Grüters A - Search Results

1

A New Multisystem Disorder Caused by the Gαs Mutation p.F376V.

Biebermann H, Kleinau G, Schnabel D, Bockenhauer D, Wilson LC, Tully I, Kiff S, Scheerer P, Reyes M, Paisdzior S, Gregory JW, Allgrove J, Krude H, Mannstadt M, Gardella TJ, Dattani M, Jüppner H, Grüters A. Biebermann H, et al. Among authors: gruters a. J Clin Endocrinol Metab. 2019 Apr 1;104(4):1079-1089. doi: 10.1210/jc.2018-01250. J Clin Endocrinol Metab. 2019. PMID: 30312418 Free PMC article.

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. Horm Res. 1994;41(1):3-9. Horm Res. 1994. PMID: 8013940 Review. No abstract available.

3

Transient congenital hypothyroidism and hyperthyrotropinemia: normal thyroid function and physical development at the ages of 6-14 years.

Köhler B, Schnabel D, Biebermann H, Gruters A. Köhler B, et al. Among authors: gruters a. J Clin Endocrinol Metab. 1996 Apr;81(4):1563-7. doi: 10.1210/jcem.81.4.8636368. J Clin Endocrinol Metab. 1996. PMID: 8636368

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. Among authors: gruters a. 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. 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: gruters a. 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. Among authors: gruters a. 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. 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

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. Among authors: gruters a. Nat Genet. 1998 Jun;19(2):155-7. doi: 10.1038/509. Nat Genet. 1998. PMID: 9620771

10

V2 vasopressin receptor dysfunction in nephrogenic diabetes insipidus caused by different molecular mechanisms.

Schöneberg T, Schulz A, Biebermann H, Grüters A, Grimm T, Hübschmann K, Filler G, Gudermann T, Schultz G. Schöneberg T, et al. Among authors: gruters a. Hum Mutat. 1998;12(3):196-205. doi: 10.1002/(SICI)1098-1004(1998)12:3<196::AID-HUMU7>3.0.CO;2-F. Hum Mutat. 1998. PMID: 9711877

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