Similar articles for PMID: 30186640

Year	Number of Results
1996	2
1997	2
1998	9
1999	7
2000	4
2001	1
2002	2
2003	4
2004	3
2005	2
2006	4
2007	3
2008	3
2010	3
2011	2
2012	2
2013	3
2014	1
2015	3
2016	6
2017	8
2018	8
2019	5
2020	2
2024	0

1

Giant Prolactinoma of Young Onset: A Clue to Diagnosis of MEN-1 Syndrome.

Subasinghe CJ, Somasundaram N, Sivatharshya P, Ranasinghe LD, Korbonits M. Subasinghe CJ, et al. Case Rep Endocrinol. 2018 Aug 14;2018:2875074. doi: 10.1155/2018/2875074. eCollection 2018. Case Rep Endocrinol. 2018. PMID: 30186640 Free PMC article.

2

Treatment-resistant pediatric giant prolactinoma and multiple endocrine neoplasia type 1.

Gan HW, Bulwer C, Jeelani O, Levine MA, Korbonits M, Spoudeas HA. Gan HW, et al. Int J Pediatr Endocrinol. 2015;2015(1):15. doi: 10.1186/s13633-015-0011-5. Epub 2015 Jul 15. Int J Pediatr Endocrinol. 2015. PMID: 26180530 Free PMC article.

3

Giant Prolactinoma Causing Hydrocephalus and Intracranial Hypertension as First Manifestations of Multiple Endocrine Neoplasia Type 1.

Dantas NCB, Soares CEL, Martins MRA, Lourenço DM Jr, Quidute ARP. Dantas NCB, et al. Front Endocrinol (Lausanne). 2019 Aug 28;10:582. doi: 10.3389/fendo.2019.00582. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 31555208 Free PMC article.

4

Germline mutations of the MEN1 gene in Korean families with multiple endocrine neoplasia type 1 (MEN1) or MEN1-related disorders.

Park JH, Kim IJ, Kang HC, Lee SH, Shin Y, Kim KH, Lim SB, Kang SB, Lee K, Kim SY, Lee MS, Lee MK, Park JH, Moon SD, Park JG. Park JH, et al. Clin Genet. 2003 Jul;64(1):48-53. doi: 10.1034/j.1399-0004.2003.00091.x. Clin Genet. 2003. PMID: 12791038

5

Multiple endocrine neoplasia type 1.

Marini F, Falchetti A, Del Monte F, Carbonell Sala S, Gozzini A, Luzi E, Brandi ML. Marini F, et al. Orphanet J Rare Dis. 2006 Oct 2;1:38. doi: 10.1186/1750-1172-1-38. Orphanet J Rare Dis. 2006. PMID: 17014705 Free PMC article. Review.

6

Sporadic pituitary adenomas: the role of germline mutations and recommendations for genetic screening.

Iacovazzo D, Hernández-Ramírez LC, Korbonits M. Iacovazzo D, et al. Expert Rev Endocrinol Metab. 2017 Mar;12(2):143-153. doi: 10.1080/17446651.2017.1306439. Expert Rev Endocrinol Metab. 2017. PMID: 30063429

7

[Multiple Endocrine Neoplasia I (Wermers Syndrome), Forms of Clinical Manifestation, 5 Case Studies].

Drbalová K, Herdová K, Krejčí P, Nývltová M, Solař S, Vedralová L, Záruba P, Netuka D, Bavor P. Drbalová K, et al. Vnitr Lek. 2016 Fall;62(9 Suppl 3):140-149. Vnitr Lek. 2016. PMID: 27734708 Czech.

8

Carcinoma of two parathyroid glands caused by a novel MEN1 gene mutation - a rare feature of the MEN 1 syndrome.

Juodelė L, Serapinas D, Sabaliauskas G, Krasauskienė A, Krasauskas V, Verkauskienė R, Barkauskienė D, Juozaitytė E. Juodelė L, et al. Medicina (Kaunas). 2011;47(11):635-9. Epub 2011 Dec 30. Medicina (Kaunas). 2011. PMID: 22207168 Free article.

9

Multiple endocrine neoplasia type 1: clinical and genetic features of the hereditary endocrine neoplasias.

Marx SJ, Agarwal SK, Kester MB, Heppner C, Kim YS, Skarulis MC, James LA, Goldsmith PK, Saggar SK, Park SY, Spiegel AM, Burns AL, Debelenko LV, Zhuang Z, Lubensky IA, Liotta LA, Emmert-Buck MR, Guru SC, Manickam P, Crabtree J, Erdos MR, Collins FS, Chandrasekharappa SC. Marx SJ, et al. Recent Prog Horm Res. 1999;54:397-438; discussion 438-9. Recent Prog Horm Res. 1999. PMID: 10548885 Review.

10

Multiple endocrine neoplasia type 1: extensive analysis of a large database of Florentine patients.

Marini F, Giusti F, Brandi ML. Marini F, et al. Orphanet J Rare Dis. 2018 Nov 14;13(1):205. doi: 10.1186/s13023-018-0938-8. Orphanet J Rare Dis. 2018. PMID: 30428914 Free PMC article.

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