Zobrazeno 1 - 6
of 6
pro vyhledávání: '"H, Orlén"'
Publikováno v:
Acta neurologica Scandinavica. 123(1)
To re-evaluate middle-aged Swedish patients diagnosed with dysequilibrium syndrome (DES) in childhood and to compare their clinical and neuroimaging features to DES with VLDLR gene mutations (DES-VLDR).Six patients from five families underwent neurol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::045e5cb895637de250f5fbf58d5d3453
https://pubmed.ncbi.nlm.nih.gov/20199520
https://pubmed.ncbi.nlm.nih.gov/20199520
Autor:
Klar J; Department of Immunology, Genetics and Pathology, The Rudbeck Laboratory and Science for Life Laboratory, Uppsala University, Uppsala, Sweden., Sobol M, Melberg A, Mäbert K, Ameur A, Johansson AC, Feuk L, Entesarian M, Orlén H, Casar-Borota O, Dahl N
Publikováno v:
Human mutation [Hum Mutat] 2013 Apr; Vol. 34 (4), pp. 572-7.
Autor:
Melberg A; Department of Neuroscience, Unit of Neurology, Uppsala University, Uppsala, Sweden., Orlén H, Raininko R, Entesarian M, Dahlqvist J, Gustavson KH, Dahl N
Publikováno v:
Acta neurologica Scandinavica [Acta Neurol Scand] 2011 Jan; Vol. 123 (1), pp. 28-33.
Autor:
Dahlqvist J; Department of Genetics and Pathology, the Rudbeck Laboratory, Uppsala University, Uppsala, Sweden., Orlén H, Matsson H, Dahl N, Lönnerholm T, Gustavson KH
Publikováno v:
Acta orthopaedica [Acta Orthop] 2009 Dec; Vol. 80 (6), pp. 711-5.
Autor:
Orlén H; Department of Genetics and Pathology, The Rudbeck Laboratory, Uppsala University and University Hospital, Uppsala, Sweden., Melberg A, Raininko R, Kumlien E, Entesarian M, Söderberg P, Påhlman M, Darin N, Kyllerman M, Holmberg E, Engler H, Eriksson U, Dahl N
Publikováno v:
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics [Am J Med Genet B Neuropsychiatr Genet] 2009 Oct 05; Vol. 150B (7), pp. 984-92.