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kw.\*:("AXENFELD SYNDROME")

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WYNIKI LECZENIA OPERACYJNEGO JASKRY W PRZYPADKU EMBRYOTOXON POSTERIOR. = RESULTATS DU TRAITEMENT CHIRURGICAL DU GLAUCOME DANS UN CAS AVEC EMBRYOTOXONE POSTERIEURKWIATKOWSKA K.1978; KLIN. OCZNA; POL; DA. 1978; VOL. 48; NO 9; PP. 473-474; ABS. RUS/ENG; BIBL. 6 REF.Article

THE AXENFELD SYNDROME AND THE RIEGER SYNDROME.FITCH N; KABACK M.1978; J. MED. GENET.; G.B.; DA. 1978; VOL. 15; NO 1; PP. 30-34; BIBL. 1 P.Article

ANIRIDIE FAMILIALE ET EMBRYOTOXON POSTERIEURMALBREL C; ALAME M; TALMUD M et al.1980; BULL. SOC. OPHTHALMOL. FR.; ISSN 0081-1270; FRA; DA. 1980; VOL. 80; NO 11; PP. 1109-1111; ABS. ENG; BIBL. 5 REF.Article

CONGENITAL ABSENCE OF LATERAL RECTUS MUSCLESANDALL GS; MORRISON JW.1979; J. PEDIATR. OPHTHALMOL. STRABISM.; USA; DA. 1979; VOL. 16; NO 1; PP. 35-39; BIBL. 23 REF.Article

ADENOME DU CORPS CILIAIRE CHEZ L'ENFANT (A PROPOS D'UN CAS)BOUDET C; MAISONGROSSE G; NAVARRE L et al.1979; BULL. SOC. OPHTALMOL. FR.; ISSN 0081-1270; FRA; DA. 1979 PUBL. 1980; VOL. 79; NO 11-12; PP. 969-972; ABS. ENG; BIBL. 10 REF.Article

JASKRA SKOJARZONA Z INNYMI WADAMI ROZWOJOWYMI OCZU W ZESPOLE STURGE'A-WEBERA = GLAUCOME ASSOCIE A D'AUTRES ANOMALIES OPHTALMOLOGIQUES DE DEVELOPPEMENT DANS LE SYNDROME DE STURGE-WEBERWIERZCHOWSKI A.1978; KLIN. OCZNA; POL; DA. 1978; VOL. 48; NO 9; PP. 475-477; ABS. RUS/ENG; BIBL. 17 REF.Article

GLAUCOME CONGENITAL-SYNDROME D'AXENFELD-COMMUNICATION INTERAURICULAIRESEKKAT A; BEC P; ARNE JL et al.1980; BULL. SOC. OPHTALMOL. FR.; FRA; DA. 1980; VOL. 80; NO 6-7; PP. 565-567; BIBL. 8 REF.Article

MANIFESTATIONS OCULAIRES ACCOMPAGNANT LES HYPOPLASIES DUCTULAIRES CONGENITALES BILIAIRESLEBUISSON DA; HERBET FRILEUX F; ARON JJ et al.1981; BULL. SOC. OPHTALMOL. FR.; ISSN 0081-1270; FRA; DA. 1981; VOL. 81; NO 2; PP. 169-170; BIBL. 2 REF.Article

UBER AUGENVERAENDERUNGEN BEI DER PIGMENTFLECKENKRANKHEIT. (PEUTZ-JEGHERS) = ALTERATIONS OCULAIRES DANS LE SYNDROME DES TACHES PIGMENTEES (PEUTZ-JEGHERS)RIEGER H; DIBOLD H.1978; KLIN. MONATSBL. AUGENHEILKDE; DEU; DA. 1978; VOL. 173; NO 6; PP. 854-857; ABS. ENG; BIBL. 12 REF.Article

OCULOCUTANEOUS ALBINISM ASSOCIATED WITH CORNEAL MESODERMAL DYSGENESISLUBIN JR.1981; AM. J. OPHTHALMOL.; ISSN 0002-9394; USA; DA. 1981; VOL. 91; NO 3; PP. 347-350; BIBL. 16 REF.Article

ARTERIOHEPATIC DYSPLASIA: A BENIGN SYNDROME OF INTRAHEPATIC CHOLESTASIS WITH MULTIPLE ORGAN INVOLVEMENTRIELY CA; COTLIER E; JENSEN PS et al.1979; ANN. INTERN. MED.; USA; DA. 1979; VOL. 91; NO 4; PP. 520-527; BIBL. 41 REF.Article

