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PNDS
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Ont pour objet de recommander des pratiques cliniques dans le champ particulier des maladies rares et permettre ainsi le remboursement des produits situés hors panier de soins de manière homogène sur l'ensemble du territoire français (déf. issu des rencontres HAS 2007)
Synonyme(s)Protocoles Nationaux de Diagnostic et de Soins |
Documents disponibles dans cette catégorie (58)
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Cintas P ; Bouhour F ; Cauquil C ; Masingue M ; Tard C ; Sacconi S ; Delmont E ; Choumert A ; Chanson JB ; Michaud M ; Sole G ; Cassereau J ; Noury JB ; Nicolas G ; Bellance R ; Pereon Y ; Camdessanché JP ; Magy L ; Attarian S | France | 03/04/2023Reco PNDS
Collectif | 10/2022Ce protocole national de diagnostic et de soins (PNDS) explicite aux professionnels concernés la prise en charge diagnostique et thérapeutique optimale et le parcours de soins d’un malade atteint de laminopathie avec atteinte cardiaque. Il a été[...]VLM
Collectif, Auteur | 01/2022"VLM" (vaincre les myopathies) est le magazine de l'AFM-Téléthon. Cette publication trimestrielle vous informe sur : - l'avancée de la recherche, -la prévention et la prise en charge médicale adaptée aux maladies neuromusculaires, - la vie q[...]Reco PNDS
The D2-mdx mouse model for Duchenne muscular dystrophy has gained popularity in the field, due to their more severely affected muscle function and histopathology when compared to the classic BL10-mdx model. This document describes recommended pr[...]Reco PNDS
The hanging wire tests that are described in this SOP can be used to assess global “subacute” muscle function and coordination over time in young and old mdx mice and their allelic variants in the C57BL/6J and DBA/2J genetic backgrounds. The tes[...]Reco PNDS
The objective of this SOP is to describe how treadmill or wheel running exercise can be used to aggravate the dystrophic phenotype in mdx mice to better determine the benefits, if any, of a specific treatment. Mdx mice have a less severe phenoty[...]Reco PNDS
objective is to determine the total hydroxyproline expressed per mg of muscle tissue wet weight (hydroxyproline content) as a quantitative measure of collagen deposition and fibrosis. The procedure is adapted from Prockop and Udenfriend (1960) a[...]Reco PNDS
The study of muscle diseases has evolved from a classical time in which a diagnosis was based on clinical and pathologic features, to a modern period when muscle biopsies were further characterized through histo- and cytochemical techniques, to [...]Reco PNDS
This document describes the methodology for performing isolated muscle function measurements for mouse extensor digitorum longus (EDL), soleus, and diaphragm, and provides reference values for isometric contractile properties of muscles from mdx[...]Reco PNDS
This document describes the methodology for performing measurements of muscle function on mouse tibialis anterior (TA) muscles, but the information is equally relevant for other hindlimb muscles, including the extensor digitorum longus (EDL), so[...]Reco PNDS
The measurement of muscle contractile function is an important end-point for assessing the efficacy of cell-, gene-, or pharmacologically-based therapies in DMD and the mdx mouse and GRMD dog models. Muscles in DMD and both the mdx mouse and GRM[...]Reco PNDS
Most DMD natural history studies have included measurements of muscle strength, joint contractures, and timed function tests. Results from these tests are used to track disease progression and offer insight on clinical milestones, such as the lo[...]Reco PNDS
This document describes the methodology for performing an evaluation of the respiratory system in adult C57 normal and mdx mice.Reco PNDS
The grip strength test is a simple non-invasive method designed to evaluate mouse muscle force in vivo, by taking advantage of the animal’s tendency to grasp a horizontal metal bar or grid while suspended by its tail. The bar or grid is attached[...]Article
Michelson D, Auteur ; Ciafaloni E ; Ashwal S ; Lewis E ; Narayanaswami P ; Oskoui M ; Armstrong MJ | 2018Article
Birnkrant DJ ; Bushby K ; Bann CM ; Apkon SD ; Blackwell A ; Brumbaugh D ; Case L ; Clemens PR ; Hadjiyannakis S ; Pandya S ; Street N ; Tomezsko J ; Wagner KR ; Ward LM ; Weber DR | 2018Comment in: Evidence-based care in Duchenne muscular dystrophy. [Lancet Neurol. 2018]Article
Birnkrant DJ ; Bushby K ; Bann CM ; Alman BA ; Apkon SD ; Blackwell A ; Case L ; Cripe L ; Hadjiyannakis S ; Olson AK ; Sheehan DW ; Bolen J ; Weber DR ; Ward LM | 2018Comment in: Evidence-based care in Duchenne muscular dystrophy. [Lancet Neurol. 2018]Article
Article
Mercuri E ; Finkel RS ; Muntoni F ; Wirth B ; Montes J ; Main M ; Mazzone ES ; Vitale M ; Snyder B ; Quijano Roy S ; Bertini E ; Davis RH ; Meyer OH ; Simonds AK ; Schroth MK ; Graham RJ ; Kirschner J ; Iannaccone ST ; Crawford TO ; Woods S ; Qian Y ; Sejersen T | 23/11/2017Article
Finkel RS ; Mercuri E ; Meyer OH ; Simonds AK ; Schroth MK ; Graham RJ ; Kirschner J ; Iannaccone ST ; Crawford TO ; Woods S ; Muntoni F ; Wirth B ; Montes J ; Main M ; Mazzone ES ; Vitale M ; Snyder B ; Quijano Roy S ; Bertini E ; Davis RH ; Qian Y ; Sejersen T | 23/11/2017Reco PNDS
Behavioural and locomotor measurements are important parameters that help to define the phenotypes of mice with neuromuscular disorders such as muscular dystrophies. These assessments are done in an open field Plexiglas chamber equipped with mul[...]Article
El-Aloul B ; Altamirano-Diaz L ; Zapata-Aldana E ; Rodrigues R ; Malvankar-Mehta MS ; Nguyen CT ; Campbell C | England | 2017