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Journal Abstract Search

205 related items for PubMed ID: 9395819

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  • 7. Severe phenotype in two half-sibs with Adams Oliver syndrome.
    Sevilla-Montoya R, Ríos-Flores B, Moreno-Verduzco E, Domínguez-Castro M, Rivera-Pedroza CI, Aguinaga-Ríos DM.
    Arch Argent Pediatr; 2014 Jun; 112(3):e108-12. PubMed ID: 24862819
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  • 8. Familial aplasia cutis congenita and coarctation of the aorta.
    Dallapiccola B, Giannotti A, Marino B, Digilio C, Obregon G.
    Am J Med Genet; 1992 Jul 01; 43(4):762-3. PubMed ID: 1621771
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  • 9. Adams-Oliver Syndrome Type 2 in Association with Compound Heterozygous DOCK6 Mutations.
    Jones KM, Silfvast-Kaiser A, Leake DR, Diaz LZ, Levy ML.
    Pediatr Dermatol; 2017 Sep 01; 34(5):e249-e253. PubMed ID: 28884918
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  • 10. Adams-Oliver syndrome associated with refractory glaucoma.
    Pillai MR, Pabolu C, R R, Chaudhary S, Sr K, Puthuran GV.
    J AAPOS; 2024 Aug 01; 28(4):103950. PubMed ID: 38866321
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  • 12. Nevocellular nevus associated with alopecia presenting as aplasia cutis congenita.
    Mastruserio DN, Cobb MA, Ross VE.
    Int J Dermatol; 1998 Jan 01; 37(1):37-9. PubMed ID: 9522236
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  • 13. Erosive pustular dermatosis of the scalp after aplasia cutis congenita in a 9-year-old patient: A 5-year follow-up.
    Fertig R, Maddy A, Cadore de Farias D, Simão Corrêa Filho S, Rigatti M, Tosti A.
    Pediatr Dermatol; 2017 Nov 01; 34(6):695-696. PubMed ID: 28925015
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  • 14. A novel DLL4 mutation in Adams-Oliver syndrome with absence of the right pulmonary artery in newborn.
    Rojnueangnit K, Phawan T, Khetkham T, Techasatid W, Sirichongkolthong B.
    Am J Med Genet A; 2022 Feb 01; 188(2):658-664. PubMed ID: 34755929
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  • 15. Adams-Oliver syndrome: a case report.
    Frantz JA, Lehmkuhl RL, Leitis LH, Uliano VG, Siementcoski GA.
    Pediatr Dermatol; 2015 Feb 01; 32(3):383-5. PubMed ID: 25556654
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  • 17. Elucidating the genetic architecture of Adams-Oliver syndrome in a large European cohort.
    Meester JAN, Sukalo M, Schröder KC, Schanze D, Baynam G, Borck G, Bramswig NC, Duman D, Gilbert-Dussardier B, Holder-Espinasse M, Itin P, Johnson DS, Joss S, Koillinen H, McKenzie F, Morton J, Nelle H, Reardon W, Roll C, Salih MA, Savarirayan R, Scurr I, Splitt M, Thompson E, Titheradge H, Travers CP, Van Maldergem L, Whiteford M, Wieczorek D, Vandeweyer G, Trembath R, Van Laer L, Loeys BL, Zenker M, Southgate L, Wuyts W.
    Hum Mutat; 2018 Sep 01; 39(9):1246-1261. PubMed ID: 29924900
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  • 18. Adams-Oliver syndrome caused by mutations of the EOGT gene.
    Schröder KC, Duman D, Tekin M, Schanze D, Sukalo M, Meester J, Wuyts W, Zenker M.
    Am J Med Genet A; 2019 Nov 01; 179(11):2246-2251. PubMed ID: 31368252
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  • 19. Epileptic Encephalopathy in Adams-Oliver Syndrome Associated to a New DOCK6 Mutation: A Peculiar Behavioral Phenotype.
    Pisciotta L, Capra V, Accogli A, Giacomini T, Prato G, Tavares P, Pinto-Basto J, Morana G, Mancardi MM.
    Neuropediatrics; 2018 Jun 01; 49(3):217-221. PubMed ID: 29631299
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  • 20. Aplasia cutis congenita--a case study of a family with two siblings with this disorder.
    Anderson SM.
    S D Med; 2013 Feb 01; 66(2):48-50. PubMed ID: 23513358
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