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Results: 1-25 | 26-50 | 51-60
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GENE CONVERSION IS A LIKELY CAUSE OF MUTATION IN PKD1
Authors: WATNICK TJ GANDOLPH MA WEBER H NEUMANN HPH GERMINO GG
Citation: Tj. Watnick et al., GENE CONVERSION IS A LIKELY CAUSE OF MUTATION IN PKD1, Human molecular genetics (Print), 7(8), 1998, pp. 1239-1243
GENOTYPE-PHENOTYPE CORRELATIONS IN VON-HIPPEL-LINDAU-DISEASE
Authors: NEUMANN HPH BENDER BU
Citation: Hph. Neumann et Bu. Bender, GENOTYPE-PHENOTYPE CORRELATIONS IN VON-HIPPEL-LINDAU-DISEASE, Journal of internal medicine, 243(6), 1998, pp. 541-545
THE HYPERTENSIVE LADY WITH ELEVATED PLASMA NOREPINEPHRINE CONCENTRATION AND NO DEMONSTRABLE TUMOR - THE SEARCH FOR PHEOCHROMOCYTOMA
Authors: BENDER B ALTEHOFER C HASSE J NEUMANN HPH
Citation: B. Bender et al., THE HYPERTENSIVE LADY WITH ELEVATED PLASMA NOREPINEPHRINE CONCENTRATION AND NO DEMONSTRABLE TUMOR - THE SEARCH FOR PHEOCHROMOCYTOMA, Nephrology, dialysis, transplantation, 13(5), 1998, pp. 1295-1296
FREQUENT PROGESTERONE-RECEPTOR IMMUNOREACTIVITY IN TUBEROUS SCLEROSIS-ASSOCIATED RENAL ANGIOMYOLIPOMAS
Authors: HENSKE EP AO X SHORT MP GREENBERG R NEUMANN HPH KWIATKOWSKI DJ RUSSO I
Citation: Ep. Henske et al., FREQUENT PROGESTERONE-RECEPTOR IMMUNOREACTIVITY IN TUBEROUS SCLEROSIS-ASSOCIATED RENAL ANGIOMYOLIPOMAS, Modern pathology, 11(7), 1998, pp. 665-668
ENDOLYMPHATIC SAC TUMORS
Authors: KEMPERMANN G NEUMANN HPH VOLK B
Citation: G. Kempermann et al., ENDOLYMPHATIC SAC TUMORS, Histopathology, 33(1), 1998, pp. 2-10
INCIDENCE OF RET PROTOONCOGENE GERMLINE MUTATIONS IN PHEOCHROMOCYTOMAPATIENTS - EXPERIENCE OF ONE MEDICAL-CENTER
Authors: JANUSZEWICZ A BENDER BU LORI I SZMIGIELSKI C LAPINSKI M FELTYNOWSKI T WOCIAL B CHODAKOWSKA J NEUMANN HPH JANUSZEWICZ W
Citation: A. Januszewicz et al., INCIDENCE OF RET PROTOONCOGENE GERMLINE MUTATIONS IN PHEOCHROMOCYTOMAPATIENTS - EXPERIENCE OF ONE MEDICAL-CENTER, Journal of hypertension, 16, 1998, pp. 429-429
PREVALENCE, MORPHOLOGY AND BIOLOGY OF RENAL-CELL CARCINOMA IN VON-HIPPEL-LINDAU-DISEASE COMPARED TO SPORADIC RENAL-CELL CARCINOMA
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
LAPAROSCOPIC SURGERY FOR PHEOCHROMOCYTOMA - ADRENALECTOMY, PARTIAL RESECTION, EXCISION OF PARAGANGLIOMAS
Authors: JANETSCHEK G FINKENSTEDT G GASSER R WAIBEL UG PESCHEL R BARTSCH G NEUMANN HPH
Citation: G. Janetschek et al., LAPAROSCOPIC SURGERY FOR PHEOCHROMOCYTOMA - ADRENALECTOMY, PARTIAL RESECTION, EXCISION OF PARAGANGLIOMAS, The Journal of urology, 160(2), 1998, pp. 330-334
AN UNUSUAL PATTERN OF MUTATION IN THE DUPLICATED PORTION OF PKD1 IS REVEALED BY USE OF A NOVEL STRATEGY FOR MUTATION DETECTION
Authors: WATNICK TJ PIONTEK KB CORDAL TM WEBER H GANDOLPH MA QIAN F LENS XM NEUMANN HPH GERMINO GG
