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Journal Abstract Search

226 related items for PubMed ID: 8952799

  • 21.
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  • 22.
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  • 23. Who's in CHARGE? Multidisciplinary management of patients with CHARGE association.
    Blake KD, Russell-Eggitt IM, Morgan DW, Ratcliffe JM, Wyse RK.
    Arch Dis Child; 1990 Feb; 65(2):217-23. PubMed ID: 2317068
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  • 24.
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  • 26. The spectrum of clinical features in CHARGE syndrome.
    Davenport SL, Hefner MA, Mitchell JA.
    Clin Genet; 1986 Apr; 29(4):298-310. PubMed ID: 2424647
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  • 29. CHARGE syndrome: report of 47 cases and review.
    Tellier AL, Cormier-Daire V, Abadie V, Amiel J, Sigaudy S, Bonnet D, de Lonlay-Debeney P, Morrisseau-Durand MP, Hubert P, Michel JL, Jan D, Dollfus H, Baumann C, Labrune P, Lacombe D, Philip N, LeMerrer M, Briard ML, Munnich A, Lyonnet S.
    Am J Med Genet; 1998 Apr 13; 76(5):402-9. PubMed ID: 9556299
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  • 30. Exclusion of PITX2 mutations as a major cause of CHARGE association.
    Martin DM, Probst FJ, Fox SE, Schimmenti LA, Semina EV, Hefner MA, Belmont JW, Camper SA.
    Am J Med Genet; 2002 Jul 22; 111(1):27-30. PubMed ID: 12124729
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  • 31. [CHARGE association: 4 case reports].
    Siala Gaigi S, Masmoudi A, Souissi MH, Chabchoub A, Chelli H, Khrouf N.
    Tunis Med; 1999 May 22; 77(5):297-302. PubMed ID: 10516817
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  • 32. Epidemiology of choanal atresia with special reference to the CHARGE association.
    Harris J, Robert E, Källén B.
    Pediatrics; 1997 Mar 22; 99(3):363-7. PubMed ID: 9041289
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  • 33. Phenotypic spectrum of CHARGE syndrome with CHD7 mutations.
    Aramaki M, Udaka T, Kosaki R, Makita Y, Okamoto N, Yoshihashi H, Oki H, Nanao K, Moriyama N, Oku S, Hasegawa T, Takahashi T, Fukushima Y, Kawame H, Kosaki K.
    J Pediatr; 2006 Mar 22; 148(3):410-4. PubMed ID: 16615981
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  • 34. Choanal atresia and associated anomalies.
    Leclerc JE, Fearon B.
    Int J Pediatr Otorhinolaryngol; 1987 Oct 22; 13(3):265-72. PubMed ID: 3679682
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  • 35. Magnesium deficiency as a cause of hypocalcemia in the CHARGE association.
    Shah BR, Santucci K, Finberg L.
    Arch Pediatr Adolesc Med; 1994 May 22; 148(5):486-9. PubMed ID: 8180639
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  • 36. CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene.
    Jongmans MC, Admiraal RJ, van der Donk KP, Vissers LE, Baas AF, Kapusta L, van Hagen JM, Donnai D, de Ravel TJ, Veltman JA, Geurts van Kessel A, De Vries BB, Brunner HG, Hoefsloot LH, van Ravenswaaij CM.
    J Med Genet; 2006 Apr 22; 43(4):306-14. PubMed ID: 16155193
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  • 37. Vestibular anomalies in CHARGE syndrome: investigations on and consequences for postural development.
    Abadie V, Wiener-Vacher S, Morisseau-Durand MP, Porée C, Amiel J, Amanou L, Peigné C, Lyonnet S, Manac'h Y.
    Eur J Pediatr; 2000 Aug 22; 159(8):569-74. PubMed ID: 10968232
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  • 38. Clinical characteristics of CHARGE syndrome.
    Ahn BS, Oh SY.
    Korean J Ophthalmol; 1998 Dec 22; 12(2):130-4. PubMed ID: 10188375
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  • 39. Choroidal neovascular membrane associated with optic nerve coloboma in a patient with CHARGE association.
    Guirgis MF, Lueder GT.
    Am J Ophthalmol; 2003 Jun 22; 135(6):919-20. PubMed ID: 12788148
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