Similar articles for PMID: 25492860

Year	Number of Results
1987	1
1988	1
1992	1
1995	1
1996	1
1998	1
2000	1
2002	5
2003	2
2004	1
2005	5
2006	5
2007	4
2008	4
2009	5
2010	5
2011	2
2012	3
2013	3
2014	4
2015	4
2016	3
2017	2
2018	6
2019	4
2020	5
2021	2
2023	1
2024	0

1

Pacak-Zhuang Syndrome: A New Kid on The Block.

Vicha A, Mercado-Asis LB. Vicha A, et al. Endocr Pract. 2014 Nov;20(11):1234-5. doi: 10.4158/endp.20.11.g37v757188j41v24. Endocr Pract. 2014. PMID: 25492860 No abstract available.

2

Polycythemia and paraganglioma with a novel somatic HIF2A mutation in a male.

Toyoda H, Hirayama J, Sugimoto Y, Uchida K, Ohishi K, Hirayama M, Komada Y. Toyoda H, et al. Pediatrics. 2014 Jun;133(6):e1787-91. doi: 10.1542/peds.2013-2419. Epub 2014 May 12. Pediatrics. 2014. PMID: 24819565

3

[More attention should be paid to Pacak-Zhuang Syndrome].

Yu H, Jia W. Yu H, et al. Zhonghua Yi Xue Za Zhi. 2015 Jul 14;95(26):2049-50. Zhonghua Yi Xue Za Zhi. 2015. PMID: 26710863 Chinese. No abstract available.

4

A new twist in neuroendocrine tumor research: Pacak-Zhuang syndrome, HIF-2α as the major player in its pathogenesis and future therapeutic options.

Jochmanova I, Lazurova I. Jochmanova I, et al. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2014 Jun;158(2):175-80. doi: 10.5507/bp.2014.021. Epub 2014 Apr 29. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2014. PMID: 24781045 Free article. Review.

5

¹²³ I-metaiodobenzylguanidine radio-guided navigation surgery for multiple recurrent paragangliomas.

Nagano Y, Inoue M, Uchida K, Otake K, Kusunoki M. Nagano Y, et al. Pediatr Int. 2020 Feb;62(2):231-232. doi: 10.1111/ped.14093. Pediatr Int. 2020. PMID: 32104990 No abstract available.

6

Genetic heterogeneity of KID syndrome: identification of a Cx30 gene (GJB6) mutation in a patient with KID syndrome and congenital atrichia.

Jan AY, Amin S, Ratajczak P, Richard G, Sybert VP. Jan AY, et al. J Invest Dermatol. 2004 May;122(5):1108-13. doi: 10.1111/j.0022-202X.2004.22518.x. J Invest Dermatol. 2004. PMID: 15140211 Free article.

7

HID and KID syndromes are associated with the same connexin 26 mutation.

van Geel M, van Steensel MA, Küster W, Hennies HC, Happle R, Steijlen PM, König A. van Geel M, et al. Br J Dermatol. 2002 Jun;146(6):938-42. doi: 10.1046/j.1365-2133.2002.04893.x. Br J Dermatol. 2002. PMID: 12072059

8

Kid-Short Marfan Score (Kid-SMS) Is a Useful Diagnostic Tool for Stratifying the Pre-Test Probability of Marfan Syndrome in Childhood.

Stark VC, Arndt F, Harring G, von Kodolitsch Y, Kozlik-Feldmann R, Mueller GC, Steiner KJ, Mir TS. Stark VC, et al. Diseases. 2015 Mar 12;3(1):24-33. doi: 10.3390/diseases3010024. Diseases. 2015. PMID: 28943606 Free PMC article.

9

Chiari Malformation Type 1 in EPAS1-Associated Syndrome.

Rosenblum JS, Maggio D, Pang Y, Nazari MA, Gonzales MK, Lechan RM, Smirniotopoulos JG, Zhuang Z, Pacak K, Heiss JD. Rosenblum JS, et al. Int J Mol Sci. 2019 Jun 10;20(11):2819. doi: 10.3390/ijms20112819. Int J Mol Sci. 2019. PMID: 31185588 Free PMC article.

10

The Kid-Short Marfan Score (Kid-SMS) - an easy executable risk score for suspected paediatric patients with Marfan syndrome.

Mueller GC, Stark V, Steiner K, Weil J, von Kodolitsch Y, Mir TS. Mueller GC, et al. Acta Paediatr. 2013 Feb;102(2):e84-9. doi: 10.1111/apa.12072. Epub 2012 Dec 7. Acta Paediatr. 2013. PMID: 23110520

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 NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

75 results

Results by year