Krude H - Search Results

1

Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency.

Krude H, Schütz B, Biebermann H, von Moers A, Schnabel D, Neitzel H, Tönnies H, Weise D, Lafferty A, Schwarz S, DeFelice M, von Deimling A, van Landeghem F, DiLauro R, Grüters A. Krude H, et al. J Clin Invest. 2002 Feb;109(4):475-80. doi: 10.1172/JCI14341. J Clin Invest. 2002. PMID: 11854319 Free PMC article.

2

[The human chorionic gonadotropin (hCG) receptor: a new class within the family of GTP protein coupled receptors. Epitope mapping of receptor-bound agonistic and antagonistic forms of hCG].

Schwarz S, Krude H. Schwarz S, et al. Among authors: krude h. Wien Klin Wochenschr. 1992;104(13):369-90. Wien Klin Wochenschr. 1992. PMID: 1636261 Review. German.

3

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.

4

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.

5

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

6

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

7

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.

8

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

9

PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis.

Macchia PE, Lapi P, Krude H, Pirro MT, Missero C, Chiovato L, Souabni A, Baserga M, Tassi V, Pinchera A, Fenzi G, Grüters A, Busslinger M, Di Lauro R. Macchia PE, et al. Among authors: krude h. Nat Genet. 1998 May;19(1):83-6. doi: 10.1038/ng0598-83. Nat Genet. 1998. PMID: 9590296

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

165 results

Search Page

Filters