Neuro-imaging characteristics of sensory impairment in cerebral palsy; a systematic review von Knijnenburg, A C S, Steinbusch, C V M, Janssen-Potten, Y J M, Defesche, A, Vermeulen, R J

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Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Famil... von Cuchel, Marina, Bruckert, Eric, Ginsberg, Henry N, Raal, Frederick J, Santos, Raul D, Hegele, Robert A, Kuivenhoven, Jan Albert, Nordestgaard, Børge G, Descamps, Olivier S, Steinhagen-Thiessen, Elisabeth, Tybjærg-Hansen, Anne, Watts, Gerald F, Averna, Maurizio, Boileau, Catherine, Borén, Jan, Catapano, Alberico L, Defesche, Joep C, Hovingh, G Kees, Humphries, Steve E, Kovanen, Petri T, Masana, Luis, Pajukanta, Päivi, Parhofer, Klaus G, Ray, Kausik K, Stalenhoef, Anton F H, Stroes, Erik, Taskinen, Marja-Riitta, Wiegman, Albert, Wiklund, Olov, Chapman, M John

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Familial hypercholesterolaemia in children and adolescents: gaining decades of life by optimizing detection and treatment von Wiegman, Albert, Gidding, Samuel S, Watts, Gerald F, Chapman, M John, Ginsberg, Henry N, Cuchel, Marina, Ose, Leiv, Averna, Maurizio, Boileau, Catherine, Borén, Jan, Bruckert, Eric, Catapano, Alberico L, Defesche, Joep C, Descamps, Olivier S, Hegele, Robert A, Hovingh, G Kees, Humphries, Steve E, Kovanen, Petri T, Kuivenhoven, Jan Albert, Masana, Luis, Nordestgaard, Børge G, Pajukanta, Päivi, Parhofer, Klaus G, Raal, Frederick J, Ray, Kausik K, Santos, Raul D, Stalenhoef, Anton F H, Steinhagen-Thiessen, Elisabeth, Stroes, Erik S, Taskinen, Marja-Riitta, Tybjærg-Hansen, Anne, Wiklund, Olov

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Home-based bimanual training based on motor learning principles in children with unilateral cerebral palsy and their parents (the COAD-study): rationale and protocols von Schnackers, Marlous, Beckers, Laura, Janssen-Potten, Yvonne, Aarts, Pauline, Rameckers, Eugène, van der Burg, Jan, de Groot, Imelda, Smeets, Rob, Geurts, Sander, Steenbergen, Bert

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Cardiac computed tomography imaging in familial hypercholesterolaemia: implications for therapy and clinical trials von Sijbrands, Eric J G, Nieman, Koen, Budoff, Matthew J

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Quality Assessment of the Genetic Test for Familial Hypercholesterolemia in The Netherlands von Kindt, Iris, Huijgen, Roeland, Boekel, Marieke, van der Gaag, Kristiaan J., Defesche, Joep C., Kastelein, John J. P., de Knijff, Peter

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Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Famil... von Cuchel, Marina, Bruckert, Eric, Ginsberg, Henry N, Raal, Frederick J, Santos, Raul D, Hegele, Robert A, Kuivenhoven, Jan Albert, Nordestgaard, Børge G, Descamps, Olivier S, Steinhagen-Thiessen, Elisabeth, Tybjaerg-Hansen, Anne, Watts, Gerald F, Averna, Maurizio, Boileau, Catherine, Borén, Jan, Catapano, Alberico L, Defesche, Joep C, Hovingh, G Kees, Humphries, Steve E, Kovanen, Petri T, Masana, Luis, Pajukanta, Päivi, Parhofer, Klaus G, Ray, Kausik K, Stalenhoef, Anton F H, Stroes, Erik, Taskinen, Marja-Riitta, Wiegman, Albert, Wiklund, Olov, Chapman, M John

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VALUED Approach to the Assessment of Design Skills in Architectural Education: a pilot study von Wolffe, Mark, Defesche, Antoine, Lans, Wendelien

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Association Between Familial Hypercholesterolemia and Prevalence of Type 2 Diabetes Mellitus von Besseling, Joost, Kastelein, John J. P, Defesche, Joep C, Hutten, Barbara A, Hovingh, G. Kees

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Homozygous autosomal dominant hypercholesterolaemia in the Netherlands: prevalence, genotype-phenotype relationship, and clinical outcome von Sjouke, Barbara, Kusters, D Meeike, Kindt, Iris, Besseling, Joost, Defesche, Joep C, Sijbrands, Eric J G, Roeters van Lennep, Jeanine E, Stalenhoef, Anton F H, Wiegman, Albert, de Graaf, Jacqueline, Fouchier, Sigrid W, Kastelein, John J P, Hovingh, G Kees

