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Results: 1-25 | 26-48
Results: 1-25/48
THE FORKHEAD TRANSCRIPTION FACTOR GENE FKHL7 IS RESPONSIBLE FOR GLAUCOMA PHENOTYPES WHICH MAP TO 6P25
Authors: NISHIMURA DY SWIDERSKI RE ALWARD WLM SEARBY CC PATIL SR BENNET SR KANIS AB GASTIER JM STONE EM SHEFFIELD VC
Citation: Dy. Nishimura et al., THE FORKHEAD TRANSCRIPTION FACTOR GENE FKHL7 IS RESPONSIBLE FOR GLAUCOMA PHENOTYPES WHICH MAP TO 6P25, Nature genetics, 19(2), 1998, pp. 140-147
A NOVEL HOMEOBOX GENE PITX3 IS MUTATED IN FAMILIES WITH AUTOSOMAL-DOMINANT CATARACTS AND ASMD
Authors: SEMINA EV FERRELL RE MINTZHITTNER HA BITOUN P ALWARD WLM REITER RS FUNKHAUSER C DAACKHIRSCH S MURRAY JC
Citation: Ev. Semina et al., A NOVEL HOMEOBOX GENE PITX3 IS MUTATED IN FAMILIES WITH AUTOSOMAL-DOMINANT CATARACTS AND ASMD, Nature genetics, 19(2), 1998, pp. 167-170
CHARACTERIZATION AND COMPARISON OF THE HUMAN AND MOUSE GLC1A GLAUCOMAGENES
Authors: FINGERT JH YING LH SWIDERSKI RE NYSTUEN AM ARBOUR NC ALWARD WLM SHEFFIELD VC STONE EM
Citation: Jh. Fingert et al., CHARACTERIZATION AND COMPARISON OF THE HUMAN AND MOUSE GLC1A GLAUCOMAGENES, PCR methods and applications, 8(4), 1998, pp. 377-384
MEDICAL-MANAGEMENT OF GLAUCOMA
Authors: ALWARD WLM
Citation: Wlm. Alward, MEDICAL-MANAGEMENT OF GLAUCOMA, The New England journal of medicine, 339(18), 1998, pp. 1298-1307
CLINICAL-FEATURES ASSOCIATED WITH MUTATIONS IN THE CHROMOSOME-1 OPEN-ANGLE GLAUCOMA GENE (GLCIA)
Authors: ALWARD WLM FINGERT JH COOTE MA JOHNSON AT LERNER SF JUNQUA D DURCAN FJ MCCARTNEY PJ MACKEY DA SHEFFIELD VC STONE EM
Citation: Wlm. Alward et al., CLINICAL-FEATURES ASSOCIATED WITH MUTATIONS IN THE CHROMOSOME-1 OPEN-ANGLE GLAUCOMA GENE (GLCIA), The New England journal of medicine, 338(15), 1998, pp. 1022-1027
AUTOSOMAL-DOMINANT IRIS HYPOPLASIA IS CAUSED BY A MUTATION IN THE RIEGER-SYNDROME (RIEG PITX2) GENE/
Authors: ALWARD WLM SEMINA EV KALENAK JW HEON E SHETH BP STONE EM MURRAY JC
Citation: Wlm. Alward et al., AUTOSOMAL-DOMINANT IRIS HYPOPLASIA IS CAUSED BY A MUTATION IN THE RIEGER-SYNDROME (RIEG PITX2) GENE/, American journal of ophthalmology, 125(1), 1998, pp. 98-100
A RANDOMIZED STUDY OF MITOMYCIN AUGMENTATION IN COMBINED PHACOEMULSIFICATION AND TRABECULECTOMY
Authors: CARLSON DW ALWARD WLM BARAD JP ZIMMERMAN MB CARNEY BL
Citation: Dw. Carlson et al., A RANDOMIZED STUDY OF MITOMYCIN AUGMENTATION IN COMBINED PHACOEMULSIFICATION AND TRABECULECTOMY, Ophthalmology, 104(4), 1997, pp. 719-724
