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
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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:
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
Citation: H. Brauch, THE HIPPEL-LINDAU SYNDROME - CLINICAL AND GENETIC-ASPECTS OF RETINAL ANGIOMATOSIS, Klinische Monatsblatter fur Augenheilkunde, 210(3), 1997, pp. 1-1
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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
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TISHERMAN S
MULVIHILL JJ
GROSS DJ
SHUIN T
WHALEY J
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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:
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NEUHAUS C
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BRAUCH H
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SELIGER B
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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
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STORKEL S
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BRAUCH H
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BRENNER W
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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
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:
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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
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
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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:
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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:
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TORY K
WENG Y
SCHMIDT L
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LI H
LATIF F
LIU S
CHEN F
DUH FM
LUBENSKY I
DUAN DR
FLORENCE C
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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
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