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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2018 | 1 |
2019 | 3 |
2020 | 3 |
2024 | 0 |
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5 results
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Page 1
Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Endocrine. 2020 Aug;69(2):262-277. doi: 10.1007/s12020-020-02323-3. Epub 2020 May 5.
Endocrine. 2020.
PMID: 32367336
Free PMC article.
Review.
Stumbling broke the spleen and unveiled pheochromocytoma, which in turn broke the heart.
Y-Hassan S, Falhammar H.
Y-Hassan S, et al.
Endocrine. 2020 Mar;67(3):727-728. doi: 10.1007/s12020-019-02169-4. Epub 2019 Dec 27.
Endocrine. 2020.
PMID: 31883060
Free PMC article.
No abstract available.
Item in Clipboard
Inverse association between glucose-lowering medications and severe hyponatremia: a Swedish population-based case-control study.
Falhammar H, Skov J, Calissendorff J, Lindh JD, Mannheimer B.
Falhammar H, et al.
Endocrine. 2020 Mar;67(3):579-586. doi: 10.1007/s12020-019-02160-z. Epub 2019 Dec 25.
Endocrine. 2020.
PMID: 31875925
Free PMC article.
Item in Clipboard
Clinical perspectives in congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase type 2 deficiency.
Al Alawi AM, Nordenström A, Falhammar H.
Al Alawi AM, et al.
Endocrine. 2019 Mar;63(3):407-421. doi: 10.1007/s12020-018-01835-3. Epub 2019 Feb 4.
Endocrine. 2019.
PMID: 30719691
Free PMC article.
Review.
Item in Clipboard
Psychological adjustment, quality of life, and self-perceptions of reproductive health in males with congenital adrenal hyperplasia: a systematic review.
Daae E, Feragen KB, Nermoen I, Falhammar H.
Daae E, et al.
Endocrine. 2018 Oct;62(1):3-13. doi: 10.1007/s12020-018-1723-0. Epub 2018 Aug 20.
Endocrine. 2018.
PMID: 30128958
Free PMC article.
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