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    Results: 1 to 20 of 223

    1.

    ARIX gene polymorphisms in patients with congenital superior oblique muscle palsy.

    Jiang Y, Matsuo T, Fujiwara H, Hasebe S, Ohtsuki H, Yasuda T.

    Br J Ophthalmol. 2004 Feb;88(2):263-7.PMID: 14736788 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    ARIX and PHOX2B polymorphisms in patients with congenital superior oblique muscle palsy.

    Jiang Y, Matsuo T, Fujiwara H, Hasebe S, Ohtsuki H, Yasuda T.

    Acta Med Okayama. 2005 Apr;59(2):55-62.PMID: 16049556 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Clinical features, ARIX and PHOX2B nucleotide changes in three families with congenital superior oblique muscle palsy.

    Imai S, Matsuo T, Itoshima E, Ohtsuki H.

    Acta Med Okayama. 2008 Feb;62(1):45-53.PMID: 18323871 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Autosomal-dominant inheritance of congenital superior oblique palsy.

    Botelho PJ, Giangiacomo JG.

    Ophthalmology. 1996 Sep;103(9):1508-11.PMID: 8841314 [PubMed - indexed for MEDLINE]Related articles

    5.

    Sequence analysis of thyroid transcription factor-1 gene reveals absence of mutations in patients with thyroid dysgenesis but presence of polymorphisms in the 5' flanking region and intron.

    Hishinuma A, Kuribayashi T, Kanno Y, Onigata K, Nagashima K, Ieiri T.

    Endocr J. 1998 Aug;45(4):563-7.PMID: 9881907 [PubMed - indexed for MEDLINE]Related articles

    6.

    A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2).

    Yazdani A, Chung DC, Abbaszadegan MR, Al-Khayer K, Chan WM, Yazdani M, Ghodsi K, Engle EC, Traboulsi EI.

    Am J Ophthalmol. 2003 Nov;136(5):861-5.PMID: 14597037 [PubMed - indexed for MEDLINE]Related articles

    7.

    Comparison of muscle volume between congenital and acquired superior oblique palsies by magnetic resonance imaging.

    Sato M, Yagasaki T, Kora T, Awaya S.

    Jpn J Ophthalmol. 1998 Nov-Dec;42(6):466-70.PMID: 9886737 [PubMed - indexed for MEDLINE]Related articles

    8.

    Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity.

    Hutcheson KA, Paluru PC, Bernstein SL, Koh J, Rappaport EF, Leach RA, Young TL.

    Mol Vis. 2005 Jul 14;11:501-8.PMID: 16052165 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    [Clinical features and surgical treatment of congenital ocular muscle palsy characterized with double elevator dysfunction]

    Xiao MY, Shou JY, Li YP.

    Zhonghua Yan Ke Za Zhi. 2004 Oct;40(10):652-4. Chinese. PMID: 16200853 [PubMed - indexed for MEDLINE]Related articles

    10.

    Magnetic resonance imaging and tendon anomaly associated with congenital superior oblique palsy.

    Sato M.

    Am J Ophthalmol. 1999 Apr;127(4):379-87.PMID: 10218689 [PubMed - indexed for MEDLINE]Related articles

    11.

    Autosomal dominant congenital superior oblique palsy.

    Bhola RM, Horne GV, Squirrell DM, Chan TK, Kumar D.

    Eye (Lond). 2001 Aug;15(Pt 4):479-84.PMID: 11767023 [PubMed - indexed for MEDLINE]Related articles

    12.

    Tendon laxity in superior oblique palsy.

    Plager DA.

    Ophthalmology. 1992 Jul;99(7):1032-8.PMID: 1495780 [PubMed - indexed for MEDLINE]Related articles

    13.

    A novel PAX6 gene mutation in a Chinese family with aniridia.

    Song S, Liu Y, Guo S, Zhang L, Zhang X, Wang S, Lu A, Li L.

    Mol Vis. 2005 May 6;11:335-7.PMID: 15889018 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Clinical features of congenital absence of the superior oblique muscle as demonstrated by orbital imaging.

    Chan TK, Demer JL.

    J AAPOS. 1999 Jun;3(3):143-50.PMID: 10428587 [PubMed - indexed for MEDLINE]Related articles

    15.

    Congenital abnormalities of cranial nerve development: overview, molecular mechanisms, and further evidence of heterogeneity and complexity of syndromes with congenital limitation of eye movements.

    Traboulsi EI.

    Trans Am Ophthalmol Soc. 2004;102:373-89.PMID: 15747768 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Two distinct compound heterozygous constellations (R277X/IVS34-1G>C and R277X/R1511X) in the thyroglobulin (TG) gene in affected individuals of a Brazilian kindred with congenital goiter and defective TG synthesis.

    Gutnisky VJ, Moya CM, Rivolta CM, Domené S, Varela V, Toniolo JV, Medeiros-Neto G, Targovnik HM.

    J Clin Endocrinol Metab. 2004 Feb;89(2):646-57.PMID: 14764776 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    A new classification of superior oblique palsy based on congenital variations in the tendon.

    Helveston EM, Krach D, Plager DA, Ellis FD.

    Ophthalmology. 1992 Oct;99(10):1609-15.PMID: 1454330 [PubMed - indexed for MEDLINE]Related articles

    18.

    Isolated superior oblique tucking: an effective procedure for superior oblique palsy with profound superior oblique underaction.

    Bhola R, Velez FG, Rosenbaum AL.

    J AAPOS. 2005 Jun;9(3):243-9.PMID: 15956944 [PubMed - indexed for MEDLINE]Related articles

    19.

    Superior oblique muscle MRI asymmetry and vertical deviation in patients with unilateral superior oblique palsy.

    Shokida F, Eleta M, Gabriel J, Sanchez C, Seclen F.

    Binocul Vis Strabismus Q. 2006;21(3):137-46.PMID: 16934025 [PubMed - indexed for MEDLINE]Related articles

    20.

    [Measurement of incomitance patterns of vertical deviation in superior oblique palsy with a synoptometer]

    Ohtsuki H, Konishi H, Hasebe S, Tadokoro Y, Watanabe S, Okano M.

    Nippon Ganka Gakkai Zasshi. 1990 Sep;94(9):833-8. Japanese. PMID: 2248169 [PubMed - indexed for MEDLINE]Related articles

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