Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment von Bosch, Annet M, Abeling, Nico G. G. M, IJlst, Lodewijk, Knoester, Hennie, van der Pol, W. Ludo, Stroomer, Alida E. M, Wanders, Ronald J, Visser, Gepke, Wijburg, Frits A, Duran, Marinus, Waterham, Hans R

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Exome Sequencing in Brown-Vialetto-Van Laere Syndrome von Johnson, Janel O., Gibbs, J. Raphael, Van Maldergem, Lionel, Houlden, Henry, Singleton, Andrew B.

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Inulin metabolism in dicots: chicory as a model system von Van Laere, A., Van Den Ende, W.

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Les Basongo - Bankutu : notes sur leur organisation domestique, sociale et politique / Adolphe van Laere von Laere, Adolphe van

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Child Neurology: Brown-Vialetto-Van Laere syndrome: Dramatic visual recovery after delayed riboflavin therapy von Bamaga, Ahmed K, Maamari, Robi N, Culican, Susan M, Shinawi, Marwan, Golumbek, Paul T

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Plant fructan exohydrolases: a role in signaling and defense? von Van den Ende, Wim, De Coninck, Barbara, Van Laere, André

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Thirteen‐month‐old girl with hyporegenerative macrocytic anemia due to Brown–Vialetto–Van Laere syndrome 2 von Naami, Nibras, Borkhardt, Arndt, Yoshimi, Ayami, Grinstein, Lev, Escherich, Gabriele

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X‐ray diffraction structure of a plant glycosyl hydrolase family 32 protein: fructan 1‐exohydrolase IIa of Cichorium intybus von Verhaest, Maureen, Ende, Wim Van den, Roy, Katrien Le, De Ranter, Camiel J., Laere, André Van, Rabijns, Anja

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zinc-adapted fungus protects pines from zinc stress von Adriaensen, K, Lelie, D. van der, Laere, A. van, Vangronsveld, J, Colpaert, J.V

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What shapes amino acid and sugar composition in Mediterranean floral nectars? von Petanidou, Theodora, Van Laere, André, N. Ellis, Willem, Smets, Erik

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Cloning, gene mapping, and functional analysis of a fructan 1-exohydrolase (1-FEH) from Lolium perenne implicated in fructan synthesis rather than in fructan mobilization von Lothier, Jérémy, Lasseur, Bertrand, Le Roy, Katrien, Van Laere, André, Prud'homme, Marie-Pascale, Barre, Philippe, Van den Ende, Wim, Morvan-Bertrand, Annette

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Towards a better understanding of the generation of fructan structure diversity in plants: molecular and functional characterization of a sucrose:fructan 6-fructosyltransferase (6-... von Lasseur, Bertrand, Lothier, Jérémy, Wiemken, Andres, Van Laere, André, Morvan-Bertrand, Annette, Van den Ende, Wim, Prud'homme, Marie-Pascale

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Cochlear Implant in Brown -- Vialetto -- Van Laere Syndrome Patient von Amaral, Maria Stella Arantes do, Massuda, Eduardo T, Fenolio, Guilherme Henrique Mitikami, Reis, Ana Claudia Mirandola Barbosa, Hyppolito, Miguel Angelo

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Corrigendum to “Brown-Vialetto-Van Laere syndrome and Fazio-Londe syndrome: A novel mutation and in silico analyses” [J. Clin. Neurosci. 72 (2020) 342–349] von Rabbani, Bahareh, Bakhshandeh, Mohammad Kazem, Navaeifar, Mohammad Reza, Abbaskhanian, Ali, Soveizi, Mahdieh, Geravandpoor, Shahpour, Mahdieh, Nejat

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Brown−Vialetto−Van Laere and Fazio−Londe syndromes: SLC52A3 mutations with puzzling phenotypes and inheritance von Gayathri, Santhalingam, Gowda, Vykuntaraju K., Udhayabanu, Tamilarasan, O'Callaghan, Benjamin, Efthymiou, Stephanie, Varalakshmi, Perumal, Benakappa, Naveen, Houlden, Henry, Ashokkumar, Balasubramaniem

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Expression analysis of a chicory fructan 1-exohydrolase gene reveals complex regulation by cold von Michiels, A, Van Laere, A, Van den Ende, W, Tucker, M

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Purification, cloning and functional characterization of a fructan 6-exohydrolase from wheat (Triticum aestivum L.) von Riet, Liesbet van, Nagaraj, Vinay, Ende, Wim van den, Clerens, Stefan, Wiemken, Andres, Laere, Andre van

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Genetic, Radiologic and Clinical Variability in Brown-Vialetto-Van Laere Syndrome von Woodcock, Ian R., MBBS MRCPCH MSc, Menezes, Manoj P., MBBS FRACP PhD, Coleman, Lee, MBCHB FRANZCR BSc, Yaplito-Lee, Joy, MD FRACP, Peters, Heidi, MBBS FRACP PhD, White, Susan M., MBBS FRACP, Stapleton, Rachel, MBBS, Phelan, Dean G., BSc, Chong, Belinda, PhD, Lunke, Sebastian, PhD, Stark, Zornitza, BM BCh FRACP MA, Pitt, James, PhD FFSc(RCPA), Ryan, Monique M., MBBS FRACP MMed, Robertson, Colin, MBBS FRACP MSc MD, Yiu, Eppie M., MBBS FRACP PhD

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Auditory neuropathy in Brown–Vialetto–Van Laere syndrome due to riboflavin transporter RFVT2 deficiency von Menezes, Manoj P, O'Brien, Katherine, Hill, Mandy, Webster, Richard, Antony, Jayne, Ouvrier, Robert, Birman, Catherine, Gardner‐Berry, Kirsty

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Severe erythroid hypoplasia and erythroblast vacuolization in a male with Brown–Vialetto–Van Laere syndrome 2 misdiagnosed as Diamond Blackfan anemia von Chen, Yanxia, Zhao, Jiwei, McLinden, A. Patrick, Luo, Meizhu, Cao, Ke, Liu, Jinlin

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