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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 20
2022
Yilmazer-Hanke, Deniz; Alami, Najwa Ouali; Fang, Lubin; Klotz, Sigried; Kovacs, Gabor G.; Pankratz, Helmut; Weis, Joachim; Katona, Istvan; Scheuerle, Angelika; Streit, Wolfgang J. und Del Tredici, Kelly
(2022):
Differential Glial Chitotriosidase 1 and Chitinase 3-like Protein 1 Expression in the Human Primary Visual Cortex and Cerebellum after Global Hypoxia-Ischemia.
In: Neuroscience, Bd. 506: S. 91-113
Jonigk, Danny; Werlein, Christopher; Acker, Till; Aepfelbacher, Martin; Amann, Kerstin U.; Baretton, Gustavo; Barth, Peter; Bohle, Rainer M.; Büttner, Andreas; Buettner, Reinhard; Dettmeyer, Reinhard; Eichhorn, Philip; Elezkurtaj, Sefer; Esposito, Irene; Evert, Katja; Evert, Matthias; Fend, Falko; Gassler, Nikolaus; Gattenloehner, Stefan; Glatzel, Markus; Göbel, Heike; Gradhand, Elise; Hansen, Torsten; Hartmann, Arndt; Heinemann, Axel; Heppner, Frank L.; Hilsenbeck, Julia; Horst, David; Kamp, Jan C.; Mall, Gita; Maerkl, Bruno; Ondruschka, Benjamin; Pablik, Jessica; Pfefferle, Susanne; Quaas, Alexander; Radbruch, Helena; Röcken, Christoph; Rosenwald, Andreas; Roth, Wilfried; Rudelius, Martina; Schirmacher, Peter; Slotta-Huspenina, Julia; Smith, Kevin; Sommer, Linna; Stock, Konrad; Ströbel, Philipp; Strobl, Stephanie; Titze, Ulf; Weirich, Gregor; Weis, Joachim; Werner, Martin; Wickenhauser, Claudia; Wiech, Thorsten; Wild, Peter; Welte, Tobias; Stillfried, Saskia von und Boor, Peter
(2022):
Organ manifestations of COVID-19: what have we learned so far (not only) from autopsies?
In: Virchows Archiv, Bd. 481, Nr. 2: S. 139-159
2021
Korinthenberg, Rudolf; Trollmann, Regina; Plecko, Barbara; Stettner, Georg M.; Blankenburg, Markus; Weis, Joachim; Schoser, Benedikt; Mueller-Felber, Wolfgang; Lochbuehler, Nina; Hahn, Gabriele und Rudnik-Schoeneborn, Sabine
(2021):
Differential Diagnosis of Acquired and Hereditary Neuropathies in Children and Adolescents-Consensus-Based Practice Guidelines.
In: Children-Basel, Bd. 8, Nr. 8, 687
Deschauer, Marcus; Hengel, Holger; Rupprich, Katrin; Kreiss, Martina; Schlotter-Weigel, Beate; Grimmel, Mona; Admard, Jakob; Schneider, Ilka; Alhaddad, Bader; Gazou, Anastasia; Sturm, Marc; Vorgerd, Matthias; Balousha, Ghassan; Balousha, Osama; Falna, Mohammed; Kirschke, Jan S.; Kornblum, Cornelia; Jordan, Berit; Kraya, Torsten; Strom, Tim M.; Weis, Joachim; Schoels, Ludger; Schara, Ulrike; Zierz, Stephan; Riess, Olaf; Meitinger, Thomas und Haack, Tobias B.
(2021):
Bi-allelic truncating mutations in VWA1 cause neuromyopathy.
In: Brain, Bd. 144: S. 574-583
2020
Herschbach, Peter; Britzelmeir, Ingrid; Dinkel, Andreas; Giesler, Jürgen M.; Herkommer, Kathleen; Nest, Alexandra; Pichler, Theresia; Reichelt, Ralf; Tanzer-Kuentzer, Sylvia; Weis, Joachim und Marten-Mittag, Birgitt
(2020):
Distress in cancer patients: Who are the main groups at risk?
