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	1.	Adrenal Function in females with low plasma HDL-C due to mutations in ABCA1 and LCAT. [electronic resource] by Bochem, Andrea E Holleboom, Adriaan G Romijn, Johannes A Hoekstra, Menno Dallinga, Geesje M Motazacker, Mahdi M Hovingh, G Kees Kuivenhoven, Jan A Stroes, Erik S G Producer: 20141231 In: PloS one vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	High density lipoprotein as a source of cholesterol for adrenal steroidogenesis: a study in individuals with low plasma HDL-C. [electronic resource] by Bochem, Andrea E Holleboom, Adriaan G Romijn, Johannes A Hoekstra, Menno Dallinga-Thie, Geesje M Motazacker, Mahdi M Hovingh, G Kees Kuivenhoven, Jan A Stroes, Erik S G Producer: 20131101 In: Journal of lipid research vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Age-related obesity and type 2 diabetes dysregulate neuronal associated genes and proteins in humans. [electronic resource] by Rahimi, Mehran Vinciguerra, Manlio Daghighi, Mojtaba Özcan, Behiye Akbarkhanzadeh, Vishtaseb Sheedfar, Fareeba Amini, Marzyeh Mazza, Tommaso Pazienza, Valerio Motazacker, Mahdi M Mahmoudi, Morteza De Rooij, Felix W M Sijbrands, Eric Peppelenbosch, Maikel P Rezaee, Farhad Producer: 20160812 In: Oncotarget vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	RELN rare variants in myoclonus-dystonia. [electronic resource] by Groen, Justus L Ritz, Katja Jalalzadeh, Hamid van der Salm, Sandra M A Jongejan, Aldo Mook, Olaf R Haagmans, Martin A Zwinderman, Aeilko H Motazacker, Mahdi M Hennekam, Raoul C Baas, Frank Tijssen, Marina A J Producer: 20151123 In: Movement disorders : official journal of the Movement Disorder Society vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A loss-of-function variant in OSBPL1A predisposes to low plasma HDL cholesterol levels and impaired cholesterol efflux capacity. [electronic resource] by Motazacker, Mahdi M Pirhonen, Juho van Capelleveen, Julian C Weber-Boyvat, Marion Kuivenhoven, Jan Albert Shah, Saundarya Hovingh, G Kees Metso, Jari Li, Shiqian Ikonen, Elina Jauhiainen, Matti Dallinga-Thie, Geesje M Olkkonen, Vesa M Producer: 20171120 In: Atherosclerosis vol. 249 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	ABCA1 mutation carriers with low high-density lipoprotein cholesterol are characterized by a larger atherosclerotic burden. [electronic resource] by Bochem, Andrea E van Wijk, Diederik F Holleboom, Adriaan G Duivenvoorden, Raphaël Motazacker, Mahdi M Dallinga-Thie, Geesje M de Groot, Eric Kastelein, John J P Nederveen, Aart J Hovingh, G Kees Stroes, Erik S G Producer: 20130703 In: European heart journal vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A rare variant in MCF2L identified using exclusion linkage in a pedigree with premature atherosclerosis. [electronic resource] by Maiwald, Stephanie Motazacker, Mahdi M van Capelleveen, Julian C Sivapalaratnam, Suthesh van der Wal, Allard C van der Loos, Chris Kastelein, John J P Ouwehand, Willem H Hovingh, G Kees Trip, Mieke D van Buul, Jaap D Dallinga-Thie, Geesje M Producer: 20160919 In: European journal of human genetics : EJHG vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Family-specific aggregation of lipid GWAS variants confers the susceptibility to familial hypercholesterolemia in a large Austrian family. [electronic resource] by Nikkola, Elina Ko, Arthur Alvarez, Marcus Cantor, Rita M Garske, Kristina Kim, Elliot Gee, Stephanie Rodriguez, Alejandra Muxel, Reinhard Matikainen, Niina Söderlund, Sanni Motazacker, Mahdi M Borén, Jan Lamina, Claudia Kronenberg, Florian Schneider, Wolfgang J Palotie, Aarno Laakso, Markku Taskinen, Marja-Riitta Pajukanta, Päivi Producer: 20180712 In: Atherosclerosis vol. 264 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardation. [electronic resource] by Mir, Asif Kaufman, Liana Noor, Abdul Motazacker, Mahdi M Jamil, Talal Azam, Matloob Kahrizi, Kimia Rafiq, Muhammad Arshad Weksberg, Rosanna Nasr, Tanveer Naeem, Farooq Tzschach, Andreas Kuss, Andreas W Ishak, Gisele E Doherty, Dan Ropers, H Hilger Barkovich, A James Najmabadi, Hossein Ayub, Muhammad Vincent, John B Producer: 20100114 In: American journal of human genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Mutation in KERA identified by linkage analysis and targeted resequencing in a pedigree with premature atherosclerosis. [electronic resource] by Maiwald, Stephanie Sivapalaratnam, Suthesh Motazacker, Mahdi M van Capelleveen, Julian C Bot, Ilze de Jager, Saskia C van Eck, Miranda Jolley, Jennifer Kuiper, Johan Stephens, Jonathon Albers, Cornelius A Vosmeer, C Ruben Kruize, Heleen Geerke, Daan P van der Wal, Allard C van der Loos, Chris M Kastelein, John J P Trip, Mieke D Ouwehand, Willem H Dallinga-Thie, Geesje M Hovingh, G Kees Producer: 20150115 In: PloS one vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)