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540 Possible Causes for wilkie

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  • Dementia

    Ross Wilkie, Abdelouahid Tajar, John McBeth and Guillermo López-Lluch , The Onset of Widespread Musculoskeletal Pain Is Associated with a Decrease in Healthy Ageing in Older[doi.org]

  • Otitis Media

    ., & Wilkie, G. ( 1984 ). Otitis media with effusion during the first three years of life and development of speech and language. Pediatrics , 74 , 282–287.[jslhr.pubs.asha.org]

  • Superior Mesenteric Artery Syndrome

    Wilkie, David P.D., Scottish surgeon, 1882-1938. Wilkie artery - the right colic artery when it occasionally crosses the duodenum.[medical-dictionary.thefreedictionary.com] […] arising from the abdominal aorta with a smaller angle than the norm ( KEYWORDS: Superior mesenteric artery; Ultrasound; Wilkie’s syndrome[ncbi.nlm.nih.gov] Abstract Wilkie's syndrome is a rare variant of small intestinal obstruction resulting from compression of third part of the duodenum by the superior mesenteric artery.[wwww.unboundmedicine.com]

  • Congenital Radioulnar Synostosis

    Classification -Wilkie Type I: Lack of proximal portion of radius Bony fusion for 3-6 cm, Radius and ulna are connected at medullary canal Type II: Normal radius Synostosis[handsurgeryresource.com] Wilkie, however, reported two types of congenital synostosis, based on the proximal radioulnar junction.[wajradiology.org] Wilkie DPD: Congenital radioulnar synostosis. Br J Surg 1914; 1:366-375. 6. Kelikian H: Congenital Deformities of the Hand and Forearm.[healio.com]

  • Microphthalmia Type Lenz

    AU - Tifft,Cynthia AU - Zhang,Liqun AU - Wilkie,Andrew O M AU - Van Der Smagt,Jasper J. AU - Gorlin,Robert J. AU - Burgess,Shawn M. AU - Bardwell,Vivian J.[research.manchester.ac.uk] 10.1038/ng1321 Author(s): Ng, David; Thakker, Nalin; Corcoran, Connie M; Donnai, Dian; Perveen, Rahat; Schneider, Adele; Hadley, Donald W; Tifft, Cynthia; Zhang, Liqun; Wilkie[plu.mx] Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR Ng D, Thakker N, Corcoran CM, Donnai D, Perveen R, Schneider A, Hadley DW, Tifft C, Zhang L, Wilkie[disorders.eyes.arizona.edu]

  • Apert Syndrome

    Wilkie in: Corresponding author Correspondence to Andrew O.M. Wilkie . Rights and permissions To obtain permission to re-use content from this article visit RightsLink .[dx.doi.org] Wilkie , Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability , The American Journal of Human Genetics , 97 , 3 , (378)[doi.org] Problems and Approaches (Springer-Verlag, Berlin, Heidelberg, 1986). 9 Wilkie, A.O.M. et al .[dx.doi.org]

  • Frontometaphyseal Dysplasia

    Cho TJ, Duba HC, Fletcher E, Kim CA, Krakow D, Morava E, Neuhann T, Superti-Furga A, Veenstra-Knol I, Wieczorek D, Wilson LC, Hennekam RC, Sutherland-Smith AJ, Strom TM, Wilkie[genome.jp] T and Mortier, Geert and NEWBURY-ECOB, R and NICHOLSON, L and SCOTT, CI and OCHMAN, K and BROZEK, I and SHEARS, DJ and SUPERTI-FURGA, A and SURI, M and WHITEFORD, M and WILKIE[biblio.ugent.be] Lewkonia R, McInnes B, van Haelst MM, Mancini G, Illés T, Mortier G, Newbury-Ecob R, Nicholson L, Scott CI, Ochman K, Brozek I, Shears DJ, Superti-Furga A, Suri M, Whiteford M, Wilkie[ghr.nlm.nih.gov]

  • Crouzon Syndrome

    AC Goos 2 , Julia Rankin 3 , Helen Lord 4 , Tracy Lester 4 , A Jeannette M Hoogeboom 5 , Ans MW van den Ouweland 5 , Steven A Wall 6 , Irene MJ Mathijssen 2 and Andrew OM Wilkie[doi.org] Goriely A, McVean GA, Pelt AM, O’Rourke AW, Wall SA, de Rooij DG, Wilkie AO (2005) Proc Natl Acad Sci USA 102:6051–6056 PubMed CrossRef Google Scholar 2.[link.springer.com] View Article PubMed PubMed Central Google Scholar Johnson D, Wilkie AO: Craniosynostosis. Eur J Hum Genet. 2011, 19: 369-376. 10.1038/ejhg.2010.235.[doi.org]

  • FGFR2-Related Bent Bone Dysplasia

    Am J Hum Genet. 2005; 76 :361–7. [ PMC free article : PMC1196382 ] [ PubMed : 15625620 ] Wilkie AO.[ncbi.nlm.nih.gov] AC Goos 2 , Julia Rankin 3 , Helen Lord 4 , Tracy Lester 4 , A Jeannette M Hoogeboom 5 , Ans MW van den Ouweland 5 , Steven A Wall 6 , Irene MJ Mathijssen 2 and Andrew OM Wilkie[bmcmedgenet.biomedcentral.com] Wilkie AOM. Cytokine Growth Factor Rev. 2005 Apr;16(2):187-203.[atlasgeneticsoncology.org]

  • Acrocephalopolysyndactyly

    Wilkie , Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization , The American Journal of Human Genetics , 10.1016[doi.org] Seelow D, Jehee FS, Perlyn CA, Alonso LG, Bueno DF, Donnai D, Josifova D, Mathijssen IM, Morton JE, Orstavik KH, Sweeney E, Wall SA, Marsh JL, Nurnberg P, Passos-Bueno MR, Wilkie[disorders.eyes.arizona.edu] Jenkins D, Baynam G, De Catte L, Elcioglu N, Gabbett MT, Hudgins L, Hurst JA, Jehee FS, Oley C, Wilkie AO.[rarediseases.org]

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