In: Psycho-Oncology, Bd. 29, Nr. 4: S. 703-710
2019
Brenner, David; Rosenbohm, Angela; Yilmaz, Ruestem; Mueller, Kathrin; Grehl, Torsten; Petri, Susanne; Meyer, Thomas; Grosskreutz, Julian; Weydt, Patrick; Ruf, Wolfgang; Neuwirth, Christoph; Weber, Markus; Pinto, Susana; Claeys, Kristl G.; Schrank, Berthold; Jordan, Berit; Knehr, Antje; Guenther, Kornelia; Huebers, Annemarie; Zeller, Daniel; Kubisch, Christian; Jablonka, Sibylle; Sendtner, Michael; Klopstock, Thomas; de Carvalho, Mamede; Sperfeld, Anne; Borck, Guntram; Volk, Alexander E.; Dorst, Johannes; Weis, Joachim; Otto, Markus; Schuster, Joachim; Del Tredici, Kelly; Braak, Heiko; Danzer, Karin M.; Freischmidt, Axel; Meitinger, Thomas; Ludolph, Albert C.; Andersen, Peter M.; Weishaupt, Jochen H.; Weyen, Ute; Hermann, Andreas; Winkler, Juergen; Hagenacker, Tim; Koch, Jan Christoph; Lingor, Paul; Goericke, Bettina; Zierz, Stephan; Baum, Petra; Wolf, Joachim; Winkler, Andrea; Young, Peter; Bogdahn, Ulrich; Prudlo, Johannes und Kassubek, Jan
(2019):
Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations.
In: Brain, Bd. 142, e67
[PDF, 190kB]
Fischbach, Felix; Nedelcu, Julia; Leopold, Patrizia; Zhan, Jiangshan; Clarner, Tim; Nellessen, Lara; Beissel, Christian; van Heuvel, Yasemin; Goswami, Anand; Weis, Joachim; Denecke, Bernd; Schmitz, Christoph; Hochstrasser, Tanja; Nyamoya, Stella; Victor, Marion; Beyer, Cordian und Kipp, Markus
(2019):
Cuprizone-induced graded oligodendrocyte vulnerability is regulated by the transcription factor DNA damage-inducible transcript 3.
In: Glia, Bd. 67, Nr. 2: S. 263-276
Koelbel, Heike; Abicht, Angela; Schwartz, Oliver; Katona, Istvan; Paulus, Werner; Neuen-Jacob, Eva; Weis, Joachim und Schara, Ulrike
(2019):
Characteristic clinical and ultrastructural findings in nesprinopathies.
In: European Journal of Paediatric Neurology, Bd. 23, Nr. 2: S. 254-261
Stengel, Helena; Vural, Atay; Brunder, Anna-Michelle; Heinius, Annika; Appeltshauser, Luise; Fiebig, Bianca; Giese, Florian; Dresel, Christian; Papagianni, Aikaterini; Birklein, Frank; Weis, Joachim; Huchtemann, Tessa; Schmidt, Christian; Koertvelyessy, Peter; Villmann, Carmen; Meinl, Edgar; Sommer, Claudia; Leypoldt, Frank und Doppler, Kathrin
(2019):
Anti-pan-neurofascin IgG3 as a marker of fulminant autoimmune neuropathy.
In: Neurology-Neuroimmunology & Neuroinflammation, Bd. 6, Nr. 5, e603
2018
Vettermann, Franziska J.; Felsberg, Jörg; Reifenberger, Guido; Hasselblatt, Martin; Forbrig, Robert; Berding, Georg; la Fougere, Christian; Galldiks, Norbert; Schittenhelm, Jens; Weis, Joachim; Albert, Nathalie L. 
ORCID: https://orcid.org/0000-0003-0953-7624 und Schüller, Ulrich
(2018):
Characterization of Diffuse Gliomas With Histone H3-G34 Mutation by MRI and Dynamic 18F-FET PET.
In: Clinical Nuclear Medicine, Bd. 43, Nr. 12: S. 895-898
[PDF, 0B]
ORCID: https://orcid.org/0000-0003-0953-7624 und Schüller, Ulrich
(2018):
Characterization of Diffuse Gliomas With Histone H3-G34 Mutation by MRI and Dynamic 18F-FET PET.
In: Clinical Nuclear Medicine, Bd. 43, Nr. 12: S. 895-898
[PDF, 0B]
Vill, Katharina; Müller-Felber, Wolfgang; Gläser, Dieter; Kuhn, Marius; Teusch, Veronika; Schreiber, Herbert; Weis, Joachim; Klepper, Jörg; Schirmacher, Anja; Blaschek, Astrid; Wiessner, Manuela; Strom, Tim M.; Draeger, Bianca; Hofmeister-Kiltz, Kristina; Tacke, Moritz; Gerstl, Lucia; Young, Peter; Horvath, Rita und Senderek, Jan
(2018):
SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy.
