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Results: 1-22 |
Results: 22
THE OCULAR PRESENTATION OF NEUROFIBROMATOSIS-2
Authors: RAGGE NK BASER ME RICCARDI VM FALK RE
Citation: Nk. Ragge et al., THE OCULAR PRESENTATION OF NEUROFIBROMATOSIS-2, Eye, 11, 1997, pp. 12-18
IDENTIFICATION OF NF2 GERM-LINE MUTATIONS AND COMPARISON WITH NEUROFIBROMATOSIS-2 PHENOTYPES (VOL 98, PG 534, 1996)
Authors: KLUWE L BAYER S BASER ME HAZIM W HAASE W FUNSTERER C MAUTNER VF
Citation: L. Kluwe et al., IDENTIFICATION OF NF2 GERM-LINE MUTATIONS AND COMPARISON WITH NEUROFIBROMATOSIS-2 PHENOTYPES (VOL 98, PG 534, 1996), Human genetics, 99(2), 1997, pp. 292-292
IMMUNOHISTOCHEMICAL DETECTION OF SCHWANNOMIN AND NEUROFIBROMIN IN VESTIBULAR SCHWANNOMAS, EPENDYMOMAS AND MENINGIOMAS
Authors: HUYNH DP MAUTNER V BASER ME STAVROU D PULST SM
Citation: Dp. Huynh et al., IMMUNOHISTOCHEMICAL DETECTION OF SCHWANNOMIN AND NEUROFIBROMIN IN VESTIBULAR SCHWANNOMAS, EPENDYMOMAS AND MENINGIOMAS, Journal of neuropathology and experimental neurology, 56(4), 1997, pp. 382-390
SKIN ABNORMALITIES IN NEUROFIBROMATOSIS .2.
Authors: MAUTNER VF LINDENAU M BASER ME KLUWE L GOTTSCHALK J
Citation: Vf. Mautner et al., SKIN ABNORMALITIES IN NEUROFIBROMATOSIS .2., Archives of dermatology, 133(12), 1997, pp. 1539-1543
MALIGNANT NERVOUS-SYSTEM TUMORS IN NEUROFIBROMATOSIS-2
Authors: BASER ME MACCOLLIN MM EVANS DGR ALLEN J JACKLER RK SUJANSKY E RUBENSTEIN AE LOUIS DN
Citation: Me. Baser et al., MALIGNANT NERVOUS-SYSTEM TUMORS IN NEUROFIBROMATOSIS-2, American journal of human genetics, 61(4), 1997, pp. 321-321
SKIN TUMORS IN NF2
Authors: KLUWE L LINDENAU M BASER ME GOTTSCHALK F MAUTNER VF
Citation: L. Kluwe et al., SKIN TUMORS IN NF2, American journal of human genetics, 61(4), 1997, pp. 578-578
GERM-LINE NF2 MUTATIONS AND TUMOR-GROWTH IN YOUNG NEUROFIBROMATOSIS-2PATIENTS
Authors: MAUTNER VF BASER ME KLUWE L FUNSTERER C SAMII M
Citation: Vf. Mautner et al., GERM-LINE NF2 MUTATIONS AND TUMOR-GROWTH IN YOUNG NEUROFIBROMATOSIS-2PATIENTS, American journal of human genetics, 61(4), 1997, pp. 2124-2124
IDENTIFICATION OF NF2 GERM-LINE MUTATIONS AND COMPARISON WITH NEUROFIBROMATOSIS-2 PHENOTYPES
Authors: KLUWE L BAYER S BASER ME HAZIM W HAASE W FUNSTERER C MAUTNER VF
Citation: L. Kluwe et al., IDENTIFICATION OF NF2 GERM-LINE MUTATIONS AND COMPARISON WITH NEUROFIBROMATOSIS-2 PHENOTYPES, Human genetics, 98(5), 1996, pp. 534-538
