Pathologic rupture of the spleen as the initial manifestation in acute lymphoblastic leukemia von Bernat, S, Garcia Boyero, R, Guinot, M, Lopez, F, Gozalbo, T, Canigral, G

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Availability, accessibility and delivery to patients of the 28 orphan medicines approved by the European Medicine Agency for hereditary metabolic diseases in the MetabERN network von Heard, Jean-Michel, Vrinten, Charlotte, Schlander, Michael, Bellettato, Cinzia Maria, van Lingen, Corine, Scarpa, Maurizio

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Management of phenylketonuria in Europe: Survey results from 19 countries von Blau, Nenad, Bélanger-Quintana, Amaya, Demirkol, Mübeccel, Feillet, François, Giovannini, Marcello, MacDonald, Anita, Trefz, Friedrich K., Spronsen, Francjan van

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Clinical pathways for inborn errors of metabolism: warranted and feasible von Demirdas, Serwet, van Kessel, Imke N, Korndewal, Marjolein J, Hollak, Carla E M, Meutgeert, Hanka, Klaren, Anja, van Rijn, Margreet, van Spronsen, Francjan J, Bosch, Annet M

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Pathologic rupture of the spleen as the initial manifestation in acute lymphoblastic leukemia von Bernat, S, García Boyero, R, Guinot, M, López, F, Gozalbo, T, Cañigral, G

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Sweet and sour: an update on classic galactosemia von Coelho, Ana I., Rubio-Gozalbo, M. Estela, Vicente, João B., Rivera, Isabel

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Low-cost ceramic membranes: A research opportunity for industrial application von Mestre, S., Gozalbo, A., Lorente-Ayza, M.M., Sánchez, E.

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White matter microstructure pathology in classic galactosemia revealed by neurite orientation dispersion and density imaging von Timmers, Inge, Zhang, Hui, Bastiani, Matteo, Jansma, Bernadette M., Roebroeck, Alard, Rubio-Gozalbo, M. Estela

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Pathophysiology and targets for treatment in hereditary galactosemia: A systematic review of animal and cellular models von Haskovic, Minela, Coelho, Ana I., Bierau, Jörgen, Vanoevelen, Jo M., Steinbusch, Laura K. M., Zimmermann, Luc J. I., Villamor‐Martinez, Eduardo, Berry, Gerard T., Rubio‐Gozalbo, M. Estela

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Impact of theta transcranial alternating current stimulation on language production in adult classic galactosemia patients von Derks, Britt, Kumar, Varsha Shashi, Yadnik, Sai, Panis, Bianca, Bosch, Annet M., Cassiman, David, Janssen, Mirian C. H., Schuhmann, Teresa, Rubio‐Gozalbo, M. Estela, Jansma, Bernadette M.

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Letermovir use may impact on the Cytomegalovirus DNA fragmentation profile in plasma from allogeneic hematopoietic stem cell transplant recipients von Giménez, Estela, Gozalbo‐Rovira, Roberto, Albert, Eliseo, Piñana, José Luis, Solano, Carlos, Navarro, David

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Galactose metabolism and health von Coelho, Ana I, Berry, Gerard T, Rubio-Gozalbo, M Estela

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Altered neural oscillations in classical galactosaemia during sentence production von Mazzini, Sara, Yadnik, Sai, Timmers, Inge, Rubio‐Gozalbo, Estela, Jansma, Bernadette M.

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International clinical guideline for the management of classical galactosemia: diagnosis, treatment, and follow-up von Welling, Lindsey, Bernstein, Laurie E., Berry, Gerard T., Burlina, Alberto B., Eyskens, François, Gautschi, Matthias, Grünewald, Stephanie, Gubbels, Cynthia S., Knerr, Ina, Labrune, Philippe, van der Lee, Johanna H., MacDonald, Anita, Murphy, Elaine, Portnoi, Pat A., Õunap, Katrin, Potter, Nancy L., Rubio-Gozalbo, M. Estela, Spencer, Jessica B., Timmers, Inge, Treacy, Eileen P., Van Calcar, Sandra C., Waisbren, Susan E., Bosch, Annet M.

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Monocarboxylate Transporter 1 Deficiency and Ketone Utilization von van Hasselt, Peter M, Ferdinandusse, Sacha, Monroe, Glen R, Ruiter, Jos P.N, Turkenburg, Marjolein, Geerlings, Maartje J, Duran, Karen, Harakalova, Magdalena, van der Zwaag, Bert, Monavari, Ardeshir A, Okur, Ilyas, Sharrard, Mark J, Cleary, Maureen, O’Connell, Nuala, Walker, Valerie, Rubio-Gozalbo, M. Estela, de Vries, Maaike C, Visser, Gepke, Houwen, Roderick H.J, van der Smagt, Jasper J, Verhoeven-Duif, Nanda M, Wanders, Ronald J.A, van Haaften, Gijs

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Hereditary galactosemia von Demirbas, Didem, Coelho, Ana I., Rubio-Gozalbo, M. Estela, Berry, Gerard T.

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The treatment of biochemical genetic diseases: From substrate reduction to nucleic acid therapies von Vos, E. Naomi, Demirbas, Didem, Mangel, Matthew, Rubio-Gozalbo, M. Estela, Levy, Harvey L., Berry, Gerard T.

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Movement disorders and nonmotor neuropsychological symptoms in children and adults with classical galactosemia von Kuiper, Anouk, Grünewald, Stephanie, Murphy, Elaine, Coenen, Maraike A., Eggink, Hendriekje, Zutt, Rodi, Rubio‐Gozalbo, Maria E., Bosch, Annet M., Williams, Monique, Derks, Terry G. J., Lachmann, Robin H. L., Brouwers, Martijn C. G. J., Janssen, Mirian C. H., Tijssen, Marina A., de Koning, Tom J.

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Presumptive brain influx of large neutral amino acids and the effect of phenylalanine supplementation in patients with Tyrosinemia type 1 von van Ginkel, Willem G, van Vliet, Danique, Burgerhof, Johannes G M, de Blaauw, Pim, Rubio Gozalbo, M Estela, Heiner-Fokkema, M Rebecca, van Spronsen, Francjan J

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An update on serine deficiency disorders von van der Crabben, S. N., Verhoeven-Duif, N. M., Brilstra, E. H., Van Maldergem, L., Coskun, T., Rubio-Gozalbo, E., Berger, R., de Koning, T. J.

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