Duchenne muscular dystrophy En

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Identifiant

Synonyme

Erb's dystrophy Pseudohypertrophic muscular dystrophy Duchenne's muscular dystrophy Zimmerlin's dystrophy Pseudohypertrophic infantile muscular dystrophy

Discipline

Psychologie (4) Sociologie (3) Sciences de l'information et de la communication (2) Droit (2) Economies et finances (1) Anthropologie sociale et ethnologie (1) Anthropologie biologique (1)

Type de document

Articles (20) Colloques et conférences (2) Billets de blog (2) Mémoires, Thèses et HDR (1) Recensions (1) Autres (1) Documents audiovisuels (1) Jeux de données (1)

Auteur

Date

28 documents
USA - FDA Approves First Gene Therapy for Treatment of Certain Patients with Duchenne Muscular Dystrophy (Catapult's regulatory round-up - June)
adelage (21 févr. 2024)
Ryanodine receptor type 1 content decrease-induced endoplasmic reticulum stress is a hallmark of myopathies.
J. Vidal et al.
Insight into the role of gut microbiota in Duchenne muscular dystrophy: an age-related study in mdx mice
Maxence Jollet et al. (27 nov. 2023)
NICE review does not recommend routine funding for Duchenne muscular dystrophy gene therapy ataluren in draft guidance
adelage (30 nov. 2022)
Quand les jeunes patients vivant avec la maladie de Duchenne négocient les actes de soin avec les adultes : personnalisation et pratiques de résistance
Adeline Perrot et al. (28 nov. 2022)
Inhibition of sphingolipid de novo synthesis counteracts muscular dystrophy.
P.P. Laurila et al. (28 janv. 2022)
Experiences of caregivers of boys with Duchenne Muscular Dystrophy: “When I look at him, my world falls apart”
Ximena Palacios-Espinosa et al. (2021)
Parole de l’enfant, parole à l’enfant : Dialogue avec Rubens
Carole Lenfant (2019)
Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database.
Z. Koeks et al. (2017)
MRI Texture-Based Classification of Dystrophic Muscles. A Search for the Most Discriminative Tissue Descriptors
Dorota Duda et al. (14 sept. 2016)
Corticosteroids for the treatment of Duchenne muscular dystrophy.
E. Matthews et al. (2016)
MRI Texture Analysis for Differentiation Between Healthy and Golden Retriever Muscular Dystrophy Dogs at Different Phases of Disease Evolution
Dorota Duda et al. (24 sept. 2015)
The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations.
C.L. Bladen et al.
MAR-Mediated Dystrophin Expression in Mesoangioblasts for Duchenne Muscular Dystrophy Cell Therapy
R.W. van Zwieten et al. (2015)
Distrofia muscular de Duchenne y defecto de oxidación de ácidos grasos en un paciente pediátrico
Alejandra Acosta-Gualandri et al. (1 sept. 2014)
The Relationship Between Sexual Function and Quality of Sleep in Caregiving Mothers of Sons with Duchenne Muscular Dystrophy
Karen T. Nozoe et al.
Back muscles activity and scoliosis in ataxic and dystrophic patients
Fawzieh Sleem (16 juin 2014)
Increased Presence of FOXP3+ Regulatory T Cells in Inflamed Muscle of Patients with Active Juvenile Dermatomyositis Compared to Peripheral Blood.
Y. Vercoulen et al. (2014)
Estudio de caso: análisis narrativo con base en el relato autobiográfico de un paciente con distrofia muscular
Gladis Fernanda Castillo Pedroza (2013)
Pérdida de heterocigocidad e identificación de portadoras de distrofia muscular de Duchenne: un caso familiar con evento de recombinación
Dora Janeth Fonseca Mendoza et al. (2012)
Marked hemiatrophy in carriers of Duchenne muscular dystrophy.
S. Rajakulendran et al. (2010)
QUALITY OF LIFE AND WISHES IN DUCHENNE MUSCULAR DYSTROPHY: THE PERCEPTION OF CHILDREN AND THEIR PARENTS
Egmar Longo Araújo de Melo et al. (2009)
Análisis de deleciones en 15 exones situados dentro y fuera del hot spot mutacional del gen de la distrofina en pacientes con distrofia muscular de Duchenne
Dora Janeth Fonseca et al. (2009)
Human muscular fetal cells: a potential cell source for muscular therapies.
N. Hirt-Burri et al. (2008)
Estudio de señales de electromiografía en niños con desordenes de movimiento en las extremidades superiores debido a parálisis cerebral, distrofia de duchenne y hemiparesia espástica
Diana Estefy Gutiérrez et al. (2005)

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