OCULAR FINDINGS IN ARTERIOHEPATIC DYSPLASIA (ALAGILLE'S SYNDROME)ROMANCHUK KG; JUDISCH GF; LABRECQUE DR et al.1981; CAN. J. OPHTHALMOL.; ISSN 0008-4182; CAN; DA. 1981; VOL. 16; NO 2; PP. 94-99; BIBL. 8 REF.Article

A family with Axenfeld-Rieger syndrome and Peters anomaly caused by a point mutation (Phe112Ser) in the FOXC1 geneHONKANEN, Robert A; NISHIMURA, Darryl Y; SWIDERSKI, Ruth E et al.American journal of ophthalmology. 2003, Vol 135, Num 3, pp 368-375, issn 0002-9394, 8 p.Article

Axenfeld-Rieger syndrome in the age of molecular geneticsALWARD, Wallace L. M.American journal of ophthalmology. 2000, Vol 130, Num 1, pp 107-115, issn 0002-9394Article

PRIMARY EMPTY SELLA AND RIEGER'S ANOMALY OF THE ANTERIOR CHAMBER OF THE EYE: A FAMILIAL SYNDROMEKLEINMANN RE; KAZARIAN EL; RAPTOPOULOS V et al.1981; N. ENGL. J. MED.; ISSN 0028-4793; USA; DA. 1981; VOL. 304; NO 2; PP. 90-93; BIBL. 25 REF.Article

Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesisBERRY, Fred B; LINES, Matthew A; OAS, J. Martin et al.Human molecular genetics (Print). 2006, Vol 15, Num 6, pp 905-919, issn 0964-6906, 15 p.Article

Axenfeld's anomaly and related disordersTHURSCHWELL, L. M; MICHELSON, M. A.Journal of the American Optometric Association. 1986, Vol 57, Num 5, pp 360-365, issn 0003-0244Article

Embryotoxon postérieur dans l'ichtyose = Posterior embryotoxon and ichtyosisRODRIGUEZ CABALLERO, M. L; PEREZ, P. U.Journal français d'ophtalmologie. 1983, Vol 6, Num 10, pp 793-795, issn 0181-5512Article

Case of chromosome 6p25 terminal deletion associated with axenfeld-rieger syndrome and persistent hyperplastic primary vitreousSUZUKI, Katsuhiro; NAKAMURA, Makoto; AMANO, Emi et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 5, pp 503-508, issn 1552-4825, 6 p.Article

Reduced human and murine corneal thickness in an axenfeld-rieger syndrome subtypeASAI-COAKWELL, Mika; BACKBOUSE, Christopher; CASEY, Ronald J et al.Investigative ophthalmology & visual science. 2006, Vol 47, Num 11, pp 4905-4909, issn 0146-0404, 5 p.Article

An unusual class of PITX2 mutations in axenfeld-rieger syndromeSAADI, Irfan; TORO, Rafael; KUBURAS, Adisa et al.Birth defects research. Clinical and molecular teratology. 2006, Vol 76, Num 3, pp 175-181, issn 1542-0752, 7 p.Article

Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinctWALTER, M. A; MIRZAYANS, F; MEARS, A. J et al.Ophthalmology (Rochester, MN). 1996, Vol 103, Num 11, pp 1907-1915, issn 0161-6420Article

Fibrotic eye muscles, Axenfeld anomaly, flat face, and mild developmental retardation : A new example of the Chitty syndromeVAN DAELE, S. G; VAN COSTER, R. N; MEIRE, F et al.American journal of medical genetics. 1996, Vol 65, Num 3, pp 205-208, issn 0148-7299Article

Axenfeld-Rieger syndrome. A spectrum of developmental disordersSHIELDS, M. B; BUCKLEY, E; KLINTWORTH, G. K et al.Survey of ophthalmology. 1985, Vol 29, Num 6, pp 387-409, issn 0039-6257Article

Anterior segment anomalies associated with the fetal alcohol syndromeMILLER, M. T; EPSTEIN, R. J; SUGAR, J et al.Journal of pediatric ophthalmology and strabismus. 1984, Vol 21, Num 1, pp 8-18, issn 0191-3913Article

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