H. Radvanyi

发表

DNA mutation size in myotonic dystrophy Correlation between decreased myocardial glucose phosphorylation and the

P. Merlet, B. Mazoyer, B. Eymard, 2011 .

Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy.

C. Junien, A. Lazarus, J. Coste, 1999, Circulation.

Severe cardiac arrhythmias in young patients with myotonic dystrophy type 1

A. Lazarus, G. Bassez, P. Laforêt, 2004, Neurology.

Blunted coronary reserve in myotonic dystrophy. An early and gene-related phenomenon.

P. Merlet, B. Mazoyer, C. Junien, 1996, Circulation.

Cranial MRI findings in myotonic dystrophy

N. Martin-Duverneuil, J. Chiras, B. Eymard, 1997, Neuroradiology.

Cognitive profile in childhood myotonic dystrophy type 1: Is there a global impairment?

B. Eymard, N. Angeard, A. Jacquette, 2007, Neuromuscular Disorders.

A new window on neurocognitive dysfunction in the childhood form of myotonic dystrophy type 1 (DM1)

B. Eymard, S. Moutier, N. Angeard, 2011, Neuromuscular Disorders.

Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenon

P. Merlet, D. Annane, S. Pappatà, 1998, Neuromuscular Disorders.

Correlation Between Decreased Myocardial Glucose Phosphorylation and the DNA Mutation Size in Myotonic Dystrophy

P. Merlet, D. Annane, B. Mazoyer, 1994, Circulation.