Delayed hemolysis, elevated liver enzymes, low platelet count syndrome in succession of switches of preventive anticoagulant treatment in a 41-year-old patient with a history of recurrent assisted implantation failures: a case report
Mikolaiczik, Katrin, Praetner, Marc, Rüth, Michael, Mark, Karlheinz
Published in Journal of medical case reports (19.01.2019)
Published in Journal of medical case reports (19.01.2019)
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Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities
Zenker, Martin, Aigner, Thomas, Wendler, Olaf, Tralau, Tim, Müntefering, Horst, Fenski, Regina, Pitz, Susanne, Schumacher, Valérie, Royer-Pokora, Brigitte, Wühl, Elke, Cochat, Pierre, Bouvier, Raymonde, Kraus, Cornelia, Mark, Karlheinz, Madlon, Henry, Dötsch, Jörg, Rascher, Wolfgang, Maruniak-Chudek, Iwona, Lennert, Thomas, Neumann, Luitgard M., Reis, André
Published in Human molecular genetics (01.11.2004)
Published in Human molecular genetics (01.11.2004)
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Journal Article
Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: An autosomal recessive syndrome
Zenker, Martin, Tralau, Tim, Lennert, Thomas, Pitz, Susanne, Mark, Karlheinz, Madlon, Henry, Dötsch, Jörg, Reis, André, Müntefering, Horst, Neumann, Luitgard M.
Published in American journal of medical genetics. Part A (01.10.2004)
Published in American journal of medical genetics. Part A (01.10.2004)
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Journal Article
Human laminin ²2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities
Zenker, Martin, Aigner, Thomas, Wendler, Olaf, Tralau, Tim, Müntefering, Horst, Fenski, Regina, Pitz, Susanne, Schumacher, Valérie, Royer-Pokora, Brigitte, Wühl, Elke, Cochat, Pierre, Bouvier, Raymonde, Kraus, Cornelia, Karlheinz, Mark, Madlon, Henry, Dötsch, Jörg
Published in Human molecular genetics (01.11.2004)
Get full text
Published in Human molecular genetics (01.11.2004)
Journal Article
Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities
Zenker, Martin, Aigner, Thomas, Wendler, Olaf, Tralau, Tim, Müntefering, Horst, Fenski, Regina, Pitz, Susanne, Schumacher, Valérie, Royer-Pokora, Brigitte, Wühl, Elke, Cochat, Pierre, Bouvier, Raymonde, Kraus, Cornelia, Mark, Karlheinz, Madlon, Henry, Dötsch, Jörg, Rascher, Wolfgang, Maruniak-Chudek, Iwona, Lennert, Thomas, Neumann, Luitgard M, Reis, André
Published in Human molecular genetics (01.11.2004)
Get full text
Published in Human molecular genetics (01.11.2004)
Journal Article