Αποτελέσματα αναζήτησης - Tobias Lindig
- Εμφανίζονται 1 - 13 Αποτελέσματα από 13
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T1ρ‐based dynamic glucose‐enhanced (DGEρ) MRI at 3 T: method development and early clinical experience in the human brain από Kai Herz, Tobias Lindig, A Deshmane, Jens Schittenhelm, Marco Skardelly, Benjamin Bender, Ulrike Ernemann, Klaus Scheffler, Moritz Zaiß
Έκδοση 2019Artigo -
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DeepCEST 3T: Robust MRI parameter determination and uncertainty quantification with neural networks—application to CEST imaging of the human brain at 3T από Felix Glang, A Deshmane, Sergey Prokudin, Florian Martin, Kai Herz, Tobias Lindig, Benjamin Bender, Klaus Scheffler, Moritz Zaiß
Έκδοση 2019Artigo -
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Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia από Rebecca Schüle, Nina Schlipf, Matthis Synofzik, Stephan Klebe, Sven Klimpe, Ute Hehr, Beate Winner, Tobias Lindig, A Dotzer, Olaf Rieß, Jürgen Winkler, Lüdger Schöls, Peter Bauer
Έκδοση 2009Artigo -
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X-linked Charcot-Marie-Tooth disease, Arts syndrome, and prelingual non-syndromic deafness form a disease continuum: evidence from a family with a novel PRPS1 mutation από Matthis Synofzik, Jennifer Müller vom Hagen, Tobias B. Haack, Christian Wilhelm, Tobias Lindig, Stefanie Beck‐Wödl, Sander B. Nabuurs, André B. P. Kuilenburg, Arjan PM de Brouwer, Lüdger Schöls
Έκδοση 2014Artigo -
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Motor protein mutations cause a new form of hereditary spastic paraplegia από Andrés Caballero-Oteyza, Esra Battaloğlu, Levent Öcek, Tobias Lindig, Jennifer Reichbauer, Adriana Rebelo, Michael Gonzalez, Yaşar Zorlu, Burçak Özeş, Dagmar Timmann, Benjamin Bender, Günther Woehlke, Stephan Züchner, Lüdger Schöls, Rebecca Schüle
Έκδοση 2014Artigo -
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Mutations in SEC24D, Encoding a Component of the COPII Machinery, Cause a Syndromic Form of Osteogenesis Imperfecta από Lutz Garbes, Kyung‐Ho Kim, Angelika Rieß, Heike Hoyer‐Kuhn, Filippo Beleggia, Andrea Bevot, Mi Jeong Kim, Yang Hoon Huh, Hee-Seok Kweon, Ravi Savarirayan, David J. Amor, Purvi M. Kakadia, Tobias Lindig, Karl Oliver Kagan, Jutta Becker, Simeon A. Boyadjiev, Bernd Wollnik, Oliver Semler, Stefan K. Bohlander, Jin Oh Kim, Christian Netzer
Έκδοση 2015Artigo -
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FAHN/SPG35: a narrow phenotypic spectrum across disease classifications από Tim W. Rattay, Tobias Lindig, Jonathan Baets, Katrien Smets, Tine Deconinck, Anne S. Söhn, Konstanze Hörtnagel, Kathrin N. Eckstein, Sarah Wiethoff, Jennifer Reichbauer, Marion Döbler‐Neumann, Ingeborg Krägeloh‐Mann, Michaela Auer‐Grumbach, Barbara Plecko, Alexander Münchau, Bernd Wilken, Marc Janauschek, Anne‐Katrin Giese, Jan De Bleecker, Els Ortibus, Martine Debyser, Adolfo López de Munaín, Aurora Pujol, Maria Teresa Bassi, Maria Grazia D’Angelo, Peter De Jonghe, Stephan Züchner, Peter Bauer, Lüdger Schöls, Rebecca Schüle
