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Results: 24

Authors: NEUMANN HPH BENDER BU BERGER DP LAUBENBERGER J SCHULTZESEEMANN W WETTERAUER U FERSTL FJ HERBST EW SCHWARZKOPF G HES FJ LIPS CJM LAMIELL JM MASEK O RIEGLER P MUELLER B GLAVAC D BRAUCH H
Citation: Hph. Neumann et al., PREVALENCE, MORPHOLOGY AND BIOLOGY OF RENAL-CELL CARCINOMA IN VON-HIPPEL-LINDAU-DISEASE COMPARED TO SPORADIC RENAL-CELL CARCINOMA, The Journal of urology, 160(4), 1998, pp. 1248-1254

Authors: SCHMIDT L DUH FM CHEN F KISHIDA T GLENN G CHOYKE P SCHERER SW ZHUANG ZP LUBENSKY I DEAN M ALLIKMETS R CHIDAMBARAM A BERGERHEIM UR FELTIS JT CASADEVALL C ZAMARRON A BERNUES M RICHARD S LIPS CJM WALTHER MM TSUI LC GEIL L ORCUTT ML STACKHOUSE T LIPAN J SLIFE L BRAUCH H DECKER J NIEHANS G HUGHSON MD MOCH H STORKEL S LERMAN MI LINEHAN WM ZBAR B
Citation: L. Schmidt et al., GERMLINE AND SOMATIC MUTATIONS IN THE TYROSINE KINASE DOMAIN OF THE MET PROTOONCOGENE IN PAPILLARY RENAL CARCINOMAS, Nature genetics, 16(1), 1997, pp. 68-73

Authors: HAMANN U BRAUCH H GARVIN AM BASTERT G SCOTT RJ
Citation: U. Hamann et al., GERMAN FAMILY STUDY ON HEREDITARY BREAST AND OR OVARIAN-CANCER - GERMLINE MUTATION ANALYSIS OF THE BRCAI GENE/, Genes, chromosomes & cancer, 18(2), 1997, pp. 126-132

Authors: WEIRICH G SCHNEIDER P FELLBAUM C BRAUCH H NATHRATH W SCHOLZ M PRAUER H HOFLER H
Citation: G. Weirich et al., P53 ALTERATIONS IN THYMIC EPITHELIAL TUMORS, Virchows Archiv, 431(1), 1997, pp. 17-23

Authors: BRUNING T WEIRICH G HORNAUER MA HOFLER H BRAUCH H
Citation: T. Bruning et al., RENAL-CELL CARCINOMAS IN TRICHLOROETHENE(TRI) EXPOSED PERSONS ARE ASSOCIATED WITH SOMATIC MUTATIONS IN THE VON-HIPPEL-LINDAU (VHL) TUMOR-SUPPRESSOR GENE, Archives of toxicology, 71(5), 1997, pp. 332-335

Authors: BRUNING T HORNAUER M WEIRICH G THIER R BOLT HM BRAUCH H
Citation: T. Bruning et al., MUTATIONS OF THE VHL (VON-HIPPEL-LINDAU) TUMOR-SUPPRESSOR GENE IN TRICHLOROETHENE EXPOSED PATIENTS WITH RENAL-CELL CARCINOMA, Naunyn-Schmiedeberg's archives of pharmacology, 355(4), 1997, pp. 617-617

Authors: BRAUCH H
Citation: H. Brauch, THE HIPPEL-LINDAU SYNDROME - CLINICAL AND GENETIC-ASPECTS OF RETINAL ANGIOMATOSIS, Klinische Monatsblatter fur Augenheilkunde, 210(3), 1997, pp. 1-1

Authors: BRAUCH H HOEPPNER W JAHNIG H WOHL T ENGELHARDT D SPELSBERG F RITTER MM
Citation: H. Brauch et al., SPORADIC PHEOCHROMOCYTOMAS ARE RARELY ASSOCIATED WITH GERMLINE MUTATIONS IN THE VHL TUMOR-SUPPRESSOR GENE OR THE RET PROTOONCOGENE, The Journal of clinical endocrinology and metabolism, 82(12), 1997, pp. 4101-4104

