125 related articles for article (PubMed ID: 12029347)
1. A probable new type of osteopenic bone disease.
Widhe TL
Pediatr Radiol; 2002 Jun; 32(6):447-51. PubMed ID: 12029347
[TBL] [Abstract][Full Text] [Related]
2. Inherited diseases of bone density in children.
Herman TE; McAlister WH
Radiol Clin North Am; 1991 Jan; 29(1):149-64. PubMed ID: 1985325
[TBL] [Abstract][Full Text] [Related]
3. Osteogenesis imperfecta. Radiographic classification, natural history, and treatment of spinal deformities.
Hanscom DA; Winter RB; Lutter L; Lonstein JE; Bloom BA; Bradford DS
J Bone Joint Surg Am; 1992 Apr; 74(4):598-616. PubMed ID: 1583055
[TBL] [Abstract][Full Text] [Related]
4. Heritable metabolic and dysplastic bone diseases.
Whyte MP
Endocrinol Metab Clin North Am; 1990 Mar; 19(1):133-73. PubMed ID: 2113470
[TBL] [Abstract][Full Text] [Related]
5. Familial congenital bowing with short thick bones and metaphyseal changes, a distinct entity. Report of the clinical and radiological findings in two siblings.
Rezza E; Iannaccone G; Lendvai D
Pediatr Radiol; 1984; 14(5):323-7. PubMed ID: 6472918
[TBL] [Abstract][Full Text] [Related]
6. Radiographic features of craniometadiaphyseal dysplasia, wormian bone type.
Langer LO; Brill PW; Afshani E; Williams CA; Thomas IT; Frias JL
Skeletal Radiol; 1991; 20(1):37-41. PubMed ID: 2000503
[TBL] [Abstract][Full Text] [Related]
7. The SPONASTRIME dysplasia: familial short-limb dwarfism with saddle nose, spinal alterations and metaphyseal striation. Report of 4 siblings.
Fanconi S; Issler C; Giedion A; Prader A
Helv Paediatr Acta; 1983 Aug; 38(3):267-80. PubMed ID: 6618893
[TBL] [Abstract][Full Text] [Related]
8. Sponastrime dysplasia. A radiologic-pathologic correlation.
Lachman RS; Stoss H; Spranger J
Pediatr Radiol; 1989; 19(6-7):417-24. PubMed ID: 2771481
[TBL] [Abstract][Full Text] [Related]
9. A new hereditary bone dysplasia with characteristic bowing and thickening of the distal ulna.
Rosenberg E; Löhr H
Eur J Pediatr; 1986 Apr; 145(1-2):40-5. PubMed ID: 3732330
[TBL] [Abstract][Full Text] [Related]
10. A new familial skeletal dysplasia with severely retarded ossification and abnormal modeling of bones especially of the epiphyses, the hands, and feet.
Eiken M; Prag J; Petersen KE; Kaufmann HJ
Eur J Pediatr; 1984 Feb; 141(4):231-5. PubMed ID: 6734674
[TBL] [Abstract][Full Text] [Related]
11. [The radiology of osteogenesis imperfecta].
Orzincolo C; Castaldi G; Scutellari PN; Ghedini M; Franceschini F; Bagni B
Radiol Med; 1992 Nov; 84(5):557-66. PubMed ID: 1475419
[TBL] [Abstract][Full Text] [Related]
12. Asymmetric and symmetric long bone bowing in two sibs: an apparently new bone dysplasia.
Moore LA; Moore CA; Smith JA; Weaver DD
Am J Med Genet; 1993 Nov; 47(7):1072-7. PubMed ID: 8291526
[TBL] [Abstract][Full Text] [Related]
13. Epiphyseal dysplasia with coxa vara, microcephaly, and normal intelligence in sibs: expanded spectrum of Lowry-Wood syndrome?
Hankenson LG; Ozonoff MB; Cassidy SB
Am J Med Genet; 1989 Jul; 33(3):336-40. PubMed ID: 2801767
[TBL] [Abstract][Full Text] [Related]
14. Mucolipidosis, probably a new variant with joint deformity and peripheral nerve dysfunction.
Bundey SE; Ashenhurst EM; Dorst JP
Birth Defects Orig Artic Ser; 1974; 10(12):484-90. PubMed ID: 4218789
[No Abstract] [Full Text] [Related]
15. Kyphomelic dysplasia in two sib fetuses.
Chen CP; Chern SR; Shih SL; Chuang CY; Huang FY
J Med Genet; 1998 Jan; 35(1):65-9. PubMed ID: 9475099
[TBL] [Abstract][Full Text] [Related]
16. [Osteopenia in childhood. Hereditary hyperphosphatasia].
Bajaj SK; Zass R; Brämswig JH; Gissler HM; von Lengerke HJ; Peters PE
Radiologe; 1995 Nov; 35(11):871-2. PubMed ID: 8657891
[No Abstract] [Full Text] [Related]
17. Results and complications of a surgical technique for correction of coxa vara in children with osteopenic bones.
Fassier F; Sardar Z; Aarabi M; Odent T; Haque T; Hamdy R
J Pediatr Orthop; 2008 Dec; 28(8):799-805. PubMed ID: 19034168
[TBL] [Abstract][Full Text] [Related]
18. Two sibs with brachyolmia type Hobaek: five year follow-up through puberty.
Hoo JJ; Oliphant M
Am J Med Genet A; 2003 Jan; 116A(1):80-4. PubMed ID: 12476457
[TBL] [Abstract][Full Text] [Related]
19. Type V osteogenesis imperfecta: a new form of brittle bone disease.
Glorieux FH; Rauch F; Plotkin H; Ward L; Travers R; Roughley P; Lalic L; Glorieux DF; Fassier F; Bishop NJ
J Bone Miner Res; 2000 Sep; 15(9):1650-8. PubMed ID: 10976985
[TBL] [Abstract][Full Text] [Related]
20. Spondylometaphyseal dysplasia, corner fracture type: a heritable condition associated with coxa vara.
Langer LO; Brill PW; Ozonoff MB; Pauli RM; Wilson WG; Alford BA; Pavlov H; Drake DG
Radiology; 1990 Jun; 175(3):761-6. PubMed ID: 2343127
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
