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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 1
1990 2
1992 2
1993 2
1994 2
1995 1
1996 3
1997 2
1998 5
1999 1
2000 1
2001 3
2002 1
2010 1
2020 0
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27 results
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Page 1
Hypercalcemia in children and adolescents.
Lietman SA, Germain-Lee EL, Levine MA. Lietman SA, et al. Curr Opin Pediatr. 2010 Aug;22(4):508-15. doi: 10.1097/MOP.0b013e32833b7c23. Curr Opin Pediatr. 2010. PMID: 20601885 Free PMC article. Review.
Determination of transgene copy number and expression level using denaturing gradient gel electrophoresis.
Ringel MD, Schwindinger WF, Saji M, Zeiger MA, Levine MA. Ringel MD, et al. Biotechniques. 1998 Jan;24(1):126, 128-31. doi: 10.2144/98241st06. Biotechniques. 1998. PMID: 9454964 Free article.
Targeted disruption of Gnas in embryonic stem cells.
Schwindinger WF, Reese KJ, Lawler AM, Gearhart JD, Levine MA. Schwindinger WF, et al. Endocrinology. 1997 Oct;138(10):4058-63. doi: 10.1210/endo.138.10.5439. Endocrinology. 1997. PMID: 9322912
Growth hormone-releasing peptide-2 stimulates GH secretion in GH-deficient patients with mutated GH-releasing hormone receptor.
Gondo RG, Aguiar-Oliveira MH, Hayashida CY, Toledo SP, Abelin N, Levine MA, Bowers CY, Souza AH, Pereira RM, Santos NL, Salvatori R. Gondo RG, et al. J Clin Endocrinol Metab. 2001 Jul;86(7):3279-83. doi: 10.1210/jcem.86.7.7694. J Clin Endocrinol Metab. 2001. PMID: 11443201
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, Espigares-Martin R, Martin De Lara I, Freeman KL, Plotnick L, Al-Ashwal A, Levine MA. Salvatori R, et al. J Clin Endocrinol Metab. 2001 Jan;86(1):273-9. doi: 10.1210/jcem.86.1.7156. J Clin Endocrinol Metab. 2001. PMID: 11232012
Familial isolated hypoparathyroidism caused by a mutation in the gene for the transcription factor GCMB.
Ding C, Buckingham B, Levine MA. Ding C, et al. J Clin Invest. 2001 Oct;108(8):1215-20. doi: 10.1172/JCI13180. J Clin Invest. 2001. PMID: 11602629 Free PMC article.
Decreased expression of the GHRH receptor gene due to a mutation in a Pit-1 binding site.
Salvatori R, Fan X, Mullis PE, Haile A, Levine MA. Salvatori R, et al. Mol Endocrinol. 2002 Mar;16(3):450-8. doi: 10.1210/mend.16.3.0785. Mol Endocrinol. 2002. PMID: 11875102
Absence of activating mutations of the genes encoding the alpha-subunits of G11 and Gq in thyroid neoplasia.
Ringel MD, Saji M, Schwindinger WF, Segev D, Zeiger MA, Levine MA. Ringel MD, et al. J Clin Endocrinol Metab. 1998 Feb;83(2):554-9. doi: 10.1210/jcem.83.2.4536. J Clin Endocrinol Metab. 1998. PMID: 9467574
Effect of severe growth hormone (GH) deficiency due to a mutation in the GH-releasing hormone receptor on insulin-like growth factors (IGFs), IGF-binding proteins, and ternary complex formation throughout life.
Aguiar-Oliveira MH, Gill MS, de A Barretto ES, Alcântara MR, Miraki-Moud F, Menezes CA, Souza AH, Martinelli CE, Pereira FA, Salvatori R, Levine MA, Shalet SM, Camacho-Hubner C, Clayton PE. Aguiar-Oliveira MH, et al. J Clin Endocrinol Metab. 1999 Nov;84(11):4118-26. doi: 10.1210/jcem.84.11.6133. J Clin Endocrinol Metab. 1999. PMID: 10566659
Deficiency of the alpha-subunit of the stimulatory G protein and severe extraskeletal ossification.
Eddy MC, Jan De Beur SM, Yandow SM, McAlister WH, Shore EM, Kaplan FS, Whyte MP, Levine MA. Eddy MC, et al. J Bone Miner Res. 2000 Nov;15(11):2074-83. doi: 10.1359/jbmr.2000.15.11.2074. J Bone Miner Res. 2000. PMID: 11092390 Free article.
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