Results 211 to 220 of about 31,854 (258)

Mortality Trends and Causes of Death in Myotonic Dystrophy Type 1 Patients From the UK Clinical Practice Research Datalink. [PDF]

Muscle Nerve
Alsaggaf R, Pfeiffer RM, Pearce EE, Greene MH, Lochmuller H, Gadalla SM.   +5 more
europepmc   +1 more source

A Novel Class of FKBP12 Ligands Rescues Premature Aging Phenotypes Associated with Myotonic Dystrophy Type 1. [PDF]

Cells
García-Puga M, Gerenu G, Bargiela A, Espinosa-Espinosa J, Mosqueira-Martín L, Sagartzazu-Aizpurua M, Aizpurua JM, Vallejo-Illarramendi A, Artero R, López de Munain A, Matheu A.   +10 more
europepmc   +1 more source

Changes in body composition revealed by bioelectrical impedance analysis reflect strength and motor performance in myotonic dystrophy type 2. [PDF]

Front Neurol
Frezza E, Merra G, Greco G, Goglia M, Seraceno S, Boffa L, Mercuri NB, De Lorenzo A, Massa R.   +8 more
europepmc   +1 more source

Longitudinal Course of Myotonic Dystrophy Type 1 With Gait Training Using a Hybrid Assistive Limb: A Case Report. [PDF]

Cureus
Nakazawa R, Koseki K, Yoshikawa K, Matsushita A, Kohno Y.   +4 more
europepmc   +1 more source

Myotonic Dystrophy type 2 unmasked by physical activity resumption following COVID-19 lockdown: case discussion and review of the literature. [PDF]

Acta Myol
Lucchiari S, Magri F, Rimoldi M, Pagliarani S, Corti S, Comi GP, Sciacco M.   +6 more
europepmc   +1 more source

CTG repeat length underlying cardiac events and sudden death in myotonic dystrophy type 1. [PDF]

Eur Heart J Open
Itoh H, Hisamatsu T, Segawa K, Takahashi T, Sato T, Takada H, Kuru S, Wada C, Suzuki M, Tamura T, Suwazono S, Kimura K, Matsumura T, Takahashi MP.   +13 more
europepmc   +1 more source

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Myotonic Dystrophy and Myotonic Dystrophy Protein Kinase

Progress in Histochemistry and Cytochemistry, 2000
Myotonic dystrophy protein kinase (DMPK) was designated as a gene responsible for myotonic dystrophy (DM) on chromosome 19, because the gene product has extensive homology to protein kinase catalytic domains. DM is the most common disease with multisystem disorders among muscular dystrophies.
Takayoshi Kobayashi, Shinichi Ohno, Hideho Ueda   +2 more
openaire   +3 more sources

Myotonic Dystrophy

CONTINUUM: Lifelong Learning in Neurology, 2022
ABSTRACT PURPOSE OF REVIEW Myotonic dystrophy type 1 (DM1) and myotonic dystrophy type 2 (DM2) are genetic disorders affecting skeletal and smooth muscle, heart, brain, eyes, and other organs. The multisystem involvement and disease variability of myotonic dystrophy have presented challenges for clinical care and ...
openaire   +2 more sources