Authors: ZBAR B KISHIDA T CHEN F SCHMIDT L MAHER ER RICHARDS FM CROSSEY PA WEBSTER AR AFFARA NA FERGUSONSMITH MA BRAUCH H GLAVAC D NEUMANN HPH TISHERMAN S MULVIHILL JJ GROSS DJ SHUIN T WHALEY J SEIZINGER B KLEY N OLSCHWANG S BOISSON C RICHARD S LIPS CHM LINEHAN WM LERMAN M
Citation: B. Zbar et al., GERMLINE MUTATIONS IN THE VON-HIPPEL-LINDAU DISEASE (VHL) GENE IN FAMILIES FROM NORTH-AMERICA, EUROPE, AND JAPAN, Human mutation, 8(4), 1996, pp. 348-357

Authors: GLAVAC D NEUMANN HPH WITTKE C JAENIG H MASEK O STREICHER T PAUSCH F ENGELHARDT D PLATE KH HOFLER H CHEN F ZBAR B BRAUCH H
Citation: D. Glavac et al., MUTATIONS IN THE VHL TUMOR-SUPPRESSOR GENE AND ASSOCIATED LESIONS IN FAMILIES WITH VON-HIPPEL-LINDAU DISEASE FROM CENTRAL-EUROPE, Human genetics, 98(3), 1996, pp. 271-280

Authors: DECKER HJH NEUHAUS C JAUCH A SPEICHER M RIED T BUJARD M BRAUCH H STORKEL S STOCKLE M SELIGER B HUBER C
Citation: Hjh. Decker et al., DETECTION OF A GERMLINE MUTATION AND SOMATIC HOMOZYGOUS LOSS OF THE VON HIPPEL-LINDAU TUMOR-SUPPRESSOR GENE IN A FAMILY WITH A DE-NOVO MUTATION - A COMBINED GENETIC-STUDY, INCLUDING CYTOGENETICS, PCR SSCP, FISH, AND CGH/, Human genetics, 97(6), 1996, pp. 770-776

Authors: NEUMANN HPH BENDER B ZAUNER I BERGER DP ENG C BRAUCH H ZBAR B
Citation: Hph. Neumann et al., MONOGENETIC HYPERTENSION AND PHEOCHROMOCYTOMA, American journal of kidney diseases, 28(3), 1996, pp. 329-333

Authors: SCHWERDTLE RF STORKEL S NEUHAUS C BRAUCH H WEIDT E BRENNER W HOHENFELLNER R HUBER C DECKER HJ
Citation: Rf. Schwerdtle et al., ALLELIC LOSSES AT CHROMOSOMES 1P, 2P, 6P, 10P, 13Q, 17P, AND 21Q SIGNIFICANTLY CORRELATE WITH THE CHROMOPHOBE SUBTYPE OF RENAL-CELL CARCINOMA, Cancer research, 56(13), 1996, pp. 2927-2930

Authors: NEUMANN HPH BRAUCH H
Citation: Hph. Neumann et H. Brauch, MOLECULAR DIAGNOSIS OF THE VON HIPPEL-LIN DAU SYNDROME, Deutsche Medizinische Wochenschrift, 120(41), 1995, pp. 1416-1416

Authors: ZAUNER I BRAUCH H ZBAR B GLAVAC D RIEGLER P MASEK O LIPS CJM NEUMANN HPH
Citation: I. Zauner et al., GERMLINE MUTATIONS IN 25 CENTRAL-EUROPEAN FAMILIES WITH VONHIPPEL-LINDAU-SYNDROME-ASSOCIATED RENAL-CELL CARCINOMA, Journal of the American Society of Nephrology, 6(3), 1995, pp. 716-716

Authors: BRAUCH H KISHIDA T GLAVAC D CHEN F PAUSCH F HOFLER H LATIF F LERMAN MI ZBAR B NEUMANN HPH
Citation: H. Brauch et al., VON HIPPEL-LINDAU (VHL) DISEASE WITH PHEOCHROMOCYTOMA IN THE BLACK-FOREST REGION OF GERMANY - EVIDENCE FOR A FOUNDER EFFECT, Human genetics, 95(5), 1995, pp. 551-556

