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Results: 1-13 |
Results: 13
Lymphangiectasia with persistent mullerian derivatives: Confirmation of autosomal recessive Urioste syndrome
Authors: van Haelst, MM Hoogeboom, J Galjaard, RJH Kleijer, WJ den Hollander, NS de Krijger, RR Hennekam, RCM Niermeijer, MF
Citation: Mm. Van Haelst et al., Lymphangiectasia with persistent mullerian derivatives: Confirmation of autosomal recessive Urioste syndrome, AM J MED G, 104(1), 2001, pp. 65-68
[I-123]metaiodobenzylguanidine and [In-111]octreotide uptake in benign andmalignant pheochromocytomas
Authors: van der Harst, E de Herder, WW Bruining, HA Bonjer, HJ de Krijger, RR Lamberts, SWJ van de Meiracker, AH Boomsma, F Stijnen, T Krenning, EP Bosman, FT Kwekkeboom, DJ
Citation: E. Van Der Harst et al., [I-123]metaiodobenzylguanidine and [In-111]octreotide uptake in benign andmalignant pheochromocytomas, J CLIN END, 86(2), 2001, pp. 685-693
Molecular genetic analysis of the von Hippel-Lindau and human peroxisome proliferator-activated receptor gamma tumor-suppressor genes in adenocarcinomas of the gastroesophageal junction
Authors: Wijnhoven, BPL Lindstedt, EW Abbou, M Ijzendoorn, Y de Krijger, RR Tilanus, HW Dinjens, WNM
Citation: Bpl. Wijnhoven et al., Molecular genetic analysis of the von Hippel-Lindau and human peroxisome proliferator-activated receptor gamma tumor-suppressor genes in adenocarcinomas of the gastroesophageal junction, INT J CANC, 94(6), 2001, pp. 891-895
Differential loss of chromosome 11q in familial and sporadic parasympathetic paragangliomas detected by comparative genomic hybridization
Authors: Dannenberg, H de Krijger, RR Zhao, JM Speel, EJM Saremaslani, P Dinjens, WNM Mooi, WJ Roth, J Heitz, PU Komminoth, P
Citation: H. Dannenberg et al., Differential loss of chromosome 11q in familial and sporadic parasympathetic paragangliomas detected by comparative genomic hybridization, AM J PATH, 158(6), 2001, pp. 1937-1942
Absence of a PDX-1 mutation and normal gastroduodenal immunohistology in achild with pancreatic agenesis
Authors: Verwest, AM Poelman, M Dinjens, WNM Batstra, MR Oostra, BA Lequin, MH Larsson, LI Aanstoot, HJ Bruining, GJ de Krijger, RR
Citation: Am. Verwest et al., Absence of a PDX-1 mutation and normal gastroduodenal immunohistology in achild with pancreatic agenesis, VIRCHOWS AR, 437(6), 2000, pp. 680-684
Adult hyperinsulinemic hypoglycemia not caused by an insulinoma: a report of two cases
Authors: van der Wal, BCH de Krijger, RR de Herder, WW Kwekkeboom, DJ van der Ham, F Bonjer, HJ van Eijck, CHJ
Citation: Bch. Van Der Wal et al., Adult hyperinsulinemic hypoglycemia not caused by an insulinoma: a report of two cases, VIRCHOWS AR, 436(5), 2000, pp. 481-486
RET is expressed but not mutated in extra-adrenal paragangliomas
Authors: de Krijger, RR van der Harst, E Muletta-Feurer, S Bruining, HA Lamberts, SWJ Dinjens, WNM Roth, J Heitz, PU Komminoth, P
Citation: Rr. De Krijger et al., RET is expressed but not mutated in extra-adrenal paragangliomas, J PATHOLOGY, 191(3), 2000, pp. 264-268
Proliferative index in phaeochromocytomas: does it predict the occurrence of metastases?
Authors: van der Harst, E Bruining, HA Bonjer, HJ van der Ham, F Dinjens, WN Lamberts, SWJ de Herder, WW Koper, JW Stijnen, T Proye, C Lecomte-Houcke, M Bosman, FT de Krijger, RR
Citation: E. Van Der Harst et al., Proliferative index in phaeochromocytomas: does it predict the occurrence of metastases?, J PATHOLOGY, 191(2), 2000, pp. 175-180
Genomic alterations in well-differentiated gastrointestinal and bronchial neuroendocrine tumors (carcinoids) - Marked differences indicating diversity in molecular pathogenesis
Authors: Zhao, JM de Krijger, RR Meier, D Speel, EJM Saremaslani, P Muletta-Feurer, S Matter, C Roth, J Heitz, PU Komminoth, P
Citation: Jm. Zhao et al., Genomic alterations in well-differentiated gastrointestinal and bronchial neuroendocrine tumors (carcinoids) - Marked differences indicating diversity in molecular pathogenesis, AM J PATH, 157(5), 2000, pp. 1431-1438
Losses of chromosomes 1p and 3q are early genetic events in the development of sporadic pheochromocytomas
Authors: Dannenberg, H Speel, EJM Zhao, JM Saremaslani, P van der Harst, E Roth, J Heitz, PU Bonjer, HJ Dinjens, WNM Mooi, WJ Kemminoth, P de Krijger, RR
Citation: H. Dannenberg et al., Losses of chromosomes 1p and 3q are early genetic events in the development of sporadic pheochromocytomas, AM J PATH, 157(2), 2000, pp. 353-359
Influence of intratumour heterogeneity in the interpretation of marker results in phaeochromocytomas - Reply
Authors: de Krijger, RR van der Harst, E van der Ham, F Stijnen, T Dinjens, WNM Koper, JW Bruining, HA Lamberts, SWJ Bosman, FT
Citation: Rr. De Krijger et al., Influence of intratumour heterogeneity in the interpretation of marker results in phaeochromocytomas - Reply, J PATHOLOGY, 189(4), 1999, pp. 628-628
Prognostic value of p53, bcl-2, and c-erbB-2 protein expression in phaeochromocytomas
Authors: de Krijger, RR van der Harst, E van der Ham, F Stijnen, T Dinjens, WNM Koper, JW Bruining, HA Lamberts, SWJ Bosman, FT
Citation: Rr. De Krijger et al., Prognostic value of p53, bcl-2, and c-erbB-2 protein expression in phaeochromocytomas, J PATHOLOGY, 188(1), 1999, pp. 51-55
Mutations and allelic deletions of the MEN1 gene are associated with a subset of sporadic endocrine pancreatic and neuroendocrine tumors and not restricted to foregut neoplasms
Authors: Gortz, B Roth, J Krahenmann, A de Krijger, RR Muletta-Feurer, S Rutimann, K Saremaslani, P Speel, EJM Heitz, PU Komminoth, P
Citation: B. Gortz et al., Mutations and allelic deletions of the MEN1 gene are associated with a subset of sporadic endocrine pancreatic and neuroendocrine tumors and not restricted to foregut neoplasms, AM J PATH, 154(2), 1999, pp. 429-436
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