Search Results - Shoukier, Moneef
- Showing 1 - 8 results of 8
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1
Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia by Shoukier, Moneef, Neesen, Juergen, Sauter, Simone M, Argyriou, Loukas, Doerwald, Nadine, Pantakani, DV Krishna, Mannan, Ashraf U
Published 2009Text -
2
Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia by Shoukier, Moneef, Neesen, Juergen, Sauter, Simone M, Argyriou, Loukas, Doerwald, Nadine, Pantakani, DV Krishna, Mannan, Ashraf U
Published 2009Text -
3
Hereditary papillary renal cell carcinoma primarily diagnosed in a cervical lymph node: a case report of a 30-year-old woman with multiple metastases by Behnes, Carl Ludwig, Schlegel, Christina, Shoukier, Moneef, Magiera, Isabella, Henschke, Frank, Schwarz, Alexander, Bremmer, Felix, Loertzer, Hagen
Published 2013Text -
4
Germline deletion of CIN85 in humans with X chromosome–linked antibody deficiency by Keller, Baerbel, Shoukier, Moneef, Schulz, Kathrin, Bhatt, Arshiya, Heine, Ines, Strohmeier, Valentina, Speckmann, Carsten, Engels, Niklas, Warnatz, Klaus, Wienands, Jürgen
Published 2018Text -
5
LMNA Mutation in a Family with a Strong History of Sudden Cardiac Death by Keil, Laura, Berisha, Filip, Knappe, Dorit, Kubisch, Christian, Shoukier, Moneef, Kirchhof, Paulus, Fabritz, Larissa, Hellenbroich, Yorck, Woitschach, Rixa, Magnussen, Christina
Published 2022Text -
6
Generalized Arterial Calcification of Infancy Type 1 (GACI1): Identification of a Novel Pathogenic Variant (c.1715T>C (p.Leu572Ser)) by Bulfamante, Gaetano Pietro, Carpenito, Laura, Bragantini, Emma, Graziani, Silvia, Bellizzi, Maria, Bagowski, Christoph Peter, Shoukier, Moneef, Rivieri, Francesca, Soffiati, Massimo, Barbareschi, Mattia
Published 2021Text -
7
The transcription factor Bcl11b promotes both canonical and adaptive NK cell differentiation by Holmes, Tim D., Pandey, Ram Vinay, Helm, Eric Y., Schlums, Heinrich, Han, Hongya, Campbell, Tessa M., Drashansky, Theodore T., Chiang, Samuel, Wu, Cheng-Ying, Tao, Christine, Shoukier, Moneef, Tolosa, Eva, Von Hardenberg, Sandra, Sun, Miao, Klemann, Christian, Marsh, Rebecca A., Lau, Colleen M., Lin, Yin, Sun, Joseph C., Månsson, Robert, Cichocki, Frank, Avram, Dorina, Bryceson, Yenan T.
Published 2021Text -
8
BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells by Lessel, Davor, Gehbauer, Christina, Bramswig, Nuria C, Schluth-Bolard, Caroline, Venkataramanappa, Sathish, van Gassen, Koen L I, Hempel, Maja, Haack, Tobias B, Baresic, Anja, Genetti, Casie A, Funari, Mariana F A, Lessel, Ivana, Kuhlmann, Leonie, Simon, Ruth, Liu, Pentao, Denecke, Jonas, Kuechler, Alma, de Kruijff, Ineke, Shoukier, Moneef, Lek, Monkol, Mullen, Thomas, Lüdecke, Hermann-Josef, Lerario, Antonio M, Kobbe, Robin, Krieger, Thorsten, Demeer, Benedicte, Lebrun, Marine, Keren, Boris, Nava, Caroline, Buratti, Julien, Afenjar, Alexandra, Shinawi, Marwan, Guillen Sacoto, Maria J, Gauthier, Julie, Hamdan, Fadi F, Laberge, Anne-Marie, Campeau, Philippe M, Louie, Raymond J, Cathey, Sara S, Prinz, Immo, Jorge, Alexander A L, Terhal, Paulien A, Lenhard, Boris, Wieczorek, Dagmar, Strom, Tim M, Agrawal, Pankaj B, Britsch, Stefan, Tolosa, Eva, Kubisch, Christian
Published 2018Text