Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Bodil Edman-Ahlbom"'
Autor:
Göran Sedvall, Lars Terenius, Agneta Gunnar, Anna Sillén, Dimitrios Andreou, Bodil Edman-Ahlbom, Håkan Hall, Peter Saetre, Ingrid Agartz, Erik G. Jönsson
Publikováno v:
Journal of Neural Transmission. 115:1695-1699
Brain-derived neurotrophic factor (BDNF) has been shown to influence monoamine transmitter synthesis, metabolism and release. We investigated possible relationships between four BDNF gene polymorphisms and cerebrospinal fluid (CSF) concentrations of
Autor:
Maria Vares, Arnoldo Frigessi, Håkan Hall, Lars Terenius, Birgitta Wode-Helgodt, Bettina Kulle, Erik G. Jönsson, Ingrid Agartz, Göran Sedvall, Anna Sillén, Sven Cichon, Birgit Ekholm, Bodil Edman-Ahlbom, Johannes Schumacher, Agneta Gunnar
Publikováno v:
Progress in Neuro-Psychopharmacology and Biological Psychiatry. 30:924-933
Polymorphisms in the brain-derived neurotrophic factor (BDNF) gene have been suggested to be associated with schizophrenia. In a replication attempt, Swedish patients with schizophrenia (n=187) and control subjects (n=275) were assessed for four BDNF
Autor:
Lore Zech, Julie R. Korenberg, Claes Wadelius, Eva Seemanova, Göran Annerén, Ulf Pettersson, Bodil Edman Ahlbom, Peter Goetz
Publikováno v:
American Journal of Medical Genetics. 63:566-572
Down syndrome (DS) is caused in most cases by the presence of an extra chromosome 21. It has been shown that the DS phenotype is produced by duplication of only a small part of the long arm of chromosome 21, the 21q22 region, including and distal to
Autor:
Göran Annerén, Agne Larsson, Hafez Ghulam Abbas, Muhammad Yaqoob, Claes Wadelius, Peter Gustavsson, Bodil Edman Ahlbom
Publikováno v:
Human genetics. 110(2)
Congenital hypothyroidism affects 1/3000-4000 newborns and it has been estimated that 10-20% are familial cases with an autosomal recessive mode of inheritance. Previous studies of mostly individual cases have led to the identification of mutations i
Publikováno v:
Clinical genetics. 48(2)
Noonan syndrome, multiple lentigines syndrome (LEOPARD syndrome), Watson syndrome and neurofibromatosis type 1 share certain clinical manifestations. We present a linkage analysis using microsatellite markers located in the neurofibromatosis type 1 r