Showing 1 - 20 results of 21 for search 'De Coo, IF', query time: 0.08s
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Loden plaquettes uit het bezit van Koning Karel I by J. de Coo
Published 1963-06-01
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Propuesta de prevención primaria de la anorexia y bulimia en la infancia by Patricia Correa, Patricia Carbia, Irene Crestar, María de-Coo, María Ángeles Diz, Tamara Fernández
Published 2015-10-01
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Healthy, mtDNA-mutation free mesoangioblasts from mtDNA patients qualify for autologous therapy by Florence van Tienen, Ruby Zelissen, Erika Timmer, Marike van Gisbergen, Patrick Lindsey, Mattia Quattrocelli, Maurilio Sampaolesi, Elvira Mulder-den Hartog, Irenaeus de Coo, Hubert Smeets
Published 2019-12-01
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Generation of three human induced pluripotent stem cell lines, LUMCi024-A, LUMCi025-A, and LUMCi026-A, from two patients with combined oxidative phosphorylation deficiency 8 and a... by Ruben W.J. van Helden, Matthew J. Birket, Christian Freund, Christaan H. Arendzen, Harald M. Mikkers, Valeria Orlova, René I. de Coo, Christine L. Mummery, Milena Bellin
Published 2021-05-01
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Anatomic & metabolic brain markers of the m.3243A>G mutation: A multi-parametric 7T MRI study by Roy A.M. Haast, Dimo Ivanov, Rutger J.T. IJsselstein, Suzanne C.E.H. Sallevelt, Jacobus F.A. Jansen, Hubert J.M. Smeets, Irenaeus F.M. de Coo, Elia Formisano, Kâmil Uludağ
Published 2018-01-01
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Renal Phenotype in Mitochondrial Diseases: A Multicenter Study by Maria Parasyri, Per Brandström, Johanna Uusimaa, Elsebet Ostergaard, Omar Hikmat, Pirjo Isohanni, Karin Naess, I.F.M. de Coo, Andrés Nascimento Osorio, Matti Nuutinen, Christopher Lindberg, Laurence A. Bindoff, Már Tulinius, Niklas Darin, Kalliopi Sofou
Published 2022-01-01
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Non-random mtDNA segregation patterns indicate a metastable heteroplasmic segregation unit in m.3243A>G cybrid cells. by Anton K Raap, Roshan S Jahangir Tafrechi, Frans M van de Rijke, Angela Pyle, Carolina Wählby, Karoly Szuhai, Raimond B G Ravelli, René F M de Coo, Harsha K Rajasimha, Mats Nilsson, Patrick F Chinnery, David C Samuels, George M C Janssen
Published 2012-01-01
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A prospective open label 2–8 year extension of the randomised controlled ICON trial on the long-term efficacy and safety of occipital nerve stimulation in medically intractable chr... by Roemer B. Brandt, Leopoldine A. Wilbrink, Ilse F. de Coo, Joost Haan, Wim M. Mulleners, Frank J.P.M. Huygen, Erik W. van Zwet, Michel D. Ferrari, Rolf Fronczek, Michel D. Ferrari, Leopoldine A. Wilbrink, Ilse F. De Coo, Patty G. Doesborg, Eveline C. Bartels, Erik W. Van Zwet, Frank J.P.M. Huygen, Wim M. Mulleners, Erkan Kurt, Robert T.M. Van Dongen, Onno P.M. Teernstra, Peter J. Koehler, Geert H. Spincemaille, Frank Wille, Katja Burger, Joost Haan, Emile G.M. Couturier, Jan Willem Kallewaard, Peter H. Veltink, R. Buschman
Published 2023-12-01
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Specific MRI abnormalities reveal severe Perrault syndrome due to CLPP defects by Tom EJ Theunissen, Tom EJ Theunissen, Radek Szklarczyk, Mike Gerards, Debby MEI Hellebrekers, Elvira NM Mulder-Den Hartog, Jo Vanoevelen, Rick Kamps, Bart de Koning, S Lane Rutledge, Thomas Schmitt-Mechelke, Carola GM van Berkel, Marjo S van der Knaap, Irenaeus FM de Coo, Hubert JM Smeets, Hubert JM Smeets, Hubert JM Smeets
Published 2016-11-01
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Preclinical Efficacy and Safety Evaluation of Hematopoietic Stem Cell Gene Therapy in a Mouse Model of MNGIE by Rana Yadak, Raquel Cabrera-Pérez, Javier Torres-Torronteras, Marianna Bugiani, Joost C. Haeck, Marshall W. Huston, Elly Bogaerts, Steffi Goffart, Edwin H. Jacobs, Merel Stok, Lorena Leonardelli, Luca Biasco, Robert M. Verdijk, Monique R. Bernsen, George Ruijter, Ramon Martí, Gerard Wagemaker, Niek P. van Til, Irenaeus F.M. de Coo
