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 *

119 related articles for article (PubMed ID: 22791316)

  • 1. Enchondromatosis revisited: new classification with molecular basis.
    Superti-Furga A; Spranger J; Nishimura G
    Am J Med Genet C Semin Med Genet; 2012 Aug; 160C(3):154-64. PubMed ID: 22791316
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Ollier disease.
    Silve C; Jüppner H
    Orphanet J Rare Dis; 2006 Sep; 1():37. PubMed ID: 16995932
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genochondromatosis type II: report of a new patient and further delineation of the phenotype.
    Isidor B; Guillard S; Hamel A; Le Caignec C; David A
    Am J Med Genet A; 2007 Aug; 143A(16):1919-21. PubMed ID: 17632779
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An intermediate phenotype in IDH related enchondromatosis spectrum.
    Yilmaz-Gulec E; Marzin P; Huber-Lequesne C; Cormier-Daire V
    Eur J Med Genet; 2023 Mar; 66(3):104697. PubMed ID: 36649847
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Acroform type of enchondromatosis associated with severe vertebral involvement and facial dysmorphism in a boy with a new variant of enchondromatosis type I1 of Spranger: case report and a review of the literature.
    Kaissi AA; Roetzer K; Klaushofer K; Grill F
    Cases J; 2008 Nov; 1(1):324. PubMed ID: 19017386
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Achondrogenesis type I: delineation of further heterogeneity and identification of two distinct subgroups.
    Borochowitz Z; Lachman R; Adomian GE; Spear G; Jones K; Rimoin DL
    J Pediatr; 1988 Jan; 112(1):23-31. PubMed ID: 3275766
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Generalized enchondromatosis in a boy with only platyspondyly in the father.
    Halal F; Azouz EM
    Am J Med Genet; 1991 Mar; 38(4):588-92. PubMed ID: 2063903
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Widespread and debilitating hemangiomas in a patient with enchondromatosis and D-2-hydroxyglutaric aciduria.
    Yeetong P; Phewplung T; Kamolvisit W; Suphapeetiporn K; Shotelersuk V
    Skeletal Radiol; 2018 Nov; 47(11):1577-1582. PubMed ID: 29744569
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hereditary multiple exostoses and enchondromatosis.
    Pannier S; Legeai-Mallet L
    Best Pract Res Clin Rheumatol; 2008 Mar; 22(1):45-54. PubMed ID: 18328980
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinics in diagnostic imaging (124). Multiple enchondromatosis in Ollier disease.
    Khoo RN; Peh WC; Guglielmi G
    Singapore Med J; 2008 Oct; 49(10):841-5; quiz 846. PubMed ID: 18946621
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exostoses, enchondromatosis and metachondromatosis; diagnosis and management.
    McFarlane J; Knight T; Sinha A; Cole T; Kiely N; Freeman R
    Acta Orthop Belg; 2016 Mar; 82(1):102-5. PubMed ID: 26984661
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ollier Disease: Pathogenesis, Diagnosis, and Management.
    Kumar A; Jain VK; Bharadwaj M; Arya RK
    Orthopedics; 2015 Jun; 38(6):e497-506. PubMed ID: 26091223
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Achondroplasia and enchondromatosis: report of three boys.
    Numakura C; Kobayashi H; Hasegawa Y; Adachi M; Kim OH; Nishimura G
    Skeletal Radiol; 2007 Jun; 36 Suppl 1():S29-33. PubMed ID: 16763840
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Unraveling the molecular diagnosis of metaphyseal enchondromatosis with D-2-hydroxyglutaric aciduria: A 22-year quest.
    Rattanapornsompong K; Chetruengchai W; Srichomthong C; Theerapanon T; Porntaveetus T; Shotelersuk V
    Am J Med Genet A; 2024 Jun; 194(6):e63557. PubMed ID: 38305044
    [No Abstract]   [Full Text] [Related]  

  • 16. [A combination of multiple cartilaginous exostoses and enchondromatosis of bone in a family].
    Tschernikoff Z; Ditscheva L
    Radiol Diagn (Berl); 1989; 30(1):53-6. PubMed ID: 2785276
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Enchondromatosis (Ollier disease, Maffucci syndrome) is not caused by the PTHR1 mutation p.R150C.
    Rozeman LB; Sangiorgi L; Briaire-de Bruijn IH; Mainil-Varlet P; Bertoni F; Cleton-Jansen AM; Hogendoorn PC; Bovée JV
    Hum Mutat; 2004 Dec; 24(6):466-73. PubMed ID: 15523647
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Symmetrical enchondromatosis of the hands and feet in two sisters.
    Mota CR; Marques L; Silva E; Fonseca M; Pinho M; Torcato M; Barbot J; Medina M; Maroteaux P
    J Pediatr Orthop B; 1997 Jan; 6(1):15-9. PubMed ID: 9039661
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dysspondyloenchondromatosis without COL2A1 mutation: possible genetic heterogeneity.
    Tran Mau-Them F; Boualam A; Barat-Houari M; Jeandel C; Cottalorda J; Cormier-Daire V; Fabre A; Dumont B; Lefort G; Baujat G; Le Merrer M; Jorgensen C; Touitou I; Geneviève D
    Am J Med Genet A; 2014 Mar; 164A(3):769-73. PubMed ID: 24357493
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ollier disease with digital enchondromatosis: anatomic and functional imaging.
    Le BB; Nguyen BD
    Clin Nucl Med; 2014 Aug; 39(8):e375-8. PubMed ID: 24152634
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.