Haas OA - Search Results

1

C-cell hyperplasia and medullary thyroid carcinoma in patients routinely screened for serum calcitonin.

Kaserer K, Scheuba C, Neuhold N, Weinhäusel A, Vierhapper H, Haas OA, Niederle B. Kaserer K, et al. Among authors: haas oa. Am J Surg Pathol. 1998 Jun;22(6):722-8. doi: 10.1097/00000478-199806000-00009. Am J Surg Pathol. 1998. PMID: 9630179

2

Distinction between sporadic and hereditary medullary thyroid carcinoma (MTC) by mutation analysis of the RET proto-oncogene. "Study Group Multiple Endocrine Neoplasia Austria (SMENA)".

Fink M, Weinhüsel A, Niederle B, Haas OA. Fink M, et al. Among authors: haas oa. Int J Cancer. 1996 Aug 22;69(4):312-6. doi: 10.1002/(SICI)1097-0215(19960822)69:4<312::AID-IJC13>3.0.CO;2-7. Int J Cancer. 1996. PMID: 8797874

3

Is medullary thyroid cancer predictable? A prospective study of 86 patients with abnormal pentagastrin tests.

Scheuba C, Kaserer K, Weinhäusl A, Pandev R, Kaider A, Passler C, Prager G, Vierhapper H, Haas OA, Niederle B. Scheuba C, et al. Among authors: haas oa. Surgery. 1999 Dec;126(6):1089-95; discussion 1096. doi: 10.1067/msy.2099.102268. Surgery. 1999. PMID: 10598192

4

A novel mutation E179K of the MEN1 gene predisposes for multiple endocrine neoplasia-type 1 (MEN1).

Weinhaeusel A, Vierhapper H, Schlegl R, Wagner T, Muhr D, Scheuba C, Niederle B, Haas OA. Weinhaeusel A, et al. Among authors: haas oa. Hum Mutat. 2000 Dec;16(6):533. doi: 10.1002/1098-1004(200012)16:6<533::AID-HUMU22>3.0.CO;2-5. Hum Mutat. 2000. PMID: 11102994 No abstract available.

5

Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCR.

Weinhäusel A, Haas OA. Weinhäusel A, et al. Among authors: haas oa. Hum Genet. 2001 Jun;108(6):450-8. doi: 10.1007/s004390100519. Hum Genet. 2001. PMID: 11499669

6

Sporadic versus familial medullary thyroid microcarcinoma: a histopathologic study of 50 consecutive patients.

Kaserer K, Scheuba C, Neuhold N, Weinhäusel A, Haas OA, Vierhapper H, Niederle B. Kaserer K, et al. Among authors: haas oa. Am J Surg Pathol. 2001 Oct;25(10):1245-51. doi: 10.1097/00000478-200110000-00004. Am J Surg Pathol. 2001. PMID: 11688458

7

Multiple endocrine neoplasia type 1 (MEN1) in Austria.

Weinhäusel A, Kaserer K, Vierhapper H, Niederle B, Haas OA; Study Group of Multiple Endocrine Neoplasia Austria. Weinhäusel A, et al. Among authors: haas oa. Wien Klin Wochenschr. 2002 Apr 15;114(7):252-7. Wien Klin Wochenschr. 2002. PMID: 12089860

8

Differential methylation pattern of the X-linked lymphoproliferative (XLP) disease gene SH2D1A correlates with the cell lineage-specific transcription.

Parolini O, Weinhäusel A, Kagerbauer B, Sassmann J, Holter W, Gadner H, Haas OA, Knapp W. Parolini O, et al. Among authors: haas oa. Immunogenetics. 2003 May;55(2):116-21. doi: 10.1007/s00251-003-0557-x. Epub 2003 Apr 23. Immunogenetics. 2003. PMID: 12709835

9

Genetic testing for familial Mediterranean fever in Austria by means of reverse-hybridization teststrips.

Oberkanins C, Weinhäusel A, Kriegshäuser G, Moritz A, Kury F, Haas OA. Oberkanins C, et al. Among authors: haas oa. Clin Chem. 2003 Nov;49(11):1948-50. doi: 10.1373/clinchem.2003.022186. Clin Chem. 2003. PMID: 14578333 No abstract available.

10

Long-term follow up of a "sporadic" unilateral pheochromocytoma revealing multiple endocrine neoplasia MEN2A-2 in an elderly woman.

Weinhäusel A, Behmel A, Ponder BA, Haas OA, Niederle B, Gessl A, Vierhapper H, Pfragner R. Weinhäusel A, et al. Among authors: haas oa. Endocr Pathol. 2003 Winter;14(4):375-82. doi: 10.1385/ep:14:4:375. Endocr Pathol. 2003. PMID: 14739494 Review.

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