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Oktober 2020 / J Genet Genomics Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation X. Su Y. Feng S.A. Rahman S. Wu G. Li F. Rüschendorf L. Zhao H. Cui J. Liang L. Fang H. Hu S. Froehler Y. Yu G. Patone O. Hummel Q. Chen K. Raile F.C. Luft S. Bähring K. Hussain W. Chen J. Zhang M. Gong 01. Januar 2001 / Am Heart J Subclinical cardiotoxic effects of anthracyclines as assessed by magnetic resonance imaging - A pilot study R. Wassmuth S. Lentzsch U. Erdbruegger J. Schulz-Menger B. Doerken R. Dietz M.G. Friedrich 01. Januar 2001 / J Med Genet Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26 R. Bayoumi K. Saar Y.A. Lee G. Nuernberg A. Reis M. Nur-E-Kamal L.I. Al Gazali 14. August 2001 / Circulation MRI versus 3D echocardiography in postinterventional patients with hypertrophic obstructive cardiomyopathy - Response J. Schulz-Menger O. Strohm J. Waigand F. Uhlich R. Dietz M.G. Friedrich 01. Januar 2001 / J Magn Reson Imaging Measurement of left ventricular dimensions and function in patients with dilated cardiomyopathy O. Strohm J. Schulz-Menger B. Pilz K.J. Osterziel R. Dietz M.G. Friedrich 01. Januar 2001 / J Magn Reson Imaging Magnetic resonance planimetry of the vena contracta as a new approach to assessment of stenotic heart valves: An in vitro study O. Strohm J. Schulz-Menger D. Haenlein R. Dietz M.G. Friedrich 23. November 2001 / Circ Res The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system M.L. Bang T. Centner F. Fornoff A.J. Geach M. Gotthardt M. McNabb C.C. Witt D. Labeit C.C. Gregorio H. Granzier S. Labeit 09. Juli 2009 / Physiol Genomics Characterization of Nob3, a major quantitative trait locus for obesity and hyperglycemia on mouse chromosome 1 H. Vogel M. Nestler F. Rueschendorf M.D. Block S. Tischer R. Kluge A. Schurmann H.G. Joost S. Scherneck 13. Februar 2009 / Am J Hum Genet Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea P. Heinz-Erian T. Mueller B. Krabichler M. Schranz C. Becker F. Rueschendorf P. Nuernberg B. Rossier M. Vujic I.W. Booth C. Holmberg C. Wijmenga G. Grigelioniene C.M. Kneepkens S. Rosipal M. Mistrik M. Kappler L. Michaud L.C. Doczy V.M. Siu M. Krantz H. Zoller G. Utermann A.R. Janecke 14. Dezember 2012 / PLoS ONE High spatial resolution and temporally resolved t(2) (*) mapping of normal human myocardium at 7.0 tesla: an ultrahigh field magnetic resonance feasibility study F. Hezel C. Thalhammer S. Waiczies J. Schulz-Menger T. Niendorf Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 … Nächste Seite Next › Letzte Seite Last »
28. Oktober 2020 / J Genet Genomics Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation X. Su Y. Feng S.A. Rahman S. Wu G. Li F. Rüschendorf L. Zhao H. Cui J. Liang L. Fang H. Hu S. Froehler Y. Yu G. Patone O. Hummel Q. Chen K. Raile F.C. Luft S. Bähring K. Hussain W. Chen J. Zhang M. Gong
01. Januar 2001 / Am Heart J Subclinical cardiotoxic effects of anthracyclines as assessed by magnetic resonance imaging - A pilot study R. Wassmuth S. Lentzsch U. Erdbruegger J. Schulz-Menger B. Doerken R. Dietz M.G. Friedrich
01. Januar 2001 / J Med Genet Localisation of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia, and distinctive facies to chromosome 15q26 R. Bayoumi K. Saar Y.A. Lee G. Nuernberg A. Reis M. Nur-E-Kamal L.I. Al Gazali
14. August 2001 / Circulation MRI versus 3D echocardiography in postinterventional patients with hypertrophic obstructive cardiomyopathy - Response J. Schulz-Menger O. Strohm J. Waigand F. Uhlich R. Dietz M.G. Friedrich
01. Januar 2001 / J Magn Reson Imaging Measurement of left ventricular dimensions and function in patients with dilated cardiomyopathy O. Strohm J. Schulz-Menger B. Pilz K.J. Osterziel R. Dietz M.G. Friedrich
01. Januar 2001 / J Magn Reson Imaging Magnetic resonance planimetry of the vena contracta as a new approach to assessment of stenotic heart valves: An in vitro study O. Strohm J. Schulz-Menger D. Haenlein R. Dietz M.G. Friedrich
23. November 2001 / Circ Res The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system M.L. Bang T. Centner F. Fornoff A.J. Geach M. Gotthardt M. McNabb C.C. Witt D. Labeit C.C. Gregorio H. Granzier S. Labeit
09. Juli 2009 / Physiol Genomics Characterization of Nob3, a major quantitative trait locus for obesity and hyperglycemia on mouse chromosome 1 H. Vogel M. Nestler F. Rueschendorf M.D. Block S. Tischer R. Kluge A. Schurmann H.G. Joost S. Scherneck
13. Februar 2009 / Am J Hum Genet Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea P. Heinz-Erian T. Mueller B. Krabichler M. Schranz C. Becker F. Rueschendorf P. Nuernberg B. Rossier M. Vujic I.W. Booth C. Holmberg C. Wijmenga G. Grigelioniene C.M. Kneepkens S. Rosipal M. Mistrik M. Kappler L. Michaud L.C. Doczy V.M. Siu M. Krantz H. Zoller G. Utermann A.R. Janecke
14. Dezember 2012 / PLoS ONE High spatial resolution and temporally resolved t(2) (*) mapping of normal human myocardium at 7.0 tesla: an ultrahigh field magnetic resonance feasibility study F. Hezel C. Thalhammer S. Waiczies J. Schulz-Menger T. Niendorf