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Results 1 to 25 of 30

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Molecular profiles of gastroenteropancreatic endocrine tumorsPERREN, Aurel; ANLAUF, Martin; KOMMINOTH, Paul et al.Virchows Archiv. 2007, Vol 451, issn 0945-6317, S39-S46, SUP1Article

Immunostaining for the tumour suppressor gene p16 product is a useful marker to differentiate melanoma metastasis from lymph-node nevusMIHIC-PROBST, Daniela; SAREMASLANI, Parvin; KOMMINOTH, Paul et al.Virchows Archiv. 2003, Vol 443, Num 6, pp 745-751, issn 0945-6317, 7 p.Article

Poorly differentiated oncocytic thyroid carcinoma ― diagnostic implications and outcomeDETTMER, Matthias; SCHMITT, Anja; STEINERT, Hans et al.Histopathology. 2012, Vol 60, Num 7, pp 1045-1051, issn 0309-0167, 7 p.Article

Insulinomatosis : A Multicentric Insulinoma Disease that Frequently Causes Early Recurrent Hyperinsulinemic HypoglycemiaANLAUF, Martin; BAUERSFELD, Juliane; KASERER, Klaus et al.The American journal of surgical pathology. 2009, Vol 33, Num 3, pp 339-346, issn 0147-5185, 8 p.Article

Glucagon Cell Adenomatosis : A Newly Recognized Disease of the Endocrine PancreasHENOPP, Tobias; ANLAUF, Martin; PELLEGATA, Natalia S et al.The Journal of clinical endocrinology and metabolism. 2009, Vol 94, Num 1, pp 213-217, issn 0021-972X, 5 p.Article

Consensus Guidelines for the Management of Patients with Digestive Neuroendocrine Tumours : Well-Differentiated Colon and Rectum Tumour/CarcinomaRAMAGE, John K; GORETZKI, Peter E; SEVILLA GARCIA, M. I et al.Neuroendocrinology (Basel). 2008, Vol 87, Num 1, pp 31-39, issn 0028-3835, 9 p.Conference Paper

WHO 2004 criteria and CK19 are reliable prognostic markers in pancreatic endocrine tumorsSCHMITT, Anja M; ANLAUF, Martin; HEITZ, Philipp U et al.The American journal of surgical pathology. 2007, Vol 31, Num 11, pp 1677-1682, issn 0147-5185, 6 p.Article

Multiple endocrine neoplasia type 1 (MEN1) : Loss of one MEN1 allele in tumors and monohormonal endocrine cell clusters but not in islet hyperplasia of the pancreasPERREN, Aurel; ANLAUF, Martin; HEITZ, Philipp U et al.The Journal of clinical endocrinology and metabolism. 2007, Vol 92, Num 3, pp 1118-1128, issn 0021-972X, 11 p.Article

Microadenomatosis of the endocrine pancreas in patients with and without the multiple endocrine neoplasia type 1 syndromeANLAUF, Martin; SCHLENGER, Regina; COUVELARD, Anne et al.The American journal of surgical pathology. 2006, Vol 30, Num 5, pp 560-574, issn 0147-5185, 15 p.Article

Genetic evidence for early divergence of small functioning and nonfunctioning endocrine pancreatic tumors: gain of 9Q34 is an early event in insulinomasSPEEL, Ernst J. M; SCHEIDWEILER, Alexander F; JIANMING ZHAO et al.Cancer research (Baltimore). 2001, Vol 61, Num 13, pp 5186-5192, issn 0008-5472Article

Spitzoid malignant melanoma with lymph-node metastasis: Is a copy-number loss on chromosome 6q a marker of malignancy?MIHIC-PROBST, Daniela; JIANMING ZHAO; SAREMASLANI, Parvin et al.Virchows Archiv. 2001, Vol 439, Num 6, pp 823-826, issn 0945-6317Article

Poorly Differentiated Thyroid Carcinomas: How Much Poorly Differentiated is Needed?DETTMER, Matthias; SCHMITT, Anja; STEINERT, Hans et al.The American journal of surgical pathology. 2011, Vol 35, Num 12, pp 1866-1872, issn 0147-5185, 7 p.Article

