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Results: 1-25 | 26-28
Results: 1-25/28
POSITIONAL CLONING OF THE GENE FOR X-LINKED RETINITIS-PIGMENTOSA-2
Authors: SCHWAHN U LENZNER S DONG J FEIL S HINZMANN B VANDUIJNHOVEN G KIRSCHNER R HEMBERGER M BERGEN AAB ROSENBERG T PINCKERS AJLG FUNDELE R ROSENTHAL A CREMERS FPM ROPERS HH BERGER W
Citation: U. Schwahn et al., POSITIONAL CLONING OF THE GENE FOR X-LINKED RETINITIS-PIGMENTOSA-2, Nature genetics, 19(4), 1998, pp. 327-332
AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA AND CONE-ROD DYSTROPHY CAUSED BY SPLICE-SITE MUTATIONS IN THE STARGARDTS-DISEASE GENE ABCR
Authors: DENHOLLANDER A VANDEPOL DJR VANDRIEL M VANHAREN FJJ KNOERS NVAM TIJMES N BERGEN AAB ROHRSCHNEIDER K BLANKENAGEL A PINCKERS AJLG DEUTMAN AF HOYNG CB CREMERS FPM
Citation: A. Denhollander et al., AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA AND CONE-ROD DYSTROPHY CAUSED BY SPLICE-SITE MUTATIONS IN THE STARGARDTS-DISEASE GENE ABCR, European journal of human genetics, 6, 1998, pp. 501-501
AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA AND CONE-ROD DYSTROPHY CAUSED BY SPLICE-SITE MUTATIONS IN THE STARGARDTS-DISEASE GENE ABCR
Authors: CREMERS FPM VANDEPOL DJR VANDRIEL M DENHOLLANDER AI VANHAREN FJJ KNOERS NVAM TIJMES N BERGEN AAB ROHRSCHNEIDER K BLANKENAGEL A PINCKERS AJLG DEUTMAN AF HOYNG CB
Citation: Fpm. Cremers et al., AUTOSOMAL RECESSIVE RETINITIS-PIGMENTOSA AND CONE-ROD DYSTROPHY CAUSED BY SPLICE-SITE MUTATIONS IN THE STARGARDTS-DISEASE GENE ABCR, Human molecular genetics, 7(3), 1998, pp. 355-362
ANOMALOSCOPE EXAMINATION IN MACULAR GLIOSIS, MACULAR HOLES AND CENTRAL SEROUS CHOROIDOPATHY
Authors: TILANUS MAD PINCKERS AJLG AANDEKERK AL
Citation: Mad. Tilanus et al., ANOMALOSCOPE EXAMINATION IN MACULAR GLIOSIS, MACULAR HOLES AND CENTRAL SEROUS CHOROIDOPATHY, Graefe's archive for clinical and experimental ophthalmology, 236(5), 1998, pp. 326-332
PARTIAL TRIPLICATION OF MTDNA IN MATERNALLY TRANSMITTED DIABETES-MELLITUS AND DEAFNESS - REPLY
Authors: BERGEN AAB PINCKERS AJLG
Citation: Aab. Bergen et Ajlg. Pinckers, PARTIAL TRIPLICATION OF MTDNA IN MATERNALLY TRANSMITTED DIABETES-MELLITUS AND DEAFNESS - REPLY, American journal of human genetics, 63(4), 1998, pp. 1232-1234
RETICULAR DYSTROPHY OF THE RETINAL-PIGMENT EPITHELIUM AND CHOROIDAL NEOVASCULARIZATION - A FLUORESCEIN AND ICGV STUDY
Authors: MARANO F DEUTMAN AF PINCKERS AJLG AANDEKERK AL RIJNEVELD WJ
Citation: F. Marano et al., RETICULAR DYSTROPHY OF THE RETINAL-PIGMENT EPITHELIUM AND CHOROIDAL NEOVASCULARIZATION - A FLUORESCEIN AND ICGV STUDY, Acta ophthalmologica Scandinavica, 75(1), 1997, pp. 22-27
MOLECULAR-BASIS OF CHOROIDEREMIA (CHM) - MUTATIONS INVOLVING THE RAB ESCORT PROTEIN-1 (REP-1) GENE
Authors: VANDENHURK JAJM SCHWARTZ M VANBOKHOVEN H VANDEPOL TJR BOGERD L PINCKERS AJLG BLEEKERWAGEMAKERS EM PAWLOWITZKI IH RUTHER K ROPERS HH CREMERS FPM
Citation: Jajm. Vandenhurk et al., MOLECULAR-BASIS OF CHOROIDEREMIA (CHM) - MUTATIONS INVOLVING THE RAB ESCORT PROTEIN-1 (REP-1) GENE, Human mutation, 9(2), 1997, pp. 110-117
PROGNOSTIC VALUE OF PATTERN-REVERSAL VISUAL-EVOKED POTENTIALS IN IDIOPATHIC EPIRETINAL MEMBRANE
