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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 2 |
2020 | 2 |
2021 | 2 |
2024 | 0 |
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5 results
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Page 1
Disorders caused by genetic defects associated with GH-dependent genes: PAPPA2 defects.
Mol Cell Endocrinol. 2020 Dec 1;518:110967. doi: 10.1016/j.mce.2020.110967. Epub 2020 Jul 30.
Mol Cell Endocrinol. 2020.
PMID: 32739295
Free PMC article.
Review.
Racial and Ethnic Disparities in the Investigation and Treatment of Growth Hormone Deficiency.
Hawkes CP, Gunturi H, Dauber A, Hirschhorn JN, Grimberg A.
Hawkes CP, et al.
J Pediatr. 2021 Sep;236:238-245. doi: 10.1016/j.jpeds.2021.04.034. Epub 2021 Apr 23.
J Pediatr. 2021.
PMID: 33901521
Free PMC article.
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Growth Hormone Stimulation Testing Patterns Contribute to Sex Differences in Pediatric Growth Hormone Treatment.
Kamoun C, Hawkes CP, Gunturi H, Dauber A, Hirschhorn JN, Grimberg A.
Kamoun C, et al.
Horm Res Paediatr. 2021;94(9-10):353-363. doi: 10.1159/000520250. Epub 2021 Oct 18.
Horm Res Paediatr. 2021.
PMID: 34662877
Free PMC article.
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Algorithm-Driven Electronic Health Record Notification Enhances the Detection of Turner Syndrome.
Alexandrou E, Cabrera-Salcedo C, Labilloy G, Tyzinski L, Smolarek TA, Andrew M, Huang Y, Backeljauw P, Dauber A.
Alexandrou E, et al.
J Pediatr. 2020 Jan;216:227-231. doi: 10.1016/j.jpeds.2019.09.023. Epub 2019 Oct 18.
J Pediatr. 2020.
PMID: 31635814
Free PMC article.
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Targeted Searches of the Electronic Health Record and Genomics Identify an Etiology in Three Patients with Short Stature and High IGF-I Levels.
Cabrera-Salcedo C, Hawkes CP, Tyzinski L, Andrew M, Labilloy G, Campos D, Feld A, Deodati A, Hwa V, Hirschhorn JN, Grimberg A, Dauber A; the Genomics Research and Innovation Network.
Cabrera-Salcedo C, et al.
Horm Res Paediatr. 2019;92(3):186-195. doi: 10.1159/000504884. Epub 2019 Dec 20.
Horm Res Paediatr. 2019.
PMID: 31865343
Free PMC article.
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