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Items: 1 to 20 of 306

1.

Autosomal dominant osteopetrosis and maxillomandibular osteomyelitis.

Junquera L, Rodríguez-Recio C, Villarreal P, García-Consuegra L.

Am J Otolaryngol. 2005 Jul-Aug;26(4):275-8.

PMID:
15991096
2.

Maxillomandibular osteomyelitis in osteopetrosis. Report of a case and review of the literature.

Vázquez E, López-Arcas JM, Navarro I, Pingarrón L, Cebrián JL.

Oral Maxillofac Surg. 2009 Jun;13(2):105-8. doi: 10.1007/s10006-009-0151-y. Review.

PMID:
19219469
3.
4.

Osteomyelitis of the mandible associated with autosomal dominant osteopetrosis: a case report.

Albuquerque MA, Melo ES, Jorge WA, Cavalcanti MG.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2006 Jul;102(1):94-8. Epub 2006 Mar 3.

PMID:
16831679
5.

Mapping of autosomal dominant osteopetrosis type II (Albers-Schönberg disease) to chromosome 16p13.3.

Bénichou O, Cleiren E, Gram J, Bollerslev J, de Vernejoul MC, Van Hul W.

Am J Hum Genet. 2001 Sep;69(3):647-54. Epub 2001 Jul 23.

6.

Marble bone disease: a review of osteopetrosis and its oral health implications for dentists.

Lam DK, Sándor GK, Holmes HI, Carmichael RP, Clokie CM.

J Can Dent Assoc. 2007 Nov;73(9):839-43. Review.

7.

Type II autosomal dominant osteopetrosis.

Senel K, Ugur M, Erdal A, Ozdemir H.

Rheumatol Int. 2002 Jul;22(3):116-8. Epub 2002 May 17.

PMID:
12111087
8.

Mandibular osteomyelitis and multiple skeletal complications in Albers-Schönberg disease.

Chattopadhyay P, Kundu AK, Saha AK, Karthak RO.

Singapore Med J. 2008 Sep;49(9):e229-33.

9.

Neurological aspects of osteopetrosis.

Steward CG.

Neuropathol Appl Neurobiol. 2003 Apr;29(2):87-97. Review.

PMID:
12662317
10.

Autosomal dominant osteopetrosis type II with "malignant" presentation: further support for heterogeneity?

Walpole IR, Nicoll A, Goldblatt J.

Clin Genet. 1990 Oct;38(4):257-63.

PMID:
2268972
11.

Type II autosomal dominant osteopetrosis: radiological features in two families containing five members with asymptomatic and uncomplicated disease.

Fotiadou A, Arvaniti M, Kiriakou V, Tsitouridis I.

Skeletal Radiol. 2009 Oct;38(10):1015-21. doi: 10.1007/s00256-009-0718-6. Epub 2009 Jun 23.

PMID:
19547970
12.

Patients with autosomal-recessive osteopetrosis presenting with hydrocephalus and hindbrain posterior fossa crowding.

Al-Tamimi YZ, Tyagi AK, Chumas PD, Crimmins DW.

J Neurosurg Pediatr. 2008 Jan;1(1):103-6. doi: 10.3171/PED-08/01/103.

PMID:
18352814
13.

Cortical bone remodeling in autosomal dominant osteopetrosis: a study of two different phenotypes.

Brockstedt H, Bollerslev J, Melsen F, Mosekilde L.

Bone. 1996 Jan;18(1):67-72.

PMID:
8717539
14.

Radiological case of the month. Osteopetrosis (Albers-Schomberg's disease) with osteomyelitis.

Gwinn JL, Lee FA.

Am J Dis Child. 1972 Jul;124(1):91-2. No abstract available.

PMID:
5033756
15.

Osteomyelitis in infantile osteopetrosis: a case report with review of literature.

Roopashri RK, Gopakumar R, Subhas BG.

J Indian Soc Pedod Prev Dent. 2008;26 Suppl 3:S125-8. Review.

16.

Osteomyelitis of the maxilla secondary to osteopetrosis: report of a case.

Barry CP, Ryan CD.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2003 Jan;95(1):12-5.

PMID:
12539021
17.

Autosomal dominant osteopetrosis: clinical severity and natural history of 94 subjects with a chloride channel 7 gene mutation.

Waguespack SG, Hui SL, Dimeglio LA, Econs MJ.

J Clin Endocrinol Metab. 2007 Mar;92(3):771-8. Epub 2006 Dec 12.

PMID:
17164308
18.

Human osteopetroses and the osteoclast V-H+-ATPase enzyme system.

Ogbureke KU, Zhao Q, Li YP.

Front Biosci. 2005 Sep 1;10:2940-54. Review.

PMID:
15970548
19.

Infantile malignant osteopetrosis: report of 2 cases with osteomyelitis of the jaws.

Sekerci AE, Sisman Y, Ertas ET, Sahman H, Aydinbelge M.

J Dent Child (Chic). 2012 May-Aug;79(2):93-9.

PMID:
22828766
20.

Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene.

Cleiren E, Bénichou O, Van Hul E, Gram J, Bollerslev J, Singer FR, Beaverson K, Aledo A, Whyte MP, Yoneyama T, deVernejoul MC, Van Hul W.

Hum Mol Genet. 2001 Dec 1;10(25):2861-7.

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