Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Claire Cannet"'
Autor:
Rubén Gil-Redondo, Ricardo Conde, Chiara Bruzzone, Maria Luisa Seco, Maider Bizkarguenaga, Beatriz González-Valle, Angela de Diego, Ana Laín, Hansjörg Habisch, Christoph Haudum, Nicolas Verheyen, Barbara Obermayer-Pietsch, Sara Margarita, Serena Pelusi, Ignacio Verde, Nádia Oliveira, Adriana Sousa, Amaia Zabala-Letona, Aida Santos-Martin, Ana Loizaga-Iriarte, Miguel Unda-Urzaiz, Jasmin Kazenwadel, Georgy Berezhnoy, Tobias Geisler, Meinrad Gawaz, Claire Cannet, Hartmut Schäfer, Tammo Diercks, Christoph Trautwein, Arkaitz Carracedo, Tobias Madl, Luca Valenti, Manfred Spraul, Shelly C. Lu, Nieves Embade, José M. Mato, Oscar Millet
Publikováno v:
Cardiovascular Diabetology, Vol 23, Iss 1, Pp 1-13 (2024)
Abstract Background Metabolic syndrome (MetS) is a cluster of medical conditions and risk factors correlating with insulin resistance that increase the risk of developing cardiometabolic health problems. The specific criteria for diagnosing MetS vary
Externí odkaz:
https://doaj.org/article/0f7d4a04add1447884a54f4d9ce65b6c
Autor:
Jasmin Kazenwadel, Georgy Berezhnoy, Claire Cannet, Hartmut Schäfer, Tobias Geisler, Anne-Katrin Rohlfing, Meinrad Gawaz, Uta Merle, Christoph Trautwein
Publikováno v:
Communications Medicine, Vol 3, Iss 1, Pp 1-15 (2023)
Abstract Background Diagnostic approaches like the nuclear magnetic resonance spectroscopy (NMR) based quantification of metabolites, lipoproteins, and inflammation markers has helped to identify typical alterations in the blood serum of COVID-19 pat
Externí odkaz:
https://doaj.org/article/18f49d0ac08c4a6ab88add1ec1b43ffb
Autor:
Georgy Berezhnoy, Rosi Bissinger, Anna Liu, Claire Cannet, Hartmut Schäfer, Katharina Kienzle, Michael Bitzer, Helene Häberle, Siri Göpel, Christoph Trautwein, Yogesh Singh
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
BackgroundDeep metabolomic, proteomic and immunologic phenotyping of patients suffering from an infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have matched a wide diversity of clinical symptoms with potential biomarkers f
Externí odkaz:
https://doaj.org/article/b1db5699b92f44e995fff750384a84cc
Autor:
Gyuntae Bae, Georgy Berezhnoy, André Koch, Claire Cannet, Hartmut Schäfer, Stefan Kommoss, Sara Brucker, Nicolas Beziere, Christoph Trautwein
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2023)
Background: Traditional diagnosis is based on histology or clinical-stage classification which provides no information on tumor metabolism and inflammation, which, however, are both hallmarks of cancer and are directly associated with prognosis and s
Externí odkaz:
https://doaj.org/article/04cc526505d84e9794ad1a8f4cbe9995
Autor:
Lucia Laugwitz, Laimdota Zizmare, Vidiyaah Santhanakumaran, Claire Cannet, Judith Böhringer, Jürgen G. Okun, Manfred Spraul, Ingeborg Krägeloh‐Mann, Samuel Groeschel, Christoph Trautwein
Publikováno v:
JIMD Reports, Vol 63, Iss 2, Pp 168-180 (2022)
Abstract Metachromatic leukodystrophy (MLD) is a lysosomal storage disease caused by a deficiency of the arylsulfatase A (ARSA). ARSA deficiency leads to an accumulation of sulfatides primarily in the nervous system ultimately causing demyelination.
