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Journal Abstract Search

168 related items for PubMed ID: 22631568

  • 1. Adams-Oliver syndrome and familial MYH9 mutation.
    Uyeda T, Echizenya T, Eto S, Ohtani K, Sato T, Takahashi T, Ito E, Yonesaka S, Kunishima S.
    Pediatr Int; 2012 Jun; 54(3):407-9. PubMed ID: 22631568
    [No Abstract] [Full Text] [Related]

  • 2. Adams-Oliver syndrome.
    Kutlubay Z, Pehlivan Ö.
    Int J Dermatol; 2014 Mar; 53(3):352-4. PubMed ID: 24320818
    [No Abstract] [Full Text] [Related]

  • 3. Adams-Oliver syndrome in a newborn infant.
    Zakanj Z, Bedek D, Kotrulja L, Ozanic Bulic S.
    Int J Dermatol; 2016 Feb; 55(2):215-7. PubMed ID: 24697559
    [No Abstract] [Full Text] [Related]

  • 4. Adams-Oliver syndrome: new evidence in variable expressivity?
    Girish M, Mujawar N, Anekar U, Bhattad S.
    Int J Dermatol; 2014 Jul; 53(7):891-3. PubMed ID: 24372423
    [No Abstract] [Full Text] [Related]

  • 5. 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; 34(5):e249-e253. PubMed ID: 28884918
    [Abstract] [Full Text] [Related]

  • 6. [Adams-Oliver syndrome].
    Bayou F, Boussofara L, Bennani ZL, Ghariani N, Saïdi W, Belajouza C, Denguezli M, Nouira R.
    Ann Dermatol Venereol; 2011 Oct; 138(10):712-4. PubMed ID: 21978514
    [No Abstract] [Full Text] [Related]

  • 7. A novel DLL4 missense mutation in a Chinese patient with Adams-Oliver syndrome.
    Yu X, Wang RR, Han SR, Bai X, Habulieti X, Sun Y, Sun LW, Zhang H, Khan A, Zhang X.
    Chin Med J (Engl); 2019 Jul 20; 132(14):1755-1757. PubMed ID: 31261205
    [No Abstract] [Full Text] [Related]

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  • 9. Adams-Oliver syndrome, a family with dominant inheritance and a severe phenotype.
    Vandersteen AM, Dixon JW.
    Clin Dysmorphol; 2011 Oct 20; 20(4):210-213. PubMed ID: 21785343
    [No Abstract] [Full Text] [Related]

  • 10. 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 20; 49(3):217-221. PubMed ID: 29631299
    [Abstract] [Full Text] [Related]

  • 11. 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 20; 188(2):658-664. PubMed ID: 34755929
    [Abstract] [Full Text] [Related]

  • 12. 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 20; 112(3):e108-12. PubMed ID: 24862819
    [Abstract] [Full Text] [Related]

  • 13. Isolated terminal limb reduction defects: extending the clinical spectrum of Adams-Oliver syndrome and ARHGAP31 mutations.
    Isrie M, Wuyts W, Van Esch H, Devriendt K.
    Am J Med Genet A; 2014 Jun 20; 164A(6):1576-9. PubMed ID: 24668619
    [Abstract] [Full Text] [Related]

  • 14. DOCK6 mutations are responsible for a distinct autosomal-recessive variant of Adams-Oliver syndrome associated with brain and eye anomalies.
    Sukalo M, Tilsen F, Kayserili H, Müller D, Tüysüz B, Ruddy DM, Wakeling E, Ørstavik KH, Snape KM, Trembath R, De Smedt M, van der Aa N, Skalej M, Mundlos S, Wuyts W, Southgate L, Zenker M.
    Hum Mutat; 2015 Jun 20; 36(6):593-8. PubMed ID: 25824905
    [Abstract] [Full Text] [Related]

  • 15. Two different management modalities in a two sibling case report of Adams Oliver syndrome.
    Al-Hadithy N, Mennie J, Stewart K.
    BMJ Case Rep; 2011 Dec 21; 2011():. PubMed ID: 22670005
    [Abstract] [Full Text] [Related]

  • 16. Adams-Oliver syndrome associated with refractory glaucoma.
    Pillai MR, Pabolu C, R R, Chaudhary S, Sr K, Puthuran GV.
    J AAPOS; 2024 Aug 21; 28(4):103950. PubMed ID: 38866321
    [Abstract] [Full Text] [Related]

  • 17. Adams-Oliver syndrome.
    Iftikhar N, Ahmad Ghumman FI, Janjua SA, Ejaz A, Butt UA.
    J Coll Physicians Surg Pak; 2014 May 21; 24 Suppl 2():S76-7. PubMed ID: 24906278
    [Abstract] [Full Text] [Related]

  • 18. Novel compound heterozygous mutations of the DOCK6 gene in a familial case of Adams-Oliver syndrome 2.
    Wang Z, Wang X, Guiyu Lou, Litao Qin, Shasha Bian, Tang X, Hongjie Zhu, Shengran Wang, Bingtao Hao, Shixiu Liao.
    Gene; 2019 Jun 05; 700():65-69. PubMed ID: 30898718
    [Abstract] [Full Text] [Related]

  • 19. Adams-Oliver Syndrome - Follow-up of a Large Scalp Defect.
    Lorenz L, Sönnichsen K, Müller-Hansen I, Poets C.
    Klin Padiatr; 2014 Jul 05; 226(4):250-1. PubMed ID: 24515817
    [No Abstract] [Full Text] [Related]

  • 20. Adams Oliver Syndrome.
    Madan A, Sardana K, Garg VK.
    Indian Pediatr; 2015 Jul 05; 52(7):633-4. PubMed ID: 26244971
    [No Abstract] [Full Text] [Related]

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