Authors: TILANUS MAD CUYPERS MH BEMELMANS NAM PINCKERS AJLG
Citation: Mad. Tilanus et al., PROGNOSTIC VALUE OF PATTERN-REVERSAL VISUAL-EVOKED POTENTIALS IN IDIOPATHIC EPIRETINAL MEMBRANE, Graefe's archive for clinical and experimental ophthalmology, 235(8), 1997, pp. 474-479
2 SIBS WITH CHORIORETINAL DYSTROPHY, HYPOGONADOTROPIC HYPOGONADISM, AND CEREBELLAR-ATAXIA - BOUCHER-NEUHAUSER-SYNDROME
Authors: RUMP P HAMEL BCJ PINCKERS AJLG VANDOP PA
Citation: P. Rump et al., 2 SIBS WITH CHORIORETINAL DYSTROPHY, HYPOGONADOTROPIC HYPOGONADISM, AND CEREBELLAR-ATAXIA - BOUCHER-NEUHAUSER-SYNDROME, Journal of Medical Genetics, 34(9), 1997, pp. 767-771
PATTERN-REVERSAL VISUAL-EVOKED POTENTIALS IN PATIENTS WITH EPIRETINALMEMBRANE
Authors: BEMELMANS NAM TILANUS MAD CUYPERS MHM PINCKERS AJLG
Citation: Nam. Bemelmans et al., PATTERN-REVERSAL VISUAL-EVOKED POTENTIALS IN PATIENTS WITH EPIRETINALMEMBRANE, American journal of ophthalmology, 123(1), 1997, pp. 97-102
LOCALIZATION OF A NOVEL X-LINKED PROGRESSIVE CONE DYSTROPHY GENE TO XQ27 - EVIDENCE FOR GENETIC-HETEROGENEITY
Authors: BERGEN AAB PINCKERS AJLG
Citation: Aab. Bergen et Ajlg. Pinckers, LOCALIZATION OF A NOVEL X-LINKED PROGRESSIVE CONE DYSTROPHY GENE TO XQ27 - EVIDENCE FOR GENETIC-HETEROGENEITY, American journal of human genetics, 60(6), 1997, pp. 1468-1473
POSITIONAL CLONING OF THE GENE FOR X-LINKED RETINITIS-PIGMENTOSA-3 - HOMOLOGY WITH THE GUANINE-NUCLEOTIDE-EXCHANGE FACTOR RCC1
Authors: ROEPMAN R VANDUIJNHOVEN G ROSENBERG T PINCKERS AJLG BLEEKERWAGEMAKERS LM BERGEN AAB POST J BECK A REINHARDT R ROPERS HH CREMERS FPM BERGER W
Citation: R. Roepman et al., POSITIONAL CLONING OF THE GENE FOR X-LINKED RETINITIS-PIGMENTOSA-3 - HOMOLOGY WITH THE GUANINE-NUCLEOTIDE-EXCHANGE FACTOR RCC1, Human molecular genetics, 5(7), 1996, pp. 1035-1041
GENETIC FINE MAPPING OF THE GENE FOR RECESSIVE STARGARDT DISEASE
Authors: HOYNG CB POPPELAARS F VANDEPOL TJR KREMER H PINCKERS AJLG DEUTMAN AF CREMERS FPM
Citation: Cb. Hoyng et al., GENETIC FINE MAPPING OF THE GENE FOR RECESSIVE STARGARDT DISEASE, Human genetics, 98(4), 1996, pp. 500-504
PROGNOSTIC VALUE OF PATTERN-REVERSAL VISUAL-EVOKED POTENTIALS IN IDIOPATHIC EPIRETINAL MEMBRANE
Authors: CUYPERS MHM TILANUS MAD PINCKERS AJLG BEMELMANS MA DEUTMAN AF
Citation: Mhm. Cuypers et al., PROGNOSTIC VALUE OF PATTERN-REVERSAL VISUAL-EVOKED POTENTIALS IN IDIOPATHIC EPIRETINAL MEMBRANE, Vision research, 36, 1996, pp. 1342-1342
GENETIC FINE MAPPING OF THE GENE FOR RECESSIVE STARGARDT DISEASE
Authors: HOYNG CB POPPELAARS F PINCKERS AJLG DEUTMAN AF CREMERS FPM
Citation: Cb. Hoyng et al., GENETIC FINE MAPPING OF THE GENE FOR RECESSIVE STARGARDT DISEASE, Vision research, 36, 1996, pp. 3234-3234
GYRATE ATROPHY AND CHOROIDAL NEOVASCULARIZATION
Authors: MARANO F DEUTMAN AF PINCKERS AJLG AANDEKERK AL
Citation: F. Marano et al., GYRATE ATROPHY AND CHOROIDAL NEOVASCULARIZATION, Archives of ophthalmology, 114(10), 1996, pp. 1295-1295
STABLE AND PROGRESSIVE HEARING-LOSS IN TYPE 2A USHERS SYNDROME
Authors: VANAAREM A HUYGEN PLM PINCKERS AJLG BLEEKERWAGEMAKERS EM KIMBERLING WJ CREMERS CWRJ
