Výsledky vyhledávání - Adeline Vanderver
- Zobrazuji výsledky 1 - 20 z 71
- Přejít na další stránku
-
1
JAK Inhibition in the Aicardi–Goutières Syndrome Autor Laura Adang, Raphaela Goldbach‐Mansky, Adeline Vanderver
Vydáno 2020Carta -
2
Therapies in Aicardi–Goutières syndrome Autor Yanick J. Crow, Adeline Vanderver, Simona Orcesi, Taco W. Kuijpers, Gillian Rice
Vydáno 2013Revisão -
3
Identification of a Novel de Novo p.Phe932Ile KCNT1 Mutation in a Patient With Leukoencephalopathy and Severe Epilepsy Autor Adeline Vanderver, Cas Simons, Johanna Schmidt, Philip Pearl, Miriam Bloom, Bennett Lavenstein, David S. Miller, Sean M. Grimmond, Ryan J. Taft
Vydáno 2013Artigo -
4
Recessive Mutations in POLR3B, Encoding the Second Largest Subunit of Pol III, Cause a Rare Hypomyelinating Leukodystrophy Autor Martine Tétreault, Karine Choquet, Simona Orcesi, Davide Tonduti, Umberto Balottin, Martin Teichmann, Sébastien Fribourg, Raphael Schiffmann, Bernard Brais, Adeline Vanderver, Geneviève Bernard
Vydáno 2011Artigo -
5
-
6
-
7
Neuroradiologic patterns and novel imaging findings in Aicardi-Goutières syndrome Autor Roberta La Piana, C. Uggetti, Federico Roncarolo, Adeline Vanderver, Ivana Olivieri, Davide Tonduti, Guy Helman, Umberto Balottin, Elisa Fazzi, Yanick J. Crow, John Livingston, Simona Orcesi
Vydáno 2015Artigo -
8
Leukodystrophy-associated POLR3A mutations down-regulate the RNA polymerase III transcript and important regulatory RNA BC200 Autor Karine Choquet, Diane Forget, Elisabeth Meloche, Marie‐Josée Dicaire, Geneviève Bernard, Adeline Vanderver, Raphael Schiffmann, Marc R. Fabian, Martin Teichmann, Benoit Coulombe, Bernard Brais, Claudia L. Kleinman
Vydáno 2019Artigo -
9
-
10
Magnetic resonance imaging pattern recognition in hypomyelinating disorders Autor Marjan E. Steenweg, Adeline Vanderver, Susan Blasér, Alberto Bizzi, Tom J. de Koning, Grazia M.S. Mancini, Wessel N. van Wieringen, Frederik Barkhof, Nicole I. Wolf, Marjo S. van der Knaap
Vydáno 2010Artigo -
11
<i>DARS</i> -associated leukoencephalopathy can mimic a steroid-responsive neuroinflammatory disorder Autor Nicole I. Wolf, Camilo Toro, Ilya Kister, Kartikasalwah Abd Latif, Richard J. Leventer, Amy Pizzino, Cas Simons, Truus E. M. Abbink, Ryan J. Taft, Marjo S. van der Knaap, Adeline Vanderver
Vydáno 2014Artigo -
12
Magnetic resonance imaging spectrum of succinate dehydrogenase–related infantile leukoencephalopathy Autor Guy Helman, Ljubica Caldovic, Matthew T. Whitehead, Cas Simons, Knut Brockmann, Simon Edvardson, Renkui Bai, Isabella Moroni, J. Michael Taylor, Keith Van Haren, Ryan J. Taft, Adeline Vanderver, Marjo S. van der Knaap
Vydáno 2015Artigo -
13
ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism Autor Sacha Ferdinandusse, Kim D. Falkenberg, Janet Koster, P. A. W. Mooyer, Richard O. Jones, Carlo W.T. van Roermund, Amy Pizzino, Michael Schrader, Ronald J. A. Wanders, Adeline Vanderver, Hans R. Waterham
