Accounts of School Nursing von Van der Moeren, Maaike, Willemsen, Leen, Muhli, Ulla Hellström

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Accounts of school nursing von Moeren, Maaike van der, Willemsen, Leen, Muhli, Ulla Hellström

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Cerebrospinal fluid glucose and lactate: age-specific reference values and implications for clinical practice von Leen, Wilhelmina G, Willemsen, Michèl A, Wevers, Ron A, Verbeek, Marcel M

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Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group von Klepper, Joerg, Akman, Cigdem, Armeno, Marisa, Auvin, Stéphane, Cervenka, Mackenzie, Cross, Helen J., De Giorgis, Valentina, Della Marina, Adela, Engelstad, Kristin, Heussinger, Nicole, Kossoff, Eric H., Leen, Wilhelmina G., Leiendecker, Baerbel, Monani, Umrao R., Oguni, Hirokazu, Neal, Elizabeth, Pascual, Juan M., Pearson, Toni S., Pons, Roser, Scheffer, Ingrid E., Veggiotti, Pierangelo, Willemsen, Michél, Zuberi, Sameer M., De Vivo, Darryl C.

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Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding von Samkar, Anusha, Leen, Willemijn G., Willemsen, Michèl A. A. P., Verrips, Aad

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Hourly analysis of cerebrospinal fluid glucose shows large diurnal fluctuations von Verbeek, Marcel M, Leen, Wilhelmina G, Willemsen, Michèl A, Slats, Diane, Claassen, Jurgen A

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Cerebrospinal Fluid Analysis in the Workup of GLUT1 Deficiency Syndrome: A Systematic Review von Leen, Wilhelmina G, Wevers, Ron A, Kamsteeg, Erik-Jan, Scheffer, Hans, Verbeek, Marcel M, Willemsen, Michèl A

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Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder von Leen, Wilhelmina G., Klepper, Joerg, Verbeek, Marcel M., Leferink, Maike, Hofste, Tom, van Engelen, Baziel G., Wevers, Ron A., Arthur, Todd, Bahi-Buisson, Nadia, Ballhausen, Diana, Bekhof, Jolita, van Bogaert, Patrick, Carrilho, Inês, Chabrol, Brigitte, Champion, Michael P., Coldwell, James, Clayton, Peter, Donner, Elizabeth, Evangeliou, Athanasios, Ebinger, Friedrich, Farrell, Kevin, Forsyth, Rob J., de Goede, Christian G. E. L., Gross, Stephanie, Grunewald, Stephanie, Holthausen, Hans, Jayawant, Sandeep, Lachlan, Katherine, Laugel, Vincent, Leppig, Kathy, Lim, Ming J., Mancini, Grazia, Marina, Adela Della, Martorell, Loreto, McMenamin, Joe, Meuwissen, Marije E. C., Mundy, Helen, Nilsson, Nils O., Panzer, Axel, Poll-The, Bwee T., Rauscher, Christian, Rouselle, Christophe M. R., Sandvig, Inger, Scheffner, Thomas, Sheridan, Eamonn, Simpson, Neil, Sykora, Parol, Tomlinson, Richard, Trounce, John, Webb, David, Weschke, Bernhard, Scheffer, Hans, Willemsen, Michél A.

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GLUT1 deficiency syndrome into adulthood: a follow-up study von Leen, W. G., Taher, M., Verbeek, M. M., Kamsteeg, E. J., van de Warrenburg, B. P., Willemsen, M. A.

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Upstream SLC2A1 translation initiation causes GLUT1 deficiency syndrome von Willemsen, Michèl A, Vissers, Lisenka Elm, Verbeek, Marcel M, van Bon, Bregje W, Geuer, Sinje, Gilissen, Christian, Klepper, Joerg, Kwint, Michael P, Leen, Wilhelmina G, Pennings, Maartje, Wevers, Ron A, Veltman, Joris A, Kamsteeg, Erik-Jan

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Head circumference in glucose transporter 1 deficiency syndrome: Normal for individuals, abnormal as a group von van Gemert, Loes A., Leen, Wilhelmina G., Draaisma, Jos M., Roeleveld, Nel, Willemsen, Michèl A.

