Resultados da busca - Carline E. Tacke
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Pasireotide treatment for severe congenital hyperinsulinism due to a homozygous ABCC8 mutation por Christiaan F. Mooij, Carline E. Tacke, Mirjam E. van Albada, Winfried Barthlen, Hennie Bikker, Klaus Mohnike, Matthijs W.N. Oomen, A.S. Paul van Trotsenburg, Nitash Zwaveling-Soonawala
Publicado em 2021-12-01
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Chondrodysplasia, enchondromas and a chest deformity causing severe pulmonary morbidity in a boy with a PTHLH duplication: A case report por Carline E. Tacke, Suzanne W.J. Terheggen-Lagro, Annemieke M. Boot, Astrid S. Plomp, Abeltje M. Polstra, Rick R. van Rijn, Peter A.A. Struijs, Henk van den Berg, Christiaan F. Mooij
Publicado em 2021-06-01
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FCGR2/3 polymorphisms are associated with susceptibility to Kawasaki disease but do not predict intravenous immunoglobulin resistance and coronary artery aneurysms por Paula Uittenbogaard, Stejara A. Netea, Stejara A. Netea, Michael W. T. Tanck, Judy Geissler, Piotr Buda, Monika Kowalczyk-Domagała, Magdalena Okarska-Napierała, Diana van Stijn, Carline E. Tacke, US Kawasaki Disease Genetics Consortium, David P. Burgner, David P. Burgner, Chisato Shimizu, Jane C. Burns, Irene M. Kuipers, Taco W. Kuijpers, Taco W. Kuijpers, Sietse Q. Nagelkerke, Sietse Q. Nagelkerke
Publicado em 2024-09-01
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Extensive Ethnic Variation and Linkage Disequilibrium at the FCGR2/3 Locus: Different Genetic Associations Revealed in Kawasaki Disease por Sietse Q. Nagelkerke, Sietse Q. Nagelkerke, Carline E. Tacke, Willemijn B. Breunis, Michael W. T. Tanck, Judy Geissler, Eileen Png, Long T. Hoang, Joris van der Heijden, Ahmad N. M. Naim, Rae S. M. Yeung, Michael L. Levin, Victoria J. Wright, David P. Burgner, David P. Burgner, Anne-Louise Ponsonby, Anne-Louise Ponsonby, Justine A. Ellis, Justine A. Ellis, Justine A. Ellis, Rolando Cimaz, Chisato Shimizu, Jane C. Burns, Karin Fijnvandraat, Karin Fijnvandraat, C. Ellen van der Schoot, Timo K. van den Berg, Timo K. van den Berg, Martin de Boer, Sonia Davila, Martin L. Hibberd, Martin L. Hibberd, Taco W. Kuijpers, Taco W. Kuijpers, The International Kawasaki Disease Genetics Consortium, Nagib Dahdah, Isabelle Kone-Paut
Publicado em 2019-03-01
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