Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Manuela Schöb"'
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e58512 (2013)
ObjectiveThe aim of this study was to evaluate the reporting of relevant prognostic information in a sample of randomized controlled trials (RCTs) that investigated treatments for patients with chronic low back pain (LBP). We also analysed how resear
Externí odkaz:
https://doaj.org/article/cd77976ec83242dc9e239abfb712a243
Autor:
Pascal Müller, Manuela Schöb, Yannick Gerth, Wolfgang Korte, Michael Brändle, Hans Rickli, Stefan Bilz, Andreas Bärlocher
Publikováno v:
Praxis. 107:1345-1353
Diagnosis and Treatment of Familial Hypercholesterolemia Abstract. Familial hypercholesterolemia secondary to heterozygous mutations in the LDL receptor, Apolipoprotein B or PCSK9 gene is characterized by 2- to 3-fold elevated LDL cholesterol levels,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::267abbe0cee90f6bfd7b6bb5ed46b0b3
https://doi.org/10.1024/1661-8157/a003134
https://doi.org/10.1024/1661-8157/a003134
Autor:
Manuela, Schöb, Pascal, Müller, Yannick, Gerth, Wolfgang, Korte, Hans, Rickli, Michael, Brändle, Andreas, Bärlocher, Stefan, Bilz
Publikováno v:
Praxis. 107(24)
Diagnosis and Treatment of Familial Hypercholesterolemia Abstract. Familial hypercholesterolemia secondary to heterozygous mutations in the LDL receptor, Apolipoprotein B or PCSK9 gene is characterized by 2- to 3-fold elevated LDL cholesterol levels,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5cd141005dd0849332043021b90bf162
https://pubmed.ncbi.nlm.nih.gov/30482120
https://pubmed.ncbi.nlm.nih.gov/30482120
Publikováno v:
Praxis. 103:899-902
Die Hemmkörperhämophilie ist eine seltene Erkrankung mit hoher Mortalität. Sie wird durch Autoantikörper meist gegen den Gerinnungsfaktor VIII verursacht und ist häufig idiopathisch. Klinisch imponieren Weichteilblutungen. Diagnostisch von Bedeu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::133a4d6d39318b62121d164a29827e09
https://doi.org/10.1024/1661-8157/a001727
https://doi.org/10.1024/1661-8157/a001727
Publikováno v:
Praxis. 103(15)
Acquired hemophilia is a rare but severe bleeding disorder caused by autoantibodies mostly against factor VIII. Clinically it mostly presents with soft tissue and muscular bleeding. Diagnostics include a prolonged aPTT, antibodies against FVIII and a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::08ad0f87f038385e51c10a9983d34f60
https://pubmed.ncbi.nlm.nih.gov/25051933
https://pubmed.ncbi.nlm.nih.gov/25051933
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 3, p e58512 (2013)
PLoS ONE, Vol 8, Iss 3, p e58512 (2013)
ObjectiveThe aim of this study was to evaluate the reporting of relevant prognostic information in a sample of randomized controlled trials (RCTs) that investigated treatments for patients with chronic low back pain (LBP). We also analysed how resear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6037aa3f2d860a131998f8f2055623a2
https://pubmed.ncbi.nlm.nih.gov/23505524
https://pubmed.ncbi.nlm.nih.gov/23505524