PHENOTYPIC VARIABILITY IN 2 FAMILIES WITH NOVEL SPLICE-SITE AND FRAMESHIFT NF2 MUTATIONS
Authors: MAUTNER VF BASER ME KLUWE L
Citation: Vf. Mautner et al., PHENOTYPIC VARIABILITY IN 2 FAMILIES WITH NOVEL SPLICE-SITE AND FRAMESHIFT NF2 MUTATIONS, Human genetics, 98(2), 1996, pp. 203-206
IDENTIFICATION OF 3 NEUROFIBROMATOSIS TYPE-2 (NF2) GENE-MUTATIONS IN VESTIBULAR SCHWANNOMAS
Authors: SAINZ J FIGUEROA K BASER ME PULST SM
Citation: J. Sainz et al., IDENTIFICATION OF 3 NEUROFIBROMATOSIS TYPE-2 (NF2) GENE-MUTATIONS IN VESTIBULAR SCHWANNOMAS, Human genetics, 97(1), 1996, pp. 121-123
PHENOTYPIC VARIABILITY IN MONOZYGOTIC TWINS WITH NEUROFIBROMATOSIS-2
Authors: BASER ME RAGGE NK RICCARDI VM JANUS T GANTZ B PULST SM
Citation: Me. Baser et al., PHENOTYPIC VARIABILITY IN MONOZYGOTIC TWINS WITH NEUROFIBROMATOSIS-2, American journal of medical genetics, 64(4), 1996, pp. 563-567
THE NEUROIMAGING AND CLINICAL SPECTRUM OF NEUROFIBROMATOSIS-2
Authors: MAUTNER VF LINDENAU M BASER ME HAZIM W TATAGIBA M HAASE W SAMII M WAIS R PULST SM
Citation: Vf. Mautner et al., THE NEUROIMAGING AND CLINICAL SPECTRUM OF NEUROFIBROMATOSIS-2, Neurosurgery, 38(5), 1996, pp. 880-885
PRESYMPTOMATIC DIAGNOSIS OF NEUROFIBROMATOSIS-2 USING LINKED GENETIC-MARKERS, NEUROIMAGING, AND OCULAR EXAMINATIONS
Authors: BASER ME MAUTNER VF RAGGE NK NECHIPORUK A RICCARDI VM KLEIN J SAINZ J PULST SM
Citation: Me. Baser et al., PRESYMPTOMATIC DIAGNOSIS OF NEUROFIBROMATOSIS-2 USING LINKED GENETIC-MARKERS, NEUROIMAGING, AND OCULAR EXAMINATIONS, Neurology, 47(5), 1996, pp. 1269-1277
A MISSENSE MUTATION IN THE NEUROFIBROMATOSIS-2 GENE OCCURS IN PATIENTS WITH MILD AND SEVERE PHENOTYPES
Authors: SCOLES DR BASER ME PULST SM
Citation: Dr. Scoles et al., A MISSENSE MUTATION IN THE NEUROFIBROMATOSIS-2 GENE OCCURS IN PATIENTS WITH MILD AND SEVERE PHENOTYPES, Neurology, 47(2), 1996, pp. 544-546
HIGH-FREQUENCY OF NONSENSE MUTATIONS IN THE NF2 GENE CAUSED BY C TO TTRANSITIONS IN 5 CGA CODONS
Authors: SAINZ J FIGUEROA K BASER ME MAUTNER VF PULST SM
Citation: J. Sainz et al., HIGH-FREQUENCY OF NONSENSE MUTATIONS IN THE NF2 GENE CAUSED BY C TO TTRANSITIONS IN 5 CGA CODONS, Human molecular genetics, 4(1), 1995, pp. 137-139
INTERINDIVIDUAL DIFFERENCES IN THE CONCENTRATION OF 1-HYDROXYPYRENE-GLUCURONIDE IN URINE AND POLYCYCLIC AROMATIC HYDROCARBON-DNA ADDUCTS INPERIPHERAL WHITE BLOOD-CELLS AFTER CHARBROILED BEEF CONSUMPTION