ENETS Consensus Guidelines for the Management of Bone and Lung Metastases from Neuroendocrine Tumors : ENETS Consensus GuidelinesKOS-KUDLA, Beata; O'TOOLE, Dermot; VAN CUSTEM, Eric et al.Neuroendocrinology (Basel). 2010, Vol 91, Num 4, pp 341-350, issn 0028-3835, 10 p.Article

A novel succinate dehydrogenase subunit B gene mutation, H132P, causes familial malignant sympathetic extraadrenal paragangliomasMAIER-WOELFLE, Margarete; BRÄNDLE, Michael; PERREN, Aurel et al.The Journal of clinical endocrinology and metabolism. 2004, Vol 89, Num 1, pp 362-367, issn 0021-972X, 6 p.Article

Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomasDANNENBERG, Hilde; DE KRIJGER, Ronald R; VAN DER HARST, Erwin et al.International journal of cancer. 2003, Vol 105, Num 2, pp 190-195, issn 0020-7136, 6 p.Article

Mutation and expression analyses reveal differential subcellular compartmentalization of PTEN in endocrine pancreatic tumors compared to normal islet cellsPERREN, Aurel; KOMMINOTH, Paul; SAREMASLANI, Parvin et al.The American journal of pathology. 2000, Vol 157, Num 4, pp 1097-1103, issn 0002-9440Article

Site-specific biology and pathology of gastroenteropancreatic neuroendocrine tumorsKLÖPPEL, Günter; RINDI, Guido; ANLAUF, Martin et al.Virchows Archiv. 2007, Vol 451, issn 0945-6317, S9-S27, SUP1Article

Hereditary neuroendocrine tumors of the gastroenteropancreatic systemANLAUF, Martin; GARBRECHT, Nele; BAUERSFELD, Juliane et al.Virchows Archiv. 2007, Vol 451, issn 0945-6317, S29-S38, SUP1Article

Clinical characteristics of pheochromocytoma patients with germline mutations in SDHDDANNENBERG, Hilde; VAN NEDERVEEN, Francien H; ABBOU, Mustaffa et al.Journal of clinical oncology. 2005, Vol 23, Num 9, pp 1894-1901, issn 0732-183X, 8 p.Article

CGH analysis shows genetic similarities and differences in Atypical fibroxanthoma and undifferentiated high grade pleomorphic sarcomaMIHIC-PROBST, Daniela; JIANMING ZHAO; SAREMASLANI, Parvin et al.Anticancer research. 2004, Vol 24, Num 1, pp 19-26, issn 0250-7005, 8 p.Article

Differential loss of chromosome 11q in familial and sporadic parasympathetic paragangliomas detected by comparative genomic hybridizationDANNENBERG, Hilde; DE KRIJGER, Ronald R; JIANMING ZHAO et al.The American journal of pathology. 2001, Vol 158, Num 6, pp 1937-1942, issn 0002-9440Article

Deletion at 3p25.3-p23 is frequently encountered in endocrine pancreatic tumours and is associated with metastatic progressionBARGHOM, André; KOMMINOTH, Paul; BACHMANN, Daniela et al.Journal of pathology. 2001, Vol 194, Num 4, pp 451-458, issn 0022-3417Article

Islet 1 (Isl1) Expression is a Reliable Marker for Pancreatic Endocrine Tumors and Their MetastasesSCHMITT, Anja M; RINIKER, Florian; ANLAUF, Martin et al.The American journal of surgical pathology. 2008, Vol 32, Num 3, pp 420-425, issn 0147-5185, 6 p.Article

Pancreatic endocrine tumors are a rare manifestation of the neurofibromatosis Type 1 phenotype : Molecular analysis of a malignant insulinoma in a NF-1 patientPERREN, Aurel; WIESLI, Peter; SCHMID, Sonja et al.The American journal of surgical pathology. 2006, Vol 30, Num 8, pp 1047-1051, issn 0147-5185, 5 p.Article

Well-differentiated gastric tumors/ carcinomasRUSZNIEWSKI, Philippe; DELLE FAVE, Gianfranco; PAUWELS, Stanislas et al.Neuroendocrinology (Basel). 2006, Vol 84, Num 3, pp 158-164, issn 0028-3835, 7 p.Article

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