151 related articles for article (PubMed ID: 10855475)
41. Spondylometaphyseal dysplasia-Sedaghatian type.
Elçioglu N; Hall CM
Am J Med Genet; 1998 Apr; 76(5):410-4. PubMed ID: 9556300
[TBL] [Abstract][Full Text] [Related]
42. A multiplex family with possible metaphyseal Spahr-type dysplasia and exclusion of RMRP and COL10A1 as candidate genes.
Mégarbané A; Chouery E; Ghanem I
Am J Med Genet A; 2008 Jul; 146A(14):1865-70. PubMed ID: 18553549
[TBL] [Abstract][Full Text] [Related]
43. Desbuquois dysplasia, a reevaluation with abnormal and "normal" hands: radiographic manifestations.
Faivre L; Cormier-Daire V; Eliott AM; Field F; Munnich A; Maroteaux P; Le Merrer M; Lachman R
Am J Med Genet A; 2004 Jan; 124A(1):48-53. PubMed ID: 14679586
[TBL] [Abstract][Full Text] [Related]
44. Mutations in the enzyme glutathione peroxidase 4 cause Sedaghatian-type spondylometaphyseal dysplasia.
Smith AC; Mears AJ; Bunker R; Ahmed A; MacKenzie M; Schwartzentruber JA; Beaulieu CL; Ferretti E; ; Majewski J; Bulman DE; Celik FC; Boycott KM; Graham GE
J Med Genet; 2014 Jul; 51(7):470-4. PubMed ID: 24706940
[TBL] [Abstract][Full Text] [Related]
45. Patterson-Lowry rhizomelic dysplasia: a potentially lethal bone dysplasia?
Kamoda T; Nakajima R; Matsui A; Nishimura G
Pediatr Radiol; 2001 Feb; 31(2):81-3. PubMed ID: 11214690
[TBL] [Abstract][Full Text] [Related]
46. Spondylometaphyseal dysplasia, east-African type: a new form of early, severe SMD with rounded vertebrae.
Verloes A; Lepage P; Baumann C; Maroteaux P; Merrer ML
Am J Med Genet; 2002 Dec; 113(4):362-6. PubMed ID: 12457408
[TBL] [Abstract][Full Text] [Related]
47. Developmental coxa vara associated with spondylometaphyseal dysplasia (DCV/SMD): "SMD-corner fracture type" (DCV/SMD-CF) demonstrated in most reported cases.
Currarino G; Birch JG; Herring JA
Pediatr Radiol; 2000 Jan; 30(1):14-24. PubMed ID: 10663502
[TBL] [Abstract][Full Text] [Related]
48. Spondylometaphyseal dysplasia: Sedaghatian type.
Koutouby A; Habibullah J; Moinuddin FA
Am J Med Genet; 2000 Jan; 90(3):199-202. PubMed ID: 10678656
[TBL] [Abstract][Full Text] [Related]
49. Japanese type of spondylo-metaphyseal dysplasia.
Hasegawa T; Kozlowski K; Nishimura G; Hara H; Hasegawa Y; Aso T; Koto S; Nagai T; Tsuchiya Y
Pediatr Radiol; 1994; 24(3):194-7. PubMed ID: 7936797
[TBL] [Abstract][Full Text] [Related]
50. Spectrum of dolichospondylic dysplasia: two new patients with distinctive findings.
Elliott AM; Graham JM; Curry CJ; Pal T; Rimoin DL; Lachman RS
Am J Med Genet; 2002 Dec; 113(4):351-61. PubMed ID: 12457407
[TBL] [Abstract][Full Text] [Related]
51. Indonesian type of metaphyseal dysplasia.
Kozlowski K; Pratomo PS; Burhan A; Firman K
Can Assoc Radiol J; 1993 Oct; 44(5):384-9. PubMed ID: 8402240
[TBL] [Abstract][Full Text] [Related]
52. New form of platyspondylic lethal chondrodysplasia.
Akaba K; Nishimura G; Hashimoto M; Wakabayashi T; Kanasugi H; Hayasaka K
Am J Med Genet; 1996 Dec; 66(4):464-7. PubMed ID: 8989469
[TBL] [Abstract][Full Text] [Related]
53. A novel type X collagen gene mutation (G595R) associated with Schmid-type metaphyseal chondrodysplasia.
Matsui Y; Yasui N; Kawabata H; Ozono K; Nakata K; Mizushima T; Tsumaki N; Kataoka E; Fujita Y; Ochi T
J Hum Genet; 2000; 45(2):105-8. PubMed ID: 10721676
[TBL] [Abstract][Full Text] [Related]
54. Severe neurologic manifestations from cervical spine instability in spondylo-megaepiphyseal-metaphyseal dysplasia.
Simon M; Campos-Xavier AB; Mittaz-Crettol L; Valadares ER; Carvalho D; Speck-Martins CE; Nampoothiri S; Alanay Y; Mihci E; van Bever Y; Garcia-Segarra N; Cavalcanti D; Mortier G; Bonafé L; Superti-Furga A
Am J Med Genet C Semin Med Genet; 2012 Aug; 160C(3):230-7. PubMed ID: 22791571
[TBL] [Abstract][Full Text] [Related]
55. Metaphyseal peg in geroderma osteodysplasticum: a new genetic bone marker and a specific finding?
Eich GF; Steinmann B; Hodler J; Exner GU; Giedion A
Am J Med Genet; 1996 May; 63(1):62-7. PubMed ID: 8723088
[TBL] [Abstract][Full Text] [Related]
56. Two unusual cases of nephrocalcinosis in infancy.
Kessel D; Hall CM; Shaw DG
Pediatr Radiol; 1992; 22(6):470-1. PubMed ID: 1437381
[TBL] [Abstract][Full Text] [Related]
57. Asphyxiating thoracic dysplasia as a complication of metaphyseal chondrodysplasia (Jansen type).
Ozonoff MB
Birth Defects Orig Artic Ser; 1974; 10(12):72-7. PubMed ID: 4461094
[No Abstract] [Full Text] [Related]
58. Axial spondylometaphyseal dysplasia.
Ehara S; Kim OH; Maisawa S; Takasago Y; Nishimura G
Eur J Pediatr; 1997 Aug; 156(8):627-30. PubMed ID: 9266195
[TBL] [Abstract][Full Text] [Related]
59. An anadysplasia-like, spontaneously remitting spondylometaphyseal dysplasia secondary to lamin B receptor (LBR) gene mutations: further definition of the phenotypic heterogeneity of LBR-bone dysplasias.
Sobreira N; Modaff P; Steel G; You J; Nanda S; Hoover-Fong J; Valle D; Pauli RM
Am J Med Genet A; 2015 Jan; 167A(1):159-63. PubMed ID: 25348816
[TBL] [Abstract][Full Text] [Related]
60. Osteosclerotic metaphyseal dysplasia: a skeletal dysplasia that may mimic lead poisoning in a child with hypotonia and seizures.
Mennel EA; John SD
Pediatr Radiol; 2003 Jan; 33(1):11-4. PubMed ID: 12497229
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]