-
1
-
-
0028080819
-
Molecular basis of familial growth hormone deficiency
-
Perez Jurado LA, Argente J. Molecular basis of familial growth hormone deficiency. Horm Res 1994; 42: 189-97.
-
(1994)
Horm Res
, vol.42
, pp. 189-197
-
-
Perez Jurado, L.A.1
Argente, J.2
-
2
-
-
0027982794
-
Genetic basis of endocrine disease 6. Molecular basis of familial human growth hormone deficiency
-
Phillips III JA, Cogan JD. Genetic basis of endocrine disease 6. Molecular basis of familial human growth hormone deficiency. J Clin Endocrinol Metab 1994; 78: 11-6.
-
(1994)
J Clin Endocrinol Metab
, vol.78
, pp. 11-16
-
-
Phillips III, J.A.1
Cogan, J.D.2
-
3
-
-
0025341416
-
Use of polymerase chain reaction in detection of growth hormone gene deletions
-
Vnencak-Jones CL, Phillips III JA, De-fen W. Use of polymerase chain reaction in detection of growth hormone gene deletions. J Clin Endocrinol Metab 1990; 70: 1550-3.
-
(1990)
J Clin Endocrinol Metab
, vol.70
, pp. 1550-1553
-
-
Vnencak-Jones, C.L.1
Phillips III, J.A.2
De-fen, W.3
-
4
-
-
0026607454
-
Detection of molecular heterogeneity in GH-1 gene deletions by analysis of polymerase chain reaction amplification products
-
Kamijo T, Phillips III JA. Detection of molecular heterogeneity in GH-1 gene deletions by analysis of polymerase chain reaction amplification products. J Clin Endocrinol Metab 1992; 74: 786-9.
-
(1992)
J Clin Endocrinol Metab
, vol.74
, pp. 786-789
-
-
Kamijo, T.1
Phillips III, J.A.2
-
5
-
-
0030043732
-
Plasma GH responses to human GHRH-antagonist in normal subjects
-
Hanew K, Tanaka A, Utsumi A, Sugawara A, Abe K. Plasma GH responses to human GHRH-antagonist in normal subjects. Eur J Endocrinol 1996; 134: 67-72.
-
(1996)
Eur J Endocrinol
, vol.134
, pp. 67-72
-
-
Hanew, K.1
Tanaka, A.2
Utsumi, A.3
Sugawara, A.4
Abe, K.5
-
6
-
-
0027257086
-
Plasma GH responses to sequential 3 day administrations of GHRH followed by arginine infusion in patients with idiopathic GH deficiency and normal short children
-
Hanew K, Utsumi A, Sugawara A, Shimizu Y, Tazawa S, Abe K. Plasma GH responses to sequential 3 day administrations of GHRH followed by arginine infusion in patients with idiopathic GH deficiency and normal short children. Tohoku J Exp Med 1993; 169: 91-101.
-
(1993)
Tohoku J Exp Med
, vol.169
, pp. 91-101
-
-
Hanew, K.1
Utsumi, A.2
Sugawara, A.3
Shimizu, Y.4
Tazawa, S.5
Abe, K.6
-
7
-
-
0028269008
-
Enhanced GH responses to combined administration of GHRP and GHRH in patients with acromegaly
-
Hanew K, Utsumi A, Sugawara A, Shimizu Y, Abe K. Enhanced GH responses to combined administration of GHRP and GHRH in patients with acromegaly. J Clin Endocrinol Metab 1994; 78: 509-12.
-
(1994)
J Clin Endocrinol Metab
, vol.78
, pp. 509-512
-
-
Hanew, K.1
Utsumi, A.2
Sugawara, A.3
Shimizu, Y.4
Abe, K.5
-
8
-
-
0029014128
-
Screening for PIT1 abnormality by PCR direct sequencing method
-
Irie Y, Tatsumi K, Kusuda S, Kawawaki H, Boyages SC, Nose O, et al. Screening for PIT1 abnormality by PCR direct sequencing method. Thyroid 1995; 5: 207-11.
