Works matching AU Albrecht, B.

Results: 56
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    The relationship between ADHD and key cognitive phenotypes is not mediated by shared familial effects with IQ.

    Published in:
    Psychological Medicine, 2011, v. 41, n. 4, p. 861, doi. 10.1017/S003329171000108X
    By:
    • Wood, A. C.;
    • Rijsdijk, F.;
    • Johnson, K. A.;
    • Andreou, P.;
    • Albrecht, B.;
    • Arias-Vasquez, A.;
    • Buitelaar, J. K.;
    • McLoughlin, G.;
    • Rommelse, N. N. J.;
    • Sergeant, J. A.;
    • Sonuga-Barke, E. J. S.;
    • Uebel, H.;
    • Van der Meere, J. J.;
    • Banaschewski, T.;
    • Gill, M.;
    • Manor, I.;
    • Miranda, A.;
    • Mulas, F.;
    • Oades, R. D.;
    • Roeyers, H.
    Publication type:
    Article
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    Präklinische Kindernotfälle.

    Published in:
    Der Anaesthesist, 2009, v. 58, n. 9, p. 876, doi. 10.1007/s00101-009-1603-3
    By:
    • Eich, C.;
    • Roessler, M.;
    • Timmermann, A.;
    • Heuer, J. F.;
    • Gentkow, U.;
    • Albrecht, B.;
    • Russo, S. G.
    Publication type:
    Article
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    Molecular and clinical studies in 8 patients with Temple syndrome.

    Published in:
    Clinical Genetics, 2018, v. 93, n. 6, p. 1179, doi. 10.1111/cge.13244
    By:
    • Gillessen‐Kaesbach, G.;
    • Albrecht, B.;
    • Eggermann, T.;
    • Elbracht, M.;
    • Mitter, D.;
    • Morlot, S.;
    • van Ravenswaaij‐Arts, C. M. A.;
    • Schulz, S.;
    • Strobl‐Wildemann, G.;
    • Buiting, K.;
    • Beygo, J.
    Publication type:
    Article
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    Arterial tortuosity syndrome: clinical and molecular findings in 12 newly identified families.

    Published in:
    Human Mutation, 2008, v. 29, n. 1, p. 150, doi. 10.1002/humu.20623
    By:
    • Callewaert, B.L.;
    • Willaert, A.;
    • Kerstjens-Frederikse, W.S.;
    • De Backer, J.;
    • Devriendt, K.;
    • Albrecht, B.;
    • Ramos-Arroyo, M.A.;
    • Doco-Fenzy, M.;
    • Hennekam, R.C.M.;
    • Pyeritz, R.E.;
    • Krogmann, O.N.;
    • Gillessen-kaesbach, G.;
    • Wakeling, E.L.;
    • Nik-zainal, S.;
    • Francannet, C.;
    • Mauran, P.;
    • Booth, C.;
    • Barrow, M.;
    • Dekens, R.;
    • Loeys, B.L.
    Publication type:
    Article
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    Monozygotic twins discordant for trisomy 18.

    Published in:
    Ultrasound in Obstetrics & Gynecology, 2011, v. 38, n. 6, p. 727, doi. 10.1002/uog.8978
    By:
    • Reuss, A.;
    • Gerlach, H.;
    • Bedow, W.;
    • Landt, S.;
    • Kuhn, U.;
    • Stein, A.;
    • Reschke, M.;
    • Albrecht, B.;
    • Westrich, V.;
    • Trawicki, W.;
    • Eiben, B.
    Publication type:
    Article
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    RAIN IN SHALLOW COMULUS OVER THE OCEAN.

    Published in:
    Bulletin of the American Meteorological Society, 2007, v. 88, n. 12, p. 1912, doi. 10.1175/BAMS-88-12-1912
    By:
    • Rauber, Robert M.;
    • Stevens, Bjorn;
    • Ochs III, Harry T.;
    • Knights, Charles;
    • Albrecht, B. A.;
    • Blyth, A. M.;
    • Fairall, C. W.;
    • Jensen, J. B.;
    • Lasher-Trapp, S. G.;
    • Mayol-Bracero, O. L.;
    • Vali, G.;
    • Anderson, J. R.;
    • Baker, B. A.;
    • Bandy, A. R.;
    • Burnet, E.;
    • Brenguier, J.-L.;
    • Brewer, W. A.;
    • Brown, P. R. A.;
    • Chuang, P.;
    • Cotton, W. R.
    Publication type:
    Article
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    Why Mie?

    Published in:
    Bulletin of the American Meteorological Society, 2002, v. 83, n. 10, p. 1471, doi. 10.1175/BAMS-83-10-1471
    By:
    • Kollias, Pavlos;
    • Albrecht, B. A.;
    • Marks, F.
    Publication type:
    Article
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    Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism.

    Published in:
    Human Genetics, 2017, v. 136, n. 2, p. 179, doi. 10.1007/s00439-016-1743-x
    By:
    • Bramswig, Nuria;
    • Lüdecke, H.-J.;
    • Pettersson, M.;
    • Albrecht, B.;
    • Bernier, R.;
    • Cremer, K.;
    • Eichler, E.;
    • Falkenstein, D.;
    • Gerdts, J.;
    • Jansen, S.;
    • Kuechler, A.;
    • Kvarnung, M.;
    • Lindstrand, A.;
    • Nilsson, D.;
    • Nordgren, A.;
    • Pfundt, R.;
    • Spruijt, L.;
    • Surowy, H.;
    • Vries, B.;
    • Wieland, T.
    Publication type:
    Article
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    Clinical and mutation data in 12 patients with the clinical diagnosis of Nager syndrome.

    Published in:
    Human Genetics, 2013, v. 132, n. 8, p. 885, doi. 10.1007/s00439-013-1295-2
    By:
    • Czeschik, J.;
    • Voigt, C.;
    • Alanay, Y.;
    • Albrecht, B.;
    • Avci, S.;
    • FitzPatrick, D.;
    • Goudie, D.;
    • Hehr, U.;
    • Hoogeboom, A.;
    • Kayserili, H.;
    • Simsek-Kiper, P.;
    • Klein-Hitpass, L.;
    • Kuechler, A.;
    • López-González, V.;
    • Martin, M.;
    • Rahmann, S.;
    • Schweiger, B.;
    • Splitt, M.;
    • Wollnik, B.;
    • Lüdecke, H.
    Publication type:
    Article
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    Slow cortical potentials neurofeedback in children with ADHD: comorbidity, self-regulation and clinical outcomes 6 months after treatment in a multicenter randomized controlled trial.

    Published in:
    European Child & Adolescent Psychiatry, 2019, v. 28, n. 8, p. 1087, doi. 10.1007/s00787-018-01271-8
    By:
    • Aggensteiner, Pascal-M.;
    • Brandeis, D.;
    • Millenet, S.;
    • Hohmann, S.;
    • Ruckes, C.;
    • Beuth, S.;
    • Albrecht, B.;
    • Schmitt, G.;
    • Schermuly, S.;
    • Wörz, S.;
    • Gevensleben, H.;
    • Freitag, C. M.;
    • Banaschewski, T.;
    • Rothenberger, A.;
    • Strehl, U.;
    • Holtmann, M.
    Publication type:
    Article
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