Le catene muscolari by Leopold Busquet, , available at Book Depository with free delivery worldwide. Discover Book Depository’s huge selection of Leopold-Busquet books online. Free delivery worldwide MichÈle Busquet-vanderheyden Le catene muscolari. Catene muscolari: 8: Michèle Busquet-Vanderheyden, M. De Rubeis, M. Lauribe, L. Hangarol: : Books.
|Published (Last):||8 June 2007|
|PDF File Size:||13.18 Mb|
|ePub File Size:||19.52 Mb|
|Price:||Free* [*Free Regsitration Required]|
Molte condizioni fisio-patologiche possono causare una riduzione della massa muscolare. L’atrofia muscolare patologica non va confusa con la normale riduzione della massa e della forza muscolare che si verifica nell’invecchiamento.
In particolare possono essere utili, a seconda dei casi:. L’atrofia muscolare esprime un’alterazione del normale rapporto fra sintesi e degradazione delle proteine. In particolare, in questa condizione si verifica un’inibizione della sintesi proteica e un’attivazione del busqust catabolismo.
Atrofia muscolare – Wikipedia
In questo sistema, alcune proteine destinate alla distruzione sono marcate dal legame con almeno quattro copie di un piccolo peptide chiamato ubiquitina. L’atrofia muscolare richiede un trattamento sistemico e non limitato ad un singolo muscolo.
Sono state effettuate promettenti ricerche sull’uomo la carnitina. Da Wikipedia, l’enciclopedia libera. Rennie, Alterations of protein turnover underlying disuse atrophy in human skeletal muscle. Busquets, Mechanisms to explain wasting of muscle and fat in cancer cachexia. Ziegler, Update on clinical trials of growth factors and anabolic steroids in cachexia and wasting.
Le catene muscolari
Kumar, Nuclear factor-kappa B signaling in skeletal muscle atrophy. Ultrastructural observations and their relationship to zidovudine treatment. Regulator of muscle wasting in heart failure and treatment target for cardiac cachexia. Molkentin, Genetic deletion of myostatin from the heart prevents skeletal muscle atrophy in heart failure.
Le Jemtel, Diagnostic usefulness of B-type natriuretic peptide and functional consequences of muscle alterations in COPD and chronic heart failure. Feiereisen, Strength training for patients with chronic heart failure. Levine, Prolonged mechanical ventilation alters diaphragmatic structure and function.
Mitch, Review of muscle wasting associated with chronic kidney disease. Mak, Inflammation and cachexia in chronic kidney disease. Mitch, Molecular mechanisms activating muscle protein degradation in chronic kidney disease and other catabolic conditions.
Tisdale, Effect of branched-chain amino acids on muscle atrophy in cancer cachexia. Tisdale, Attenuation of muscle atrophy in a murine model of cachexia by inhibition of the dsRNA-dependent protein kinase.
Bird, Hereditary motor-sensory neuropathies. Conchin, The hypertrophic forms of hereditary motor and sensory neuropathy. Sauer, [Investigations of peripheral and central somatosensory pathways in peroneal muscular atrophy and Friedreich’s heredoataxia author’s transl ]in Arch Psychiatr Nervenkrvol. Strehle, Long-term management of children with neuromuscular disorders. Levi, Role of intrinsic muscle atrophy in the etiology of claw toe deformity in diabetic neuropathy may not be as straightforward as widely believed.
Cavanagh, Intrinsic muscle atrophy and toe deformity in the diabetic neuropathic foot: Mitsumoto, Study of patients indicates progressive muscular atrophy is a form of ALS.
Floyd, Quantitative objective markers for upper and lower motor neuron dysfunction in ALS. Gehrig, Lou Gehrig, rawhide, and Rowland, Objective tests for upper motor neuron involvement in amyotrophic lateral sclerosis ALS. Hays, Amyotrophic lateral sclerosis.
Neubauer, The “Child in the Barrel syndrome”–severe pharyngeal-cervical-brachial variant of Guillain-Barre Syndrome in a toddler. Prior, Spinal muscular atrophy: Isacson, Global gene expression profiling of somatic motor neuron populations with different vulnerability identify molecules and pathways of degeneration and protection. Pelissier, Aging and sequelae of poliomyelitis.