PROGRESS IN RIEGER-SYNDROME GENES SEARCH AND MUTATION SCREENING
Authors: SEMINA EV REITER R ALWARD WLM BITOUN P MURRAY JC
Citation: Ev. Semina et al., PROGRESS IN RIEGER-SYNDROME GENES SEARCH AND MUTATION SCREENING, Investigative ophthalmology & visual science, 38(4), 1997, pp. 3725-3725
IDENTIFICATION OF THE GENE CAUSING 1Q-LINKED JUVENILE-ONSET OPEN-ANGLE GLAUCOMA (GLC1A) AND EVIDENCE FOR ITS INVOLVEMENT IN ADULT PRIMARY OPEN-ANGLE GLAUCOMA
Authors: FINGERT JH ALWARD WLM SUNDEN SLF NISHIMURA D NYSTUEN A NICHOLS BE MACKEY DA RITCH R KALENAK JW CRAVEN ER BECK GE STREB LM SHEFFIELD VC STONE EM
Citation: Jh. Fingert et al., IDENTIFICATION OF THE GENE CAUSING 1Q-LINKED JUVENILE-ONSET OPEN-ANGLE GLAUCOMA (GLC1A) AND EVIDENCE FOR ITS INVOLVEMENT IN ADULT PRIMARY OPEN-ANGLE GLAUCOMA, Investigative ophthalmology & visual science, 38(4), 1997, pp. 4333-4333
THE PHENOTYPE OF PRIMARY OPEN-ANGLE GLAUCOMA PATIENT WITH MUTATIONS IN THE GLC1A GENE
Authors: ALWARD WLM FINGERT JH JOHNSON AT KWON YH HAYREH SS LOVE TM VANDENBURGH K SHEFFIELD VC STONE EM
Citation: Wlm. Alward et al., THE PHENOTYPE OF PRIMARY OPEN-ANGLE GLAUCOMA PATIENT WITH MUTATIONS IN THE GLC1A GENE, Investigative ophthalmology & visual science, 38(4), 1997, pp. 4335-4335
3-YEAR FOLLOW-UP OF MITOMYCIN VS PLACEBO IN COMBINED PHACOEMULSIFICATION AND TRABECULECTOMY
Authors: BIAS MF BARAD JP CARLSON DW ALWARD WLM
Citation: Mf. Bias et al., 3-YEAR FOLLOW-UP OF MITOMYCIN VS PLACEBO IN COMBINED PHACOEMULSIFICATION AND TRABECULECTOMY, Investigative ophthalmology & visual science, 38(4), 1997, pp. 1225-1225
IDENTIFICATION OF A GENE THAT CAUSES PRIMARY OPEN-ANGLE GLAUCOMA
Authors: STONE EM FINGERT JH ALWARD WLM NGUYEN TD POLANSKY JR SUNDEN SLF NISHIMURA D CLARK AF NYSTUEN A NICHOLS BE MACKEY DA RITCH R KALENAK JW CRAVEN ER SHEFFIELD VC
Citation: Em. Stone et al., IDENTIFICATION OF A GENE THAT CAUSES PRIMARY OPEN-ANGLE GLAUCOMA, Science, 275(5300), 1997, pp. 668-670
UNILATERAL PIGMENT DISPERSION AND GLAUCOMA CAUSED BY ANGLE-RECESSION
Authors: MCKINNEY JK ALWARD WLM
Citation: Jk. Mckinney et Wlm. Alward, UNILATERAL PIGMENT DISPERSION AND GLAUCOMA CAUSED BY ANGLE-RECESSION, Archives of ophthalmology, 115(11), 1997, pp. 1478-1479
CHARACTERIZATION OF THE GLAUCOMA PHENOTYPES ASSOCIATED WITH 2 MUTATIONS IN THE GLC1A GENE
Authors: FINGERT JH CLARK TD BECK G HOCKEY R ALWARD WLM SHEFFIELD VC STONE EM
