Striatal volume deficits in children with ADHD who present a poor response to methylphenidate von Moreno, A., Duñó, L., Hoekzema, E., Picado, M., Martín, L. M., Fauquet, J., Vives-Gilabert, Y., Bulbena, A., Vilarroya, O.

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Comparison of Cell Wall Polysaccharide Composition and Structure Between Strains of Sporothrix schenckii and Sporothrix brasiliensis von Villalobos-Duno, Héctor L., Barreto, Laura A., Alvarez-Aular, Álvaro, Mora-Montes, Héctor M., Lozoya-Pérez, Nancy E., Franco, Bernardo, Lopes-Bezerra, Leila M., Niño-Vega, Gustavo A.

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Sleep architecture disturbances in children with bipolar disorder versus attention deficit and hyperactivity disorder: a pilot study von Estrada Prat, X, Alvarez Guerrico, I, Principe, A, Batlle Vila, S, Martín López, L, Duñó Ambrós, L

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Intra- and inter-field compositional changes of oils from the Misoa B4 reservoir in the Ceuta Southeast Area (Lake Maracaibo, Venezuela) von Márquez, G., Escobar, M., Lorenzo, E., Duno, L., Esquinas, N., Gallego, J.R.

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Characterization of tar-like material and producible oil in Misoa C2 and C3 reservoir sands of the Area 2 South (Ceuta Field, Venezuela) von Márquez, G., Escobar, M., Esquinas, N., Duno, L., Martín-Martín, J.D., Permanyer, A.

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Topological features dictate the mechanics of the mammalian brains von Sáez, P., Duñó, C., Sun, L.Y., Antonovaite, N., Malvè, M., Tost, D., Goriely, A.

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Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease von Lindquist, SG, Duno, M, Batbayli, M, Puschmann, A, Braendgaard, H, Mardosiene, S, Svenstrup, K, Pinborg, LH, Vestergaard, K, Hjermind, LE, Stokholm, J, Andersen, BB, Johannsen, P, Nielsen, JE

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Osteogenesis imperfecta and the teeth, eyes, and ears—a study of non-skeletal phenotypes in adults von Hald, J.D., Folkestad, L., Swan, C.Z., Wanscher, J., Schmidt, M., Gjørup, H., Haubek, D., Leonhard, C.-H., Larsen, D.A., Hjortdal, J.Ø., Harsløf, T., Duno, M., Lund, A.M., Jensen, J.-E.B., Brixen, K., Langdahl, B.

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Lecocytes mutation load declines with age in carriers of the m.3243A>G mutation: A 10‐year Prospective Cohort von Langdahl, J.H., Larsen, M., Frost, M., Andersen, P.H., Yderstræde, K.B., Vissing, J., Dunø, M., Thomassen, M., Frederiksen, A.L.

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Primary failure of eruption of teeth in two siblings with a novel mutation in the PTH1R gene von Aziz, S., Hermann, N. V., Dunø, M., Risom, L., Daugaard-Jensen, J., Kreiborg, S.

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Skeletal phenotypes in adult patients with osteogenesis imperfecta—correlations with COL1A1/COL1A2 genotype and collagen structure von Hald, J. D., Folkestad, L., Harsløf, T., Lund, A. M., Duno, M., Jensen, J. B., Neghabat, S., Brixen, K., Langdahl, B.

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Mitochondrial dysfunction and risk of cancer von Lund, M, Melbye, M, Diaz, L J, Duno, M, Wohlfahrt, J, Vissing, J

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Transmission of Guanarito and Pirital viruses among wild rodents, Venezuela von Milazzo, Mary L, Cajimat, Maria N B, Duno, Gloria, Duno, Freddy, Utrera, Antonio, Fulhorst, Charles F

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Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations von Ostergaard, Elsebet, Hansen, Flemming J., Sorensen, Nicolina, Duno, Morten, Vissing, John, Larsen, Pernille L., Faeroe, Oddmar, Thorgrimsson, Sigurdur, Wibrand, Flemming, Christensen, Ernst, Schwartz, Marianne

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A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy von Vissing, John, Barresi, Rita, Witting, Nanna, Van Ghelue, Marijke, Gammelgaard, Lise, Bindoff, Laurence A, Straub, Volker, Lochmüller, Hanns, Hudson, Judith, Wahl, Christoph M, Arnardottir, Snjolaug, Dahlbom, Kathe, Jonsrud, Christoffer, Duno, Morten

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Molecular mechanics of E525K dilated cardiomyopathy mutant human cardiac myosin von Duno-Miranda, Sebastian, Nelson, Shane R., Rasicci, David, Bodt, Skylar M.L., Vang, Duha, Sivaramakrishnan, Sivaraj, Yengo, Christopher M., Warshaw, David M.

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Tail length and E525K dilated cardiomyopathy mutant alter human β-cardiac myosin super-relaxed state von Duno-Miranda, Sebastian, Nelson, Shane R, Rasicci, David V, Bodt, Skylar M L, Cirilo, Jr, Joseph A, Vang, Duha, Sivaramakrishnan, Sivaraj, Yengo, Christopher M, Warshaw, David M

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Respiratory chain complex I deficiency due to NDUFA12 mutations as a new cause of Leigh syndrome von Ostergaard, Elsebet, Rodenburg, Richard J, van den Brand, Mariël, Thomsen, Lise Lykke, Duno, Morten, Batbayli, Mustafa, Wibrand, Flemming, Nijtmans, Leo

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Ocular, bulbar, limb, and cardiopulmonary involvement in oculopharyngeal muscular dystrophy von Witting, N., Mensah, A., Køber, L., Bundgaard, H., Petri, H., Duno, M., Milea, D., Vissing, J.

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A novel mitochondrial mutation m.8989G>C associated with neuropathy, ataxia, retinitis pigmentosa — The NARP syndrome von Duno, Morten, Wibrand, Flemming, Baggesen, Kirsten, Rosenberg, Thomas, Kjaer, Niels, Frederiksen, Anja L.

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