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Results 1 to 25 of 76

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A KINDRED SHOWING HYPOCALCIFIED AMELOGENESIS IMPERFECTA: REPORT OF CASE = FAMILLE PRESENTANT UNE AMELOGENESE IMPARFAITE HYPOCALCIFIEE. PRESENTATION D'UN CASGIANSANTI JS.1973; J. AMER. DENT. ASS.; U.S.A.; DA. 1973; VOL. 86; NO 3; PP. 675-678; BIBL. 13REF.Serial Issue

AMELOGENESIS IMPERFECTA. REPORT OF TWO CASES = AMELOGENESE IMPARFAITE. PRESENTATION DE DEUX CASDRUCK JS.1975; ORAL SURG. ORAL MED. ORAL PATHOL.; U.S.A.; DA. 1975; VOL. 39; NO 3; PP. 502-505; BIBL. 2 REF.Article

AMELOGENESIS IMPERFECTA. REPORT OF TWO CASES = AMELOGENESE IMPARFAITE. PRESENTATION DE DEUX CASDRUCK JS.1975; ORAL SURG. ORAL MED. ORAL PATHOL.; U.S.A.; DA. 1975; VOL. 39; NO 3; PP. 502-505; BIBL. 2 REF.Article

MINERALISATION DEFECTS OF THE PRIMARY TEETH IN INTRA-UTERINE UNDERNUTRITION. I.RESULTS OF A CLINICAL INVESTIGATION = DEFAUTS DE MINERALISATION DES DENTS DE LAIT DANS LA SOUS-NUTRITION INTRAUTERINE. I.RESULTATS D'UNE ENQUETE CLINIQUEGRAHNEN H; HOLM AK; MAGNUSSON B et al.1972; CARIES RES.; SWITZ.; DA. 1972; VOL. 6; NO 3; PP. 224-228; BIBL. 12REF.Serial Issue

X-LINKED RECESSIVE HYPOMATURATION AMELOGENESIS IMPERFECTA: REPORT OF CASEHAUG RH; FERGUSON FS.1981; J. AM. DENT. ASSOC.; ISSN 0002-8177; USA; DA. 1981; VOL. 102; NO 6; PP. 865-867; BIBL. 7 REF.Article

THE SURFACE OF GENETICALLY DETERMINED HYPOPLASTIC ENAMEL IN HUMAN TEETH = LA SURFACE DE L'EMAIL DES DENTS HUMAINES ATTEINT D'HYPOPLASIE GENETIQUEMENT DETERMINEESAUK JJ JR; VICKERS RA; COPELAND JS et al.1972; ORAL SURG. ORAL MED. ORAL PATHOL.; U.S.A.; DA. 1972; VOL. 34; NO 1; PP. 60-68; BIBL. 19REF.Serial Issue

AN ESTHETIC TRANSITIONAL TREATMENT FOR AMELOGENESIS IMPERFECTA: REPORT OF TWO CASES.LIGHT EI; RAKOW B; FRAZE RL et al.1975; J. AMER. DENT. ASS.; U.S.A.; DA. 1975; VOL. 90; NO 1; PP. 166-170; BIBL. 15 REF.Article

Variable expression in Amelogenesis imperfecta with taurodontismALRED, M. J; CRAWFORD, P. J. M.Journal of oral pathology. 1988, Vol 17, Num 5, pp 327-333, issn 0300-9777Article

Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classificationWITKOP, C. J. JR.Journal of oral pathology. 1988, Vol 17, Num 9-10, pp 547-553, issn 0300-9777Article

THE TRICHO-DENTO-OSSEOUS (TDO) SYNDROME = LE SYNDROME TRICHO-ODONTO-OSSEUXLICHTENSTEIN J; WARSON R; JORGENSON R et al.1972; AMER. J. HUM. GENET.; U.S.A.; DA. 1972; VOL. 24; NO 5; PP. 569-582; BIBL. 1P.1/2Serial Issue

AMELOGENESIS IMPERFECTA AMONG ISRAELI JEWS AND THE DESCRIPTION OF A NEW TYPE OF LOCAL HYPOPLASTIC AUTOSOMAL RECESSIVE AMELOGENESIS IMPERFECTACHOSACK A; EIDELMAN E; WISOTSKI I et al.1979; ORAL SURG. ORAL MED. ORAL PATHOL.; USA; DA. 1979; VOL. 47; NO 2; PP. 148-156; BIBL. 13 REF.Article

