অনুসন্ধান ফলাফলগুলি - Heinz Jungbluth
- প্রদর্শন 1 - 20 ফলাফল এর 58
- পরবর্তী পৃষ্ঠায় যান
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Multi-minicore Disease অনুযায়ী Heinz Jungbluth
প্রকাশিত 2007Revisão -
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Central core disease অনুযায়ী Heinz Jungbluth
প্রকাশিত 2007Revisão -
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Pathogenic Mechanisms in Centronuclear Myopathies অনুযায়ী Heinz Jungbluth, Mathias Gautel
প্রকাশিত 2014Revisão -
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Congenital myopathies: not only a paediatric topic অনুযায়ী Heinz Jungbluth, Nicol C. Voermans
প্রকাশিত 2016Revisão -
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Centronuclear (myotubular) myopathy অনুযায়ী Heinz Jungbluth, Carina Wallgren‐Pettersson, Jocelyn Laporte
প্রকাশিত 2008Revisão -
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Vici syndrome: a review অনুযায়ী Susan Byrne, Carlo Dionisi‐Vici, Luke J. Smith, Mathias Gautel, Heinz Jungbluth
প্রকাশিত 2016Revisão -
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Congenital disorders of autophagy: an emerging novel class of inborn errors of neuro-metabolism অনুযায়ী Darius Ebrahimi‐Fakhari, Afshin Saffari, Lara Wahlster, Jenny Lu, Susan Byrne, Georg F. Hoffmann, Heinz Jungbluth, Mustafa Şahin
প্রকাশিত 2015Revisão -
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Polymyositis without Beneficial Response to Steroid Therapy: Should Miyoshi Myopathy be a Differential Diagnosis? অনুযায়ী R. Scalco, Paulo José Lorenzoni, David S. Lynch, William Alves Martins, Heinz Jungbluth, Rosaline C. M. Quinlivan, Jéfferson Becker, Henry Houlden
প্রকাশিত 2017Artigo -
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Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy অনুযায়ী Lilli Winter, Matthias Türk, Patrick N. Harter, Michel Mittelbronn, Cornelia Kornblum, Fiona Norwood, Heinz Jungbluth, Christian T. Thiel, Ursula Schlötzer‐Schrehardt, Rolf Schröder
প্রকাশিত 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 অনুযায়ী 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
প্রকাশিত 2025Artigo -
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Congenital myopathies অনুযায়ী 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
প্রকাশিত 2014Artigo -
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The spectrum of neurodevelopmental, neuromuscular and neurodegenerative disorders due to defective autophagy অনুযায়ী 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
প্রকাশিত 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 অনুযায়ী 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
প্রকাশিত 2023Artigo -
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Nebulin (NEB) mutations in a childhood onset distal myopathy with rods and cores uncovered by next generation sequencing অনুযায়ী 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
প্রকাশিত 2013Artigo -
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Fetal acetylcholine receptor inactivation syndrome অনুযায়ী 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
প্রকাশিত 2014Artigo -
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Stall in Canonical Autophagy-Lysosome Pathways Prompts Nucleophagy-Based Nuclear Breakdown in Neurodegeneration অনুযায়ী 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
প্রকাশিত 2017Artigo
অনুসন্ধান সাধনীগুলি:
সম্পর্কিত বিষয়
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