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63 Possible Causes for talvik

  • Baraitser Syndrome

    Talvik, T ; view all (2017) New SMARCA2 mutation in a patient with Nicolaides–Baraitser syndrome and myoclonic astatic epilepsy.[discovery.ucl.ac.uk]

  • Partial Trisomy 13 in Patau Syndrome

    Talvik T, Mikelsaar AV, Mikelsaar R, Kaosaar M, Tuiir S: Inherited translocations in two families t(14q ;10q-) and t(13q-;21q ).[link.springer.com] Genet. 9 , 105–110 (1972) Google Scholar Talvik, T., Mikelsaar, A.[link.springer.com]

  • Deletion of the Long Arm of Chromosome 18

    Talvik 2 1. Karyological Laboratory Institute of Molecular Biology of Academy of Sciences of UdSSR Moscow 2.[link.springer.com]

  • Nicolaides-Baraitser Syndrome

    Talvik, T ; view all (2017) New SMARCA2 mutation in a patient with Nicolaides–Baraitser syndrome and myoclonic astatic epilepsy.[discovery.ucl.ac.uk] MA, Pal DK, Marini C, Guerrini R, Neubauer B, Korff CM, Craiu D, Pal D, Caglayan H, Helbig I, De Jonghe P, Thomas R, Moller RS, Sisodiya S, von Spiczak S, Weckhuysen S, Talvik[eprint.ncl.ac.uk]

  • Multiple Congenital Anomalies

    Talvik T 6 .[ncbi.nlm.nih.gov] Vaher U 1 , Nõukas M 2 , Nikopensius T 2 , Kals M 3 , Annilo T 2 , Nelis M 3 , Ounap K 4 , Reimand T 5 , Talvik I 6 , Ilves P 7 , Piirsoo A 8 , Seppet E 9 , Metspalu A 2 ,[ncbi.nlm.nih.gov]

  • Epilepsy with Continuous Spike-and-Slow-Waves during Sleep

    Muhle H, Boor R, Van Paesschen W, Caraballo R, Fejerman N, Weckhuysen S, De Jonghe P, Larsen J, Moller RS, Hjalgrim H, Addis L, Tang S, Hughes E, Pal DK, Veri K, Vaher U, Talvik[genome.jp] Kadi Veri , Ulvi Vaher & Tiina Talvik Clinic of Child Neurology, St. Naum University Hospital of Neurology and Psychiatry, Sofia, Bulgaria.[nature.com] Reinthaler , Johanna A Jähn , Hiltrud Muhle , Sarah Weckhuysen , Peter De Jonghe , Jan Larsen , Rikke S Møller , Helle Hjalgrim , Deb K Pal , Kadi Veri , Ulvi Vaher , Tiina Talvik[nature.com]

  • Ring Chromosome 13

    I....Talvik T. 2000 21 Skin pigmentation anomalies in ring chromosome 13. ( 9664214 ) Fryns J.P....Legius E. 1998 22 Retinal detachment in an infant with the ring chromosome[malacards.org] […] congenital anomalies. ( 11590457 ) Venugopalan P....Kenue R.K. 2001 20 Boy with celiac disease, malformations, and ring chromosome 13 with deletion 13q32-->qter. ( 10951464 ) Talvik[malacards.org]

  • Emery-Dreifuss Muscular Dystrophy

    Talkop UA, Talvik I, Sõnajalg M, Sibul H, Kolk A, Piirsoo A, Warzok R, Wulff K, Wehnert MS, Talvik T: Early onset of cardiomyopathy in two brothers with X-linked Emery-Dreifuss[karger.com] Hum Mol Genet. 1998; 7 :135–9. [ PubMed : 9384614 ] Talkop UA, Talvik I, Sonajalg M, Sibul H, Kolk A, Piirsoo A, Warzok R, Wulff K, Wehnert MS, Talvik T.[ncbi.nlm.nih.gov] ., Talvik, I., Sõnajalg, M., Sibul, H., Kolk, A., Piirsoo, A., Warzok, R., Wulff, K., Wehnert, M.S., Talvik, T. Neuromuscul.[wikigenes.org]

  • Ring Chromosome 19

    . , Talvik , T. A. , Sitska , M. E. ( 1967 ). A ring shaped chromosome (presumably N. 18) and its bearing on the multiple congenital anomalies in man .[cambridge.org] N., Talvik, T. A.: Partial deletion of the long arm of chromosome 18. Humangenetik 7 , 359–360 (1969). Google Scholar Moore, M.[link.springer.com] ., Talvik, T. A., Sitska, M. E.: A ring-shaped chromosome (presumably No. 18) and its bearing on multiple congenital anomalies in man.[link.springer.com]

  • Paroxysmal Hemicrania

    ( 17119794 ) Fragoso Y.D. 2006 50 Chronic paroxysmal hemicrania in a 3-year, 10-month-old female. ( 16504793 ) Talvik I....Talvik T. 2006[malacards.org] I....Talvik T. 2009 31 Paroxysmal hemicrania and POEMS syndrome: further evidence that neuropeptides are implicated in primary headache?[malacards.org] […] hemicrania with visual aura in a 17-year-old boy. ( 19348039 ) Seidel S....WAPber C. 2009 30 Three-year follow-up of a girl with chronic paroxysmal hemicrania. ( 19068259 ) Talvik[malacards.org]

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