AMELOGENESIS IMPERFECTA WITH TAURODONTISMCONGLETON J; BURKES EJ JR.1979; ORAL SURG. ORAL MED. ORAL PATHOL.; USA; DA. 1979; VOL. 48; NO 6; PP. 540-544; BIBL. 16 REF.Article

Prise en charge précoce de l'amélogenèse imparfaite : Une prévention des complications à l'adolescence et à l'âge adulte = Early management of Amelogenesis Imperfecta : Prevention of complications in teenagers and young adultsBESLOT, Aurélie; VILLETTE, Francoise.RFOP Revue francophone d'odontologie pédiatrique. 2008, Vol 3, Num 3, pp 136-143, issn 1954-5010, 8 p.Article

Amelogenesis imperfecta: a genetic studyBACKMAN, B; HOLMGREN, G.Human heredity. 1988, Vol 38, Num 4, pp 189-206, issn 0001-5652Article

Amelogenesis imperfecta with taurodontism and the tricho-dento-osseous syndrome : separate conditions or a spectrum of disease ?CRAWFORD, P. J. M; ALDRED, M. J.Clinical genetics. 1990, Vol 38, Num 1, pp 44-50, issn 0009-9163, 7 p.Article

Autosomal recessive rough hypoplastic amelogenesis imperfecta: a case report with clinical, light microscopic, radiographic, and electron microscopic observationsOOYA, K; NALBANDIAN, J; NOIKURA, T et al.Oral surgery, oral medicine, oral pathology. 1988, Vol 65, Num 4, pp 449-458, issn 0030-4220Article

MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfectaKIM, J.-W; SIMMER, J. P; HART, T. C et al.Journal of medical genetics. 2005, Vol 42, Num 3, pp 271-275, issn 0022-2593, 5 p.Article

Open bite deformity in amelogenesis imperfecta. Part 2 : Le Fort I osteotomies and treatment resultsHOPPENREIJS, T. J. M; VOORSMIT, R. A. C. A; FREIHOFER, H. P. M et al.Journal of cranio-maxillo-facial surgery. 1998, Vol 26, Num 5, pp 286-293, issn 1010-5182Article

Molecular basis and consequences of a deletion in the amelogenin gene, analyzed by capture PCRLAGERSTRÖM-FERMER, M; PETTERSSON, U; LANDEGREN, U et al.Genomics (San Diego, Calif.). 1993, Vol 17, Num 1, pp 89-92, issn 0888-7543Article

Enamel ultrastructure in pigmented hypomaturation amelogenesis imperfectaTIMOTHY WRIGHT, J; LORD, V; ROBINSON, C et al.Journal of oral pathology & medicine. 1992, Vol 21, Num 9, pp 390-394, issn 0904-2512Article

A progressive cone-rod dystrophy and amelogenesis imperfecta: a new syndromeJALILI, I. K; SMITH, M. J. D.Journal of medical genetics. 1988, Vol 25, Num 11, pp 738-740, issn 0022-2593Article

Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia SyndromeO'SULLIVAN, James; BITU, Carolina C; COLETTA, Ricardo D et al.American journal of human genetics. 2011, Vol 88, Num 5, pp 616-620, issn 0002-9297, 5 p.Article

Enamelin (Enam) is essential for amelogenesis : ENU-induced mouse mutants as models for different clinical subtypes of human amelogenesis imperfecta (Al)MASUYA, Hiroshi; SHIMIZU, Kunihiko; KOBAYASHI, Kimio et al.Human molecular genetics (Print). 2005, Vol 14, Num 5, pp 575-583, issn 0964-6906, 9 p.Article

A spontaneous mutation: Amelogenesis imperfecta with cysts in ratsKATSUTA, Osamu; HOSHINO, Nobuhito; TAKEDA, Midori et al.Toxicologic pathology. 2003, Vol 31, Num 4, pp 411-416, issn 0192-6233, 6 p.Article

A new form of skeletal dysplasia with amelogenesis imperfecta and platyspondylyVERLOES, A; JAMBLIN, P; KOULISCHER, L et al.Clinical genetics. 1996, Vol 49, Num 1, pp 2-5, issn 0009-9163Article

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