Vydáno 2016Artigo -
14
Developmental Outcomes of Aicardi Goutières Syndrome Autor Laura Adang, Francesco Gavazzi, Micaela De Simone, Elisa Fazzi, Jessica Galli, Jamie Koh, Julia Kramer-Golinkoff, Valentina De Giorgis, Simona Orcesi, Kyle Peer, Nicole Ulrick, Sarah Woidill, Justine Shults, Adeline Vanderver
Vydáno 2019Artigo -
15
Lysosomal abnormalities in hereditary spastic paraplegia types <scp>SPG</scp> 15 and <scp>SPG</scp> 11 Autor Benoît Renvoisé, Jaerak Chang, Rajat Singh, Sayuri Yonekawa, Edmond J. FitzGibbon, Ami Mankodi, Adeline Vanderver, Alice B. Schindler, Camilo Toro, William A. Gahl, Don J. Mahuran, Craig Blackstone, Tyler Mark Pierson
Vydáno 2014Artigo -
16
Aicardi goutières syndrome is associated with pulmonary hypertension Autor Laura Adang, David B. Frank, Ahmed Gilani, Asako Takanohashi, Nicole Ulrick, Abigail Collins, Zachary Cross, Csaba Galambos, Guy Helman, Usama Kanaan, Stephanie Keller, Dawn M. Simon, Omar Sherbini, Brian D. Hanna, Adeline Vanderver
Vydáno 2018Artigo -
17
Hypomyelinating leukodystrophies: Translational research progress and prospects Autor Petra J. W. Pouwels, Adeline Vanderver, Geneviève Bernard, Nicole I. Wolf, Steffi F. Dreha‐Kulczewksi, Sean Deoni, Enrico Bertini, Alfried Kohlschütter, William D. Richardson, Charles ffrench‐Constant, Wolfgang Köhler, David H. Rowitch, A. James Barkovich
Vydáno 2014Revisão -
18
Comprehensive Immunophenotyping of Cerebrospinal Fluid Cells in Patients with Neuroimmunological Diseases Autor Sungpil Han, Yen Chih Lin, Tianxia Wu, Alan D. Salgado, Ina Mexhitaj, Simone C. Wuest, Elena Romm, Joan Ohayon, Raphaela Goldbach‐Mansky, Adeline Vanderver, Adriana Marques, Camilo Toro, Peter R. Williamson, Irene Cortese, Bibiana Bielekova
Vydáno 2014Artigo -
19
POLR3-Related Leukodystrophy: A Qualitative Study on Parents’ Experiences with the Healthcare System Autor Adam Le, Kelly-Ann Thibault, Pouneh Amir-Yazdani, Enrico Bertini, Francesco Nicita, Daniela Pohl, Sunita Venkateswaran, Stephanie Keller, Deborah L. Renaud, Dolores Gonzales Moron, Marcelo Kauffman, Danilo de Assis Pereira, Adeline Vanderver, Maxime Morsa, Geneviève Bernard
Vydáno 2025Artigo -
20
A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies Autor Sumit Parikh, Geneviève Bernard, Richard J. Leventer, Marjo S. van der Knaap, Johan Van Hove, Amy Pizzino, Nathan H. McNeill, Guy Helman, Cas Simons, Johanna Schmidt, William B. Rizzo, Marc C. Patterson, Ryan J. Taft, Adeline Vanderver
Vydáno 2014Revisão
Vyhledávací nástroje:
Související témata
Medicine
Biology
Genetics
Gene
Pathology
Disease
Internal medicine
Leukodystrophy
Mutation
Magnetic resonance imaging
Phenotype
Radiology
Psychiatry
White matter
Neuroscience
Pediatrics
Leukoencephalopathy
Compound heterozygosity
Immunology
Allele
Bioinformatics
Exome sequencing
Missense mutation
RNA
Atrophy
Central nervous system
Psychology
Ataxia
Immune system
Interferon