Ohcanbohtosat - Huebner, Angela

Triple A syndrome: two novel mutations in the AAAS gene Dahkki Thümmler, Susanne, Huebner, Angela, Baechler-Sadoul, Elisabeth

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Mutations of the AAAS gene in an Indian family with Allgrove's syndrome Dahkki Mukhopadhya, Ashis, Danda, Sumita, Huebner, Angela, Chacko, Ashok

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Identification of a novel putative interaction partner of the nucleoporin ALADIN Dahkki Jühlen, Ramona, Landgraf, Dana, Huebner, Angela, Koehler, Katrin

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Triple A patient cells suffering from mitotic defects fail to localize PGRMC1 to mitotic kinetochore fibers Dahkki Jühlen, Ramona, Landgraf, Dana, Huebner, Angela, Koehler, Katrin

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SAT-254 Combination of Octreotide and Dexamphetamine to Control Weight Gain in Pediatric Patients with Hypothalamic Obesity Dahkki Reschke, Felix, Knoefler, Ralf, Smitka, Martin, Huebner, Angela

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Triple A (Allgrove) syndrome: an unusual association with syringomyelia Dahkki Bizzarri, Carla, Benevento, Danila, Terzi, Cesare, Huebner, Angela, Cappa, Marco

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MON-175 Structural Instability as an Underlying Pathomechanism in Congenital Adrenal Hyperplasia Dahkki Meese, Nicolas, Paul, Pallabi Sil, Haslbeck, Martin, Huebner, Angela, Reisch, Nicole

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“Crying without tears” as an early diagnostic sign-post of triple A (Allgrove) syndrome: two case reports Dahkki Tibussek, Daniel, Ghosh, Sujal, Huebner, Angela, Schaper, Joerg, Mayatepek, Ertan, Koehler, Katrin

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Compensation for chronic oxidative stress in ALADIN null mice Dahkki Jühlen, Ramona, Peitzsch, Mirko, Gärtner, Sebastian, Landgraf, Dana, Eisenhofer, Graeme, Huebner, Angela, Koehler, Katrin

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MON-185 ACTH-Derived Peptide Antagonists as an Alternative Treatment Strategy for Congenital Adrenal Hyperplasia Dahkki Schubert, Tina, Nicke, Lennart, Schanze, André, Reisch, Nicole, Geyer, Armin, Koehler, Katrin, Huebner, Angela

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Role of ALADIN in Human Adrenocortical Cells for Oxidative Stress Response and Steroidogenesis Dahkki Jühlen, Ramona, Idkowiak, Jan, Taylor, Angela E., Kind, Barbara, Arlt, Wiebke, Huebner, Angela, Koehler, Katrin

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ALADIN is required for the production of fertile mouse oocytes Dahkki Carvalhal, Sara, Stevense, Michelle, Koehler, Katrin, Naumann, Ronald, Huebner, Angela, Jessberger, Rolf, Griffis, Eric R.

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SUN-222 Pre- and Post-Pubertal Reference Ranges for Oxygenated Androgens in Saliva Dahkki Adaway, Joanne, Eisenhofer, Graeme, Huebner, Angela, Krone, Nils, McTaggart, Malcolm, Peitzsch, Mirko, Keevil, Brian George

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The nucleoporin ALADIN regulates Aurora A localization to ensure robust mitotic spindle formation Dahkki Carvalhal, Sara, Ribeiro, Susana Abreu, Arocena, Miguel, Kasciukovic, Taciana, Temme, Achim, Koehler, Katrin, Huebner, Angela, Griffis, Eric R.

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Deficiency of Ferritin Heavy-Chain Nuclear Import in Triple A Syndrome Implies Nuclear Oxidative Damage as the Primary Disease Mechanism Dahkki Storr, Helen L., Kind, Barbara, Parfitt, David A., Chapple, J. Paul, Lorenz, M., Koehler, Katrin, Huebner, Angela, Clark, Adrian J. L.

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Mice Lacking the Nuclear Pore Complex Protein ALADIN Show Female Infertility but Fail To Develop a Phenotype Resembling Human Triple A Syndrome Dahkki Huebner, Angela, Mann, Philipp, Rohde, Elvira, Kaindl, Angela M., Witt, Martin, Verkade, Paul, Jakubiczka, Sibylle, Menschikowski, Mario, Stoltenburg-Didinger, Gisela, Koehler, Katrin

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Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation Dahkki Farag, Heba Gamal, Froehler, Sebastian, Oexle, Konrad, Ravindran, Ethiraj, Schindler, Detlev, Staab, Timo, Huebner, Angela, Kraemer, Nadine, Chen, Wei, Kaindl, Angela M

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Salbutamol-responsive limb-girdle congenital myasthenic syndrome due to a novel missense mutation and heteroallelic deletion in MUSK Dahkki Gallenmüller, Constanze, Müller-Felber, Wolfgang, Dusl, Marina, Stucka, Rolf, Guergueltcheva, Velina, Blaschek, Astrid, von der Hagen, Maja, Huebner, Angela, Müller, Juliane S., Lochmüller, Hanns, Abicht, Angela

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Cancer Stem Cells in Pheochromocytoma and Paraganglioma Dahkki Scriba, Laura D., Bornstein, Stefan R., Santambrogio, Alice, Mueller, Gregor, Huebner, Angela, Hauer, Julia, Schedl, Andreas, Wielockx, Ben, Eisenhofer, Graeme, Andoniadou, Cynthia L., Steenblock, Charlotte

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Diabetes and Neurodegeneration in Wolfram Syndrome: A multicenter study of phenotype and genotype Dahkki Rohayem, Julia, Ehlers, Christian, Wiedemann, Bärbel, Holl, Reinhard, Oexle, Konrad, Kordonouri, Olga, Salzano, Giuseppina, Meissner, Thomas, Burger, Walter, Schober, Edith, Huebner, Angela, Lee-Kirsch, Min Ae

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