Authors: KANG DH ROTHMAN N POIRIER MC GREENBERG A HSU CH SCHWARTZ BS BASER ME GROOPMAN JD WESTON A STRICKLAND PT
Citation: Dh. Kang et al., INTERINDIVIDUAL DIFFERENCES IN THE CONCENTRATION OF 1-HYDROXYPYRENE-GLUCURONIDE IN URINE AND POLYCYCLIC AROMATIC HYDROCARBON-DNA ADDUCTS INPERIPHERAL WHITE BLOOD-CELLS AFTER CHARBROILED BEEF CONSUMPTION, Carcinogenesis, 16(5), 1995, pp. 1079-1085
OCULAR ABNORMALITIES IN NEUROFIBROMATOSIS-2
Authors: RAGGE NK BASER ME KLEIN J NECHIPORUK A SAINZ J PULST SM RICCARDI VM
Citation: Nk. Ragge et al., OCULAR ABNORMALITIES IN NEUROFIBROMATOSIS-2, American journal of ophthalmology, 120(5), 1995, pp. 634-641
MUTATIONS OF THE NEUROFIBROMATOSIS TYPE-2 GENE AND LACK OF THE GENE-PRODUCT IN VESTIBULAR SCHWANNOMAS
Authors: SAINZ J HUYNH DP FIGUEROA K RAGGE NK BASER ME PULST SM
Citation: J. Sainz et al., MUTATIONS OF THE NEUROFIBROMATOSIS TYPE-2 GENE AND LACK OF THE GENE-PRODUCT IN VESTIBULAR SCHWANNOMAS, Human molecular genetics, 3(6), 1994, pp. 885-891
COMPREHENSIVE MANAGEMENT OF BILATERAL ACOUSTIC NEUROMAS - CURRENT PERSPECTIVES
Authors: BRIGGS RJS BRACKMANN DE BASER ME HITSELBERGER WE
Citation: Rjs. Briggs et al., COMPREHENSIVE MANAGEMENT OF BILATERAL ACOUSTIC NEUROMAS - CURRENT PERSPECTIVES, Archives of otolaryngology, head & neck surgery, 120(12), 1994, pp. 1307-1314
LOSS OF ALLELES IN VESTIBULAR SCHWANNOMAS - USE OF MICROSATELLITE MARKERS ON CHROMOSOME-22
Authors: SAINZ J BASER ME RAGGE NK NELSON RA PULST SM
Citation: J. Sainz et al., LOSS OF ALLELES IN VESTIBULAR SCHWANNOMAS - USE OF MICROSATELLITE MARKERS ON CHROMOSOME-22, Archives of otolaryngology, head & neck surgery, 119(12), 1993, pp. 1285-1288
MUTATIONS IN THE NEUROFIBROMATOSIS-2 GENE IN 31 VESTIBULAR SCHWANNOMAS
Authors: SAINZ J FIGUEROA C BASER ME PULAT SM
Citation: J. Sainz et al., MUTATIONS IN THE NEUROFIBROMATOSIS-2 GENE IN 31 VESTIBULAR SCHWANNOMAS, American journal of human genetics, 53(3), 1993, pp. 354-354
PRESYMPTOMATIC DIAGNOSIS IN NF2 - USE OF NOVEL MICROSATELLITE MARKERS, NEUROIMAGING AND OCULAR EXAMINATIONS
Authors: PULST SM BASER ME MAUTNER V SAINZ J NECHIPORUK A KLEIN J NELSON RA RAGGE NK RICCARDI VM
Citation: Sm. Pulst et al., PRESYMPTOMATIC DIAGNOSIS IN NF2 - USE OF NOVEL MICROSATELLITE MARKERS, NEUROIMAGING AND OCULAR EXAMINATIONS, American journal of human genetics, 53(3), 1993, pp. 488-488
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