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Lactate and its many faces von Taher, Marjan, Leen, Wilhelmina G, Wevers, Ron A, Willemsen, Michèl A

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Child Neurology: Differential diagnosis of a low CSF glucose in children and young adults von Leen, Wilhelmina G, de Wit, Cornelis J, Wevers, Ron A, van Engelen, Baziel G, Kamsteeg, Erik-Jan, Klepper, Joerg, Verbeek, Marcel M, Willemsen, Michèl A

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A novel SLC2A1 mutation linking hemiplegic migraine with alternating hemiplegia of childhood von Weller, Claudia M, Leen, Wilhelmina G, Neville, Brian GR, Duncan, John S, Vries, Boukje de, Geilenkirchen, Marije A, Haan, Joost, Kamsteeg, Erik-Jan, Ferrari, Michel D, Maagdenberg, Arn MJM van den, Willemsen, Michèl AAP, Scheffer, Hans, Terwindt, Gisela M

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Gene Variants in the Novel Type 2 Diabetes Loci CDC123/CAMK1D, THADA, ADAMTS9, BCL11A, and MTNR1B Affect Different Aspects of Pancreatic β-Cell Function von Simonis-Bik, Annemarie M, Nijpels, Giel, van Haeften, Timon W, Houwing-Duistermaat, Jeanine J, Boomsma, Dorret I, Reiling, Erwin, van Hove, Els C, Diamant, Michaela, Kramer, Mark H H, Heine, Robert J, Maassen, J Antonie, Slagboom, P Eline, Willemsen, Gonneke, Dekker, Jacqueline M, Eekhoff, Elisabeth M, de Geus, Eco J, 't Hart, Leen M

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Effects of alagebrium, an advanced glycation endproduct breaker, on exercise tolerance and cardiac function in patients with chronic heart failure von Hartog, Jasper W.L., Willemsen, Suzan, van Veldhuisen, Dirk J., Posma, Jan L., van Wijk, Leen M., Hummel, Yoran M., Hillege, Hans L., Voors, Adriaan A.

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Movement disorders in GLUT1 deficiency syndrome respond to the modified Atkins diet von Leen, Wilhelmina G., Mewasingh, Leena, Verbeek, Marcel M., Kamsteeg, Erik-Jan, van de Warrenburg, Bart P., Willemsen, Michel A.

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CIAO1 and MMS19 deficiency: A lethal neurodegenerative phenotype caused by cytosolic Fe-S cluster protein assembly disorders von van Karnebeek, Clara D.M., Tarailo-Graovac, Maja, Leen, René, Meinsma, Rutger, Correard, Solenne, Jansen-Meijer, Judith, Prykhozhij, Sergey V., Pena, Izabella A., Ban, Kevin, Schock, Sarah, Saxena, Vishal, Pras-Raves, Mia L., Drögemöller, Britt I., Grootemaat, Anita E., van der Wel, Nicole N., Dobritzsch, Doreen, Roseboom, Winfried, Schomakers, Bauke V., Jaspers, Yorrick R.J., Zoetekouw, Lida, Roelofsen, Jeroen, Ferreira, Carlos R., van der Lee, Robin, Ross, Colin J., Kochan, Jakub, McIntyre, Rebecca L., van Klinken, Jan B., van Weeghel, Michel, Kramer, Gertjan, Weschke, Bernhard, Labrune, Philippe, Willemsen, Michèl A., Riva, Daria, Garavaglia, Barbara, Moeschler, John B., Filiano, James J., Ekker, Marc, Berman, Jason N., Dyment, David, Vaz, Frédéric M., Wasserman, Wyeth W., Houtkooper, Riekelt H., van Kuilenburg, André B.P.

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Metabolite ratios as potential biomarkers for type 2 diabetes: a DIRECT study von Molnos, Sophie, Wahl, Simone, Haid, Mark, Eekhoff, E. Marelise W., Pool, René, Floegel, Anna, Deelen, Joris, Much, Daniela, Prehn, Cornelia, Breier, Michaela, Draisma, Harmen H., van Leeuwen, Nienke, Simonis-Bik, Annemarie M. C., Jonsson, Anna, Willemsen, Gonneke, Bernigau, Wolfgang, Wang-Sattler, Rui, Suhre, Karsten, Peters, Annette, Thorand, Barbara, Herder, Christian, Rathmann, Wolfgang, Roden, Michael, Gieger, Christian, Kramer, Mark H. H., van Heemst, Diana, Pedersen, Helle K., Gudmundsdottir, Valborg, Schulze, Matthias B., Pischon, Tobias, de Geus, Eco J. C., Boeing, Heiner, Boomsma, Dorret I., Ziegler, Anette G., Slagboom, P. Eline, Hummel, Sandra, Beekman, Marian, Grallert, Harald, Brunak, Søren, McCarthy, Mark I., Gupta, Ramneek, Pearson, Ewan R., Adamski, Jerzy, ’t Hart, Leen M.

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Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome von Riestra, Maria Rodrigo, Pillay, Bethany A., Willemsen, Mathijs, Kienapfel, Verena, Ehlers, Lisa, Delafontaine, Selket, Pinton, Antoine, Wouters, Marjon, Hombrouck, Anneleen, Sauer, Kate, Bossuyt, Xavier, Voet, Arnout, Soenen, Stefaan J., Conde, Cecilia Dominguez, Bucciol, Giorgia, Boztug, Kaan, Humblet-Baron, Stephanie, Touzart, Aurore, Rieux-Laucat, Frédéric, Notarangelo, Luigi D., Moens, Leen, Meyts, Isabelle

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