-
2
-
-
33845577005
-
Recombinant human insulin-like growth factor-I (rhIGF-I) and rhIGF-I/rhIGF-binding-protein-3:new growth treatment options?
-
Rosenbloom AL: Recombinant human insulin-like growth factor-I (rhIGF-I) and rhIGF-I/rhIGF-binding-protein-3:new growth treatment options? J Pediatr 2007;150:7-11.
-
(2007)
J Pediatr
, vol.150
, pp. 7-11
-
-
Rosenbloom, A.L.1
-
4
-
-
0026488334
-
Saltation and stasis: A model of human growth
-
Lampl M, Veldhuis JD, Johnson ML: Saltation and stasis: a model of human growth. Science 1992;258:801-803.
-
(1992)
Science
, vol.258
, pp. 801-803
-
-
Lampl, M.1
Veldhuis, J.D.2
Johnson, M.L.3
-
5
-
-
84886618830
-
Shifting linear growth during infancy: Illustration of genetic factors in growth from fetal life through infancy
-
Smith DW, Truog W, Rogers JE, et al: Shifting linear growth during infancy: illustration of genetic factors in growth from fetal life through infancy. J Pediatr 1976;89:225-230.
-
(1976)
J Pediatr
, vol.89
, pp. 225-230
-
-
Smith, D.W.1
Truog, W.2
Rogers, J.E.3
-
7
-
-
41349090258
-
Overgrowth syndromes: Evaluation and management of the child with excessive linear growth; in Lifshitz F (ed): Pediatric Endocrinology
-
ed 5
-
Root AW, Diamond FB Jr: Overgrowth syndromes: evaluation and management of the child with excessive linear growth; in Lifshitz F (ed): Pediatric Endocrinology, ed 5. New York, Informa Health Care, 2007, vol 2, pp 163-194.
-
(2007)
New York, Informa Health Care
, vol.2
, pp. 163-194
-
-
Root, A.W.1
Diamond Jr, F.B.2
-
8
-
-
0016401794
-
Height and weight standards for preschool children
-
Habicht J-P, Martorelli R, Yarborough C, et al: Height and weight standards for preschool children. Lancet 1974;i:1051-1052.
-
(1974)
Lancet
, vol.1
, pp. 1051-1052
-
-
Habicht, J.-P.1
Martorelli, R.2
Yarborough, C.3
-
9
-
-
10144241062
-
Genetics, environment and growth: Issues in the assessment of nutritional status
-
Velazquez A, Bourges H eds, New York, Academic Press
-
Martorelli R: Genetics, environment and growth: Issues in the assessment of nutritional status; in Velazquez A, Bourges H (eds): Genetic Factors in Nutrition. New York, Academic Press, 1985.
-
(1985)
Genetic Factors in Nutrition
-
-
Martorelli, R.1
-
10
-
-
33646035837
-
Heterozygous mutations in natriuretic peptide receptor-B (NPR2) are associated with short stature
-
Olney RC, Bukulmez H, Bartels CF, et al: Heterozygous mutations in natriuretic peptide receptor-B (NPR2) are associated with short stature. J. Clin Endocrinol Metab 2006;91:1229-1232.
-
(2006)
J. Clin Endocrinol Metab
, vol.91
, pp. 1229-1232
-
-
Olney, R.C.1
Bukulmez, H.2
Bartels, C.F.3
-
11
-
-
0017376279
-
Hypopituitarism following extirpation of a pharyngeal pituitary
-
Weber FT, Donnelley WH, Behar RL: Hypopituitarism following extirpation of a pharyngeal pituitary. Am J Dis Child 1977;131:525-528.
-
(1977)
Am J Dis Child
, vol.131
, pp. 525-528
-
-
Weber, F.T.1
Donnelley, W.H.2
Behar, R.L.3
-
13
-
-
0034043216
-
Genetic regulation of the embryology of the pituitary gland and somatotrophs
-
Cohen LE: Genetic regulation of the embryology of the pituitary gland and somatotrophs. Endocrine 2000;12:99-106.
-
(2000)
Endocrine
, vol.12
, pp. 99-106
-
-
Cohen, L.E.1
-
14
-
-
17344362762
-
Mutations in the homeobox gene HESX1/HESX1 associated with septo optic dysplasia in human and in mouse
-
Dattani M, Martinez-Barbera J-P, Thomas PQ: Mutations in the homeobox gene HESX1/HESX1 associated with septo optic dysplasia in human and in mouse. Nat Genet 1998;19:125-133.
