Nucleic acids potentiate Factor VII-activating protease (FSAP)-mediated cleavage of platelet-derived growth factor-BB and inhibition of vascular smooth muscle cell proliferation

nork Shibamiya, Aya, Muhl, Lars, Tannert-Otto, Susanne, Preissner, Klaus T., Kanse, Sandip M.
Argitaratua 2007

Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP)

nork Karle, Kathrin N, Schüle, Rebecca, Klebe, Stephan, Otto, Susanne, Frischholz, Christian, Liepelt-Scarfone, Inga, Schöls, Ludger
Argitaratua 2013

Guideline Adherence and Registry Recruitment of Congenital Primary Hypothyroidism: Data from the German Registry for Congenital Hypothyroidism (HypoDok)

nork Thomann, Julia, Tittel, Sascha R., Voss, Egbert, Oeverink, Rudolf, Palm, Katja, Fricke-Otto, Susanne, Kapelari, Klaus, Holl, Reinhard W., Woelfle, Joachim, Bettendorf, Markus
Argitaratua izan da Int J Neonatal Screen (2021)

Evaluation of the EFNS/PNS diagnostic criteria in a cohort of CIDP patients

nork Athanasopoulos, Diamantis, Motte, Jeremias, Grüter, Thomas, Köse, Nuray, Yoon, Min‐Suk, Otto, Susanne, Schneider‐Gold, Christiane, Gold, Ralf, Fisse, Anna L., Pitarokoili, Kalliopi
Argitaratua izan da Ann Clin Transl Neurol (2021)

Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency

nork Montalbano, Antonino, Juergensen, Lonny, Roeth, Ralph, Weiss, Birgit, Fukami, Maki, Fricke‐Otto, Susanne, Binder, Gerhard, Ogata, Tsutomu, Decker, Eva, Nuernberg, Gudrun, Hassel, David, Rappold, Gudrun A
Argitaratua izan da EMBO Mol Med (2016)

Treatment response to cyclophosphamide, rituximab, and bortezomib in chronic immune-mediated sensorimotor neuropathies: a retrospective cohort study

nork Motte, Jeremias, Fisse, Anna Lena, Köse, Nuray, Grüter, Thomas, Mork, Hannah, Athanasopoulos, Diamantis, Fels, Miriam, Otto, Susanne, Siglienti, Ines, Schneider-Gold, Christiane, Hellwig, Kerstin, Yoon, Min-Suk, Gold, Ralf, Pitarokoili, Kalliopi
Argitaratua izan da Ther Adv Neurol Disord (2021)

Genotype/phenotype correlations in 538 congenital adrenal hyperplasia patients from Germany and Austria: discordances in milder genotypes and in screened versus prescreening patien...

nork Riedl, Stefan, Röhl, Friedrich-Wilhelm, Bonfig, Walter, Brämswig, Jürgen, Richter-Unruh, Annette, Fricke-Otto, Susanne, Bettendorf, Markus, Riepe, Felix, Kriegshäuser, Gernot, Schönau, Eckhard, Even, Gertrud, Hauffa, Berthold, Dörr, Helmuth-Günther, Holl, Reinhard W, Mohnike, Klaus
Argitaratua izan da Endocr Connect (2019)

Quality of Life of Short-Statured Children Born Small for Gestational Age or Idiopathic Growth Hormone Deficiency Within 1 Year of Growth Hormone Treatment

nork Quitmann, Julia, Bloemeke, Janika, Silva, Neuza, Bullinger, Monika, Witt, Stefanie, Akkurt, Ilker, Dunstheimer, Desiree, Vogel, Christian, Böttcher, Volker, Kuhnle Krahl, Ursula, Bettendorf, Markus, Schönau, Eckhard, Fricke-Otto, Susanne, Keller, Alexandra, Mohnike, Klaus, Dörr, Helmuth-Günther
Argitaratua izan da Front Pediatr (2019)

A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42)

nork Schlipf, Nina A, Beetz, Christian, Schüle, Rebecca, Stevanin, Giovanni, Erichsen, Anne Kjersti, Forlani, Sylvie, Zaros, Cécile, Karle, Kathrin, Klebe, Stephan, Klimpe, Sven, Durr, Alexandra, Otto, Susanne, Tallaksen, Chantal M E, Riess, Olaf, Brice, Alexis, Bauer, Peter, Schöls, Ludger
Argitaratua 2010

REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31

nork Beetz, Christian, Schüle, Rebecca, Deconinck, Tine, Tran-Viet, Khanh-Nhat, Zhu, Hui, Kremer, Berry P. H., Frints, Suzanna G. M., van Zelst-Stams, Wendy A. G., Byrne, Paula, Otto, Susanne, Nygren, Anders O. H., Baets, Jonathan, Smets, Katrien, Ceulemans, Berten, Dan, Bernard, Nagan, Narasimhan, Kassubek, Jan, Klimpe, Sven, Klopstock, Thomas, Stolze, Henning, Smeets, Hubert J. M., Schrander-Stumpel, Constance T. R. M., Hutchinson, Michael, van de Warrenburg, Bart P., Braastad, Corey, Deufel, Thomas, Pericak-Vance, Margaret, Schöls, Ludger, de Jonghe, Peter, Züchner, Stephan
Argitaratua 2008