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MEN1
LE WE PMID CA
MEN11747MEN1

Adrenal gland (Neoplasia)

Adrenal gland (Primary pigmented nodular adrenocortical disease)

Beckwith Wiedemann syndrome

Carney s complex

Congenital adrenal hyperplasia

Glucocorticoid remediable aldosteronism

Li Fraumeni syndrome

MEN1

Menin

Neuroendocrine System (Neoplasia Carcinoid)

Neuroendocrine system (Neoplasia)

PRKAR1A

Receptor (ACTH Melanocortin2 Receptor MC2R)

1998  
1
The ultimate biochemical diagnosis of endocrine pancreatic tumours in MEN-1.
[9681845] J Intern Med 243(6): 471-6 (1998)
1998  
2
Pathology of MEN-1: morphology, clinicopathologic correlations and tumour development.
[9681843] J Intern Med 243(6): 455-64 (1998)
2000  
3
Duodenopancreatic resections in patients with multiple endocrine neoplasia type 1.
[10816635] Ann Surg 231(6): 909-18 (2000)
1998  
4
Thymic carcinoids in multiple endocrine neoplasia type 1.
[9671073] Ann Surg 228(1): 99-105 (1998)
2005  
5
Bronchopulmonary carcinoid in multiple endocrine neoplasia type 1.
[15611976] Cancer 103(3): 509-15 (2005)
1998  
6
Multiple endocrine neoplasia type 1: clinical and genetic topics.
[9735087] Ann Intern Med 129(6): 484-94 (1998)
2006  
7
Natural course of small, asymptomatic neuroendocrine pancreatic tumours in multiple endocrine neoplasia type 1: an endoscopic ultrasound imaging study.
[17158764] Endocr Relat Cancer 13(4): 1195-202 (2006)
1999  
8
Multiple endocrine neoplasia type 1.
[10730900] Endocr Relat Cancer 6(4): 449-73 (1999)
2008  
9
The appearance of the adrenal glands on computed tomography in multiple endocrine neoplasia type 1.
[18827064] Eur J Endocrinol 159(6): 819-24 (2008)
2007  
10
The parathyroid/pituitary variant of multiple endocrine neoplasia type 1 usually has causes other than p27Kip1 mutations.
[17299066] J Clin Endocrinol Metab 92(5): 1948-51 (2007)
2007  
11
The multiple endocrine neoplasia type-1 (MEN-1) syndrome and its effect on the pancreas.
[17341576] J Clin Endocrinol Metab 92(3): 811-2 (2007)
2003  
12
Prospective study of thymic carcinoids in patients with multiple endocrine neoplasia type 1.
[12629087] J Clin Endocrinol Metab 88(3): 1066-81 (2003)
2001  
13
Molecular and genetic mechanisms of tumorigenesis in multiple endocrine neoplasia type-1.
[11579199] Mol Endocrinol 15(10): 1653-64 (2001)
2006  
14
Multiple endocrine neoplasia type 1.
[17014705] Orphanet J Rare Dis 1(-): 38 (2006)
2011  
15
Menin represses tumorigenesis via repressing cell proliferation.
[22016823] Am J Cancer Res 1(6): 726-39 (2011)
2009  
16
Asymptomatic children with multiple endocrine neoplasia type 1 mutations may harbor nonfunctioning pancreatic neuroendocrine tumors.
[19622622] J Clin Endocrinol Metab 94(10): 3640-6 (2009)
2005  
17
Molecular genetics of adrenocortical tumours, from familial to sporadic diseases.
[16189167] Eur J Endocrinol 153(4): 477-87 (2005)

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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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