-
(1998)
Nat Genet
, vol.19
, pp. 125-133
-
-
Dattani, M.1
Martinez-Barbera, J.-P.2
Thomas, P.Q.3
-
15
-
-
0242383356
-
Enhanced repression by HESX1 as a cause of hypopituitarism and septooptic dysplasia
-
Cohen RN, Cohen LE, Botero D, et al: Enhanced repression by HESX1 as a cause of hypopituitarism and septooptic dysplasia. J Clin Endocrinol Metab 2003;88:4832-4839.
-
(2003)
J Clin Endocrinol Metab
, vol.88
, pp. 4832-4839
-
-
Cohen, R.N.1
Cohen, L.E.2
Botero, D.3
-
16
-
-
0036668183
-
Molecular basis of combined pituitary hormone deficiencies
-
Cohen LE, Radovick S: Molecular basis of combined pituitary hormone deficiencies. Endocr Rev 2002;23:431-442.
-
(2002)
Endocr Rev
, vol.23
, pp. 431-442
-
-
Cohen, L.E.1
Radovick, S.2
-
17
-
-
0028929541
-
Expression pattern of the murine LIM class homeobox gene Lhx3 in subsets of neural and neuroendocrine tissues
-
Zhadanov AB, Bertuzzi S, Taira M, et al: Expression pattern of the murine LIM class homeobox gene Lhx3 in subsets of neural and neuroendocrine tissues. Dev Dyn 1995;202:354-364.
-
(1995)
Dev Dyn
, vol.202
, pp. 354-364
-
-
Zhadanov, A.B.1
Bertuzzi, S.2
Taira, M.3
-
18
-
-
0034040904
-
Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency
-
Netchine I, Sobrier M-L, Krude H, et al: Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency. Nat Genet 2000;25:182-186.
-
(2000)
Nat Genet
, vol.25
, pp. 182-186
-
-
Netchine, I.1
Sobrier, M.-L.2
Krude, H.3
-
19
-
-
0034760533
-
Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4
-
Machinis K, Pantel J, Netchine I, et al: Syndromic short stature in patients with a germline mutation in the LIM homeobox LHX4. Am J Hum Genet 2001;69:961-968.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 961-968
-
-
Machinis, K.1
Pantel, J.2
Netchine, I.3
-
20
-
-
0344392285
-
Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features
-
Roessler EYZ, Mullor JL, Casas E, et al: Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features. Proc Natl Acad Sci USA 2003;100:13424-13429.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 13424-13429
-
-
Roessler, E.Y.Z.1
Mullor, J.L.2
Casas, E.3
-
21
-
-
0036212222
-
Increased gene dosage at Xq26-q27 is associated with X-linked hypopituitarism
-
Solomon NM, Nouri S, Warne GL, et al: Increased gene dosage at Xq26-q27 is associated with X-linked hypopituitarism. Genomics 2002;79:553-559.
-
(2002)
Genomics
, vol.79
, pp. 553-559
-
-
Solomon, N.M.1
Nouri, S.2
Warne, G.L.3
-
22
-
-
4444236951
-
Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3
-
Solomon NM, Ross SA, Morgan T, et al: Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3. J Med Genet 2004;41:669-678.
-
(2004)
J Med Genet
, vol.41
, pp. 669-678
-
-
Solomon, N.M.1
Ross, S.A.2
Morgan, T.3
-
23
-
-
0036913192
-
Transcription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiency
-
Laumonnier F, Ronce N, Hamel BC, et al: Transcription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiency. Am J Hum Genet 2002;71:1450-1455.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1450-1455
-
-
Laumonnier, F.1
Ronce, N.2
Hamel, B.C.3
-
24
-
-
20244386714
-
Overand underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism
-
Woods KS, Cundall M, Turton J, et al: Overand underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism. Am J Hum Genet 2005;76:833-849.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 833-849
-
-
Woods, K.S.1
Cundall, M.2
Turton, J.3
-
25
-
-
6344282311
-
PROP1 mutations cause progressive deterioration of anterior function including adrenal insufficiency: A longitudinal analysis
-
Bottner A, Keller E, Kratzsch J, et al: PROP1 mutations cause progressive deterioration of anterior function including adrenal insufficiency: a longitudinal analysis. J Clin Endocrinol Metab 2004;89:5256-5265.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 5256-5265
-
-
Bottner, A.1
Keller, E.2
Kratzsch, J.3
-
26
-
-
8744315604
-
A familial form of congenital hypopituitarism due to a PROP1 mutation in a large kindred: Phenotypic and in vitro functional studies
-
Reynaud R, Chadli-Chaieb M, Vallette-Kasic S, et al: A familial form of congenital hypopituitarism due to a PROP1 mutation in a large kindred: phenotypic and in vitro functional studies. J Clin Endocrinol Metab 2004;89:5779-5786.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 5779-5786
-
-
Reynaud, R.1
Chadli-Chaieb, M.2
Vallette-Kasic, S.3
-
27
-
-
2442568583
-
Pituitary magnetic resonance imaging in fifteen patients with PROP1 gene mutations: Pituitary enlargement may originate from the intermediate lobe
-
Voutetakis A, Argyropoulou M, Sertedaki A, et al: Pituitary magnetic resonance imaging in fifteen patients with PROP1 gene mutations: pituitary enlargement may originate from the intermediate lobe. J Clin Endocrinol Metab 2004;89:2200-2206.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 2200-2206
-
-
Voutetakis, A.1
Argyropoulou, M.2
Sertedaki, A.3
-
28
-
-
0032926727
-
Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of PROP-1 gene
-
Rosenbloom AL, Selman-Almonte A, Brown MR, et al: Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of PROP-1 gene. J Clin Endocrinol Metab 1999;84:50-57.