Authors: LAI SL BRAUCH H KNUTSEN T JOHNSON BE NAU MM MITSUDOMI T TSAI CM WHANGPENG J ZBAR B KAYE FJ GAZDAR AF
Citation: Sl. Lai et al., MOLECULAR-GENETIC CHARACTERIZATION OF NEUROENDOCRINE LUNG-CANCER CELL-LINES, Anticancer research, 15(2), 1995, pp. 225-231

Authors: BRAUCH H BOHM J HOFLER H
Citation: H. Brauch et al., VONHIPPEL-LINDAU-DISEASE AND SPORADIC REN AL-CELL CARCINOMA - REVIEW OF PATHOGENESIS, MORPHOLOGICAL SPECTRUM AND MOLECULAR-GENETICS, Der Pathologe, 16(5), 1995, pp. 321-327

Authors: NEUMANN HPH ENG C MULLIGAN LM GLAVAC D ZAUNER I PONDER BAJ CROSSEY PA MAHER ER BRAUCH H
Citation: Hph. Neumann et al., CONSEQUENCES OF DIRECT GENETIC TESTING FOR GERMLINE MUTATIONS IN THE CLINICAL MANAGEMENT OF FAMILIES WITH MULTIPLE ENDOCRINE NEOPLASIA, TYPE-II, JAMA, the journal of the American Medical Association, 274(14), 1995, pp. 1149-1151

Authors: KELLER G ROTTER M VOGELSANG H BISCHOFF P BECKER KF MUELLER J BRAUCH H SIEWERT JR HOFLER H
Citation: G. Keller et al., MICROSATELLITE INSTABILITY IN ADENOCARCINOMAS OF THE UPPER GASTROINTESTINAL-TRACT - RELATION TO CLINICOPATHOLOGICAL DATA AND FAMILY HISTORY, The American journal of pathology, 147(3), 1995, pp. 593-600

Authors: GNARRA JR TORY K WENG Y SCHMIDT L WEI MH LI H LATIF F LIU S CHEN F DUH FM LUBENSKY I DUAN DR FLORENCE C POZZATTI R WALTHER MM BANDER NH GROSSMAN HB BRAUCH H POMER S BROOKS JD ISAACS WB LERMAN MI ZBAR B LINEHAN WM
Citation: Jr. Gnarra et al., MUTATIONS OF THE VHL TUMOR-SUPPRESSOR GENE IN RENAL-CARCINOMA, Nature genetics, 7(1), 1994, pp. 85-90

Authors: NEUMANN HPH PAUSCH F GLAVAC D BRAUCH H
Citation: Hph. Neumann et al., GERM-LINE MUTATIONS IN RENAL-CELL CARCINOMA (RCC) ASSOCIATED WITH VONHIPPEL-LINDAU DISEASE (VHL), Journal of the American Society of Nephrology, 5(3), 1994, pp. 632-632

Authors: BRAUCH H POMER S HIERONYMUS T SCHADT T LOHRKE H KOMITOWSKI D
Citation: H. Brauch et al., GENETIC ALTERATIONS IN SPORADIC RENAL-CELL CARCINOMA - MOLECULAR ANALYSES OF TUMOR-SUPPRESSOR GENE HARBORING CHROMOSOMAL REGIONS 3P, 5Q, AND 17P, World journal of urology, 12(3), 1994, pp. 162-168

Authors: BRAUCH H MASEK O KOOP H LERMAN MI HOFLER H
Citation: H. Brauch et al., CHROMOSOME-3P HAPLOTYPE ANALYSIS IN 2 SLOVAKIAN PEDIGREES WITH VONHIPPEL-LINDAU DISEASE - PRESYMPTOMATIC DIAGNOSIS OF GENE CARRIERS, American journal of human genetics, 53(3), 1993, pp. 277-277
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