-
1
-
-
0018360949
-
Osteopetrosis in South Africa. The benign, lethal and intermediate forms
-
Beighton P, Hamersma H, Cremin BJ (1979). Osteopetrosis in South Africa. The benign, lethal and intermediate forms. S Afr Med J 55: 659-665.
-
(1979)
S Afr Med J
, vol.55
, pp. 659-665
-
-
Beighton, P.1
Hamersma, H.2
Cremin, B.J.3
-
2
-
-
0023900049
-
Radiological, biochemical and hereditary evidence of two types of autosomal dominant osteopetrosis
-
Bollerslev J, Andersen PE Jr (1988). Radiological, biochemical and hereditary evidence of two types of autosomal dominant osteopetrosis. Bone 9: 7-13.
-
(1988)
Bone
, vol.9
, pp. 7-13
-
-
Bollerslev, J.1
Andersen Jr., P.E.2
-
3
-
-
0027662076
-
Osteopetrose: Relate de dois casos e revisão da literature
-
Colônia AMN, Schaimberg CG, Yoshinari NH, Santos M, Jorgetti V, Cossermelli W (1993). Osteopetrose: Relate de dois casos e revisão da literature. Rev Hasp Clin Fac Med S Paulo 48: 242-247.
-
(1993)
Rev Hasp Clin Fac Med S Paulo
, vol.48
, pp. 242-247
-
-
Colônia, A.M.N.1
Schaimberg, C.G.2
Yoshinari, N.H.3
Santos, M.4
Jorgetti, V.5
Cossermelli, W.6
-
4
-
-
0025778915
-
Cranial osteopetrosis: MR findings
-
Demirci A, Sze G (1991). Cranial osteopetrosis: MR findings. Am J Neuroradiol 12: 781-782.
-
(1991)
Am J Neuroradiol
, vol.12
, pp. 781-782
-
-
Demirci, A.1
Sze, G.2
-
5
-
-
0033946477
-
Defects in TCIRG1 subunit of the vacuolar proton pump are responsible subset of human autosomal recessive osteopetrosis
-
Frattini A, Orchard PJ, Sobacchi C, Giliani S, Abinum M, Mattsson et al (2000). Defects in TCIRG1 subunit of the vacuolar proton pump are responsible subset of human autosomal recessive osteopetrosis. Nat Genet 25: 343-346.
-
(2000)
Nat Genet
, vol.25
, pp. 343-346
-
-
Frattini, A.1
Orchard, P.J.2
Sobacchi, C.3
Giliani, S.4
Abinum, M.5
Mattsson6
-
6
-
-
0027236586
-
Bone densitometry observations of osteopetrosis in response to bone marrow transplantation
-
Kaplan FS, August CS, Dalinka MK, Karp J, Fallon MD, Haddad JG (1993). Bone densitometry observations of osteopetrosis in response to bone marrow transplantation. Clin Orthop 294: 79-84.
-
(1993)
Clin Orthop
, vol.294
, pp. 79-84
-
-
Kaplan, F.S.1
August, C.S.2
Dalinka, M.K.3
Karp, J.4
Fallon, M.D.5
Haddad, J.G.6
-
7
-
-
0035951282
-
Loss of the CIC-7 chloride channel leads to osteopetrosis in mice and man
-
Kornak U, Kasper D, Bosl MR, Kaiser E, Schweizer M, Schulz A et al (2001). Loss of the CIC-7 chloride channel leads to osteopetrosis in mice and man. Cell 104: 205-215.
-
(2001)
Cell
, vol.104
, pp. 205-215
-
-
Kornak, U.1
Kasper, D.2
Bosl, M.R.3
Kaiser, E.4
Schweizer, M.5
Schulz, A.6
-
9
-
-
0025002765
-
Benign osteopetrosis
-
Rosenthal L (1990). Benign osteopetrosis. Clin Nucl Med 15: 412-414.
-
(1990)
Clin Nucl Med
, vol.15
, pp. 412-414
-
-
Rosenthal, L.1
-
10
-
-
0020084567
-
Osteomyelitis of the mandible. An initial feature in late-onset osteopetrosis
-
Shaff MI, Mathis JM (1982). Osteomyelitis of the mandible. An initial feature in late-onset osteopetrosis. Arch Otolaryngol 108: 120-121.
-
(1982)
Arch Otolaryngol
, vol.108
, pp. 120-121
-
-
Shaff, M.I.1
Mathis, J.M.2
-
11
-
-
0027304954
-
Osteopetrosis. Current clinical considerations
-
Shapiro F (1993). Osteopetrosis. Current clinical considerations. Clin Orthop 294: 34-44.
-
(1993)
Clin Orthop
, vol.294
, pp. 34-44
-
-
Shapiro, F.1
-
12
-
-
0027429167
-
Benign osteopetrosis: A review of 42 cases showing two different patterns
-
el-Tawil T, Stoker DJ (1993). Benign osteopetrosis: a review of 42 cases showing two different patterns. Skeletal Radiol 22: 587-593.
-
(1993)
Skeletal Radiol
, vol.22
, pp. 587-593
-
-
El-Tawil, T.1
Stoker, D.J.2
-
13
-
-
0035204519
-
Molecular and radiological diagnosis of sclerosing bone dysplasias
-
Van Hul W, Vanhoenacker F, Balemans W, Janssens, De Schepper AM (2001). Molecular and radiological diagnosis of sclerosing bone dysplasias. Eur J Radiol 40: 198-207.
-
(2001)
Eur J Radiol
, vol.40
, pp. 198-207
-
-
Van Hul, W.1
Vanhoenacker, F.2
Balemans, W.3
Janssens4
De Schepper, A.M.5
-
14
-
-
0035999445
-
Localization of the gene causing autosomal dominant osteopetrosis type I chromosome 11q12-13
-
Van Hul E, Gram J, Bollerslev J et al (2002). Localization of the gene causing autosomal dominant osteopetrosis type I chromosome 11q12-13. J Bone Miner Res 17: 1111-1117.
-
(2002)
J Bone Miner Res
, vol.17
, pp. 1111-1117
-
-
Van Hul, E.1
Gram, J.2
Bollerslev, J.3
|