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 50-57
-
-
Rosenbloom, A.L.1
Selman-Almonte, A.2
Brown, M.R.3
-
29
-
-
23844487385
-
Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency
-
Turton JP, Reynaud R, Mehta A, et al: Novel mutations within the POU1F1 gene associated with variable combined pituitary hormone deficiency. J Clin Endocrinol Metab 2005;90:4762-4770.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 4762-4770
-
-
Turton, J.P.1
Reynaud, R.2
Mehta, A.3
-
30
-
-
0031732361
-
Phenotypic and genetic analysis of a syndrome caused by an inactivating mutation in the GH releasing hormone receptor: Dwarfism of Sindh
-
Maheshwari HG, Silverman BL, Dupuis J, Baumann G: Phenotypic and genetic analysis of a syndrome caused by an inactivating mutation in the GH releasing hormone receptor: dwarfism of Sindh. J Clin Endocrinol Metab 1998;83:4065-4074.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 4065-4074
-
-
Maheshwari, H.G.1
Silverman, B.L.2
Dupuis, J.3
Baumann, G.4
-
31
-
-
0034090514
-
Pituitary hypoplasia in patients with a mutation in the growth hormone-releasing hormone receptor gene
-
Murray RA, Maheshwari HG, Russell EJ, Baumann G: Pituitary hypoplasia in patients with a mutation in the growth hormone-releasing hormone receptor gene. Am J Neuroradiol 2000;21:685-689.
-
(2000)
Am J Neuroradiol
, vol.21
, pp. 685-689
-
-
Murray, R.A.1
Maheshwari, H.G.2
Russell, E.J.3
Baumann, G.4
-
32
-
-
0035142279
-
Three new mutations in the gene for the growth hormone (GH)-releasing hormone receptor in familial isolated GH deficiency type Ib
-
Salvatori R, Fan X, Phillips JA 3rd, et al: Three new mutations in the gene for the growth hormone (GH)-releasing hormone receptor in familial isolated GH deficiency type Ib. J Clin Endocrinol Metab 2001;86:273-279.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 273-279
-
-
Salvatori, R.1
Fan, X.2
Phillips 3rd, J.A.3
-
33
-
-
0023141980
-
Isolated growth hormone deficiency after cerebral edema complicating diabetic ketoacidosis
-
Keller RJ, Wolfsdorf JI: Isolated growth hormone deficiency after cerebral edema complicating diabetic ketoacidosis. N Engl J Med 1987;316:857-859.
-
(1987)
N Engl J Med
, vol.316
, pp. 857-859
-
-
Keller, R.J.1
Wolfsdorf, J.I.2
-
34
-
-
41349123418
-
-
Netter FH: The CIBA Collection of Medical Illustrations. 4: Endocrine System and Selected Metabolic Diseases. Chicago, Donnelley & Sons, 1964, section 1, plate 2.1.
-
Netter FH: The CIBA Collection of Medical Illustrations. Vol 4: Endocrine System and Selected Metabolic Diseases. Chicago, Donnelley & Sons, 1964, section 1, plate 2.1.