Published 2018-03-01
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Selection and Characterization of Palmitic Acid Responsive Patients with an OXPHOS Complex I Defect by Tom E. J. Theunissen, Tom E. J. Theunissen, Mike Gerards, Debby M. E. I. Hellebrekers, Florence H. van Tienen, Rick Kamps, Suzanne C. E. H. Sallevelt, Elvira N. M. M.-D. Hartog, Hans R. Scholte, Robert M. Verdijk, Kees Schoonderwoerd, Irenaeus F. M. de Coo, Radek Szklarczyk, Hubert J. M. Smeets, Hubert J. M. Smeets, Hubert J. M. Smeets
Published 2017-10-01
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Human mutations in integrator complex subunits link transcriptome integrity to brain development. by Renske Oegema, David Baillat, Rachel Schot, Leontine M van Unen, Alice Brooks, Sima Kheradmand Kia, A Jeannette M Hoogeboom, Zheng Xia, Wei Li, Matteo Cesaroni, Maarten H Lequin, Marjon van Slegtenhorst, William B Dobyns, Irenaeus F M de Coo, Frans W Verheijen, Andreas Kremer, Peter J van der Spek, Daphne Heijsman, Eric J Wagner, Maarten Fornerod, Grazia M S Mancini
Published 2017-05-01
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Correction: Human mutations in integrator complex subunits link transcriptome integrity to brain development. by Renske Oegema, David Baillat, Rachel Schot, Leontine M van Unen, Alice Brooks, Sima Kheradmand Kia, A Jeannette M Hoogeboom, Zheng Xia, Wei Li, Matteo Cesaroni, Maarten H Lequin, Marjon van Slegtenhorst, William B Dobyns, Irenaeus F M de Coo, Debbie van den Berg, Frans W Verheijen, Andreas Kremer, Peter J van der Spek, Daphne Heijsman, Eric J Wagner, Maarten Fornerod, Grazia M S Mancini
Published 2017-08-01
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Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome by J.M. van Hagen, J.N. van der Geest, R.S. van der Giessen, G.C. Lagers-van Haselen, H.J.F.M.M. Eussen, J.J.P. Gille, L.C.P. Govaerts, C.H. Wouters, I.F.M. de Coo, C.C. Hoogenraad, S.K.E. Koekkoek, M.A. Frens, N. van Camp, A. van der Linden, M.C.E. Jansweijer, S.S. Thorgeirsson, C.I. De Zeeuw
Published 2007-04-01
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Mitochondrial DNA D-loop variants correlate with a primary open-angle glaucoma subgroup by Antoni Vallbona-Garcia, Antoni Vallbona-Garcia, Antoni Vallbona-Garcia, Patrick J. Lindsey, Rick Kamps, Alphons P. M. Stassen, Nhan Nguyen, Florence H. J. van Tienen, Florence H. J. van Tienen, Ilse H. J. Hamers, Rianne Hardij, Marike W. van Gisbergen, Marike W. van Gisbergen, Birke J. Benedikter, Birke J. Benedikter, Irenaeus F. M. de Coo, Carroll A. B. Webers, Carroll A. B. Webers, Theo G. M. F. Gorgels, Theo G. M. F. Gorgels, Hubert J. M. Smeets, Hubert J. M. Smeets
Published 2024-01-01
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A Delphi Survey Study to Formulate Statements on the Treatability of Inherited Metabolic Disorders to Decide on Eligibility for Newborn Screening by Abigail Veldman, M. B. Gea Kiewiet, Dineke Westra, Annet M. Bosch, Marion M. G. Brands, René I. F. M. de Coo, Terry G. J. Derks, Sabine A. Fuchs, Johanna. M. P. van den Hout, Hidde H. Huidekoper, Leo A. J. Kluijtmans, Klaas Koop, Charlotte M. A. Lubout, Margaretha F. Mulder, Bianca Panis, M. Estela Rubio-Gozalbo, Monique G. de Sain-van der Velden, Jaqueline Schaefers, Andrea B. Schreuder, Gepke Visser, Ron A. Wevers, Frits A. Wijburg, M. Rebecca Heiner-Fokkema, Francjan J. van Spronsen
Published 2023-10-01
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Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective? by Mastantuono, E, Repp, B, Alston, CL, Schiff, M, Haack, TB, Rotig, A, Ardissone, A, Lombes, A, Catarino, CB, Diodato, D, Schottmann, G, Poulton, J, Burlina, A, Jonckheere, A, Munnich, A, Ghezzi, D, Rokicki, D, Wellesley, D, Martinelli, D, Lamantea, E, Ostergaard, E, Pronicka, E, Pierre, G, Smeets, HJ, Scurr, I, De Coo, IF, Moroni, I, Smet, J, Mayr, JA, De Meirleir, L, Schuelke, M, Zeviani, M, McFarland, R, Seneca, S, Klopstock, T, Meitinger, T, Strom, TM, Herberg, U, Sperl, W, Nassogne, M, Ling, H, Fang, F, Freisinger, P, Van Coster, R, Taylor, RW, Haberle, J, Vockley, J, Prokisch, H, Wortmann, S
Published 2019Conference item