Krude H - Search Results

1

European Society for Paediatric Endocrinology consensus guidelines on screening, diagnosis, and management of congenital hypothyroidism.

Léger J, Olivieri A, Donaldson M, Torresani T, Krude H, van Vliet G, Polak M, Butler G; ESPE-PES-SLEP-JSPE-APEG-APPES-ISPAE; Congenital Hypothyroidism Consensus Conference Group. Léger J, et al. Among authors: krude h. J Clin Endocrinol Metab. 2014 Feb;99(2):363-84. doi: 10.1210/jc.2013-1891. Epub 2014 Jan 21. J Clin Endocrinol Metab. 2014. PMID: 24446653 Free PMC article.

2

The gene for the thyrotropin receptor (TSHR) as a candidate gene for congenital hypothyroidism with thyroid dysgenesis.

Krude H, Biebermann H, Göpel W, Grüters A. Krude H, et al. Exp Clin Endocrinol Diabetes. 1996;104 Suppl 4:117-20. doi: 10.1055/s-0029-1211717. Exp Clin Endocrinol Diabetes. 1996. PMID: 8981017 Review.

3

Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidism.

Grüters A, Köhler B, Wolf A, Söling A, de Vijlder L, Krude H, Biebermann H. Grüters A, et al. Among authors: krude h. Exp Clin Endocrinol Diabetes. 1996;104 Suppl 4:121-3. doi: 10.1055/s-0029-1211718. Exp Clin Endocrinol Diabetes. 1996. PMID: 8981018

4

Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidism.

Biebermann H, Schöneberg T, Krude H, Schultz G, Gudermann T, Grüters A. Biebermann H, et al. Among authors: krude h. J Clin Endocrinol Metab. 1997 Oct;82(10):3471-80. doi: 10.1210/jcem.82.10.4286. J Clin Endocrinol Metab. 1997. PMID: 9329388

5

Long-term consequences of congenital hypothyroidism in the era of screening programmes.

Grüters A, Jenner A, Krude H. Grüters A, et al. Among authors: krude h. Best Pract Res Clin Endocrinol Metab. 2002 Jun;16(2):369-82. doi: 10.1053/beem.2002.0202. Best Pract Res Clin Endocrinol Metab. 2002. PMID: 12064898 Review.

6

The use of L-T4 as liquid solution improves the practicability and individualized dosage in newborns and infants with congenital hypothyroidism.

von Heppe JH, Krude H, L'Allemand D, Schnabel D, Grüters A. von Heppe JH, et al. Among authors: krude h. J Pediatr Endocrinol Metab. 2004 Jul;17(7):967-74. doi: 10.1515/jpem.2004.17.7.967. J Pediatr Endocrinol Metab. 2004. PMID: 15301044

7

Molecular genetic defects in congenital hypothyroidism.

Grüters A, Krude H, Biebermann H. Grüters A, et al. Among authors: krude h. Eur J Endocrinol. 2004 Nov;151 Suppl 3:U39-44. doi: 10.1530/eje.0.151u039. Eur J Endocrinol. 2004. PMID: 15554885 Review.

8

Childhood obesity.

Speiser PW, Rudolf MC, Anhalt H, Camacho-Hubner C, Chiarelli F, Eliakim A, Freemark M, Gruters A, Hershkovitz E, Iughetti L, Krude H, Latzer Y, Lustig RH, Pescovitz OH, Pinhas-Hamiel O, Rogol AD, Shalitin S, Sultan C, Stein D, Vardi P, Werther GA, Zadik Z, Zuckerman-Levin N, Hochberg Z; Obesity Consensus Working Group. Speiser PW, et al. Among authors: krude h. J Clin Endocrinol Metab. 2005 Mar;90(3):1871-87. doi: 10.1210/jc.2004-1389. Epub 2004 Dec 14. J Clin Endocrinol Metab. 2005. PMID: 15598688 Review.

9

Update on the management of congenital hypothyroidism.

Grüters A, Krude H. Grüters A, et al. Among authors: krude h. Horm Res. 2007;68 Suppl 5:107-11. doi: 10.1159/000110591. Epub 2007 Dec 10. Horm Res. 2007. PMID: 18174723 Review.

10

Screening chromosomal aberrations by array comparative genomic hybridization in 80 patients with congenital hypothyroidism and thyroid dysgenesis.

Thorwarth A, Mueller I, Biebermann H, Ropers HH, Grueters A, Krude H, Ullmann R. Thorwarth A, et al. Among authors: krude h. J Clin Endocrinol Metab. 2010 Jul;95(7):3446-52. doi: 10.1210/jc.2009-2195. Epub 2010 Apr 28. J Clin Endocrinol Metab. 2010. PMID: 20427504

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