-
-
-
-
36
-
-
0021322884
-
On the in vitro and in vivo activity of a new synthetic hexapeptide that acts on the pituitary to specifically release growth hormone
-
Bowers CY, Momany F, Reynolds GA, Hong A: On the in vitro and in vivo activity of a new synthetic hexapeptide that acts on the pituitary to specifically release growth hormone. Endocrinology 1984;114:1531-1536.
-
(1984)
Endocrinology
, vol.114
, pp. 1531-1536
-
-
Bowers, C.Y.1
Momany, F.2
Reynolds, G.A.3
Hong, A.4
-
37
-
-
0026607276
-
Pituitary adenylate cyclase activating polypeptides, growth hormone (GH) releasing peptide and GH releasing hormone stimulate GH release through distinct pituitary receptors
-
Goth MI, Lyons CE, Canny BJ, Thorner MO: Pituitary adenylate cyclase activating polypeptides, growth hormone (GH) releasing peptide and GH releasing hormone stimulate GH release through distinct pituitary receptors. Endocrinology 1992;130:939-944.
-
(1992)
Endocrinology
, vol.130
, pp. 939-944
-
-
Goth, M.I.1
Lyons, C.E.2
Canny, B.J.3
Thorner, M.O.4
-
38
-
-
0033540056
-
Ghrelin is a growth hormone releasing acetylated peptide from stomach
-
Kojima M, Hosada H, Date Y, et al: Ghrelin is a growth hormone releasing acetylated peptide from stomach. Nature 1999;402:656-660.
-
(1999)
Nature
, vol.402
, pp. 656-660
-
-
Kojima, M.1
Hosada, H.2
Date, Y.3
-
39
-
-
0035039474
-
Unnatural growth hormone-releasing peptide begets natural ghrelin
-
Bowers CY: Unnatural growth hormone-releasing peptide begets natural ghrelin. J Clin Endocrinol Metab 2001;86:1464-1469.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 1464-1469
-
-
Bowers, C.Y.1
-
40
-
-
0035097594
-
The expression of the growth hormone secretagogue receptor ligand ghrelin in normal and abnormal human pituitary and other neuroendocrine tumors
-
Korbonits M, Bustin SA, Kojima M, et al: The expression of the growth hormone secretagogue receptor ligand ghrelin in normal and abnormal human pituitary and other neuroendocrine tumors. J Clin Endocrinol Metab 2001;86:881-887.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 881-887
-
-
Korbonits, M.1
Bustin, S.A.2
Kojima, M.3
-
41
-
-
31044451656
-
Neuro-hormonal control of food intake; basic mechanisms and clinical implications
-
Konturek PC, Konturek JW, Czesnikiewicz-Guzik M, et al: Neuro-hormonal control of food intake; basic mechanisms and clinical implications. J Physiol Pharmacol 2005;56(suppl 6):5-25.
-
(2005)
J Physiol Pharmacol
, vol.56
, Issue.SUPPL. 6
, pp. 5-25
-
-
Konturek, P.C.1
Konturek, J.W.2
Czesnikiewicz-Guzik, M.3
-
43
-
-
0021876594
-
Evidence for the specific binding of growth hormone to a receptor like protein in rabbit serum
-
Ymer SI, Herrington AC: Evidence for the specific binding of growth hormone to a receptor like protein in rabbit serum. Mol Cell Endocrinol 1985;41:153-161.
-
(1985)
Mol Cell Endocrinol
, vol.41
, pp. 153-161
-
-
Ymer, S.I.1
Herrington, A.C.2
-
44
-
-
2342488722
-
Absence of serum growth hormone binding protein in patients with growth hormone receptor deficiency (Laron dwarfism)
-
Daughaday WH, Trivedi B: Absence of serum growth hormone binding protein in patients with growth hormone receptor deficiency (Laron dwarfism). Proc Natl Acad Sci USA 1987;84:4636-4640.
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 4636-4640
-
-
Daughaday, W.H.1
Trivedi, B.2
-
45
-
-
0023627925
-
Absence of plasma growth hormone-binding protein in Laron-type dwarfism
-
Baumann G, Shaw MA, Winter RJ: Absence of plasma growth hormone-binding protein in Laron-type dwarfism. J Clin Endocrinol Metab 1987;65:814-816.
-
(1987)
J Clin Endocrinol Metab
, vol.65
, pp. 814-816
-
-
Baumann, G.1
Shaw, M.A.2
Winter, R.J.3
-
46
-
-
0023635603
-
Growth hormone receptor and serum binding protein: Purification, cloning and expression
-
Leung DW, Spencer SA, Cachianes G, et al: Growth hormone receptor and serum binding protein: purification, cloning and expression. Nature 1987;330:537-543.
