Torthaí cuardaigh - Knöfler, Ralf

Strategies in Clinical and Laboratory Diagnosis of Inherited Platelet Function Disorders in Children de réir Knöfler, Ralf, Streif, Werner

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Investigations of Platelet Function in Whole Blood with BAPA as Anticoagulant de réir Tauer, Josephine Tabea, Lohse, Judith, König, Silvia, Knöfler, Ralf

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Real-Time Live Confocal Fluorescence Microscopy as a New Tool for Assessing Platelet Vitality de réir Hermann, Martin, Nussbaumer, Oliver, Knöfler, Ralf, Hengster, Paul, Nussbaumer, Walter, Streif, Werner

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Treatment of high-grade osteoblastic osteosarcoma of the humerus in a 5-year-old boy with cystic fibrosis: A case report de réir Okuda, Kenichi V., Hammermann, Jutta, Lange, Björn S., Fischer, Jana C., Thielemann, Falk, Knöfler, Ralf, Suttorp, Meinolf

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Novel Mutation in Bernard-Soulier Syndrome de réir Sandrock, Kirstin, Knöfler, Ralf, Greinacher, Andreas, Fürll, Birgitt, Gerisch, Sebastian, Schuler, Ulrich, Gehrisch, Siegmund, Busse, Anja, Zieger, Barbara

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Severe Bleeding Diathesis in Siblings with Platelet Dysfunction due to a Novel Nonsense RASGRP2 Mutation de réir Körholz, Julia, Lucas, Nadja, Boiti, Franziska, Althaus, Karina, Tiebel, Oliver, Fang, Mingyan, Berner, Reinhard, Lee-Kirsch, Min Ae, Knöfler, Ralf

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MEDB-34. A very rare case: medulloblastoma relapse with bone marrow infiltration in a toddler de réir Zinke, Claudia, Fleischhack, Gudrun, Hauer, Julia, Lange, Björn Sönke, Dörnemann, Jenny, Hahn, Gabriele, Schackert, Gabriele, Gurtner, Kristin, Meinhardt, Matthias, Jöhrens, Korinna, Knöfler, Ralf

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Risk factors for recurrent venous thromboembolism in the European collaborative paediatric database on cerebral venous thrombosis: a multicentre cohort study de réir Kenet, Gili, Kirkham, Fenella, Niederstadt, Thomas, Heinecke, Achim, Saunders, Dawn, Stoll, Monika, Brenner, Benjamin, Bidlingmaier, Christoph, Heller, Christine, Knöfler, Ralf, Schobess, Rosemarie, Zieger, Barbara, Sébire, Guillaume, Nowak-Göttl, Ulrike

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A rare PALB2 germline variant causing G2/M cell cycle arrest is associated with isolated myelosarcoma in infancy de réir Beer, Angelina, Beck, Ricardo, Schedel, Anne, von Bonin, Malte, Meinel, Jörn, Friedrich, Ulrike Anne, Menzel, Maria, Suttorp, Meinolf, Brenner, Sebastian, Fitze, Guido, Lange, Björn, Knöfler, Ralf, Hauer, Julia, Auer, Franziska

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Use of Targeted High-Throughput Sequencing for Genetic Classification of Patients with Bleeding Diathesis and Suspected Platelet Disorder de réir Andres, Oliver, König, Eva-Maria, Althaus, Karina, Bakchoul, Tamam, Bugert, Peter, Eber, Stefan, Knöfler, Ralf, Kunstmann, Erdmute, Manukjan, Georgi, Meyer, Oliver, Strauß, Gabriele, Streif, Werner, Thiele, Thomas, Wiegering, Verena, Klopocki, Eva, Schulze, Harald

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Correction of a Factor VIII genomic inversion with designer-recombinases de réir Lansing, Felix, Mukhametzyanova, Liliya, Rojo-Romanos, Teresa, Iwasawa, Kentaro, Kimura, Masaki, Paszkowski-Rogacz, Maciej, Karpinski, Janet, Grass, Tobias, Sonntag, Jan, Schneider, Paul Martin, Günes, Ceren, Hoersten, Jenna, Schmitt, Lukas Theo, Rodriguez-Muela, Natalia, Knöfler, Ralf, Takebe, Takanori, Buchholz, Frank

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One Gene, Many Facets: Multiple Immune Pathway Dysregulation in SOCS1 Haploinsufficiency de réir Körholz, Julia, Gabrielyan, Anastasia, Sowerby, John M., Boschann, Felix, Chen, Lan-Sun, Paul, Diana, Brandt, David, Kleymann, Janina, Kolditz, Martin, Toepfner, Nicole, Knöfler, Ralf, Jacobsen, Eva-Maria, Wolf, Christine, Conrad, Karsten, Röber, Nadja, Lee-Kirsch, Min Ae, Smith, Kenneth G. C., Mundlos, Stefan, Berner, Reinhard, Dalpke, Alexander H., Schuetz, Catharina, Rae, William

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Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia de réir Latham, Sharissa L., Ehmke, Nadja, Reinke, Patrick Y. A., Taft, Manuel H., Eicke, Dorothee, Reindl, Theresia, Stenzel, Werner, Lyons, Michael J., Friez, Michael J., Lee, Jennifer A., Hecker, Ramona, Frühwald, Michael C., Becker, Kerstin, Neuhann, Teresa M., Horn, Denise, Schrock, Evelin, Niehaus, Indra, Sarnow, Katharina, Grützmann, Konrad, Gawehn, Luzie, Klink, Barbara, Rump, Andreas, Chaponnier, Christine, Figueiredo, Constanca, Knöfler, Ralf, Manstein, Dietmar J., Di Donato, Nataliya

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Author Correction: Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia de réir Latham, Sharissa L., Ehmke, Nadja, Reinke, Patrick Y. A., Taft, Manuel H., Eicke, Dorothee, Reindl, Theresia, Stenzel, Werner, Lyons, Michael J., Friez, Michael J., Lee, Jennifer A., Hecker, Ramona, Frühwald, Michael C., Becker, Kerstin, Neuhann, Teresa M., Horn, Denise, Schrock, Evelin, Niehaus, Indra, Sarnow, Katharina, Grützmann, Konrad, Gawehn, Luzie, Klink, Barbara, Rump, Andreas, Chaponnier, Christine, Figueiredo, Constanca, Knöfler, Ralf, Manstein, Dietmar J., Di Donato, Nataliya

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