Ohcanbohtosat - Heinz Jungbluth
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Multi-minicore Disease Dahkki Heinz Jungbluth
Almmustuhtton 2007Revisão -
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Central core disease Dahkki Heinz Jungbluth
Almmustuhtton 2007Revisão -
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Pathogenic Mechanisms in Centronuclear Myopathies Dahkki Heinz Jungbluth, Mathias Gautel
Almmustuhtton 2014Revisão -
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Congenital myopathies: not only a paediatric topic Dahkki Heinz Jungbluth, Nicol C. Voermans
Almmustuhtton 2016Revisão -
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Centronuclear (myotubular) myopathy Dahkki Heinz Jungbluth, Carina Wallgren‐Pettersson, Jocelyn Laporte
Almmustuhtton 2008Revisão -
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Vici syndrome: a review Dahkki Susan Byrne, Carlo Dionisi‐Vici, Luke J. Smith, Mathias Gautel, Heinz Jungbluth
Almmustuhtton 2016Revisão -
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Congenital disorders of autophagy: an emerging novel class of inborn errors of neuro-metabolism Dahkki Darius Ebrahimi‐Fakhari, Afshin Saffari, Lara Wahlster, Jenny Lu, Susan Byrne, Georg F. Hoffmann, Heinz Jungbluth, Mustafa Şahin
Almmustuhtton 2015Revisão -
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Polymyositis without Beneficial Response to Steroid Therapy: Should Miyoshi Myopathy be a Differential Diagnosis? Dahkki R. Scalco, Paulo José Lorenzoni, David S. Lynch, William Alves Martins, Heinz Jungbluth, Rosaline C. M. Quinlivan, Jéfferson Becker, Henry Houlden
Almmustuhtton 2017Artigo -
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Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy Dahkki Lilli Winter, Matthias Türk, Patrick N. Harter, Michel Mittelbronn, Cornelia Kornblum, Fiona Norwood, Heinz Jungbluth, Christian T. Thiel, Ursula Schlötzer‐Schrehardt, Rolf Schröder
Almmustuhtton 2016Artigo -
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Integrated single‐cell functional‐proteomic profiling reveals a shift in myofibre specificity in human nemaline myopathy: A proof‐of‐principle study Dahkki Robert A. Seaborne, Roger Moreno‐Justicia, Jenni Laitila, Christopher T. A. Lewis, Lola Savoure, Edmar Zanoteli, Michael W. Lawlor, Heinz Jungbluth, Atul S. Deshmukh, Julien Ochala
Almmustuhtton 2025Artigo -
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Congenital myopathies Dahkki Irene Colombo, Mariacristina Scoto, Adnan Y. Manzur, S. Robb, Lorenzo Maggi, Vasantha Gowda, Thomas Cullup, Michael Yau, Rahul Phadke, Caroline A. Sewry, Heinz Jungbluth, Francesco Muntoni
Almmustuhtton 2014Artigo -
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The spectrum of neurodevelopmental, neuromuscular and neurodegenerative disorders due to defective autophagy Dahkki Celine Deneubourg, Mauricio Ramm, Luke J. Smith, Olga Baron, Kritarth Singh, Susan Byrne, Michael R. Duchen, Mathias Gautel, Eeva‐Liisa Eskelinen, Manolis Fanto, Heinz Jungbluth
Almmustuhtton 2021Artigo -
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Abnormal myosin post‐translational modifications and <scp>ATP</scp> turnover time associated with human congenital myopathy‐related <i>RYR1</i> mutations Dahkki Alexander Sonne, Anna Katarina Antonovic, Elise G. Melhedegaard, Fariha Akter, Jesper L. Andersen, Heinz Jungbluth, Nanna Witting, John Vissing, Edmar Zanoteli, Arianna Fornili, Julien Ochala
Almmustuhtton 2023Artigo -
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Nebulin (NEB) mutations in a childhood onset distal myopathy with rods and cores uncovered by next generation sequencing Dahkki Mariacristina Scoto, Thomas Cullup, Sebahattin Çirak, Shu Yau, Adnan Y. Manzur, Lucy Feng, Thomas S. Jacques, Glenn Anderson, Stephen Abbs, Caroline A. Sewry, Heinz Jungbluth, Francesco Muntoni
Almmustuhtton 2013Artigo -
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Fetal acetylcholine receptor inactivation syndrome Dahkki Yael Hacohen, Leslie Jacobson, Susan Byrne, Fiona Norwood, Abhimanu Lall, S. Robb, Robertino Dilena, Monica Fumagalli, Alfred Peter Born, D Clarke, Ming Lim, Angela Vincent, Heinz Jungbluth
Almmustuhtton 2014Artigo -
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Stall in Canonical Autophagy-Lysosome Pathways Prompts Nucleophagy-Based Nuclear Breakdown in Neurodegeneration Dahkki Olga Baron, Adel Boudi, Catarina Dias, Michael Schilling, Anna Nölle, Gema Vizcay‐Barrena, Ivan Rattray, Heinz Jungbluth, Wiep Scheper, Roland A. Fleck, Gillian P. Bates, Manolis Fanto
Almmustuhtton 2017Artigo
Ohcanreaiddut:
Laktáseaddji fáttát
Medicine
Biology
Genetics
Internal medicine
Gene
Myopathy
Pathology
RYR1
Ryanodine receptor
Biopsy
Muscle biopsy
Cell biology
Congenital myopathy
Mutation
Skeletal muscle
Endocrinology
Anatomy
Malignant hyperthermia
Pediatrics
Receptor
Neuroscience
Surgery
Central core disease
Disease
Phenotype
Bioinformatics
Rhabdomyolysis
Weakness
Calcium
Hypotonia