-
(1995)
Thyroid
, vol.5
, pp. 207-211
-
-
Irie, Y.1
Tatsumi, K.2
Kusuda, S.3
Kawawaki, H.4
Boyages, S.C.5
Nose, O.6
-
9
-
-
0027284128
-
A new mutation causing inherited growth hormone deficiency: A compound heterozygote of a 6.7 kb deletion and a two base deletion in the third exon of the GH-1 gene
-
Igarashi Y, Ogawa M, Kamijo T, Iwatani N, Nishi Y, Kohno H, et al. A new mutation causing inherited growth hormone deficiency: a compound heterozygote of a 6.7 kb deletion and a two base deletion in the third exon of the GH-1 gene. Hum Mol Genet 1993; 2: 1073-4.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1073-1074
-
-
Igarashi, Y.1
Ogawa, M.2
Kamijo, T.3
Iwatani, N.4
Nishi, Y.5
Kohno, H.6
-
10
-
-
0027212155
-
Heterogeneous growth hormone (GH) gene mutations in familial GH deficiency
-
Cogan JD, Phillips III JA, Sakati N, Frisch H, Schober E, Milner RDG. Heterogeneous growth hormone (GH) gene mutations in familial GH deficiency. J Clin Endocrinol Metab 1993; 76: 1224-8.
-
(1993)
J Clin Endocrinol Metab
, vol.76
, pp. 1224-1228
-
-
Cogan, J.D.1
Phillips III, J.A.2
Sakati, N.3
Frisch, H.4
Schober, E.5
Milner, R.D.G.6
-
11
-
-
0028037298
-
Familial growth hormone deficiency: A model of dominant and recessive mutations affecting a monomeric protein
-
Cogan JD, Phillips III JA, Schenkman SS, Milner RDG, Sakati N. Familial growth hormone deficiency: a model of dominant and recessive mutations affecting a monomeric protein. J Clin Endocrinol Metab 1994; 79:1261-5.
-
(1994)
J Clin Endocrinol Metab
, vol.79
, pp. 1261-1265
-
-
Cogan, J.D.1
Phillips III, J.A.2
Schenkman, S.S.3
Milner, R.D.G.4
Sakati, N.5
-
12
-
-
0028811675
-
A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency - A clinical research center study
-
Cogan JD, Ramel B, Lehto M, Phillips III JA, Prince M, Blizzard RM, et al. A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency- a clinical research center study. J Clin Endocrinol Metab 1995; 80: 3591-5.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 3591-3595
-
-
Cogan, J.D.1
Ramel, B.2
Lehto, M.3
Phillips III, J.A.4
Prince, M.5
Blizzard, R.M.6
-
13
-
-
0028955078
-
Screening for growth hormone (GH) gene splice-site mutations in sporadic cases with severe isolated GH deficiency using ectopic transcript analysis
-
Binder G, Ranke MB. Screening for growth hormone (GH) gene splice-site mutations in sporadic cases with severe isolated GH deficiency using ectopic transcript analysis. J Clin Endocrinol Metab 1995; 80: 1247-52.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 1247-1252
-
-
Binder, G.1
Ranke, M.B.2
-
14
-
-
0029839542
-
Mechanisms responsible for dominant expression of human growth hormone gene mutations
-
Binder G, Brown M, Parks JS. Mechanisms responsible for dominant expression of human growth hormone gene mutations. J Clin Endocrinol Metab 1996; 81: 4047-50.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 4047-4050
-
-
Binder, G.1
Brown, M.2
Parks, J.S.3
-
15
-
-
0021223874
-
Isolated growth hormone deficiency type 1A in a Japanese family
-
Nishi Y, Aihara K, Usui T, Phillips JA 3d, Mallonee RL, Migeon CJ. Isolated growth hormone deficiency type 1A in a Japanese family. J Pediatr 1984; 104: 885-9.
-
(1984)
J Pediatr
, vol.104
, pp. 885-889
-
-
Nishi, Y.1
Aihara, K.2
Usui, T.3
Phillips III, J.A.4
Mallonee, R.L.5
Migeon, C.J.6
-
16
-
-
0023413904
-
Heterogeneous phenotypes of Japanese cases with a growth hormone gene deletion
-
Matsuda I, Hata A, Jinno Y, Endo F, Akaboshi I, Nishi Y, et al. Heterogeneous phenotypes of Japanese cases with a growth hormone gene deletion. Jinrui Idengaku Zasshi 1987; 32: 227-35.
-
(1987)
Jinrui Idengaku Zasshi
, vol.32
, pp. 227-235
-
-
Matsuda, I.1
Hata, A.2
Jinno, Y.3
Endo, F.4
Akaboshi, I.5
Nishi, Y.6
|