Krude H - Search Results

1

Autosomal-dominant mode of inheritance of a melanocortin-4 receptor mutation in a patient with severe early-onset obesity is due to a dominant-negative effect caused by receptor dimerization.

Biebermann H, Krude H, Elsner A, Chubanov V, Gudermann T, Grüters A. Biebermann H, et al. Among authors: krude h. Diabetes. 2003 Dec;52(12):2984-8. doi: 10.2337/diabetes.52.12.2984. Diabetes. 2003. PMID: 14633860

2

Etiological grouping of permanent congenital hypothyroidism with a thyroid gland in situ.

Grüters A, Finke R, Krude H, Meinhold H. Grüters A, et al. Among authors: krude h. Horm Res. 1994;41(1):3-9. Horm Res. 1994. PMID: 8013940 Review. No abstract available.

3

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.

4

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

5

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

6

Congenital hyperthyroidism.

Krude H, Biebermann H, Krohn HP, Dralle H, Grüters A. Krude H, et al. Exp Clin Endocrinol Diabetes. 1997;105 Suppl 4:6-11. doi: 10.1055/s-0029-1211924. Exp Clin Endocrinol Diabetes. 1997. PMID: 9439907 Review.

7

Severe congenital hyperthyroidism caused by a germ-line neo mutation in the extracellular portion of the thyrotropin receptor.

Grüters A, Schöneberg T, Biebermann H, Krude H, Krohn HP, Dralle H, Gudermann T. Grüters A, et al. Among authors: krude h. J Clin Endocrinol Metab. 1998 May;83(5):1431-6. doi: 10.1210/jcem.83.5.4776. J Clin Endocrinol Metab. 1998. PMID: 9589634

8

Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans.

Krude H, Biebermann H, Luck W, Horn R, Brabant G, Grüters A. Krude H, et al. Nat Genet. 1998 Jun;19(2):155-7. doi: 10.1038/509. Nat Genet. 1998. PMID: 9620771

9

Alterations of neonatal thyroid function.

Grüters A, Krude H, Biebermann H, Liesenkötter KP, Schöneberg T, Gudermann T. Grüters A, et al. Among authors: krude h. Acta Paediatr Suppl. 1999 Feb;88(428):17-22. doi: 10.1111/j.1651-2227.1999.tb14346.x. Acta Paediatr Suppl. 1999. PMID: 10102047 Review.

10

Implications of proopiomelanocortin (POMC) mutations in humans: the POMC deficiency syndrome.

Krude H, Grüters A. Krude H, et al. Trends Endocrinol Metab. 2000 Jan-Feb;11(1):15-22. doi: 10.1016/s1043-2760(99)00213-1. Trends Endocrinol Metab. 2000. PMID: 10652501 Review.

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