-
(1987)
Nature
, vol.330
, pp. 537-543
-
-
Leung, D.W.1
Spencer, S.A.2
Cachianes, G.3
-
47
-
-
0346628520
-
Characterization of the human growth hormone receptor gene and demonstration of a partial gene deletion in two patients with Laron-type dwarfism
-
Godowski PJ, Leung DW, Meacham LR, et al: Characterization of the human growth hormone receptor gene and demonstration of a partial gene deletion in two patients with Laron-type dwarfism. Proc Natl Acad Sci USA 1989;86:8083-8087.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 8083-8087
-
-
Godowski, P.J.1
Leung, D.W.2
Meacham, L.R.3
-
48
-
-
2042466343
-
Growth hormone-prolactin receptor gene family
-
Shiverick KT, Rosenbloom AL eds, Boca Raton, CRC Press
-
Kelly PA, Nagano M, Sotiropoulos A, et al: Growth hormone-prolactin receptor gene family; in Shiverick KT, Rosenbloom AL (eds): Human Growth Hormone Pharmacology: Basic and Clinical Aspects. Boca Raton, CRC Press, 1995, pp 13-28.
-
(1995)
Human Growth Hormone Pharmacology: Basic and Clinical Aspects
, pp. 13-28
-
-
Kelly, P.A.1
Nagano, M.2
Sotiropoulos, A.3
-
49
-
-
0026598960
-
Human growth hormone and extracellular domain of its receptor: Crystal structure of the complex
-
de Vos AM, Ultsch M, Kossiakoff AA: Human growth hormone and extracellular domain of its receptor: crystal structure of the complex. Science 1992;255:306-312.
-
(1992)
Science
, vol.255
, pp. 306-312
-
-
de Vos, A.M.1
Ultsch, M.2
Kossiakoff, A.A.3
-
50
-
-
0030665990
-
Growth-hormone signal transduction
-
Campbell GS: Growth-hormone signal transduction. J Pediatr 1997;131:S42-S44.
-
(1997)
J Pediatr
, vol.131
-
-
Campbell, G.S.1
-
52
-
-
0029780688
-
Alternative spliced forms in the cytoplasmic domain of the human growth hormone (GH) receptor regulate its ability to generate a soluble GH binding protein
-
Dastot F, Sobrier ML, Duquesnoy P, et al: Alternative spliced forms in the cytoplasmic domain of the human growth hormone (GH) receptor regulate its ability to generate a soluble GH binding protein. Proc Natl Acad Sci USA 1996;93:10723-10728.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 10723-10728
-
-
Dastot, F.1
Sobrier, M.L.2
Duquesnoy, P.3
-
53
-
-
0035092767
-
Gene expression of a truncated and the full-length growth hormone (GH) receptor in subcutaneous fat and skeletal muscle in GH-deficient adults: Impact of GH treatment
-
Fisker S, Kristensen K, Rosenfalck AM, et al: Gene expression of a truncated and the full-length growth hormone (GH) receptor in subcutaneous fat and skeletal muscle in GH-deficient adults: impact of GH treatment. J Clin Endocrinol Metab 2001;86:792-796.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 792-796
-
-
Fisker, S.1
Kristensen, K.2
Rosenfalck, A.M.3
-
54
-
-
41349114742
-
Hypopituitarism and other disorders of the growth hormone-insulin-like growth factor-I axis; in Lifshitz F (ed): Pediatric Endocrinology
-
ed 5
-
Rosenbloom AL, Connor EL: Hypopituitarism and other disorders of the growth hormone-insulin-like growth factor-I axis; in Lifshitz F (ed): Pediatric Endocrinology, ed 5. New York, Informa Health Care, 2007, vol 2, pp 65-99.
-
(2007)
New York, Informa Health Care
, vol.2
, pp. 65-99
-
-
Rosenbloom, A.L.1
Connor, E.L.2
-
55
-
-
33749074521
-
Founder effect of E180-splice mutation in growth hormone receptor gene (GHR) identified in Brazilian patients with GH insensitivity. Arq Bras Endocrinol
-
de Lima Jorge AA, de Menezes Filho HC, Soares Lins TS, et al: Founder effect of E180-splice mutation in growth hormone receptor gene (GHR) identified in Brazilian patients with GH insensitivity. Arq Bras Endocrinol Metabol 2005;49:384-389.
