182 related articles for article (PubMed ID: 23188049)
1. A new double substitution mutation in the MEN1 gene: a limited penetrance and a specific phenotype.
Ullmann U; Unuane D; Velkeniers B; Lissens W; Wuyts W; Bonduelle M
Eur J Hum Genet; 2013 Jun; 21(6):695-7. PubMed ID: 23188049
[TBL] [Abstract][Full Text] [Related]
2. A new mutation in the menin gene causes the multiple endocrine neoplasia type 1 syndrome with adrenocortical carcinoma.
Haase M; Anlauf M; Schott M; Schinner S; Kaminsky E; Scherbaum WA; Willenberg HS
Endocrine; 2011 Apr; 39(2):153-9. PubMed ID: 21069576
[TBL] [Abstract][Full Text] [Related]
3. A Novel Germline c.1267T>A
Gierlikowski W; Skwarek-Szewczyk A; Popow M
Genes (Basel); 2020 Nov; 11(11):. PubMed ID: 33233395
[TBL] [Abstract][Full Text] [Related]
4. Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders.
Giraud S; Zhang CX; Serova-Sinilnikova O; Wautot V; Salandre J; Buisson N; Waterlot C; Bauters C; Porchet N; Aubert JP; Emy P; Cadiot G; Delemer B; Chabre O; Niccoli P; Leprat F; Duron F; Emperauger B; Cougard P; Goudet P; Sarfati E; Riou JP; Guichard S; Rodier M; Meyrier A; Caron P; Vantyghem MC; Assayag M; Peix JL; Pugeat M; Rohmer V; Vallotton M; Lenoir G; Gaudray P; Proye C; Conte-Devolx B; Chanson P; Shugart YY; Goldgar D; Murat A; Calender A
Am J Hum Genet; 1998 Aug; 63(2):455-67. PubMed ID: 9683585
[TBL] [Abstract][Full Text] [Related]
5. p.Ala541Thr variant of MEN1 gene: a non deleterious polymorphism or a pathogenic mutation?
Nozières C; Zhang CX; Buffet A; Dupasquier S; Vargas-Poussou R; Guillaud-Bataille M; Cordier-Bussat M; Ruszniewski P; Christin-Maitre S; Murat A; Groussin L; Vezzosi D; Cardot-Bauters C; Hervieu V; Joly MO; Giraud S; Odou MF; Gimenez-Roqueplo AP; Goudet P; Borson-Chazot F; Calender A;
Ann Endocrinol (Paris); 2014 Jul; 75(3):133-40. PubMed ID: 24997771
[TBL] [Abstract][Full Text] [Related]
6. Menin mutations in the diagnosis and prediction of multiple endocrine neoplasia type 1.
Karges W; Ludwig L; Kessler H; Wissmann A; Wagner PK; Boehm BO
Langenbecks Arch Surg; 1998 Apr; 383(2):183-6. PubMed ID: 9641896
[TBL] [Abstract][Full Text] [Related]
7. Age-related penetrance of endocrine tumours in multiple endocrine neoplasia type 1 (MEN1): a multicentre study of 258 gene carriers.
Machens A; Schaaf L; Karges W; Frank-Raue K; Bartsch DK; Rothmund M; Schneyer U; Goretzki P; Raue F; Dralle H
Clin Endocrinol (Oxf); 2007 Oct; 67(4):613-22. PubMed ID: 17590169
[TBL] [Abstract][Full Text] [Related]
8. Analysis of MEN1 c.482G>A (p.Gly161Asp) mutation in a pedigree with familial multiple endocrine neoplasia type 1.
Luo Y; Sun Y; Zhu X; Li X
Mol Med Rep; 2017 Dec; 16(6):8973-8976. PubMed ID: 29039523
[TBL] [Abstract][Full Text] [Related]
9. Multiple endocrine neoplasia type 1 associated with a new germline Men1 mutation in a family with atypical tumor phenotype.
