Ertl DA - Search Results

1

Lethal Encephalopathy in an Infant with Hypophosphatasia despite Enzyme Replacement Therapy.

Raimann A, Haberler C, Patsch J, Ertl DA, Sadeghi K, Freilinger M, Lang S, Schmook M, Plecko B, Haeusler G. Raimann A, et al. Among authors: ertl da. Horm Res Paediatr. 2021;94(9-10):390-398. doi: 10.1159/000520341. Epub 2021 Oct 21. Horm Res Paediatr. 2021. PMID: 34673643 Free article.

2

A novel homozygous mutation in the parathyroid hormone gene (PTH) in a girl with isolated hypoparathyroidism.

Ertl DA, Stary S, Streubel B, Raimann A, Haeusler G. Ertl DA, et al. Bone. 2012 Sep;51(3):629-32. doi: 10.1016/j.bone.2012.06.009. Epub 2012 Jun 18. Bone. 2012. PMID: 22722080

3

Fibroblast growth factor 23 and Klotho are present in the growth plate.

Raimann A, Ertl DA, Helmreich M, Sagmeister S, Egerbacher M, Haeusler G. Raimann A, et al. Among authors: ertl da. Connect Tissue Res. 2013;54(2):108-17. doi: 10.3109/03008207.2012.753879. Epub 2013 Jan 18. Connect Tissue Res. 2013. PMID: 23206185

4

Determining the normal range for IGF-I, IGFBP-3, and ALS: new reference data based on current internal standards.

Ertl DA, Gleiss A, Sagmeister S, Haeusler G. Ertl DA, et al. Wien Med Wochenschr. 2014 Sep;164(17-18):343-52. doi: 10.1007/s10354-014-0299-4. Epub 2014 Sep 4. Wien Med Wochenschr. 2014. PMID: 25186253

5

A Pediatric Patient with a CYP24A1 Mutation: Four Years of Clinical, Biochemical, and Imaging Follow-Up.

Ertl DA, Raimann A, Csaicsich D, Patsch JM, Laccone F, Haeusler G. Ertl DA, et al. Horm Res Paediatr. 2017;87(3):196-204. doi: 10.1159/000450947. Epub 2016 Nov 1. Horm Res Paediatr. 2017. PMID: 27798933

6

Care of girls and women with Turner syndrome: beyond growth and hormones.

Culen C, Ertl DA, Schubert K, Bartha-Doering L, Haeusler G. Culen C, et al. Among authors: ertl da. Endocr Connect. 2017 May;6(4):R39-R51. doi: 10.1530/EC-17-0036. Epub 2017 Mar 23. Endocr Connect. 2017. PMID: 28336768 Free PMC article. Review.

7

Health status, quality of life and medical care in adult women with Turner syndrome.

Ertl DA, Gleiss A, Schubert K, Culen C, Hauck P, Ott J, Gessl A, Haeusler G. Ertl DA, et al. Endocr Connect. 2018 Apr;7(4):534-543. doi: 10.1530/EC-18-0053. Epub 2018 Mar 7. Endocr Connect. 2018. PMID: 29514898 Free PMC article.

8

Diagnostic Value of Serum Acid-Labile Subunit Alone and in combination with IGF-I and IGFBP-3 in the Diagnosis of Growth Hormone Deficiency.

Ertl DA, Chen J, Gleiss A, Janu D, Sagmeister S, Raimann A, Riedl S, Haeusler G. Ertl DA, et al. Horm Res Paediatr. 2020;93(6):371-379. doi: 10.1159/000512336. Epub 2020 Dec 18. Horm Res Paediatr. 2020. PMID: 33341813

9

Bone and growth: basic principles behind rare disorders.

Raimann A, Ertl DA, Haeusler G. Raimann A, et al. Among authors: ertl da. Wien Med Wochenschr. 2021 Apr;171(5-6):86-93. doi: 10.1007/s10354-020-00809-3. Epub 2021 Jan 27. Wien Med Wochenschr. 2021. PMID: 33502636 English.

10

Growth pattern in children with X-linked hypophosphatemia treated with burosumab and growth hormone.

Ertl DA, Le Lorier J, Gleiss A, Trabado S, Bensignor C, Audrain C, Zhukouskaya V, Coutant R, Berkenou J, Rothenbuhler A, Haeusler G, Linglart A. Ertl DA, et al. Orphanet J Rare Dis. 2022 Nov 12;17(1):412. doi: 10.1186/s13023-022-02562-9. Orphanet J Rare Dis. 2022. PMID: 36371259 Free PMC article.

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