-
1
-
-
0001473635
-
Syndrome characterized by osteitis fibrosa disseminata, areas of pigmentation and endocrine dysfunction, with precocious puberty in females: Report of five cases
-
Albright F, Butler AM, Hampton AO, Smith P: Syndrome characterized by osteitis fibrosa disseminata. areas of pigmentation and endocrine dysfunction, with precocious puberty in females: Report of five cases. N Engl J Med 1937:216:727-746.
-
(1937)
N Engl J Med
, vol.216
, pp. 727-746
-
-
Albright, F.1
Butler, A.M.2
Hampton, A.O.3
Smith, P.4
-
2
-
-
0000439832
-
Osteitis fibrosa cystica: The case of a nine-year-old girl who also exhibits precocious puberty, multiple pigmentation of the skin and hyperthyroidism
-
McCune DJ: Osteitis fibrosa cystica: The case of a nine-year-old girl who also exhibits precocious puberty, multiple pigmentation of the skin and hyperthyroidism. Am J Dis Child 1936:52:743-744.
-
(1936)
Am J Dis Child
, vol.52
, pp. 743-744
-
-
Mc Cune, D.J.1
-
4
-
-
0028323562
-
An unusual presentation of McCunc-Albright syndrome confirmed by an activating mutation of the G, a-subunit from a bone lesion
-
Malchoff CD. Reardon G. MacGillivray DC, et al: An unusual presentation of McCunc-Albright syndrome confirmed by an activating mutation of the G, a-subunit from a bone lesion. J Clin Endocrinol Metab 1994:78: 803-806.
-
(1994)
J Clin Endocrinol Metab
, vol.78
, pp. 803-806
-
-
Malchoff, C.D.1
Reardon, G.2
Macgillivray, D.C.3
-
5
-
-
0028169341
-
An activating G, a mutation is present in fibrous dysplasia of bone in the McCune-Albright syndrome
-
Shenker A, Weinstein LS, Sweet DE, et al: An activating G, a mutation is present in fibrous dysplasia of bone in the McCune-Albright syndrome. J Clin Endocrinol Metab 1994:79:750-755.
-
(1994)
J Clin Endocrinol Metab
, vol.79
, pp. 750-755
-
-
Shenker, A.1
Weinstein, L.S.2
Sweet, D.E.3
-
6
-
-
0017156603
-
Alopecia with fibrous dysplasia and osteomas of skin: A sign of polyostotic fibrous dysplasia
-
Shelley WB, Wood MG: Alopecia with fibrous dysplasia and osteomas of skin: A sign of polyostotic fibrous dysplasia. Arch Dermatol 1976:112:715-719.
-
(1976)
Arch Dermatol
, vol.112
, pp. 715-719
-
-
Shelley, W.B.1
Wood, M.G.2
-
7
-
-
0026003074
-
Activating mutations of the stimulatory C protein in the McCunc-Albright syndrome
-
Weinstein LS, Shenker A. Gejman PV. et al: Activating mutations of the stimulatory C protein in the McCunc-Albright syndrome. N Engl J Med 1991:325:1688-1695.
-
(1991)
N Engl J Med
, vol.325
, pp. 1688-1695
-
-
Weinstein, L.S.1
Shenker, A.2
Gejman, P.V.3
-
8
-
-
0026075596
-
The McCune-Albright syndrome: The whys and wherefores of abnormal signal transduction
-
Levine MA: The McCune-Albright syndrome: The whys and wherefores of abnormal signal transduction. N Engl J Med 1991;325: 1738-1740.
-
(1991)
N Engl J Med
, vol.325
, pp. 1738-1740
-
-
Levine, M.A.1
-
9
-
-
0027482950
-
Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein G
-
Shenker A, Weinstein LS. Moran A, et al: Severe endocrine and nonendocrine manifestations of the McCune-Albright syndrome associated with activating mutations of stimulatory G protein G,. J Pediatr 1993:123:509-518.
-
(1993)
J Pediatr
, vol.123
, pp. 509-518
-
-
Shenker, A.1
Weinstein, L.S.2
Moran, A.3
-
10
-
-
84909453751
-
Diagnostic importance of cafe-au-lait spot in neurofibromatosis
-
Crowe FW, Schull WJ: Diagnostic importance of cafe-au-lait spot in neurofibromatosis. Arch Intern Med 1953:91:758-766.
-
(1953)
Arch Intern Med
, vol.91
, pp. 758-766
-
-
Crowe, F.W.1
Schull, W.J.2
-
11
-
-
0014431125
-
Melanotic macules in Albright’s syndrome and in neurofibromatosis
-
Benedict PH. Szabo G, Fitzpatrick TC. et al: Melanotic macules in Albright’s syndrome and in neurofibromatosis. J Am Med Assoc 1968; 205:618-626.
-
(1968)
J am Med Assoc
, vol.205
, pp. 618-626
-
-
Benedict, P.H.1
Szabo, G.2
Fitzpatrick, T.C.3
-
12
-
-
0023128723
-
Neurofibromatosis and Albright’s syndrome
-
Riccardi VM: Neurofibromatosis and Albright’s syndrome. Dermatol Clin 1987:5: 193-203.
-
(1987)
Dermatol Clin
, vol.5
, pp. 193-203
-
-
Riccardi, V.M.1
-
14
-
-
0015173235
-
Albright's hereditary osteodystrophy with cutaneous bone formation
-
Eyre WG, Reed WB: Albright's hereditary osteodystrophy with cutaneous bone formation. Arch Dermatol 1971; 104:635-642.
-
(1971)
Arch Dermatol
, vol.104
, pp. 635-642
-
-
Eyre, W.G.1
Reed, W.B.2
-
15
-
-
0025323257
-
Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy
-
Patten JL. Johns DR. Valle D. et al: Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy. N Engl J Med 1990:322: 1412-1419.
-
(1990)
N Engl J Med
, vol.322
, pp. 1412-1419
-
-
Patten, J.L.1
Johns, D.R.2
Valle, D.3
-
16
-
-
0027210606
-
Heterogenous mutations in the gene encoding the alpha-subunit of the stimulatory G protein of adenylyl cyclase in Albright hereditary osteodystrophy
-
Mirie A, Vechio JD, Levine MA: Heterogenous mutations in the gene encoding the alpha-subunit of the stimulatory G protein of adenylyl cyclase in Albright hereditary osteodystrophy. J Clin Endocrinol Metab 1993; 76:1560-1568.
-
(1993)
J Clin Endocrinol Metab
, vol.76
, pp. 1560-1568
-
-
Mirie, A.1
Vechio, J.D.2
Levine, M.A.3
|