Grüters A - Search Results

1

Constitutively activating TSH-receptor mutations as a molecular cause of non-autoimmune hyperthyroidism in childhood.

Biebermann H, Schöneberg T, Krude H, Gudermann T, Grüters A. Biebermann H, et al. Among authors: gruters a. Langenbecks Arch Surg. 2000 Oct;385(6):390-2. doi: 10.1007/s004230000145. Langenbecks Arch Surg. 2000. PMID: 11127522

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 TSH receptor as cause of congenital hyperthyroidism.

Schwab KO, Söhlemann P, Gerlich M, Broecker M, Petrykowski W, Holzapfel HP, Paschke R, Grüters A, Derwahl M. Schwab KO, et al. Among authors: gruters a. Exp Clin Endocrinol Diabetes. 1996;104 Suppl 4:124-8. doi: 10.1055/s-0029-1211719. Exp Clin Endocrinol Diabetes. 1996. PMID: 8981019

7

Congenital hypothyroidism caused by mutations in the thyrotropin-receptor gene.

Biebermann H, Grüters A, Schöneberg T, Gudermann T. Biebermann H, et al. Among authors: gruters a. N Engl J Med. 1997 May 8;336(19):1390-1. doi: 10.1056/NEJM199705083361914. N Engl J Med. 1997. PMID: 9139226 No abstract available.

8

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

9

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.

10

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

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