Citation: Tj. Watnick et al., AN UNUSUAL PATTERN OF MUTATION IN THE DUPLICATED PORTION OF PKD1 IS REVEALED BY USE OF A NOVEL STRATEGY FOR MUTATION DETECTION, Human molecular genetics, 6(9), 1997, pp. 1473-1481
LATE OCCURRENCE OF CYSTS IN AUTOSOMAL-DOMINANT MEDULLARY CYSTIC KIDNEY-DISEASE
Authors: NEUMANN HPH ZAUNER I STRAHM B BENDER BU SCHOLLMEYER P BLUM U ROHRBACH R HILDEBRANDT F
Citation: Hph. Neumann et al., LATE OCCURRENCE OF CYSTS IN AUTOSOMAL-DOMINANT MEDULLARY CYSTIC KIDNEY-DISEASE, Nephrology, dialysis, transplantation, 12(6), 1997, pp. 1242-1246
AN INCIDENTAL FINDING - BILATERAL MULTIFOCAL RENAL ONCOCYTOMA
Authors: BENDER BU WETTERAUER U SCHOLLMEYER P NEUMANN HPH
Citation: Bu. Bender et al., AN INCIDENTAL FINDING - BILATERAL MULTIFOCAL RENAL ONCOCYTOMA, Nephrology, dialysis, transplantation, 12(5), 1997, pp. 1034-1036
OCTREOTIDE SCINTIGRAPHY AND CATECHOLAMINE RESPONSE TO AN OCTREOTIDE CHALLENGE IN MALIGNANT PHEOCHROMOCYTOMA
Authors: KOPF D BOCKISCH A STEINERT H HAHN K BEYER J NEUMANN HPH HENSEN J LEHNERT H
Citation: D. Kopf et al., OCTREOTIDE SCINTIGRAPHY AND CATECHOLAMINE RESPONSE TO AN OCTREOTIDE CHALLENGE IN MALIGNANT PHEOCHROMOCYTOMA, Clinical endocrinology, 46(1), 1997, pp. 39-44
RENAL CYSTS, RENAL-CANCER AND VONHIPPEL-LINDAU DISEASE
Authors: NEUMANN HPH ZBAR B
Citation: Hph. Neumann et B. Zbar, RENAL CYSTS, RENAL-CANCER AND VONHIPPEL-LINDAU DISEASE, Kidney international, 51(1), 1997, pp. 16-26
MOLECULAR-GENETIC IDENTIFICATION OF FAMILIES WITH JUVENILE NEPHRONOPHTHISIS TYPE-1 - RATE OF PROGRESSION TO RENAL-FAILURE
Authors: HILDEBRANDT F STRAHM B NOTHWANG HG GRETZ N SCHNIEDERS B SINGHSAWHNEY I KUTT R VOLLMER M BRANDIS M BODE U BRODEHL J LATTA K BROUHARD B DIPPEL J FELDHOFF C WINGEN M FILLER G GHIGGERI GM GUAYWOODFORD L HOPPE B KLARE B KUIJTEN RH KUHN K LEUMANN E NEUMANN HPH VOSSMERBAUMER U NEUMAYER HH RASCHER W SCHARER K STOLPE HJ
Citation: F. Hildebrandt et al., MOLECULAR-GENETIC IDENTIFICATION OF FAMILIES WITH JUVENILE NEPHRONOPHTHISIS TYPE-1 - RATE OF PROGRESSION TO RENAL-FAILURE, Kidney international, 51(1), 1997, pp. 261-269
RESULTS OF RENAL-TRANSPLANTATION IN PATIENTS WITH RENAL-CELL CARCINOMA AND VONHIPPEL-LINDAU-DISEASE
Authors: GOLDFARB DA NEUMANN HPH PENN I NOVICK AC
Citation: Da. Goldfarb et al., RESULTS OF RENAL-TRANSPLANTATION IN PATIENTS WITH RENAL-CELL CARCINOMA AND VONHIPPEL-LINDAU-DISEASE, Transplantation, 64(12), 1997, pp. 1726-1729
MUTATION ANALYSIS OF GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR, A LIGAND FOR AN RET CORECEPTOR COMPLEX, IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-2 AND SPORADIC NEUROENDOCRINE TUMORS/
Authors: MARSH DJ ZHENG ZM ARNOLD A ANDREW SD LEAROYD D FRILLING A KOMMINOTH P NEUMANN HPH PONDER BAJ ROLLINS BJ SHAPIRO GI ROBINSON BG MULLIGAN LM ENG C
Citation: Dj. Marsh et al., MUTATION ANALYSIS OF GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR, A LIGAND FOR AN RET CORECEPTOR COMPLEX, IN MULTIPLE ENDOCRINE NEOPLASIA TYPE-2 AND SPORADIC NEUROENDOCRINE TUMORS/, The Journal of clinical endocrinology and metabolism, 82(9), 1997, pp. 3025-3028
