Wedell A - Search Results

1

Male sex determination and prenatal differentiation of the testis.

Töhönen V, Ritzén EM, Nordqvist K, Wedell A. Töhönen V, et al. Among authors: wedell a. Endocr Dev. 2003;5:1-23. doi: 10.1159/000069299. Endocr Dev. 2003. PMID: 12629889 Review. No abstract available.

2

Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations.

Wedell A, Ritzén EM, Haglund-Stengler B, Luthman H. Wedell A, et al. Proc Natl Acad Sci U S A. 1992 Aug 1;89(15):7232-6. doi: 10.1073/pnas.89.15.7232. Proc Natl Acad Sci U S A. 1992. PMID: 1496017 Free PMC article.

3

Early growth is not increased in untreated moderately severe 21-hydroxylase deficiency.

Thilén A, Woods KA, Perry LA, Savage MO, Wedell A, Ritzén EM. Thilén A, et al. Among authors: wedell a. Acta Paediatr. 1995 Aug;84(8):894-8. doi: 10.1111/j.1651-2227.1995.tb13788.x. Acta Paediatr. 1995. PMID: 7488813

4

Mutational spectrum of the steroid 21-hydroxylase gene in Sweden: implications for genetic diagnosis and association with disease manifestation.

Wedell A, Thilén A, Ritzén EM, Stengler B, Luthman H. Wedell A, et al. J Clin Endocrinol Metab. 1994 May;78(5):1145-52. doi: 10.1210/jcem.78.5.8175971. J Clin Endocrinol Metab. 1994. PMID: 8175971

5

The use of adrenalectomy as a treatment for congenital adrenal hyperplasia.

Van Wyk JJ, Gunther DF, Ritzén EM, Wedell A, Cutler GB Jr, Migeon CJ, New MI. Van Wyk JJ, et al. Among authors: wedell a. J Clin Endocrinol Metab. 1996 Sep;81(9):3180-90. doi: 10.1210/jcem.81.9.8784066. J Clin Endocrinol Metab. 1996. PMID: 8784066 No abstract available.

6

Prophylactic adrenalectomy of a three-year-old girl with congenital adrenal hyperplasia: pre- and postoperative studies.

Gunther DF, Bukowski TP, Ritzén EM, Wedell A, Van Wyk JJ. Gunther DF, et al. Among authors: wedell a. J Clin Endocrinol Metab. 1997 Oct;82(10):3324-7. doi: 10.1210/jcem.82.10.4281. J Clin Endocrinol Metab. 1997. PMID: 9329362

7

Long-term somatic follow-up of prenatally treated children with congenital adrenal hyperplasia.

Lajic S, Wedell A, Bui TH, Ritzén EM, Holst M. Lajic S, et al. Among authors: wedell a. J Clin Endocrinol Metab. 1998 Nov;83(11):3872-80. doi: 10.1210/jcem.83.11.5233. J Clin Endocrinol Metab. 1998. PMID: 9814461 Clinical Trial.

8

Functional characterisation of mutations in the ligand-binding domain of the androgen receptor gene in patients with androgen insensitivity syndrome.

Lundberg Giwercman Y, Nikoshkov A, Lindsten K, Byström B, Pousette A, Chibalin AV, Arvidsson S, Tiulpakov A, Semitcheva TV, Peterkova V, Hagenfeldt K, Ritzén EM, Wedell A. Lundberg Giwercman Y, et al. Among authors: wedell a. Hum Genet. 1998 Oct;103(4):529-31. doi: 10.1007/s004390050864. Hum Genet. 1998. PMID: 9856504

9

Failure of cortisone acetate treatment in congenital adrenal hyperplasia because of defective 11beta-hydroxysteroid dehydrogenase reductase activity.

Nordenström A, Marcus C, Axelson M, Wedell A, Ritzén EM. Nordenström A, et al. Among authors: wedell a. J Clin Endocrinol Metab. 1999 Apr;84(4):1210-3. doi: 10.1210/jcem.84.4.5584. J Clin Endocrinol Metab. 1999. PMID: 10199755

10

How can molecular biology contribute to the management of congenital adrenal hyperplasia?

Ritzén EM, Lajic S, Wedell A. Ritzén EM, et al. Among authors: wedell a. Horm Res. 2000;53 Suppl 1:34-7. doi: 10.1159/000053202. Horm Res. 2000. PMID: 10895040 Review.

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

161 results

Search Page

Filters