Έκδοση 2019Artigo -
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Spinal cord damage in Friedreich’s ataxia: Results from the ENIGMA-Ataxia από Thiago Junqueira Ribeiro de Rezende, Isaac Adanyeguh, Filippo Arrigoni, Benjamin Bender, Fernando Cendes, Louise A. Corben, Andreas Deistung, Martin B. Delatycki, Imis Dogan, Gary F. Egan, Sophia Göricke, Nellie Georgiou‐Karistianis, Pierre‐Gilles Henry, Diane Hutter, Neda Jahanshad, James M. Joers, Christophe Lenglet, Tobias Lindig, Alberto RM Martinez, Andrea Martinuzzi, Gabriella Paparella, Denis Peruzzo, Kathrin Reetz, Sandro Romanzetti, Lüdger Schöls, Jörg B. Schulz, Matthis Synofzik, Sophia I. Thomopoulos, Paul M. Thompson, Dagmar Timmann, Ian H. Harding, Marcondes C. França
Έκδοση 2022Pré-impressão -
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Progressive Spinal Cord Degeneration in Friedreich's Ataxia: Results from <scp>ENIGMA‐Ataxia</scp> από Thiago Junqueira Ribeiro de Rezende, Isaac Adanyeguh, Filippo Arrigoni, Benjamin Bender, Fernando Cendes, Louise A. Corben, Andreas Deistung, Martin B. Delatycki, Imis Dogan, Gary F. Egan, Sophia Göricke, Nellie Georgiou‐Karistianis, Pierre‐Gilles Henry, Diane Hutter, Neda Jahanshad, James M. Joers, Christophe Lenglet, Tobias Lindig, Alberto Martínez, Andrea Martinuzzi, Gabriella Paparella, Denis Peruzzo, Kathrin Reetz, Sandro Romanzetti, Lüdger Schöls, Jörg B. Schulz, Matthis Synofzik, Sophia I. Thomopoulos, Paul M. Thompson, Dagmar Timmann, Ian H. Harding, Marcondes C. França
Έκδοση 2022Artigo -
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Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia από Martina Minnerop, Delia Kurzwelly, Holger Wagner, Anne S. Soehn, Jennifer Reichbauer, Feifei Tao, Tim W. Rattay, Michael Peitz, Kristina Rehbach, Alejandro Giorgetti, Angela Pyle, Holger Thiele, Janine Altmüller, Dagmar Timmann, Ilker Karaca, Martina Lennarz, Jonathan Baets, Holger Hengel, Matthis Synofzik, Burcu Atasu, Shawna Feely, Marina Kennerson, Claudia Stendel, Tobias Lindig, Michael Gonzalez, Rüdiger Stirnberg, Marc Sturm, Sandra Roeske, Johanna Jung, Peter Bauer, Ebba Lohmann, Stefan Herms, Stefanie Heilmann‐Heimbach, Garth A. Nicholson, Muhammad Mahanjah, Rajech Sharkia, Paolo Carloni, Oliver Brüstle, Thomas Klopstock, Katherine D. Mathews, Michael E. Shy, Peter De Jonghe, Patrick F. Chinnery, Rita Horváth, Jürgen Kohlhase, Ina Schmitt, Michael Wolf, Susanne Greschus, Katrin Amunts, Wolfgang Maier, Lüdger Schöls, Peter Nürnberg, Stephan Züchner, Thomas Klockgether, Alfredo Ramı́rez, Rebecca Schüle
Έκδοση 2017Artigo
Εργαλεία αναζήτησης:
Σχετικά θέματα
Biology
Medicine
Genetics
Psychology
Gene
Neuroscience
Computer science
Pathology
Phenotype
Artificial intelligence
Ataxia
Anatomy
Compound heterozygosity
Computer vision
Disease
Hereditary spastic paraplegia
Image (mathematics)
Mathematics
Missense mutation
Mutation
Physics
Psychiatry
Radiology
Sociology
Spinal cord
Algorithm
Allele
Amygdala
Anterior commissure
Arithmetic