Grüters A - Search Results

1

[Hypothyroidism in dizygotic premature twins due to excessive prepartal vaginal iodine application].

Müther S, Krude H, Jäger R, Rhode W, Grüters A, Rossi R. Müther S, et al. Among authors: gruters a. Zentralbl Gynakol. 2003 Jun;125(6):226-8. doi: 10.1055/s-2003-42907. Zentralbl Gynakol. 2003. PMID: 14556121 German.

2

Iodine in contrast agents and skin disinfectants is the major cause for hypothyroidism in premature infants during intensive care.

l'Allemand D, Grüters A, Beyer P, Weber B. l'Allemand D, et al. Among authors: gruters a. Horm Res. 1987;28(1):42-9. doi: 10.1159/000180924. Horm Res. 1987. PMID: 3447940

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. 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. 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

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

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