FUNCTIONING THORACIC PARAGANGLIOMA - ASSOCIATION WITH VON-HIPPEL-LINDAU-SYNDROME
Authors: BENDER BU ALTEHOFER C JANUSZEWICZ A GARTNER R SCHMIDT K HOFFMANN MM HEIDEMANN PH NEUMANN HPH
Citation: Bu. Bender et al., FUNCTIONING THORACIC PARAGANGLIOMA - ASSOCIATION WITH VON-HIPPEL-LINDAU-SYNDROME, The Journal of clinical endocrinology and metabolism, 82(10), 1997, pp. 3356-3360
PROBABLE GENE CONVERSION BETWEEN PKD1 AND ITS HOMOLOGS AS A CAUSE OF ADPKD
Authors: WATNICK TJ GANDOLPH MA WEBER H NEUMANN HPH GERMINO GG
Citation: Tj. Watnick et al., PROBABLE GENE CONVERSION BETWEEN PKD1 AND ITS HOMOLOGS AS A CAUSE OF ADPKD, American journal of human genetics, 61(4), 1997, pp. 2050-2050
PRIMARY PIGMENTED NODULAR ADRENOCORTICAL DYSPLASIA - A RARE CAUSE OF CUSHINGS-SYNDROME
Authors: ANDING K KOHLER G BOHM N PETERSON KG SCHOLLMEYER P NEUMANN HPH
Citation: K. Anding et al., PRIMARY PIGMENTED NODULAR ADRENOCORTICAL DYSPLASIA - A RARE CAUSE OF CUSHINGS-SYNDROME, Deutsche Medizinische Wochenschrift, 121(43), 1996, pp. 1321-1324
GERMLINE MUTATIONS IN THE VON-HIPPEL-LINDAU DISEASE (VHL) GENE IN FAMILIES FROM NORTH-AMERICA, EUROPE, AND JAPAN
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
MUTATION DETECTION WITHIN THE DUPLICATED REGION OF THE PKD1 GENE
Authors: WATNICK T LANDES G NEUMANN HPH PIONTEK K VANRAAY T WEBER H GERMINO G
Citation: T. Watnick et al., MUTATION DETECTION WITHIN THE DUPLICATED REGION OF THE PKD1 GENE, Journal of the American Society of Nephrology, 7(9), 1996, pp. 1883-1883
USE OF A FUNCTIONAL ASSAY FOR EVALUATING SEQUENCE VARIANTS IN EXON-45-46 OF PKD1
Authors: WATNICK TJ QIAN F SOMLO S NEUMANN HPH WEBER H GERMINO GG
Citation: Tj. Watnick et al., USE OF A FUNCTIONAL ASSAY FOR EVALUATING SEQUENCE VARIANTS IN EXON-45-46 OF PKD1, Journal of the American Society of Nephrology, 7(9), 1996, pp. 1885-1885
IDENTIFICATION OF 17 MUTATIONS IN 10 EXONS IN THE COL4A5 COLLAGEN GENE, BUT NO MUTATIONS FOUND IN 4 EXONS IN COL4A6 - A STUDY OF 250 PATIENTS WITH HEMATURIA AND SUSPECTED OF HAVING ALPORT SYNDROME
Authors: HEISKARI N ZHANG X ZHOU J LEINONEN A BARKER D GREGORY M ATKIN CL NETZER KO WEBER M REEDERS S GRONHAGENRISKA C NEUMANN HPH TREMBATH R TRYGGVASON K
Citation: N. Heiskari et al., IDENTIFICATION OF 17 MUTATIONS IN 10 EXONS IN THE COL4A5 COLLAGEN GENE, BUT NO MUTATIONS FOUND IN 4 EXONS IN COL4A6 - A STUDY OF 250 PATIENTS WITH HEMATURIA AND SUSPECTED OF HAVING ALPORT SYNDROME, Journal of the American Society of Nephrology, 7(5), 1996, pp. 702-709
MUTATIONS IN THE VHL TUMOR-SUPPRESSOR GENE AND ASSOCIATED LESIONS IN FAMILIES WITH VON-HIPPEL-LINDAU DISEASE FROM CENTRAL-EUROPE
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
MONOGENETIC HYPERTENSION AND PHEOCHROMOCYTOMA
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
Risultati: 1-25 | 26-50 | 51-60