-
1
-
-
10544256602
-
Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism
-
Sornson MW, Wu W, Dasen JS, et al. Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism. Nature 1996, 384: 327-33.
-
(1996)
Nature
, vol.384
, pp. 327-333
-
-
Sornson, M.W.1
Wu, W.2
Dasen, J.S.3
-
2
-
-
17344371881
-
Mutations in PROP1 cause familial combined pituitary hormone deficiency
-
Wu W, Cogan JD, Pfaffle RW, et al. Mutations in PROP1 cause familial combined pituitary hormone deficiency. Nat Genet 1998, 18: 147-9.
-
(1998)
Nat Genet
, vol.18
, pp. 147-149
-
-
Wu, W.1
Cogan, J.D.2
Pfaffle, R.W.3
-
3
-
-
0037155604
-
Pituitary development: Regulatory codes in mammalian organogenesis
-
Scully KM, Rosenfeld MG. Pituitary development: regulatory codes in mammalian organogenesis. Science 2002, 295: 2231-5.
-
(2002)
Science
, vol.295
, pp. 2231-2235
-
-
Scully, K.M.1
Rosenfeld, M.G.2
-
4
-
-
0036668183
-
Molecular basis of combined pituitary hormone deficiencies
-
Cohen LE, Radovick S. Molecular basis of combined pituitary hormone deficiencies. Endocr Rev 2002, 23: 431-42.
-
(2002)
Endocr Rev
, vol.23
, pp. 431-442
-
-
Cohen, L.E.1
Radovick, S.2
-
5
-
-
0033305649
-
Heritable disorders of pituitary development
-
Parks JS, Brown MR, Hurley DL, Phelps CJ, Wajnrajch MP. Heritable disorders of pituitary development. J Clin Endocrinol Metab 1999, 84: 4362-70.
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 4362-4370
-
-
Parks, J.S.1
Brown, M.R.2
Hurley, D.L.3
Phelps, C.J.4
Wajnrajch, M.P.5
-
6
-
-
0032989717
-
Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301, G302 in the PROP1 gene
-
Mendonca BB, Osorio MG, Latronico AC, Estefan V, Lo LS, Arnhold IJ. Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301, G302 in the PROP1 gene. J Clin Endocrinol Metab 1999, 84: 942-5.
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 942-945
-
-
Mendonca, B.B.1
Osorio, M.G.2
Latronico, A.C.3
Estefan, V.4
Lo, L.S.5
Arnhold, I.J.6
-
7
-
-
0033971815
-
MR imaging of the pituitary gland in children and young adults with congenital combined pituitary hormone deficiency associated with PROP1 mutations
-
Fofanova O, Takamura N, Kinoshita E, et al. MR imaging of the pituitary gland in children and young adults with congenital combined pituitary hormone deficiency associated with PROP1 mutations. AJR Am J Roentgenol 2000, 174: 555-9.
-
(2000)
AJR Am J Roentgenol
, vol.174
, pp. 555-559
-
-
Fofanova, O.1
Takamura, N.2
Kinoshita, E.3
-
8
-
-
0034853603
-
Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutation
-
Riepe FG, Partsch CJ, Blankenstein O, Monig H, Pfaffle RW, Sippell WG. Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutation. J Clin Endocrinol Metab 2001, 86: 4353-7.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 4353-4357
-
-
Riepe, F.G.1
Partsch, C.J.2
Blankenstein, O.3
Monig, H.4
Pfaffle, R.W.5
Sippell, W.G.6
-
9
-
-
2442568583
-
Pituitary MR imaging in 15 patients with PROP1 gene mutations: Pituitary enlargement may originate from the intermediate lobe
-
Voutetakis A, Argyropoulou MI, Sertedaki A, et al. Pituitary MR imaging in 15 patients with PROP1 gene mutations: pituitary enlargement may originate from the intermediate lobe. J Clin Endocrinol Metab 2004, 89: 2200-6.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 2200-2206
-
-
Voutetakis, A.1
Argyropoulou, M.I.2
Sertedaki, A.3
-
10
-
-
85039325201
-
Pituitary enlargement in patients with PROP1 gene mutations originate from the intermediate lobe. Evidence from long term pituitary MR Imaging in 18 patients
-
(European Society for Paediatric Endocrinology, 43rd Annual Meeting, Basel 2004)
-
Sertedaki A, Voutetakis A, Argyropoulou M, et al. Pituitary enlargement in patients with PROP1 gene mutations originate from the intermediate lobe. Evidence from long term pituitary MR Imaging in 18 patients (European Society for Paediatric Endocrinology, 43rd Annual Meeting, Basel 2004). Horm Res 2004, 62 (Suppl 2): 21.
-
(2004)
Horm Res
, vol.62
, Issue.SUPPL. 2
, pp. 21
-
-
Sertedaki, A.1
Voutetakis, A.2
Argyropoulou, M.3
-
11
-
-
0025911051
-
Height of normal pituitary gland as a function of age evaluated by magnetic resonance imaging in children
-
Argyropoulou M, Perignon F, Brunelle F, Brauner R, Rappaport R. Height of normal pituitary gland as a function of age evaluated by magnetic resonance imaging in children. Pediatr Radiol 1991, 21: 247-9.
