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Items: 1 to 20 of 72

1.

A puzzling case of phospho-soda-induced hypocalcemia in a patient with multiple endocrine neoplasia type 1-associated primary hyperparathyroidism.

Ozveren A, Akinci B, Makay O, Sarsik B, Simsir IY, Berdeli A, Akyildiz M.

Intern Med. 2012;51(22):3145-9. Epub 2012 Nov 15.

2.

Novel 14 base-pair deletion of the MEN1 gene in a patient with recurrent primary hyperparathyroidism.

Katai M, Sakurai A, Uchino S, Minemura K, Hashizume K, Fukushima Y.

Jpn J Clin Oncol. 2006 Jun;36(6):395-7. Epub 2006 May 19.

PMID:
16714299
3.

Severe hypocalcemia complicated by postsurgical hypoparathyroidism and hungry bone syndrome in a patient with primary hyperparathyroidism, Graves' disease, and acromegaly.

Tachibana S, Sato S, Yokoi T, Nagaishi R, Akehi Y, Yanase T, Yamashita H.

Intern Med. 2012;51(14):1869-73. Epub 2012 Jul 15.

4.

Diagnostic challenges due to phenocopies: lessons from Multiple Endocrine Neoplasia type1 (MEN1).

Turner JJ, Christie PT, Pearce SH, Turnpenny PD, Thakker RV.

Hum Mutat. 2010 Jan;31(1):E1089-101. doi: 10.1002/humu.21170.

PMID:
19953642
5.

Unusual presentation of multiple endocrine neoplasia type 1 in a young woman with a novel mutation of the MEN1 gene.

Balogh K, Patócs A, Majnik J, Varga F, Illyés G, Hunyady L, Rácz K.

J Hum Genet. 2004;49(7):380-6. Epub 2004 Jun 16.

PMID:
15205994
6.

Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain.

Belar O, De La Hoz C, Pérez-Nanclares G, Castaño L, Gaztambide S; Spanish MEN1 Group.

Clin Endocrinol (Oxf). 2012 May;76(5):719-24. doi: 10.1111/j.1365-2265.2011.04269.x.

PMID:
22026581
7.

Characteristics of the Danish families with multiple endocrine neoplasia type 1.

Jäger AC, Friis-Hansen L, Hansen TV, Eskildsen PC, Sølling K, Knigge U, Hansen CP, Andersen PH, Brixen K, Feldt-Rasmussen U, Kroustrup JP, Mollerup CL, Rehfeld JF, Blichert-Toft M, Nielsen FC.

Mol Cell Endocrinol. 2006 Apr 25;249(1-2):123-32. Epub 2006 Mar 23.

PMID:
16563611
8.

Germline mutation of the multiple endocrine neoplasia type 1 (MEN1) gene in a family with primary hyperparathyroidism.

Ohye H, Sato M, Matsubara S, Miyauchi A, Imachi H, Murao K, Takahara J.

Endocr J. 1998 Dec;45(6):719-23.

9.

Sarcomatoid carcinoma of the kidney in a MEN1 patient: case report and genetic profile.

Cavalli T, Giudici F, Nesi G, Marini F, Giusti F, Cavalli L, Brandi ML, Tonelli F.

Endocr J. 2014;61(8):781-7. Epub 2014 May 30.

10.

Clinical testing for multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory.

Klein RD, Salih S, Bessoni J, Bale AE.

Genet Med. 2005 Feb;7(2):131-8.

PMID:
15714081
11.

A novel missense mutation in the MEN1 gene in a patient with multiple endocrine neoplasia type 1.

Hou R, Manwaring LP, Moley JF, Whelan A.

Endocr Pract. 2011 May-Jun;17(3):e63-7. doi: 10.4158/EP10291.CR.

PMID:
21454242
12.

Novel deletional mutation of the MEN 1 gene in a kindred with multiple endocrine neoplasia type 1.

Kakizawa T, Sakurai A, Ikeo Y, Ueno I, Hashizume K.

Clin Genet. 2000 Jul;58(1):61-3.

PMID:
10945663
13.

Gene symbol: MEN1. Disease: MEN1.

Costa MH, Candida M, Fragoso BV, Mendonca BB.

Hum Genet. 2005 Dec;118(3-4):541. No abstract available.

PMID:
16521275
14.

Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases.

Poncin J, Abs R, Velkeniers B, Bonduelle M, Abramowicz M, Legros JJ, Verloes A, Meurisse M, Van Gaal L, Verellen C, Koulischer L, Beckers A.

Hum Mutat. 1999;13(1):54-60.

PMID:
9888389
15.

A novel germline mutation of multiple endocrine neoplasia type 1 (MEN1) gene in a Japanese MEN1 patient and her daughter.

Ohye H, Sato M, Matsubara S, Miyauchi A, Kishi-Imai K, Murao K, Takahara J.

Endocr J. 1999 Apr;46(2):325-9.

16.

MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1.

Balogh K, Hunyady L, Patocs A, Gergics P, Valkusz Z, Toth M, Racz K.

Clin Endocrinol (Oxf). 2007 Nov;67(5):727-34.

PMID:
17953629
17.

Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states.

Agarwal SK, Kester MB, Debelenko LV, Heppner C, Emmert-Buck MR, Skarulis MC, Doppman JL, Kim YS, Lubensky IA, Zhuang Z, Green JS, Guru SC, Manickam P, Olufemi SE, Liotta LA, Chandrasekharappa SC, Collins FS, Spiegel AM, Burns AL, Marx SJ.

Hum Mol Genet. 1997 Jul;6(7):1169-75.

PMID:
9215689
18.

Hyperparathyroidism in hereditary syndromes: special expressions and special managements.

Marx SJ, Simonds WF, Agarwal SK, Burns AL, Weinstein LS, Cochran C, Skarulis MC, Spiegel AM, Libutti SK, Alexander HR Jr, Chen CC, Chang R, Chandrasekharappa SC, Collins FS.

J Bone Miner Res. 2002 Nov;17 Suppl 2:N37-43. Review.

PMID:
12412776
19.

Somatic mutations of the multiple endocrine neoplasia type 1 (MEN1) gene in patients with sporadic, nonfamilial primary hyperparathyroidism.

Sato K, Yamazaki K, Zhu H, Kanbe M, Iihara M, Wada Y, Tanaka R, Okamoto T, Ito Y, Obara T.

Surgery. 2000 Mar;127(3):337-41.

PMID:
10715991
20.

A Novel Missense Mutation of the MEN1 Gene in a Patient with Multiple Endocrine Neoplasia Type 1 with Glucagonoma and Obesity.

Murakami T, Usui T, Nakajima A, Mochida Y, Saito S, Nambu T, Kato T, Matsuda Y, Yonemitsu S, Muro S, Oki S.

Intern Med. 2015;54(19):2475-81. doi: 10.2169/internalmedicine.54.4886. Epub 2015 Oct 1.

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