Bond AP
    BMC Musculoskelet Disord; 2021 Jan; 22(1):96. PubMed ID: 33478453
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Metachondromatosis. Report of a family with 4 cases].
    Hinkel GK; Rupprecht E; Harzer W
    Helv Paediatr Acta; 1984 Dec; 39(5-6):481-9. PubMed ID: 6336171
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Enchondromatosis: insights on the different subtypes.
    Pansuriya TC; Kroon HM; Bovée JV
    Int J Clin Exp Pathol; 2010 Jun; 3(6):557-69. PubMed ID: 20661403
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Hereditary multiple exostoses and solitary osteochondroma associated with growth hormone deficiency: to treat or not to treat?
    Bozzola M; Gertosio C; Gnoli M; Baronio F; Pedrini E; Meazza C; Sangiorgi L
    Ital J Pediatr; 2015 Aug; 41():53. PubMed ID: 26239617
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Roentgen rounds #89. Metachondromatosis.
    McAlister WH; Cacciarelli AA; Gilula LA
    Orthop Rev; 1987 Jul; 16(7):498-500. PubMed ID: 3502612
    [No Abstract]   [Full Text] [Related]  

  • 38. Recessive mutations in PTHR1 cause contrasting skeletal dysplasias in Eiken and Blomstrand syndromes.
    Duchatelet S; Ostergaard E; Cortes D; Lemainque A; Julier C
    Hum Mol Genet; 2005 Jan; 14(1):1-5. PubMed ID: 15525660
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Novel EXT1 mutation identified in a pedigree with hereditary multiple exostoses.
    Cao L; Liu F; Kong M; Fang Y; Gu H; Chen Y; Zhao C; Zhang S; Bi Q
    Oncol Rep; 2014 Feb; 31(2):713-8. PubMed ID: 24297320
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Otofaciocervical syndrome and metachondromatosis in a girl: Presentation of a novel association and remarks on clinical variability of branchial-arch disorders.
    Salinas-Torres VM; Salinas-Torres RA
    Int J Pediatr Otorhinolaryngol; 2016 Jun; 85():19-21. PubMed ID: 27240490
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.