Externí odkaz:
https://doaj.org/article/0f1efdd0ccc549398ca53844ee8f0043
Autor:
Matteo Stocchero, Claire Cannet, Claudia Napoli, Elena Demetrio, Eugenio Baraldi, Giuseppe Giordano
Publikováno v:
Metabolites, Vol 13, Iss 9, p 1029 (2023)
Low-field (LF) benchtop NMR is a new family of instruments available on the market, promising for fast metabolic fingerprinting and targeted quantification of specific metabolites despite a lack of sensitivity and resolution with respect to high-fiel
Externí odkaz:
https://doaj.org/article/fc82defb131c4474baff9a542cb59b20
Autor:
Afshin Saffari, Claire Cannet, Astrid Blaschek, Andreas Hahn, Georg F. Hoffmann, Jessika Johannsen, Romy Kirsten, Musa Kockaya, Stefan Kölker, Wolfgang Müller-Felber, Andreas Roos, Hartmut Schäfer, Ulrike Schara, Manfred Spraul, Friedrich K. Trefz, Katharina Vill, Wolfgang Wick, Markus Weiler, Jürgen G. Okun, Andreas Ziegler
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-16 (2021)
Abstract Background 5q spinal muscular atrophy (SMA) is a disabling and life-limiting neuromuscular disease. In recent years, novel therapies have shown to improve clinical outcomes. Yet, the absence of reliable biomarkers renders clinical assessment
Externí odkaz:
https://doaj.org/article/d1420f1c464d4e51b184e3fd1fc57e55
Autor:
Claire Cannet, Allan Bayat, Georg Frauendienst-Egger, Peter Freisinger, Manfred Spraul, Nastassja Himmelreich, Musa Kockaya, Kirsten Ahring, Markus Godejohann, Anita MacDonald, Friedrich Trefz
Publikováno v:
Molecules, Vol 28, Iss 13, p 4916 (2023)
Phenylketonuria (PKU) is a rare metabolic disorder caused by mutations in the phenylalanine hydroxylase gene. Depending on the severity of the genetic mutation, medical treatment, and patient dietary management, elevated phenylalanine (Phe) may occur
Externí odkaz:
https://doaj.org/article/79d4e93690414af8a5b7ad7677919e00
Autor:
Chiara Bruzzone, Rubén Gil-Redondo, Marisa Seco, Rocío Barragán, Laura de la Cruz, Claire Cannet, Hartmut Schäfer, Fang Fang, Tammo Diercks, Maider Bizkarguenaga, Beatriz González-Valle, Ana Laín, Arantza Sanz-Parra, Oscar Coltell, Ander López de Letona, Manfred Spraul, Shelly C. Lu, Elisabetta Buguianesi, Nieves Embade, Quentin M. Anstee, Dolores Corella, José M. Mato, Oscar Millet
Publikováno v:
Cardiovascular Diabetology, Vol 20, Iss 1, Pp 1-13 (2021)
Abstract Background Metabolic syndrome (MetS) is a multimorbid long-term condition without consensual medical definition and a diagnostic based on compatible symptomatology. Here we have investigated the molecular signature of MetS in urine. Methods
Externí odkaz:
https://doaj.org/article/fdd2825fb92b43c38b52b9294746026e
Autor:
Claire Cannet, Andrea Pilotto, Júlio César Rocha, Hartmut Schäfer, Manfred Spraul, Daniela Berg, Peter Nawroth, Christian Kasperk, Gwendolyn Gramer, Dorothea Haas, David Piel, Stefan Kölker, Georg Hoffmann, Peter Freisinger, Friedrich Trefz
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)
Abstract Background Phenylketonuria (PKU; OMIM#261600) is a rare metabolic disorder caused by mutations in the phenylalanine hydroxylase (PAH) gene resulting in high phenylalanine (Phe) in blood and brain. If not treated early this results in intelle
Externí odkaz:
https://doaj.org/article/8b6f46eb86264e03ba005cf5a9db5cf9