Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ronald H. Lekanne Dit Deprez"'
Autor:
Matthew J. O’Neill, Suet Nee Chen, Lynne Rumping, Renee Johnson, Marjon van Slegtenhorst, Andrew M. Glazer, Tao Yang, Joseph F. Solus, Julie Laudeman, Devyn W. Mitchell, Loren R. Vanags, Brett M. Kroncke, Katherine Anderson, Shanshan Gao, Job A.J. Verdonschot, Han Brunner, Debby Hellebrekers, Matthew R.G. Taylor, Dan M. Roden, Marja W. Wessels, Ronald H. Lekanne Dit Deprez, Diane Fatkin, Luisa Mestroni, M. Benjamin Shoemaker
Publikováno v:
Heart Rhythm.
Background: Truncating variants in filamin C (FLNC) can cause arrhythmogenic cardiomyopathy (ACM) through haploinsufficiency. Noncanonical splice-altering variants may contribute to this phenotype. Objective: The purpose of this study was to investig
Autor:
Marijke H. van der Meulen, Johanna C. Herkert, Susanna L. den Boer, Gideon J. du Marchie Sarvaas, Nico Blom, Arend D.J. ten Harkel, Hans M.P.J. Breur, Lukas A.J. Rammeloo, Ronald Tanke, Carlo Marcelis, Ingrid M.B.H. van de Laar, Judith M.A. Verhagen, Ronald H. Lekanne dit Deprez, Daniela Q.C.M. Barge-Schaapveld, Annette Baas, Arjan Sammani, Imke Christiaans, J. Peter van Tintelen, Michiel Dalinghaus
Publikováno v:
Circulation. Genomic and Precision Medicine, 15, 5, pp. 375-385
van der Meulen, M H, Herkert, J C, den Boer, S L, du Marchie Sarvaas, G J, Blom, N A, ten Harkel, A D J, Breur, H M P J, Rammeloo, L A J, Tanke, R B, Marcelis, C, van de Laar, I M B H, Verhagen, J M A, Lekanne Dit Deprez, R H, Barge-Schaapveld, D Q C M, Baas, A F, Sammani, A, Christiaans, I, van Tintelen, J P & Dalinghaus, M 2022, ' Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort : The Use of Genetic Testing in Risk Stratification ', Circulation: Genomic and Precision Medicine, vol. 15, no. 5, pp. 375-385 . https://doi.org/10.1161/CIRCGEN.120.002981
Circulation. Genomic and precision medicine, 15(5), 375-385. Lippincott Williams and Wilkins Ltd.
Circulation. Genomic and precision medicine, 15(5), 375-385. Lippincott Williams & Wilkins
Circulation. Genomic and precision medicine, 15(5):e002981. LIPPINCOTT WILLIAMS & WILKINS
Circulation: Genomic and Precision Medicine, 15(5), 375-385. Lippincott Williams and Wilkins Ltd.
Circulation. Genomic and Precision Medicine, 15, 375-385
Circulation: Genomic and Precision Medicine, 15(5), 375-385. LIPPINCOTT WILLIAMS & WILKINS
van der Meulen, M H, Herkert, J C, den Boer, S L, du Marchie Sarvaas, G J, Blom, N A, ten Harkel, A D J, Breur, H M P J, Rammeloo, L A J, Tanke, R B, Marcelis, C, van de Laar, I M B H, Verhagen, J M A, Lekanne Dit Deprez, R H, Barge-Schaapveld, D Q C M, Baas, A F, Sammani, A, Christiaans, I, van Tintelen, J P & Dalinghaus, M 2022, ' Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort : The Use of Genetic Testing in Risk Stratification ', Circulation: Genomic and Precision Medicine, vol. 15, no. 5, pp. 375-385 . https://doi.org/10.1161/CIRCGEN.120.002981
Circulation. Genomic and precision medicine, 15(5), 375-385. Lippincott Williams and Wilkins Ltd.
Circulation. Genomic and precision medicine, 15(5), 375-385. Lippincott Williams & Wilkins
Circulation. Genomic and precision medicine, 15(5):e002981. LIPPINCOTT WILLIAMS & WILKINS
Circulation: Genomic and Precision Medicine, 15(5), 375-385. Lippincott Williams and Wilkins Ltd.
Circulation. Genomic and Precision Medicine, 15, 375-385
Circulation: Genomic and Precision Medicine, 15(5), 375-385. LIPPINCOTT WILLIAMS & WILKINS
Background: This study aimed to describe the current practice and results of genetic evaluation in Dutch children with dilated cardiomyopathy and to evaluate genotype-phenotype correlations that may guide prognosis. Methods: We performed a multicente
Autor:
Chris M. van der Loos, Christian Rust, Hennie Bikker, Gerald Denk, Thomas Pusl, Ronald H. Lekanne dit Deprez, Ulrich Beuers, Valeska Terpstra
Publikováno v:
Hepatology Research. 40:937-941
Gallstones are very common. However, there is a small group of patients with low phospholipid-associated cholelithiasis (LPAC) that is characterized by symptomatic cholelithiasis at a young age ( A) in the ABCB4 gene.
Autor:
Gerald U, Denk, Hennie, Bikker, Ronald H, Lekanne Dit Deprez, Valeska, Terpstra, Chris, van der Loos, Ulrich, Beuers, Christian, Rust, Thomas, Pusl
Publikováno v:
Hepatology research : the official journal of the Japan Society of Hepatology. 40(9)
Gallstones are very common. However, there is a small group of patients with low phospholipid-associated cholelithiasis (LPAC) that is characterized by symptomatic cholelithiasis at a young age (40 years), recurrence of biliary symptoms despite chole