-
(2005)
Metabol
, vol.49
, pp. 384-389
-
-
de Lima Jorge, A.A.1
de Menezes Filho, H.C.2
Soares Lins, T.S.3
-
57
-
-
0023446097
-
Mechanism of the stimulatory effect of growth hormone on longitudinal bone growth
-
Isaksson OG, Lindahl A, Nilsson A, Isgaard J: Mechanism of the stimulatory effect of growth hormone on longitudinal bone growth. Endocr Rev 1987;8:426-438.
-
(1987)
Endocr Rev
, vol.8
, pp. 426-438
-
-
Isaksson, O.G.1
Lindahl, A.2
Nilsson, A.3
Isgaard, J.4
-
58
-
-
0018184054
-
The amino acid sequence of human insulin like growth factor I and its structural homology with proinsulin
-
Rinderknecht E, Humbel RE: The amino acid sequence of human insulin like growth factor I and its structural homology with proinsulin. J Biol Chem 1978;253:2769-2776.
-
(1978)
J Biol Chem
, vol.253
, pp. 2769-2776
-
-
Rinderknecht, E.1
Humbel, R.E.2
-
59
-
-
0017887021
-
Primary structure of human insulin like growth factor II
-
Rinderknecht E, Humbel RE: Primary structure of human insulin like growth factor II. FEBS Lett 1978;89:283-287.
-
(1978)
FEBS Lett
, vol.89
, pp. 283-287
-
-
Rinderknecht, E.1
Humbel, R.E.2
-
60
-
-
0031792813
-
Recommendations for nomenclature of the insulin-like growth factor binding proteins superfamily
-
Baxter RG, Binoux MA, Clemmons DR, et al: Recommendations for nomenclature of the insulin-like growth factor binding proteins superfamily. J Clin Endocrinol Metab 1998;83:3213.
-
(1998)
J Clin Endocrinol Metab
, vol.83
, pp. 3213
-
-
Baxter, R.G.1
Binoux, M.A.2
Clemmons, D.R.3
-
61
-
-
27744468209
-
Acid-labile subunit deficiency: Phenotypic similarities and differences between human and mouse
-
Domene HM, Bengolea SV, Jasper HG, Boisclair YR: Acid-labile subunit deficiency: phenotypic similarities and differences between human and mouse. J Endocrinol Invest 2005;28(suppl):43-46.
-
(2005)
J Endocrinol Invest
, vol.28
, Issue.SUPPL.
, pp. 43-46
-
-
Domene, H.M.1
Bengolea, S.V.2
Jasper, H.G.3
Boisclair, Y.R.4
-
62
-
-
0027272980
-
Hormonal and metabolic effects and pharmacokinetics of recombinant human insulin-like growth factor-I in GH receptor deficiency/Laron syndrome
-
Vaccarello MA, Diamond FB Jr, Guevara-Aguirre J, et al: Hormonal and metabolic effects and pharmacokinetics of recombinant human insulin-like growth factor-I in GH receptor deficiency/Laron syndrome. J Clin Endocrinol Metab 1993;77:273-280.
-
(1993)
J Clin Endocrinol Metab
, vol.77
, pp. 273-280
-
-
Vaccarello, M.A.1
Diamond Jr, F.B.2
Guevara-Aguirre, J.3
-
63
-
-
0034131121
-
Genetics, chemistry, and function of the IGF/IGFBP system
-
Collett-Solberg PF, Cohen P: Genetics, chemistry, and function of the IGF/IGFBP system. Endocrine 2000;12:121-136.
-
(2000)
Endocrine
, vol.12
, pp. 121-136
-
-
Collett-Solberg, P.F.1
Cohen, P.2
-
64
-
-
0029065857
-
Insulin like growth factors and their binding proteins in the term and preterm human fetus and neonate with normal and extremes of intrauterine growth
-
Giudice LC, de Zegher F, Gargosky SE, et al: Insulin like growth factors and their binding proteins in the term and preterm human fetus and neonate with normal and extremes of intrauterine growth. J Clin Endocrinol Metab 1995;80:1548-1555.
-
(1995)
J Clin Endocrinol Metab
, vol.80
, pp. 1548-1555
-
-
Giudice, L.C.1
de Zegher, F.2
Gargosky, S.E.3
-
65
-
-
0029787983
-
The growth without growth hormone syndrome
-
Geffner ME: The growth without growth hormone syndrome. Endocrinol Metab Clin North Am 1996;25:649-663.
-
(1996)
Endocrinol Metab Clin North Am
, vol.25
, pp. 649-663
-
-
Geffner, M.E.1
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