Citation: A. Vanaarem et al., STABLE AND PROGRESSIVE HEARING-LOSS IN TYPE 2A USHERS SYNDROME, The Annals of otology, rhinology & laryngology, 105(12), 1996, pp. 962-967
OPHTHALMOLOGIC FINDINGS IN USHER SYNDROME TYPE 2A
Authors: VANAAREM A WAGENAAR M PINCKERS AJLG HUYGEN PLM BLEEKERWAGEMAKERS EM KIMBERLING BJ CREMERS CWRJ
Citation: A. Vanaarem et al., OPHTHALMOLOGIC FINDINGS IN USHER SYNDROME TYPE 2A, Ophthalmic genetics, 16(4), 1995, pp. 151-158
MULTIPOINT LINKAGE ANALYSIS AND HOMOGENEITY TESTS IN 15 DUTCH X-LINKED RETINITIS-PIGMENTOSA FAMILIES
Authors: BERGEN AAB VANDENBORN LI SCHUURMAN EJM PINCKERS AJLG VANOMMEN GJB BLEEKERSWAGEMAKERS EM SANDKUIJL LA
Citation: Aab. Bergen et al., MULTIPOINT LINKAGE ANALYSIS AND HOMOGENEITY TESTS IN 15 DUTCH X-LINKED RETINITIS-PIGMENTOSA FAMILIES, Ophthalmic genetics, 16(2), 1995, pp. 63-70
PATTERN-REVERSAL VISUAL-EVOKED POTENTIALS - INFLUENCE OF AGE, GENDER AND CHECK SIZE IN THE DIAGNOSIS OF MULTIPLE-SCLEROSIS
Authors: BEMELMANS NAM CUYPERS MHM PINCKERS AJLG HOMMES OR
Citation: Nam. Bemelmans et al., PATTERN-REVERSAL VISUAL-EVOKED POTENTIALS - INFLUENCE OF AGE, GENDER AND CHECK SIZE IN THE DIAGNOSIS OF MULTIPLE-SCLEROSIS, Neuro-ophthalmology, 15(2), 1995, pp. 83-91
THE USHER-SYNDROME TYPE-2A - CLINICAL FINDINGS IN OBLIGATE CARRIERS
Authors: VANAAREM A CREMERS CWRJ PINCKERS AJLG HUYGEN PLM HOMBERGEN GCJH KIMBERLING BJ
Citation: A. Vanaarem et al., THE USHER-SYNDROME TYPE-2A - CLINICAL FINDINGS IN OBLIGATE CARRIERS, International journal of pediatric otorhinolaryngology, 31(2-3), 1995, pp. 159-174
CARRIER DETECTION OF BATTEN-DISEASE (JUVENILE NEURONAL CEROID-LIPOFUSCINOSIS)
Authors: TASCHNER PEM DEVOS N POST JG MEIJERSHEIJBOER EJ HOFMAN I LOONEN MCB PINCKERS AJLG WAGEMAKERS EM GARDINER RM BREUNING MH
Citation: Pem. Taschner et al., CARRIER DETECTION OF BATTEN-DISEASE (JUVENILE NEURONAL CEROID-LIPOFUSCINOSIS), American journal of medical genetics, 57(2), 1995, pp. 333-337
AUTOSOMAL RECESSIVE MELNICK-NEEDLES SYNDROME OR TER HAAR SYNDROME - REPORT OF A PATIENT AND REAPPRAISAL OF AN EARLIER REPORT
Authors: HAMEL BCJ DRAAISMA JMT PINCKERS AJLG BOETES C HOPPE RLE ROPERS HH BRUNNER HG
Citation: Bcj. Hamel et al., AUTOSOMAL RECESSIVE MELNICK-NEEDLES SYNDROME OR TER HAAR SYNDROME - REPORT OF A PATIENT AND REAPPRAISAL OF AN EARLIER REPORT, American journal of medical genetics, 56(3), 1995, pp. 312-316
VARIABILITY OF PATTERN-REVERSAL VISUAL-EVOKED POTENTIALS IN MULTIPLE-SCLEROSIS - LATENCY JITTER AND SIGNAL-TO-NOISE RATIO
Authors: CUYPERS MHM THIJSSEN JM BOURGONJE R PINCKERS AJLG DEUTMAN AF
Citation: Mhm. Cuypers et al., VARIABILITY OF PATTERN-REVERSAL VISUAL-EVOKED POTENTIALS IN MULTIPLE-SCLEROSIS - LATENCY JITTER AND SIGNAL-TO-NOISE RATIO, Vision research, 35, 1995, pp. 4241-4241
ALTERATION OF PATTERN-REVERSAL VISUAL-EVOKED POTENTIALS IN EYES WITH MACULAR HOLES AND THEIR FELLOW EYES
Authors: TILANUS MAD BEMELMANS NAM PINCKERS AJLG CUYPERS MHM DEUTMAN AF
Citation: Mad. Tilanus et al., ALTERATION OF PATTERN-REVERSAL VISUAL-EVOKED POTENTIALS IN EYES WITH MACULAR HOLES AND THEIR FELLOW EYES, Vision research, 35, 1995, pp. 4244-4244
Risultati: 1-25 | 26-28