Andrew M - Search Results

1

Five-Year Therapy with Recombinant Human Insulin-Like Growth Factor-1 in a Patient with PAPP-A2 Deficiency.

Muthuvel G, Dauber A, Alexandrou E, Tyzinski L, Andrew M, Hwa V, Backeljauw P. Muthuvel G, et al. Among authors: andrew m. Horm Res Paediatr. 2023;96(5):449-457. doi: 10.1159/000529071. Epub 2023 Jan 16. Horm Res Paediatr. 2023. PMID: 36646053

2

Severe Short Stature in Two Siblings as the Presenting Sign of ACP5 Deficiency.

de Bruin C, Orbak Z, Andrew M, Hwa V, Dauber A. de Bruin C, et al. Among authors: andrew m. Horm Res Paediatr. 2016;85(5):358-62. doi: 10.1159/000443684. Epub 2016 Jan 21. Horm Res Paediatr. 2016. PMID: 26789720 Free PMC article.

3

Pharmacokinetics of IGF-1 in PAPP-A2-Deficient Patients, Growth Response, and Effects on Glucose and Bone Density.

Cabrera-Salcedo C, Mizuno T, Tyzinski L, Andrew M, Vinks AA, Frystyk J, Wasserman H, Gordon CM, Hwa V, Backeljauw P, Dauber A. Cabrera-Salcedo C, et al. Among authors: andrew m. J Clin Endocrinol Metab. 2017 Dec 1;102(12):4568-4577. doi: 10.1210/jc.2017-01411. J Clin Endocrinol Metab. 2017. PMID: 29029190 Free PMC article. Clinical Trial.

4

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. Among authors: andrew m. 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.

5

Treatment of Short Stature in Aggrecan-deficient Patients With Recombinant Human Growth Hormone: 1-Year Response.

Muthuvel G, Dauber A, Alexandrou E, Tyzinski L, Andrew M, Hwa V, Backeljauw P. Muthuvel G, et al. Among authors: andrew m. J Clin Endocrinol Metab. 2022 Apr 19;107(5):e2103-e2109. doi: 10.1210/clinem/dgab904. J Clin Endocrinol Metab. 2022. PMID: 34922359 Free PMC article.

6

Two Patients with Severe Short Stature due to a FBN1 Mutation (p.Ala1728Val) with a Mild Form of Acromicric Dysplasia.

de Bruin C, Finlayson C, Funari MF, Vasques GA, Lucheze Freire B, Lerario AM, Andrew M, Hwa V, Dauber A, Jorge AA. de Bruin C, et al. Among authors: andrew m. Horm Res Paediatr. 2016;86(5):342-348. doi: 10.1159/000446476. Epub 2016 Jun 2. Horm Res Paediatr. 2016. PMID: 27245183 Free PMC article.

7

PAPPA2 as a Therapeutic Modulator of IGF-I Bioavailability: in Vivo and in Vitro Evidence.

Andrew M, Liao L, Fujimoto M, Khoury J, Hwa V, Dauber A. Andrew M, et al. J Endocr Soc. 2018 May 28;2(7):646-656. doi: 10.1210/js.2018-00106. eCollection 2018 Jul 1. J Endocr Soc. 2018. PMID: 29942928 Free PMC article.

8

Disorders caused by genetic defects associated with GH-dependent genes: PAPPA2 defects.

Fujimoto M, Andrew M, Dauber A. Fujimoto M, et al. Among authors: andrew m. 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.

9

Clinical phenotype and musculoskeletal characteristics of patients with aggrecan deficiency.

Alexandrou E, Dauber A, Tyzinski L, Hwa V, Andrew M, Kim H, Elangovan S, Gubanich P, Taylor-Haas JA, Paterno M, Backeljauw P. Alexandrou E, et al. Among authors: andrew m. Am J Med Genet A. 2022 Apr;188(4):1193-1203. doi: 10.1002/ajmg.a.62639. Epub 2022 Jan 9. Am J Med Genet A. 2022. PMID: 35001504

10

Isolated growth hormone deficiency due to the R183H mutation in GH1: Clinical analysis of a four-generation family.

Cabrera-Salcedo C, Shah AS, Andrew M, Tyzinski L, Hwa V, Gutmark-Little I, Backeljauw P, Dauber A. Cabrera-Salcedo C, et al. Among authors: andrew m. Clin Endocrinol (Oxf). 2017 Dec;87(6):874-876. doi: 10.1111/cen.13400. Epub 2017 Jul 21. Clin Endocrinol (Oxf). 2017. PMID: 28626954 Free PMC article. No abstract available.

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