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Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel von Sturm, Amy C, Knowles, Joshua W, Gidding, Samuel S, Ahmad, Zahid S, Ahmed, Catherine D, Ballantyne, Christie M, Baum, Seth J, Bourbon, Mafalda, Carrié, Alain, Cuchel, Marina, de Ferranti, Sarah D, Defesche, Joep C, Freiberger, Tomas, Hershberger, Ray E, Hovingh, G Kees, Karayan, Lala, Kastelein, Johannes Jacob Pieter, Kindt, Iris, Lane, Stacey R, Leigh, Sarah E, Linton, MacRae F, Mata, Pedro, Neal, William A, Nordestgaard, Børge G, Santos, Raul D, Harada-Shiba, Mariko, Sijbrands, Eric J, Stitziel, Nathan O, Yamashita, Shizuya, Wilemon, Katherine A, Ledbetter, David H, Rader, Daniel J

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Rationale and design of two trials assessing the efficacy, safety, and tolerability of inclisiran in adolescents with homozygous and heterozygous familial hypercholesterolaemia von Reijman, M Doortje, Schweizer, Anja, Peterson, Amy L H, Bruckert, Eric, Stratz, Christian, Defesche, Joep C, Hegele, Robert A, Wiegman, Albert

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Clinical Genetic Testing for Familial Hypercholesterolemia von Sturm, Amy C., Knowles, Joshua W., Gidding, Samuel S., Ahmad, Zahid S., Ahmed, Catherine D., Ballantyne, Christie M., Baum, Seth J., Bourbon, Mafalda, Carrié, Alain, Cuchel, Marina, de Ferranti, Sarah D., Defesche, Joep C., Freiberger, Tomas, Hershberger, Ray E., Hovingh, G. Kees, Karayan, Lala, Kastelein, Johannes Jacob Pieter, Kindt, Iris, Lane, Stacey R., Leigh, Sarah E., Linton, MacRae F., Mata, Pedro, Neal, William A., Nordestgaard, Børge G., Santos, Raul D., Harada-Shiba, Mariko, Sijbrands, Eric J., Stitziel, Nathan O., Yamashita, Shizuya, Wilemon, Katherine A., Ledbetter, David H., Rader, Daniel J.

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ClinVar database of global familial hypercholesterolemia‐associated DNA variants von Iacocca, Michael A., Chora, Joana R., Carrié, Alain, Freiberger, Tomáš, Leigh, Sarah E., Defesche, Joep C., Kurtz, C. Lisa, DiStefano, Marina T., Santos, Raul D., Humphries, Steve E., Mata, Pedro, Jannes, Cinthia E., Hooper, Amanda J., Wilemon, Katherine A., Benlian, Pascale, O'Connor, Robert, Garcia, John, Wand, Hannah, Tichy, Lukáš, Sijbrands, Eric J., Hegele, Robert A., Bourbon, Mafalda, Knowles, Joshua W.

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Next-generation sequencing to confirm clinical familial hypercholesterolemia von Reeskamp, Laurens F, Tromp, Tycho R, Defesche, Joep C, Grefhorst, Aldo, Stroes, Erik S G, Hovingh, G Kees, Zuurbier, Linda

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Mutations in LPL, APOC2, APOA5, GPIHBP1 and LMF1 in patients with severe hypertriglyceridaemia von Surendran, R. P., Visser, M. E., Heemelaar, S., Wang, J., Peter, J., Defesche, J. C., Kuivenhoven, J. A., Hosseini, M., Péterfy, M., Kastelein, J. J. P., Johansen, C. T., Hegele, R. A., Stroes, E. S. G., Dallinga-Thie, G. M.

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ABCG5 and ABCG8 genetic variants in familial hypercholesterolemia von Reeskamp, Laurens F., Volta, Andrea, Zuurbier, Linda, Defesche, Joep C., Hovingh, G. Kees, Grefhorst, Aldo

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Cardiovascular risk in relation to functionality of sequence variants in the gene coding for the low-density lipoprotein receptor: a study among 29,365 individuals tested for 64 sp... von Huijgen, Roeland, Kindt, Iris, Defesche, Joep C, Kastelein, John J P

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Next-generation sequencing to confirm clinical familial hypercholesterolemia von Reeskamp, Laurens F, Tromp, Tycho R, Defesche, Joep C, Grefhorst, Aldo, Stroes, Erik Sg, Hovingh, G Kees, Zuurbier, Linda

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Efficacy of statins in familial hypercholesterolaemia: a long term cohort study von Versmissen, Jorie, Oosterveer, Daniëlla M, Yazdanpanah, Mojgan, Defesche, Joep C, Basart, Dick C G, Liem, Anho H, Heeringa, Jan, Witteman, Jacqueline C, Lansberg, Peter J, Kastelein, John J P, Sijbrands, Eric J G

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