Pattern of lymph node metastases in papillary thyroid carcinomaGIMM, O; RATH, F. W; DRALLE, H et al.British journal of surgery. 1998, Vol 85, Num 2, pp 252-254, issn 0007-1323Article

Clinical significance of E-cadherin as a prognostic marker in thyroid carcinomasSCHEUMMAN, G. F. W; CUONG HOANG-VU; BRABANT, G et al.The Journal of clinical endocrinology and metabolism. 1995, Vol 80, Num 7, pp 2168-2172, issn 0021-972XArticle

Ectopic intrathyroidal thymus diagnosed as a solid thyroid lesion : Case report and review of the literatureGIMM, O; KRAUSE, U; WESSEL, H et al.Journal of pediatric surgery. 1997, Vol 32, Num 8, pp 1241-1243, issn 0022-3468Article

Over-representation of PPARγ sequence variants in sporadic cases of glioblastoma multiforme : preliminary evidence for common low penetrance modifiers for brain tumour risk in the general populationZHOU, X.-P; SMITH, W. M; YATES, A. J et al.Journal of medical genetics. 2000, Vol 37, Num 6, pp 410-414, issn 0022-2593Article

Prognostic significance and surgical management of locoregional lymph node metastases in papillary thyroid cancer. CommentarySCHEUMANN, G. F. W; GIMM, O; WEGENER, G et al.World journal of surgery. 1994, Vol 18, Num 4, pp 559-568, issn 0364-2313Conference Paper

HRPT2 mutations are associated with malignancy in sporadic parathyroid tumoursHOWELL, V. M; HAVEN, C. J; NELSON, A. E et al.Journal of medical genetics. 2003, Vol 40, Num 9, pp 657-663, issn 0022-2593, 7 p.Article

Expression of the PTEN tumour suppressor protein during human developmentGIMM, O; ATTIE-BITACH, T; LEES, J. A et al.Human molecular genetics (Print). 2000, Vol 9, Num 11, pp 1633-1639, issn 0964-6906Article

Mutation and deletion analysis of GFRα-1, encoding the co-receptor for the GDNF/RET complex, in human brain tumoursGIMM, O; GÖSSLING, A; MARSH, D. J et al.British journal of cancer. 1999, Vol 80, Num 3-4, pp 383-386, issn 0007-0920Article

Advances in the management of hereditary medullary thyroid cancerMACHENS, A; UKKAT, J; BRAUCKHOFF, M et al.Journal of internal medicine. 2005, Vol 257, Num 1, pp 50-59, issn 0954-6820, 10 p.Conference Paper

RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung diseaseBORREGO, S; RUIZ, A; SAEZ, M. E et al.Journal of medical genetics. 2000, Vol 37, Num 8, pp 572-578, issn 0022-2593Article

Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutationGIMM, O; NEUBERG, D. S; MARSH, D. J et al.Oncogene (Basingstoke). 1999, Vol 18, Num 6, pp 1369-1373, issn 0950-9232Article

Differences in allelic distribution of two polymorphisms in the VHL-associated gene CUL2 in pheochromocytoma patients without somatic CUL2 mutationsDUERR, E.-M; GIMM, O; NEUBERG, D. S et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 9, pp 3207-3211, issn 0021-972XArticle

Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosisZHOU, X.-P; MARSH, D. J; HAMPEL, H et al.Human molecular genetics (Print). 2000, Vol 9, Num 5, pp 765-768, issn 0964-6906Article

Mutation analysis reveals novel sequence variants in NTRK1 in sporadic human medullary thyroid carcinomaGIMM, O; GRECO, A; HOANG-VU, C et al.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 8, pp 2784-2787, issn 0021-972XArticle

Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expressionBORREGO, S; SAEZ, M. E; RUIZ, A et al.Journal of medical genetics. 1999, Vol 36, Num 10, pp 771-774, issn 0022-2593Article

Primary hereditary medullary thyroid carcinoma : C-cell morphology and correlation with preoperative calcitonin levelsHINZE, R; HOLZHAUSEN, H.-J; GIMM, O et al.Virchows Archiv. 1998, Vol 433, Num 3, pp 203-208, issn 0945-6317Article

Reoperation in metastasizing medullary thyroid carcinoma : Is a tumor stage-oriented approach justified? DiscussionGIMM, O; DRALLE, H; CADY, R. B et al.Surgery. 1997, Vol 122, Num 6, pp 1124-1131, issn 0039-6060Conference Paper

Allelic deletion of the MEN1 gene in duodenal gastrin and somatostatin cell neoplasms and their precursor lesions. CommentaryPRITCHARD, D. M; ANLAUF, M; KNOEFEL, W. T et al.Gut. 2007, Vol 56, Num 5, issn 0017-5749, 606-607,637-644 [10 p.]Article

Frequent promoter methylation of tumor-related genes in sporadic and Men2-associated pheochromocytomasDAMMANN, R; SCHAGDARSURENGIN, U; SEIDEL, C et al.Experimental and clinical endocrinology & diabetes. 2005, Vol 113, Num 1, pp 1-7, issn 0947-7349, 7 p.Article

An update on thyroid surgeryGIMM, O; BRAUCKHOFF, M; THANH, P. N et al.European journal of nuclear medecine and molecular imaging Print. 2002, Vol 29, pp S447-S452, issn 1619-7070, SUP2Article

Differential nuclear and cytoplasmic expression of PTEN in normal thyroid tissue, and benign and malignant epithelial thyroid tumorsGIMM, O; PERREN, A; MUTTER, G. L et al.The American journal of pathology. 2000, Vol 156, Num 5, pp 1693-1700, issn 0002-9440Article

Improved prediction of calcitonin normalization in medullary thyroid carcinoma patients by quantitative lymph node analysisMACHENS, A; GIMM, O; UKKAT, J et al.Cancer. 2000, Vol 88, Num 8, pp 1909-1915, issn 0008-543XArticle

Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutationGIMM, O; MARSH, D. J; ANDREW, S. D et al.The Journal of clinical endocrinology and metabolism. 1997, Vol 82, Num 11, pp 3902-3904, issn 0021-972XArticle

Completion thyroidectomy in 131 patients with differentiated thyroid carcinomaSCHEUMANN, G. F. W; SEELIGER, H; MUSHOLT, T. J et al.The European journal of surgery. 1996, Vol 162, Num 9, pp 677-684, issn 1102-4151Article