In: Human Genetics, Bd. 137, Nr. 11-12: S. 911-919
Emons, Guenter; Steiner, Eric; Vordermark, Dirk; Uleer, Christoph; Bock, Nina; Paradies, Kerstin; Ortmann, Olaf; Aretz, Stefan; Mallmann, Peter; Kurzeder, Christian; Hagen, Volker; Oorschot, Birgitt van; Hoecht, Stefan; Feyer, Petra; Egerer, Gerlinde; Friedrich, Michael; Cremer, Wolfgang; Prott, Franz-Josef; Horn, Lars-Christian; Prompeler, Heinrich; Langrehr, Jan; Leinung, Steffen; Beckmann, Matthias W.; Kimmig, Rainer; Letsch, Anne; Reinhardt, Michael; Alt-Epping, Bernd; Kiesel, Ludwig; Menke, Jan; Gebhardt, Marion; Steinke-Lange, Verena; Rahner, Nils; Lichtenegger, Werner; Zeimet, Alain; Hanf, Volker; Weis, Joachim; Müller, Michael; Henscher, Ulla; Schmutzler, Rita K.; Meindl, Alfons; Hilpert, Felix; Panke, Joan Elisabeth; Strnad, Vratislav; Niehues, Christiane; Dauelsberg, Timm; Niehoff, Peter; Mayr, Doris; Grab, Dieter; Kreissl, Michael; Witteler, Ralf; Schorsch, Annemarie; Mustea, Alexander; Petru, Edgar; Hübner, Jutta; Rose, Anne Derke; Wight, Edward; Tholen, Reina; Bauerschmitz, Gerd J.; Fleisch, Markus; Juhasz-Boess, Ingolf; Lax, Sigurd; Runnebaum, Ingo; Tempfer, Clemens; Nothacker, Monika J.; Bloedt, Susanne; Follmann, Markus; Langer, Thomas; Raatz, Heike; Wesselmann, Simone und Erdogan, Saskia
(2018):
Interdisciplinary Diagnosis, Therapy and Follow-up of Patients with Endometrial Cancer. Guideline (S3-Level, AWMF Registry Number 032/034-OL, April 2018) - Part 2 with Recommendations on the Therapy and Follow-up of Endometrial Cancer, Palliative Care, Psycho-oncological/Psychosocial Care/Rehabilitation/Patient Information and Healthcare Facilities.
In: Geburtshilfe und Frauenheilkunde, Bd. 78, Nr. 11: S. 1089-1109
Emons, Guenter; Steiner, Eric; Vordermark, Dirk; Uleer, Christoph; Bock, Nina; Paradiess, Kerstin; Ortmann, Olaf; Aretz, Stefan; Mallmann, Peter; Kurzeder, Christian; Hagen, Volker; Oorschot, Birgitt van; Hoecht, Stefan; Feyer, Petra; Egerer, Gerlinde; Friedrich, Michael; Cremer, Wolfgang; Prott, Franz-Josef; Horn, Lars-Christian; Proempeler, Heinrich; Langrehr, Jan; Leinung, Steffen; Beckmann, Matthias W.; Kimmig, Rainer; Letsch, Anne; Reinhardt, Michael; Alt-Epping, Bernd; Kiesel, Ludwig; Menke, Jan; Gebhardt, Marion; Steinke-Lange, Verena; Rahner, Nils; Lichtenegger, Werner; Zeimet, Alain; Hanf, Volker; Weis, Joachim; Müller, Michael; Henscher, Ulla; Schmutzler, Rita K.; Meindl, Alfons; Hilpert, Felix; Panke, Joan Elisabeth; Strnad, Vratislav; Niehues, Christiane; Dauelsberg, Timm; Niehoff, Peter; Mayr, Doris; Grab, Dieter; Kreissl, Michael; Witteler, Ralf; Schorsch, Annemarie; Mustea, Alexander; Petru, Edgar; Hübner, Jutta; Rose, Anne Derke; Wight, Edward; Tholen, Reina; Bauerschmitz, Gerd J.; Fleisch, Markus; Juhasz-Boess, Ingolf; Sigurd, Lax; Runnebaum, Ingo; Tempfer, Clemens; Nothacker, Monika J.; Bloedt, Susanne; Follmann, Markus; Langer, Thomas; Raatz, Heike; Wesselmann, Simone und Erdogan, Saskia
(2018):
Interdisciplinary Diagnosis, Therapy and Follow-up of Patients with Endometrial Cancer. Guideline (S3-Level, AWMF Registry Nummer 032/034-OL, April 2018) - Part 1 with Recommendations on the Epidemiology, Screening, Diagnosis and Hereditary Factors of Endometrial Cancer.