-
(1991)
Pediatr Radiol
, vol.21
, pp. 247-249
-
-
Argyropoulou, M.1
Perignon, F.2
Brunelle, F.3
Brauner, R.4
Rappaport, R.5
-
12
-
-
0031741771
-
Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg - >Cys at codon 120 (R120C)
-
Fluck C, Deladoey J, Rutishauser K, et al. Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg - >Cys at codon 120 (R120C). J Clin Endocrinol Metab 1998, 83: 3727-34.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 3727-3734
-
-
Fluck, C.1
Deladoey, J.2
Rutishauser, K.3
-
13
-
-
0036360499
-
A unique case of combined pituitary hormone deficiency caused by a PROP1 gene mutation (R120C) associated with normal height and absent puberty
-
Arroyo A, Pernasetti F, Vasilyev VV, Amato P, Yen SS, Mellon PL. A unique case of combined pituitary hormone deficiency caused by a PROP1 gene mutation (R120C) associated with normal height and absent puberty. Clin Endocrinol (Oxf) 2002, 57: 283-91.
-
(2002)
Clin Endocrinol (Oxf)
, vol.57
, pp. 283-291
-
-
Arroyo, A.1
Pernasetti, F.2
Vasilyev, V.V.3
Amato, P.4
Yen, S.S.5
Mellon, P.L.6
-
14
-
-
6344282311
-
PROP1 mutations cause progressive deterioration of anterior pituitary function including adrenal insufficiency: A longitudinal analysis
-
Bottner A, Keller E, Kratzsch J, et al. PROP1 mutations cause progressive deterioration of anterior pituitary function including adrenal insufficiency: a longitudinal analysis. J Clin Endocrinol Metab 2004, 89: 5256-65.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 5256-5265
-
-
Bottner, A.1
Keller, E.2
Kratzsch, J.3
-
15
-
-
0036745788
-
Lhx4 and PROP1 are required for cell survival and expansion of the pituitary primordia
-
Raetzman LT, Ward R, Camper SA. Lhx4 and PROP1 are required for cell survival and expansion of the pituitary primordia. Development 2002, 129: 4229-39.
-
(2002)
Development
, vol.129
, pp. 4229-4239
-
-
Raetzman, L.T.1
Ward, R.2
Camper, S.A.3
-
16
-
-
14844322343
-
Role of PROP1 in pituitary gland growth
-
Ward RD, Raetzman LT, Suh H, Stone BM, Nasonkin IO, Camper SA. Role of PROP1 in pituitary gland growth. Mol Endocrinol 2005, 19: 698-710.
-
(2005)
Mol Endocrinol
, vol.19
, pp. 698-710
-
-
Ward, R.D.1
Raetzman, L.T.2
Suh, H.3
Stone, B.M.4
Nasonkin, I.O.5
Camper, S.A.6
-
17
-
-
0035576879
-
Temporal regulation of a paired-like homeodomain repressor/TLE corepressor complex and a related activator is required for pituitary organogenesis
-
Dasen JS, Barbera JP, Herman TS, et al. Temporal regulation of a paired-like homeodomain repressor/TLE corepressor complex and a related activator is required for pituitary organogenesis. Genes Dev 2001, 15: 3193-207.
-
(2001)
Genes Dev
, vol.15
, pp. 3193-3207
-
-
Dasen, J.S.1
Barbera, J.P.2
Herman, T.S.3
-
18
-
-
0018092337
-
Familial hypopituitarism with large sella turcica
-
Parks JS, Tenore A, Bongiovanni AM, Kirkland RT. Familial hypopituitarism with large sella turcica. N Engl J Med 1978, 298: 698-702.
-
(1978)
N Engl J Med
, vol.298
, pp. 698-702
-
-
Parks, J.S.1
Tenore, A.2
Bongiovanni, A.M.3
Kirkland, R.T.4
-
19
-
-
22044451892
-
Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD)
-
Turton JP, Mehta A, Raza J, et al. Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD). Clin Endocrinol (Oxf) 2005, 63: 10-8.
-
(2005)
Clin Endocrinol (Oxf)
, vol.63
, pp. 10-18
-
-
Turton, J.P.1
Mehta, A.2
Raza, J.3
-
20
-
-
0002546131
-
Natural history and molecular mechanisms of hypopituitarism with large sella turcica
-
(abstract)
-
Parks JS, Baumbach L, Sanchez JC, Stanley CA, Gianella-Neto D. Natural history and molecular mechanisms of hypopituitarism with large sella turcica. Proccedings of the 80th Annual Meeting of the Endocrine Society. 1998, P470 (abstract).
-
(1998)
Proccedings of the 80th Annual Meeting of the Endocrine Society
-
-
Parks, J.S.1
Baumbach, L.2
Sanchez, J.C.3
Stanley, C.A.4
Gianella-Neto, D.5
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