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PUBMED FOR HANDHELDS

Journal Abstract Search


136 related items for PubMed ID: 7715155

  • 1. [Rieger's syndrome in a 12 year old girl].
    Ginter M, Krawczyński M.
    Klin Oczna; 1994; 96(10-11):347-50. PubMed ID: 7715155
    [Abstract] [Full Text] [Related]

  • 2. [Variability of clinical manifestations in the family with Axenfeld-Rieger syndrome].
    Kamińska A, Sokołowska-Oracz A, Pawluczyk-Dyjecińska M, Szaflik JP.
    Klin Oczna; 2007; 109(7-9):321-6. PubMed ID: 18260289
    [Abstract] [Full Text] [Related]

  • 3. [A case of Rieger's syndrome].
    Poirier A, Mascrès C.
    J Dent Que; 1981; 18():35-8. PubMed ID: 6793650
    [No Abstract] [Full Text] [Related]

  • 4. Rieger's syndrome.
    Pang GX, Mao WS.
    Chin Med J (Engl); 1984 Jan; 97(1):29-31. PubMed ID: 6428830
    [No Abstract] [Full Text] [Related]

  • 5. [Surgical treatment of glaucoma in Rieger's syndrome].
    Murzin AA.
    Vestn Oftalmol; 1979 Jan; (2):74-5. PubMed ID: 107646
    [No Abstract] [Full Text] [Related]

  • 6. Dental anomalies in Axenfeld-Rieger syndrome.
    O'Dwyer EM, Jones DC.
    Int J Paediatr Dent; 2005 Nov; 15(6):459-63. PubMed ID: 16238657
    [Abstract] [Full Text] [Related]

  • 7. [Congenital glaucoma with dominant heredity associated with ocular and somatic malformations (Rieger's syndrome)].
    Deimarcelle Y.
    Ann Ocul (Paris); 1968 Feb; 201(2):132-57. PubMed ID: 4970667
    [No Abstract] [Full Text] [Related]

  • 8. Rieger's syndrome.
    Kumta NB, Agarwal U, Savliwala AS.
    Indian Pediatr; 1982 Feb; 19(2):183-5. PubMed ID: 6811430
    [No Abstract] [Full Text] [Related]

  • 9. Bone and joint manifestations of Rieger's syndrome: a report of a family.
    Koshino T, Konno T, Ohzeki T.
    J Pediatr Orthop; 1989 Feb; 9(2):224-30. PubMed ID: 2494224
    [Abstract] [Full Text] [Related]

  • 10. PHACE: a neurocutaneous syndrome with important ophthalmologic implications: case report and literature review.
    Coats DK, Paysse EA, Levy ML.
    Ophthalmology; 1999 Sep; 106(9):1739-41. PubMed ID: 10485544
    [Abstract] [Full Text] [Related]

  • 11. [Diagnostic and therapeutic difficulties concerning glaucoma in Rieger's syndrome].
    Chwirot R, Remlein-Mozolewska G.
    Klin Oczna; 1971 Sep; 41(6):821-5. PubMed ID: 5159027
    [No Abstract] [Full Text] [Related]

  • 12. Rieger's syndrome.
    Feingold M, Shiere F, Fogels HR, Donaldson D.
    Pediatrics; 1969 Oct; 44(4):564-9. PubMed ID: 5346635
    [No Abstract] [Full Text] [Related]

  • 13. Rieger syndrome: a clinical, molecular, and biochemical analysis.
    Amendt BA, Semina EV, Alward WL.
    Cell Mol Life Sci; 2000 Oct; 57(11):1652-66. PubMed ID: 11092457
    [Abstract] [Full Text] [Related]

  • 14. [The Rieger syndrome. A clinical study. A study of 4 generations in one family with the Rieger syndrome].
    Rusu V.
    Oftalmologia; 1997 Oct; 41(3):234-7. PubMed ID: 9409970
    [Abstract] [Full Text] [Related]

  • 15. [Clinical observation on Rieger's syndrome (report of 4 cases) (author's transl)].
    Deng HJ.
    Zhonghua Yan Ke Za Zhi; 1981 Nov; 17(6):359-61. PubMed ID: 6806034
    [No Abstract] [Full Text] [Related]

  • 16. [The clinical characteristics of Rieger's syndrome].
    Sidorov EG, Perchikova OI, Polutornov AL, Baranovskiĭ EE.
    Vestn Oftalmol; 1990 Nov; 106(1):56-9. PubMed ID: 2378040
    [No Abstract] [Full Text] [Related]

  • 17. [Hypoplasia of the pulmonary artery in Rieger's Syndrome (author's transl)].
    Schmidt-Redemann B, Vogt J.
    Klin Padiatr; 1976 Nov; 188(6):554-7. PubMed ID: 826736
    [Abstract] [Full Text] [Related]

  • 18. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
    Vieira V, David G, Roche O, de la Houssaye G, Boutboul S, Arbogast L, Kobetz A, Orssaud C, Camand O, Schorderet DF, Munier F, Rossi A, Delezoide AL, Marsac C, Ricquier D, Dufier JL, Menasche M, Abitbol M.
    Mol Vis; 2006 Dec 01; 12():1448-60. PubMed ID: 17167399
    [Abstract] [Full Text] [Related]

  • 19. Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss: a provisionally unique genetic syndrome?
    Grosso S, Farnetani MA, Berardi R, Vivarelli R, Vanni M, Morgese G, Balestri P.
    Am J Med Genet; 2002 Aug 01; 111(2):182-6. PubMed ID: 12210347
    [Abstract] [Full Text] [Related]

  • 20. [Anterior cleavage syndrome associated with endocrine orbitopathy (author's transl)].
    Binder K, Müller-Jensen K.
    Klin Monbl Augenheilkd; 1981 Jun 01; 178(6):457-9. PubMed ID: 6973664
    [Abstract] [Full Text] [Related]


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