Citation: Jh. Fingert et al., CHARACTERIZATION OF THE GLAUCOMA PHENOTYPES ASSOCIATED WITH 2 MUTATIONS IN THE GLC1A GENE, American journal of human genetics, 61(4), 1997, pp. 102-102
CHARACTERIZATION OF 6P25 CHROMOSOMAL-ANOMALIES IN 2 PATIENTS IDENTIFIES A POTENTIAL CANDIDATE GENE CAUSING CONGENITAL GLAUCOMA
Authors: NISHIMURA DY ALWARD WLM BECK G HOCKEY R PATIL S STONE EM SHEFFIELD VC
Citation: Dy. Nishimura et al., CHARACTERIZATION OF 6P25 CHROMOSOMAL-ANOMALIES IN 2 PATIENTS IDENTIFIES A POTENTIAL CANDIDATE GENE CAUSING CONGENITAL GLAUCOMA, American journal of human genetics, 61(4), 1997, pp. 103-103
CHARACTERIZATION OF THE PITX REIG HOMEOBOX-CONTAINING GENE FAMILY ANDITS INVOLVEMENT IN THE FORMATION OF ANTERIOR EYE STRUCTURES/
Authors: SEMINA EV REITER R ALWARD WLM BITOUN P FERRELL R DAACKHIRSCH S WISE M FUNKHAUSER CD NISHIMURA CJ LUDWIG B MURRAY JC
Citation: Ev. Semina et al., CHARACTERIZATION OF THE PITX REIG HOMEOBOX-CONTAINING GENE FAMILY ANDITS INVOLVEMENT IN THE FORMATION OF ANTERIOR EYE STRUCTURES/, American journal of human genetics, 61(4), 1997, pp. 2027-2027
CLONING AND CHARACTERIZATION OF A NOVEL BICOID-RELATED HOMEOBOX TRANSCRIPTION FACTOR GENE, RIEG, INVOLVED IN RIEGER SYNDROME
Authors: SEMINA EV REITER R LEYSENS NJ ALWARD WLM SMALL KW DATSON NA SIEGELBARTELT J BIERKENELSON D BITOUN P ZABEL BU CAREY JC MURRAY JC
Citation: Ev. Semina et al., CLONING AND CHARACTERIZATION OF A NOVEL BICOID-RELATED HOMEOBOX TRANSCRIPTION FACTOR GENE, RIEG, INVOLVED IN RIEGER SYNDROME, Nature genetics, 14(4), 1996, pp. 392-399
MOLECULAR-GENETICS OF GLAUCOMA - CURRENT STATUS
Authors: ALWARD WLM JOHNSON AT NISHIMURA DY SHEFFIELD VC STONE EM
Citation: Wlm. Alward et al., MOLECULAR-GENETICS OF GLAUCOMA - CURRENT STATUS, Journal of glaucoma, 5(4), 1996, pp. 276-284
FINE MAPPING OF THE AUTOSOMAL-DOMINANT JUVENILE OPEN-ANGLE GLAUCOMA (GLCLA) REGION AND EVALUATION OF CANDIDATE GENES
Authors: SUNDEN SLF ALWARD WLM NICHOLS BE ROKHLINA TR NYSTUEN A STONE EM SHEFFIELD VC
Citation: Slf. Sunden et al., FINE MAPPING OF THE AUTOSOMAL-DOMINANT JUVENILE OPEN-ANGLE GLAUCOMA (GLCLA) REGION AND EVALUATION OF CANDIDATE GENES, PCR methods and applications, 6(9), 1996, pp. 862-869
HIGH-DENSITY MAPPING OF THE JUVENILE OPEN-ANGLE GLAUCOMA REGION
Authors: SHEFFIELD VC SUNDEN SLF ALWARD WLM ROHKLINA RT NICHOLS BE STONE EM
Citation: Vc. Sheffield et al., HIGH-DENSITY MAPPING OF THE JUVENILE OPEN-ANGLE GLAUCOMA REGION, Investigative ophthalmology & visual science, 37(3), 1996, pp. 2078-2078