Perakakis N; Flohr F; Kayser G; Thomusch O; Parsons L; Billmann F; von Dobschuetz E; Rondot S; Seufert J; Laubner K
Hormones (Athens); 2016; 15(1):113-7. PubMed ID: 26732163
[TBL] [Abstract][Full Text] [Related]
10. MEN1 c.825‑1G>A mutation in a family with multiple endocrine neoplasia type 1: A case report.
Ning Z; Wang O; Meng X; Xing X; Xia W; Jiang Y; Li M; Xu Y
Mol Med Rep; 2015 Oct; 12(4):6152-6. PubMed ID: 26239674
[TBL] [Abstract][Full Text] [Related]
11. New splicing mutation of MEN1 gene affecting the translocation of menin to the nucleus.
Tala HP; Carvajal CA; González AA; Garrido JL; Tobar J; Solar A; Campino C; Arteaga E; Fardella CE
J Endocrinol Invest; 2006 Nov; 29(10):888-93. PubMed ID: 17185897
[TBL] [Abstract][Full Text] [Related]
12. Heterogeneity of the Clinical Presentation of the MEN1 LRG_509 c.781C>T (p.Leu261Phe) Variant Within a Three-Generation Family.
Gilis-Januszewska A; Bogusławska A; Hasse-Lazar K; Jurecka-Lubieniecka B; Jarząb B; Sowa-Staszczak A; Opalińska M; Godlewska M; Grochowska A; Skalniak A; Hubalewska-Dydejczyk A
Genes (Basel); 2021 Mar; 12(4):. PubMed ID: 33807230
[TBL] [Abstract][Full Text] [Related]
13. Multiple endocrine neoplasia type 1 (MEN1): clinical heterogeneity in a large family with a nonsense mutation in the MEN1 gene (Trp471Stop).
Valdés N; Pérez de Nanclares G; Alvarez V; Castaño L; Díaz-Cadórniga F; Aller J; Coto E
Clin Endocrinol (Oxf); 1999 Mar; 50(3):309-13. PubMed ID: 10435055
[TBL] [Abstract][Full Text] [Related]
14. Novel Germline c.105_107dupGCT
Stasiak M; Dedecjus M; Zawadzka-Starczewska K; Adamska E; Tomaszewska M; Lewiński A
Genes (Basel); 2020 Aug; 11(9):. PubMed ID: 32847108
[TBL] [Abstract][Full Text] [Related]
15. Mutation analysis in a Chinese family with multiple endocrine neoplasia type 1.
Zha BB; Liang W; Liu J; Cheng J; Hong XW; Liu J; Li YM; Ma D
Chin Med J (Engl); 2010 Mar; 123(5):569-73. PubMed ID: 20367983
[TBL] [Abstract][Full Text] [Related]
16. Novel Germline p.Gly42Val
Koehler VF; Jungheim K; Groß U; Iacovazzo D; Mann A; Korbonits M
Ann Clin Lab Sci; 2017 Sep; 47(5):606-610. PubMed ID: 29066490
[TBL] [Abstract][Full Text] [Related]
17. Multiple endocrine neoplasia type 1.
Marini F; Falchetti A; Del Monte F; Carbonell Sala S; Gozzini A; Luzi E; Brandi ML
Orphanet J Rare Dis; 2006 Oct; 1():38. PubMed ID: 17014705
[TBL] [Abstract][Full Text] [Related]
18. MEN1 gene and its mutations: basic and clinical implications.
Tsukada T; Nagamura Y; Ohkura N
Cancer Sci; 2009 Feb; 100(2):209-15. PubMed ID: 19068082
[TBL] [Abstract][Full Text] [Related]
19. Distinct clinical phenotypes in a family with a novel truncating MEN1 frameshift mutation.
Welsch C; Flügel AK; Rondot S; Schulze E; Sircar I; Nußbaumer J; Bojunga J
BMC Endocr Disord; 2022 Mar; 22(1):64. PubMed ID: 35287658
[TBL] [Abstract][Full Text] [Related]
20. Multiple endocrine neoplasia type 1: extensive analysis of a large database of Florentine patients.
Marini F; Giusti F; Brandi ML
Orphanet J Rare Dis; 2018 Nov; 13(1):205. PubMed ID: 30428914
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
