Search Results - Hehr, Ute

Fertility preservation for patients with malignant disease. Guideline of the DGGG, DGU and DGRM (S2k-Level, AWMF Registry No. 015/082, November 2017): recommendations and statement... by Dittrich, Ralf (Author) , Kliesch, Sabine (Author) , Balcerek, Magdalena (Author) , Beckmann, Matthias Wilhelm (Author) , Behringer, Karolin (Author) , Denzer, Christian (Author) , Diemer, Thorsten (Author) , Dorn, Almut (Author) , Fehm, Tanja (Author) , Germeyer, Ariane (Author) , Geue, Kristina (Author) , Ghadjar, Pirus (Author) , Goeckenjan, Maren (Author) , Guth, Dagmar (Author) , Hauffa, Berthold (Author) , Hehr, Ute (Author) , Hetzer, Franc (Author) , Hoffmann, Wilfried (Author) , Jantke, Andreas (Author) , Kentenich, Heribert (Author) , Köhn, Frank-Michael (Author) , Meißner, Julia (Author) , Micke, Oliver (Author) , Nawroth, Frank (Author) , Nordhoff, Verena (Author) , Ochsendorf, Falk (Author) , Oppelt, Patricia G. (Author) , Pelz, Jörg (Author) , Rau, Beate (Author) , Reisch, Nicole (Author) , Riesenbeck, Dorothea (Author) , Schwab, Roxana Michaela (Author) , Siedentopf, Friederike (Author) , Wimberger, Pauline (Author) , Wischmann, Tewes (Author) , Wolff, Michael von (Author) , Lotz, Laura (Author) ,

• Verlag, kostenfrei, Volltext
• Verlag, kostenfrei, Volltext

47 patients with FLNA associated periventricular nodular heterotopia by Lange, Max (Author) , Kasper, Burkhard (Author) , Bohring, Axel (Author) , Rutsch, Frank (Author) , Kluger, Gerhard (Author) , Hoffjan, Sabine (Author) , Spranger, Stephanie (Author) , Behnecke, Anne (Author) , Ferbert, Andreas (Author) , Hahn, Andreas (Author) , Oehl-Jaschkowitz, Barbara (Author) , Graul-Neumann, Luitgard (Author) , Diepold, Katharina (Author) , Schreyer, Isolde (Author) , Bernhard, Matthias K. (Author) , Mueller, Franziska (Author) , Siebers-Renelt, Ulrike (Author) , Beleza-Meireles, Ana (Author) , Uyanik, Goekhan (Author) , Janssens, Sandra (Author) , Boltshauser, Eugen (Author) , Winkler, Juergen (Author) , Schuierer, Gerhard (Author) , Hehr, Ute (Author) ,

• Resolving-System, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Craniofrontonasal syndrome in a male due to chromosomal mosaicism involving EFNB1: further insights into a genetic paradox by Evers, Christina (Author) , Jungwirth, Maria Sophia (Author) , Morgenthaler, J. (Author) , Hinderhofer, Katrin (Author) , Maas, B. (Author) , Janssen, Johannes W. G. (Author) , Jauch, Anna (Author) , Hehr, Ute (Author) , Steinbeisser, Herbert (Author) , Moog, Ute (Author) ,

• Resolving-System, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Fukutin mutations in non-Japanese patients with congenital muscular dystrophy: less severe mutations predominate in patients with a non-Walker-Warburg phenotype by Yiş, Uluç (Author) , Uyanik, Gökhan (Author) , Bambul Heck, Pinar (Author) , Smitka, Martin (Author) , Nobel, Hannes (Author) , Ebinger, Friedrich (Author) , Dirik, Eray (Author) , Feng, Lucy (Author) , Kurul, Semra H. (Author) , Brocke, Katja (Author) , Unalp, Aycan (Author) , Özer, Erdener (Author) , Cakmakci, Handan (Author) , Sewry, Caroline (Author) , Cirak, Sebahattin (Author) , Muntoni, Francesco (Author) , Hehr, Ute (Author) , Morris-Rosendahl, Deborah J. (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Fukutin mutations in non-Japanese patients with congenital muscular dystrophy: less severe mutations predominate in patients with a non-Walker-Warburg phenotype

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