Idali, Farah, Wahlström, Jan, Dahlberg, Benita, Khademi, Mohsen, Olsson, Tomas, Eklund, Anders, ...
Abstract Background Activated T helper (Th)-1 pulmonary CD4 + cells and their mediators are essential for the inflammation and granulomatous process in sarcoidosis. Recently, T-cell immunoglobulin...
Inerot, Annica, Enerbäck, Charlotta, Enlund, Fredrik, Martinsson, Tommy, Samuelsson, Lena, Wahlström, Jan, ...
Abstract Background The aim of the present study was to describe the clinical characteristics of a population of psoriatics sampled from a patient organisation and not from hospitals or out-patient...
Autosomal dominant myopathy: Missense mutation (Glu-706 → Lys) in the myosin heavy chain IIa gene
Martinsson, Tommy, Oldfors, Anders, Darin, Niklas, Berg, Kerstin, Tajsharghi, Homa, Kyllerman, Mårten, ...
We here report on a human myopathy associated with a mutation in a fast myosin heavy chain (MyHC) gene, and also the genetic defect in a hereditary inclusion body myopathy. The disorder has...
Inerot, Annica, Enerbäck, Charlotta, Enlund, Fredrik, Martinsson, Tommy, Samuelsson, Lena, Wahlström, Jan, ...
A Major Locus for Myoclonus-Dystonia Maps to Chromosome 7q in Eight Families
Klein, Christine, Schilling, Karla, Saunders-Pullman, Rachel J., Garrels, Jennifer, Breakefield, Xandra O., Brin, Mitchell F., ...
Myoclonus-dystonia (M-D) is an autosomal dominant disorder characterized by myoclonic and dystonic muscle contractions that are often responsive to alcohol. The dopamine D2 receptor gene (DRD2) on...
Autosomal dominant myopathy: Missense mutation (Glu-706 → Lys) in the myosin heavy chain IIa gene
Martinsson, Tommy, Oldfors, Anders, Darin, Niklas, Berg, Kerstin, Tajsharghi, Homa, Kyllerman, Mårten, ...
We here report on a human myopathy associated with a mutation in a fast myosin heavy chain (MyHC) gene, and also the genetic defect in a hereditary inclusion body myopathy. The disorder has...
Inerot, Annica, Enerbäck, Charlotta, Enlund, Fredrik, Martinsson, Tommy, Samuelsson, Lena, Wahlström, Jan, ...
A Major Locus for Myoclonus-Dystonia Maps to Chromosome 7q in Eight Families
Klein, Christine, Schilling, Karla, Saunders-Pullman, Rachel J., Garrels, Jennifer, Breakefield, Xandra O., Brin, Mitchell F., ...
Myoclonus-dystonia (M-D) is an autosomal dominant disorder characterized by myoclonic and dystonic muscle contractions that are often responsive to alcohol. The dopamine D2 receptor gene (DRD2) on...
Wahlström, Jan, Dengjel, Jörn, Persson, Bengt, Duyar, Hüseyin, Rammensee, Hans-Georg, Stevanoviδc, Stefan, ...
Sarcoidosis is an inflammatory disease of unknown etiology, most commonly affecting the lungs. Activated CD4+ T cells accumulate in the lungs of individuals with sarcoidosis and are considered to be...