In: Geburtshilfe und Frauenheilkunde, Bd. 78, Nr. 10: S. 949-970
Esser, Peter; Hartung, Tim J.; Friedrich, Michael; Johansen, Christoffer; Wittchen, Hans-Ulrich; Faller, Hermann; Koch, Uwe; Härter, Martin; Keller, Monika; Schulz, Holger; Wegscheider, Karl; Weis, Joachim und Mehnert, Anja
(2018):
The Generalized Anxiety Disorder Screener (GAD-7) and the anxiety module of the Hospital and Depression Scale (HADS-A) as screening tools for generalized anxiety disorder among cancer patients.
In: Psycho-Oncology, Bd. 27, Nr. 6: S. 1509-1516
Müller, Kathrin; Brenner, David; Weydt, Patrick; Meyer, Thomas; Grehl, Torsten; Petri, Susanne; Grosskreutz, Julian; Schuster, Joachim; Volk, Alexander E.; Borck, Guntram; Kubisch, Christian; Klopstock, Thomas; Zeller, Daniel; Jablonka, Sibylle; Sendtner, Michael; Klebe, Stephan; Knehr, Antje; Günther, Kornelia; Weis, Joachim; Claeys, Kristl G.; Schrank, Berthold; Sperfeld, Anne-Dorte; Hübers, Annemarie; Otto, Markus; Dorst, Johannes; Meitinger, Thomas; Strom, Tim M.; Andersen, Peter M.; Ludolph, Albert C. und Weishaupt, Jochen H.
(2018):
Comprehensive analysis of the mutation spectrum in 301 German ALS families.
In: Journal of Neurology Neurosurgery and Psychiatry, Bd. 89, Nr. 8: S. 817-827
[PDF, 637kB]
Naumann, Marcel; Pal, Arun; Goswami, Anand; Lojewski, Xenia; Japtok, Julia; Vehlow, Anne; Naujock, Maximilian; Günther, Rene; Jin, Mengmeng; Stanslowsky, Nancy; Reinhardt, Peter; Sterneckert, Jared; Frickenhaus, Marie; Pan-Montojo, Francisco; Storkebaum, Erik; Poser, Ina; Freischmidt, Axel; Weishaupt, Jochen H.; Holzmann, Karlheinz; Troost, Dirk; Ludolph, Albert C.; Böckers, Tobias M.; Liebau, Stefan; Petri, Susanne; Cordes, Nils; Hyman, Anthony A.; Wegner, Florian; Grill, Stephan W.; Weis, Joachim; Storch, Alexander und Hermann, Andreas
(2018):
Impaired DNA damage response signaling by FUS-NLS mutations leads to neurodegeneration and FUS aggregate formation.
In: Nature Communications, Bd. 9, 335
[PDF, 6MB]
2017
Brauers, Eva; Roos, Andreas; Kollipara, Laxmikanth; Zahedi, René P.; Beckmann, Alf; Mohanadas, Nilane; Bauer, Hartmut; Häusler, Martin; Thoma, Stéphanie; Kress, Wolfram; Senderek, Jan und Weis, Joachim
(2017):
The Caveolin-3 G56S sequence variant of unknown significance: Muscle biopsy findings and functional cell biological analysis.
In: Proteomics Clinical Applications, Bd. 11, Nr. 43132, 1600007
Kollipara, Laxmikanth; Buchkremer, Stephan; Coraspe, Jose Andres Gonzalez; Hathazi, Denisa; Senderek, Jan; Weis, Joachim; Zahedi, Rene P. und Roos, Andreas
(2017):
In-depth phenotyping of lymphoblastoid cells suggests selective cellular vulnerability in Marinesco-Sjogren syndrome.
In: Oncotarget, Bd. 8, Nr. 40: S. 68493-68516
Weis, Joachim; Claeys, Kristl G.; Roos, Andreas; Azzedine, Hamid; Katona, Istvan; Schröder, J. Michael und Senderek, Jan
(2017):
Towards a functional pathology of hereditary neuropathies.
In: Acta Neuropathologica, Bd. 133, Nr. 4: S. 493-515
2016
Altmann, Judith; Büchner, Boriana; Nadaj-Pakleza, Aleksandra; Schäfer, Jochen; Jackson, Sandra; Lehmann, Diana; Deschauer, Marcus; Kopajtich, Robert; Lautenschläger, Ronald; Kuhn, Klaus A.; Karle, Kathrin; Schöls, Ludger; Schulz, Jörg B.; Weis, Joachim; Prokisch, Holger; Kornblum, Cornelia; Claeys, Kristl G. und Klopstock, Thomas
(2016):
Expanded phenotypic spectrum of the m.8344A > G "MERRF" mutation: data from the German mitoNET registry.
In: Journal of Neurology, Bd. 263, Nr. 5: S. 961-972