Spencer, Late functional deterioration following paralytic poliomyelitis. Nollet, The course of functional status and muscle strength in patients with late-onset sequelae of poliomyelitis: Neuen-Jacob, Morphologic changes in the vastus medialis muscle in patients with osteoarthritis of the knee.
Fitzgerald, Neuromuscular electrical stimulation and volitional exercise for individuals with rheumatoid arthritis: Pestronk, Myopathy with anti-Jo-1 antibodies: Chan, Understanding acute ankle ligamentous sprain injury in sports. Phototherapy in peripheral nerve injury: Curi, Sympathetic hyperactivity differentially affects skeletal muscle mass in developing heart failure: Patterson, Muscle ring finger 1 mediates cardiac atrophy in vivo.
Fukuda, Disuse-induced preferential loss of the giant protein titin depresses muscle performance via abnormal sarcomeric organization. European consensus on definition and diagnosis: Moraes, Increased muscle PGC-1alpha expression protects from sarcopenia and metabolic disease during aging. Fouret, Overexpression of the mitochondrial T3 receptor induces skeletal muscle atrophy during aging. Rasmussen, Dietary protein recommendations and the prevention of sarcopenia.
Francia, Functional and molecular effects of arginine butyrate and prednisone on muscle and heart in the mdx mouse model of Duchenne Muscular Dystrophy. Lindberg, Depression in Myotonic Dystrophy type 1: Tawil, Facioscapulohumeral muscular dystrophy.
Timmer, A Dutch guideline for the treatment of scoliosis in neuromuscular disorders. Wang, A novel functional assessment of the differentiation of micropatterned muscle cells. Palencia, [Critical illness myopathy.
Neurophysiological and muscular biopsy assessment in 33 patients]in Rev Neurolvol. Montgomery, The effect of high-altitude on human skeletal muscle energetics: Nolte, [Neurogenic muscular atrophy and selective mudcolari type atrophies: Groundbreaking findings in the biopsy diagnosis of neuromuscular disease]in Pathologevol.
Sandri, Signaling in muscle atrophy and hypertrophy. Sandri, Smad2 and 3 transcription factors control muscle mass in adulthood. Vatene, Mitochondrial function in physically active elders with sarcopenia. Ezaki, Overexpression of peroxisome proliferator-activated receptor gamma co-activator-1alpha leads to muscle atrophy with depletion of ATP. Yao, Microarray gene expression analysis in atrophying rainbow trout muscle: Gerrard, Mitogen-activated protein kinase signaling is necessary for the maintenance of skeletal muscle mass.
Rubin, Dynamic skeletal muscle stimulation and its potential muscolaru bone adaptation. Roussos, Electrical muscle stimulation preserves the muscle mass of critically ill patients: Cendes, Electrical stimulation during gait promotes increase of muscle cross-sectional area in quadriplegics: Dudley, The role of pulse duration and stimulation duration in maximizing the normalized torque during neuromuscular electrical stimulation. Fondamenti del movimento umano, Scienza e traumatologia dello sport, principi di trattamento riabilitativo.
Edizioni Medico Scientifiche, Torino. Bernard, Branched-chain aminoacids and retraining of patients with chronic muscoari lung disease. Leidy, Dietary protein and resistance training effects on muscle and body composition in older persons. Volpi, Amino acid metabolism and regulatory effects in aging.
Op ‘t Eijnde, B. Hespel, Effect of oral creatine supplementation on human muscle GLUT4 protein content after immobilization.
Bach, Growth hormone secretagogues: Estratto da ” https: Menu di navigazione Strumenti personali Accesso non effettuato discussioni contributi registrati entra. Visite Leggi Modifica Modifica wikitesto Cronologia. Vedi le condizioni d’uso per i dettagli. Le informazioni riportate non sono consigli medici e potrebbero non essere accurate.
I contenuti hanno solo fine illustrativo e non sostituiscono il parere medico: Prigioniero di guerra che mostra gli effetti dell’atrofia muscolare.