189 related articles for article (PubMed ID: 12788869)
1. Autosomal dominant hyperostosis/osteosclerosis with high serum alkaline phosphatase activity.
Hernandez-Cassis C; Vogel CK; Hernandez TP; Econs MJ; Iglesias M; Iglesias A; Levis S; Roos BA; Howard GA; Iglesias Gamarra A
J Clin Endocrinol Metab; 2003 Jun; 88(6):2650-5. PubMed ID: 12788869
[TBL] [Abstract][Full Text] [Related]
2. Autosomal dominant osteosclerosis.
Gorlin RJ; Glass L
Radiology; 1977 Nov; 125(2):547-8. PubMed ID: 198847
[TBL] [Abstract][Full Text] [Related]
3. Bone metabolic activity in hyperostosis cranialis interna measured with 18F-fluoride PET.
Waterval JJ; Van Dongen TM; Stokroos RJ; Teule JG; Kemerink GJ; Brans B; Nieman FH; Manni JJ
Eur J Nucl Med Mol Imaging; 2011 May; 38(5):884-93. PubMed ID: 21079950
[TBL] [Abstract][Full Text] [Related]
4. Autosomal dominant osteosclerosis.
Gelman MI
Radiology; 1977 Nov; 125(2):289-96. PubMed ID: 198844
[TBL] [Abstract][Full Text] [Related]
5. Phenotypic manifestations and management of hyperostosis cranialis interna, a hereditary bone dysplasia affecting the calvaria and the skull base.
Waterval JJ; Stokroos RJ; Bauer NJ; De Bondt RB; Manni JJ
Am J Med Genet A; 2010 Mar; 152A(3):547-55. PubMed ID: 20140965
[TBL] [Abstract][Full Text] [Related]
6. Autosomal dominant osteosclerosis: report of a kindred.
Curran AE; Pfeffle RC; Miller E
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 1999 May; 87(5):600-4. PubMed ID: 10348520
[TBL] [Abstract][Full Text] [Related]
7. Expansile skeletal hyperphosphatasia: a new familial metabolic bone disease.
Whyte MP; Mills BG; Reinus WR; Podgornik MN; Roodman GD; Gannon FH; Eddy MC; McAlister WH
J Bone Miner Res; 2000 Dec; 15(12):2330-44. PubMed ID: 11127198
[TBL] [Abstract][Full Text] [Related]
8. Autosomal dominant osteosclerosis associated with familial spinal canal stenosis.
Yasuda Y; Dokoh S; Seko K; Imai T; Akiguchi I; Kameyama M
Neurology; 1986 May; 36(5):687-92. PubMed ID: 3703268
[TBL] [Abstract][Full Text] [Related]
9. Localization of the gene for hyperostosis cranialis interna to chromosome 8p21 with analysis of three candidate genes.
Borra VM; Waterval JJ; Stokroos RJ; Manni JJ; Van Hul W
Calcif Tissue Int; 2013 Jul; 93(1):93-100. PubMed ID: 23640157
[TBL] [Abstract][Full Text] [Related]
10. Idiopathic acquired diffuse osteosclerosis in a young woman.
Beyer HS; Parfitt AM; Shih MS; Anderson Q; Heath H
J Bone Miner Res; 1990 Dec; 5(12):1257-63. PubMed ID: 2075839
[TBL] [Abstract][Full Text] [Related]
11. Bone densitometry of a patient with osteosclerosis.
Bagur A; Dobrovsky V; Mautalen C
J Clin Densitom; 2003; 6(1):67-71. PubMed ID: 12665704
[TBL] [Abstract][Full Text] [Related]
12. Distal osteosclerosis.
Beighton P; Macrae M; Kozlowski K
Clin Genet; 1980 Oct; 18(4):298-304. PubMed ID: 7438509
[TBL] [Abstract][Full Text] [Related]
13. Prostaglandin induced cortical hyperostosis in neonates with cyanotic heart disease.
Nadroo AM; Shringari S; Garg M; al-Sowailem AM
J Perinat Med; 2000; 28(6):447-52. PubMed ID: 11155430
[TBL] [Abstract][Full Text] [Related]
14. Osteosclerotic metaphyseal dysplasia.
Nishimura G; Kozlowski K
Pediatr Radiol; 1993; 23(6):450-2. PubMed ID: 8255649
[TBL] [Abstract][Full Text] [Related]
15. Autosomal dominant osteosclerosis type Stanescu: the third family.
Horovitz DD; Barbosa Neto JG; Boy R; Vargas FR; Llerena Júnior JC; de Almeida JC
Am J Med Genet; 1995 Jul; 57(4):605-9. PubMed ID: 7573138
[TBL] [Abstract][Full Text] [Related]
16. Osteomesopyknosis: report of a new case with bone histology.
Hardouin P; Flautre B; Sutter B; Leclet H; Grardel B; Fauquert P
Bone; 1994; 15(1):81-3. PubMed ID: 8024856
[TBL] [Abstract][Full Text] [Related]
17. [Osteomesopycnosis. A new autosomal dominant osteosclerosing bone disease (author's transl)].
Maroteaux P
Arch Fr Pediatr; 1980 Mar; 37(3):153-7. PubMed ID: 7469692
[TBL] [Abstract][Full Text] [Related]
18. [Hyperostosis cranialis interna; a new syndrome with autosomal dominant inheritance].
Manni JJ; Scaf JJ; Huygen PL; Cruysberg JR; Verhagen WI
Ned Tijdschr Geneeskd; 1990 Sep; 134(35):1697-701. PubMed ID: 2215719
[TBL] [Abstract][Full Text] [Related]
19. Autosomal dominant endosteal hyperostosis. Report of a Spanish family with neurological involvement.
Perez-Vicente JA; Rodríguez de Castro E; Lafuente J; Mateo MM; Giménez-Roldán S
Clin Genet; 1987 Mar; 31(3):161-9. PubMed ID: 3568443
[TBL] [Abstract][Full Text] [Related]
20. An autosomal dominant high bone mass phenotype in association with craniosynostosis in an extended family is caused by an LRP5 missense mutation.
Kwee ML; Balemans W; Cleiren E; Gille JJ; Van Der Blij F; Sepers JM; Van Hul W
J Bone Miner Res; 2005 Jul; 20(7):1254-60. PubMed ID: 15940380
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]