Davis JG - Search Results

1

Bone mineral density determinations by dual-energy x-ray absorptiometry in the management of patients with Marfan syndrome--some factors which affect the measurement.

Giampietro PF, Peterson MG, Schneider R, Davis JG, Burke SW, Boachie-Adjei O, Mueller CM, Raggio CL. Giampietro PF, et al. Among authors: davis jg. HSS J. 2007 Feb;3(1):89-92. doi: 10.1007/s11420-006-9030-3. HSS J. 2007. PMID: 18751776 Free PMC article.

2

Assessment of bone mineral density in adults and children with Marfan syndrome.

Giampietro PF, Peterson M, Schneider R, Davis JG, Raggio C, Myers E, Burke SW, Boachie-Adjei O, Mueller CM. Giampietro PF, et al. Among authors: davis jg. Osteoporos Int. 2003 Jul;14(7):559-63. doi: 10.1007/s00198-003-1433-0. Epub 2003 Jul 3. Osteoporos Int. 2003. PMID: 12845424

3

The incidence of protrusio acetabuli in Marfan's syndrome and its relationship to bone mineral density.

Do T, Giampietro PF, Burke SW, Davis JG, Raggio C, Schneider R, Boachie-Adjei O, Brill P. Do T, et al. Among authors: davis jg. J Pediatr Orthop. 2000 Nov-Dec;20(6):718-21. doi: 10.1097/00004694-200011000-00004. J Pediatr Orthop. 2000. PMID: 11097242

4

Marfan syndrome: orthopedic and genetic review.

Giampietro PF, Raggio C, Davis JG. Giampietro PF, et al. Among authors: davis jg. Curr Opin Pediatr. 2002 Feb;14(1):35-41. doi: 10.1097/00008480-200202000-00006. Curr Opin Pediatr. 2002. PMID: 11880731 Review.

5

The Kathryn O. and Alan C. Greenberg Center for Skeletal Dysplasias: an interdisciplinary approach.

Carter EM, Montuori L, Davis JG, Raggio CL. Carter EM, et al. Among authors: davis jg. HSS J. 2008 Sep;4(2):112-6. doi: 10.1007/s11420-008-9076-5. Epub 2008 May 28. HSS J. 2008. PMID: 18815853 Free PMC article.

6

Advances in understanding etiology of achondroplasia and review of management.

Carter EM, Davis JG, Raggio CL. Carter EM, et al. Among authors: davis jg. Curr Opin Pediatr. 2007 Feb;19(1):32-7. doi: 10.1097/MOP.0b013e328013e3d9. Curr Opin Pediatr. 2007. PMID: 17224659 Review.

7

Fanconi's anemia.

Giampietro PF, Davis JG, Auerbach AD. Giampietro PF, et al. Among authors: davis jg. N Engl J Med. 1994 Mar 10;330(10):720-1. doi: 10.1056/NEJM199403103301021. N Engl J Med. 1994. PMID: 8107737 No abstract available.

8

Diagnosis of Fanconi anemia in patients without congenital malformations: an international Fanconi Anemia Registry Study.

Giampietro PF, Verlander PC, Davis JG, Auerbach AD. Giampietro PF, et al. Among authors: davis jg. Am J Med Genet. 1997 Jan 10;68(1):58-61. Am J Med Genet. 1997. PMID: 8986277

9

New recessive syndrome characterized by increased chromosomal breakage and several findings which overlap with Fanconi anemia.

Giampietro PF, Auerbach AD, Elias ER, Gutman A, Zellers NJ, Davis JG. Giampietro PF, et al. Among authors: davis jg. Am J Med Genet. 1998 Jun 16;78(1):70-5. Am J Med Genet. 1998. PMID: 9637428

10

Novel missense ACAN gene variants linked to familial osteochondritis dissecans cluster in the C-terminal globular domain of aggrecan.

Stattin EL, Lindblom K, Struglics A, Önnerfjord P, Goldblatt J, Dixit A, Sarkar A, Randell T, Suri M, Raggio C, Davis J, Carter E, Aspberg A. Stattin EL, et al. Sci Rep. 2022 Mar 25;12(1):5215. doi: 10.1038/s41598-022-09211-y. Sci Rep. 2022. PMID: 35338222 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

204 results

Search Page

Filters