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Results: 26-50/60
Authors:
NEUMANN HPH
ENG C
MULLIGAN LM
Citation: Hph. Neumann et al., VON HIPPEL-LINDAU DISEASE AND PHEOCHROMOCYTOMA - REPLY, JAMA, the journal of the American Medical Association, 275(11), 1996, pp. 840-840
Authors:
KEMPERMANN G
NEUMANN HPH
SCHEREMET R
VOLK B
MANN W
GILSBACH J
LASZIG R
Citation: G. Kempermann et al., DEAFNESS DUE TO BILATERAL ENDOLYMPHATIC SAC TUMORS IN A CASE OF VON-HIPPEL-LINDAU SYNDROME, Journal of Neurology, Neurosurgery and Psychiatry, 61(3), 1996, pp. 318-320
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:
HENSKE EP
NEUMANN HPH
SCHEITHAUER BW
HERBST EW
SHORT MP
KWIATKOWSKI DJ
Citation: Ep. Henske et al., LOSS OF HETEROZYGOSITY IN THE TUBEROUS SCLEROSIS (TSC2) REGION OF CHROMOSOME BAND 16P13 OCCURS IN SPORADIC AS WELL AS TSC-ASSOCIATED RENAL ANGIOMYOLIPOMAS, Genes, chromosomes & cancer, 13(4), 1995, pp. 295-298
Authors:
ENG C
MULLIGAN LM
SMITH DP
HEALEY CS
FRILLING A
RAUE F
NEUMANN HPH
PFRAGNER R
BEHMEL A
LORENZO MJ
STONEHOUSE TJ
PONDER MA
PONDER BAJ
Citation: C. Eng et al., MUTATION OF THE RET PROTOONCOGENE IN SPORADIC MEDULLARY-THYROID CARCINOMA, Genes, chromosomes & cancer, 12(3), 1995, pp. 209-212
Authors:
NEUMANN HPH
LIPS CJM
HSIA YE
ZBAR B
Citation: Hph. Neumann et al., VON HIPPEL-LINDAU SYNDROME, Brain pathology, 5(2), 1995, pp. 181-193
Authors:
NEUMANN HPH
Citation: Hph. Neumann, VON HIPPEL-LINDAU SYNDROME - A RARE SYNDROME AS THE CLUE FOR THE MOLECULAR-BASIS OF COMMON RENAL DISORDERS, Nephrology, dialysis, transplantation, 10(9), 1995, pp. 1498-1499
Authors:
NEUMANN HPH
BRUGGEN V
BERGER DP
HERBST E
BLUM U
MORGENROTH A
SCHOLLMEYER P
WETTERAUER U
Citation: Hph. Neumann et al., TUBEROUS SCLEROSIS COMPLEX WITH END-STAGE RENAL-FAILURE, Nephrology, dialysis, transplantation, 10(3), 1995, pp. 349-353
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:
ENG C
MULLIGAN LM
SMITH DP
HEALEY CS
FRILLING A
RAUE F
NEUMANN HPH
PONDER MA
PONDER BAJ
Citation: C. Eng et al., LOW-FREQUENCY OF GERMLINE MUTATIONS IN THE RET PROTOONCOGENE IN PATIENTS WITH APPARENTLY SPORADIC MEDULLARY-THYROID CARCINOMA, Clinical endocrinology, 43(1), 1995, pp. 123-127
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:
ZAUNER I
GERLING J
NEUMANN HPH
Citation: I. Zauner et al., OSSEOUS MALFORMATIONS ASSOCIATED WITH NEPHRONOPHTHISIS, Kidney international, 47(3), 1995, pp. 1008-1008
Authors:
CROSSEY PA
RICHARDS FM
GREEN JS
NEUMANN HPH
FOSTER K
PROWSE A
AFFARA NA
FERGUSONSMITH MA
MAHER ER
Citation: Pa. Crossey et al., GENOTYPE-PHENOTYPE CORRELATIONS IN VONHIPPEL-LINDAU (VHL)-DISEASE, Journal of Medical Genetics, 32(2), 1995, pp. 137-138
Authors:
SCHMIDT D
NEUMANN HPH
Citation: D. Schmidt et Hph. Neumann, RETINAL VASCULAR HAMARTOMA IN VON HIPPEL-LINDAU DISEASE, Archives of ophthalmology, 113(9), 1995, pp. 1163-1167
Authors:
HENSKE EP
NEUMANN HPH
SCHEITHAUER BW
SHORT MP
HERBST EW
KWIATKOWSKI DJ
Citation: Ep. Henske et al., FREQUENT CHROMOSOME 16P13 LOSS OF HETEROZYGOSITY IN TUBEROUS SCLEROSIS ANGIOMYOLIPOMAS SUPPORTS A TUMOR-SUPPRESSOR ROLE FOR TSC2 BUT NOT TSC1, American journal of human genetics, 57(4), 1995, pp. 117-117
Authors:
NEUMANN HPH
Citation: Hph. Neumann, RISK OF RUPTURE IN THE CASE OF RENAL CYST S, Deutsche Medizinische Wochenschrift, 119(43), 1994, pp. 1486-1486
Authors:
ZERRES K
MUCHER G
BACHNER L
DESCHENNES G
EGGERMANN T
KAARIAINEN H
KNAPP M
LENNERT T
MISSELWITZ J
VONMUHLENDAHL KE
NEUMANN HPH
PIRSON Y
RUDNIKSCHONEBORN S
STEINBICKER V
WIRTH B
SCHARER K
Citation: K. Zerres et al., MAPPING OF THE GENE FOR AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE(ARPKD) TO CHROMOSOME 6P21-CEN, Nature genetics, 7(3), 1994, pp. 429-432
Authors:
MULLIGAN LM
ENG C
HEALEY CS
CLAYTON D
KWOK JBJ
GARDNER E
PONDER MA
FRILLING A
JACKSON CE
LEHNERT H
NEUMANN HPH
THIBODEAU SN
PONDER BAJ
Citation: Lm. Mulligan et al., SPECIFIC MUTATIONS OF THE RET PROTOONCOGENE ARE RELATED TO DISEASE PHENOTYPE IN MEN 2A AND FMTC, Nature genetics, 6(1), 1994, pp. 70-74
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:
NEUMANN HPH
Citation: Hph. Neumann, GENETICS OF HYPERTENSION - THE PHEOCHROMOCYTOMA MODEL, The Clinical investigator, 72(9), 1994, pp. 729-730
Authors:
NEUMANN HPH
Citation: Hph. Neumann, POSTOPERATIVE FLANK PAIN AFTER SURGERY OF PHEOCHROMOCYTOMA, Nephrology, dialysis, transplantation, 9(6), 1994, pp. 721-722
Authors:
NEUMANN HPH
Citation: Hph. Neumann, VON HIPPEL-LINDAU SYNDROME, Nephrology, dialysis, transplantation, 9(3), 1994, pp. 313-315
Authors:
NEUMANN HPH
WIESTLER OD
Citation: Hph. Neumann et Od. Wiestler, VON HIPPEL-LINDAU DISEASE - A SYNDROME PROVIDING INSIGHTS INTO GROWTH-CONTROL AND TUMORIGENESIS, Nephrology, dialysis, transplantation, 9(12), 1994, pp. 1832-1833
Authors:
BATHMANN J
NEUMANN HPH
SIGMUND G
MOSER E
Citation: J. Bathmann et al., FALSE-POSITIVE DIAGNOSIS OF A PHEOCHROMOCYTOMA WITH I-123 METAIODOBENZYLGUANIDINE, Clinical nuclear medicine, 19(3), 1994, pp. 221-223