5-YEAR FOLLOW-UP OF THE FLUOROURACIL FILTERING SURGERY STUDY
Authors: ALWARD WLM FARRELL T HAYREH S KOLDER H CARNEY B PHELPS C GRESSEL M COSTIN J CRAVEN P ZGRABIK M SCHREMP P SIMASHKEVICH B HEUER DK BAERVELDT G MINCKLER D IRVINE J GREEN R MCDONNELL P SADUN A WALONKER F PADILLA M MARTONE J LLOYD MA LIGGETT P LEAN J OBER RR GRIFFAY E MILLERSCHOLTE A KASS M KOLKER A FARBER M GANS L SMITH M JONES A KLENKE S OWENSBY A PARRISH RK HODAPP E PALMBERG PF ANDERSON DR DELCALVO M MULE M CARTER A FAJARDO A ROSARIO Y SHERWOOD M STERN G DRIEBE W GUY J SMITH MF DOYLE W SHAMIS D ENGEL H ADI M FANOUS M MAMES R CRAWFORD P BENEKE J WILENSKY J TESSLER H FROHLICHSTEIN D BARNES R HIGGINBOTHAM E LIU S SHAHBAZI M SCHOLES G MOWERY RL SURAN A GOLDBERG I DUDLEY P SCHIFFMAN J FEURER W GUAL L ANDERSON P SCHWELM R GILLINGS D FURBERG C DUEKER D GREEN SB LATIES AM PERES KE TAYLOR RF HART WM LESKE C
Citation: Wlm. Alward et al., 5-YEAR FOLLOW-UP OF THE FLUOROURACIL FILTERING SURGERY STUDY, American journal of ophthalmology, 121(4), 1996, pp. 349-366
LINKAGE OF AUTOSOMAL-DOMINANT IRIS HYPOPLASIA TO THE REGION OF THE RIEGER SYNDROME LOCUS (4Q25)
Authors: HEON E SHETH BP KALENAK JW SUNDEN SLF STREB LM TAYLOR CM ALWARD WLM SHEFFIELD VC STONE EM
Citation: E. Heon et al., LINKAGE OF AUTOSOMAL-DOMINANT IRIS HYPOPLASIA TO THE REGION OF THE RIEGER SYNDROME LOCUS (4Q25), Human molecular genetics, 4(8), 1995, pp. 1435-1439
LINKAGE OF POSTERIOR POLYMORPHOUS CORNEAL-DYSTROPHY TO 20Q11
Authors: HEON E MATHERS WD ALWARD WLM WEISENTHAL RW SUNDEN SLF FISHBAUGH JA TAYLOR CM KRACHMER JH SHEFFIELD VC STONE EM
Citation: E. Heon et al., LINKAGE OF POSTERIOR POLYMORPHOUS CORNEAL-DYSTROPHY TO 20Q11, Human molecular genetics, 4(3), 1995, pp. 485-488
CIRCULAR PERIODIC IRIS FURROWS SEEN BY TRANSILLUMINATION IN PATIENTS WITH UNILATERAL PSEUDOEXFOLIATION
Authors: MAWN LA ALWARD WLM VERDICK R
Citation: La. Mawn et al., CIRCULAR PERIODIC IRIS FURROWS SEEN BY TRANSILLUMINATION IN PATIENTS WITH UNILATERAL PSEUDOEXFOLIATION, Investigative ophthalmology & visual science, 36(4), 1995, pp. 460-460
FINE MAPPING OF THE CHROMOSOMAL BREAKPOINTS IN AN INDIVIDUAL WITH CONGENITAL GLAUCOMA AND A 6-13 TRANSLOCATION
Authors: NISHIMURA DYS PATIL S ALWARD WLM STONE EM SHEFFIELD VC
Citation: Dys. Nishimura et al., FINE MAPPING OF THE CHROMOSOMAL BREAKPOINTS IN AN INDIVIDUAL WITH CONGENITAL GLAUCOMA AND A 6-13 TRANSLOCATION, Investigative ophthalmology & visual science, 36(4), 1995, pp. 554-554
Risultati: 1-25 | 26-48