Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anneke Joosten"'
Autor:
João Caria, Francisco Vara-Luiz, Inês Maia, Anneke Joosten, Luís Val-Flores, Hélder Pinheiro, Diana Póvoas, Nuno Germano, Fernando Maltez
Publikováno v:
Infectious Disease Reports, Vol 15, Iss 2, Pp 171-179 (2023)
We report a fatal case of disseminated mpox infection that progressed over more than three months in an HIV-infected patient with acquired immunodeficiency syndrome (AIDS). Mucocutaneous, pleuropulmonary, central nervous system, and gastrointestinal
Externí odkaz:
https://doaj.org/article/bb1a36f6fc1a4d1ea3aeda7c30e718fa
Publikováno v:
European Journal of Case Reports in Internal Medicine (2021)
Granulomatosis with polyangiitis (Wegener’s granulomatosis) is a systemic vasculitis that primarily affects small and medium vessels. Its manifestations are usually confined to the upper airway, lower airway and kidney. It can also affect other org
Externí odkaz:
https://doaj.org/article/0cf69caf2cd340b6a004ff8307d66b9a
Publikováno v:
Cureus
Hypereosinophilic syndrome is a rare condition characterized by eosinophilia associated with organ damage, most commonly affecting the skin, lung, gastrointestinal, cardiovascular and central nervous system. The idiopathic form is characterized by th
Publikováno v:
Eur J Case Rep Intern Med
European Journal of Case Reports in Internal Medicine (2021)
European Journal of Case Reports in Internal Medicine (2021)
Granulomatosis with polyangiitis (Wegener’s granulomatosis) is a systemic vasculitis that primarily affects small and medium vessels. Its manifestations are usually confined to the upper airway, lower airway and kidney. It can also affect other org
Autor:
J.H.A.J. Curfs, Laura N. Bull, Roderick H. J. Houwen, Janneke M. Stapelbroek, Bert G. A. van Zanten, Theo A. Peters, Andy J. Beynon, Ronald P.J. Oude Elferink, Anneke Joosten, Bibian M. van Leeuwen, Denis H. A. van Beurden, Leo W. J. Klomp, Lieke M. van der Velden
Publikováno v:
Proceedings of the National Academy of Sciences USA, 106, 24, pp. 9709-14
Proceedings of the National Academy of Sciences of the United States of America, 106(24), 9709-9714. National Academy of Sciences
Proceedings of the National Academy of Sciences USA, 106, 9709-14
Proceedings of the National Academy of Sciences of the United States of America, 106(24), 9709-9714. National Academy of Sciences
Proceedings of the National Academy of Sciences USA, 106, 9709-14
ATP8B1 deficiency is caused by autosomal recessive mutations in ATP8B1 , which encodes the putative phospatidylserine flippase ATP8B1 (formerly called FIC1). ATP8B1 deficiency is primarily characterized by cholestasis, but extrahepatic symptoms are a