Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotype

By Mercuri E.   Cini C.   Pichiecchio A.   Allsop J.   Counsell S.   Zolkipli Z.   Messina S.   Kinali M.   Brown S.C.   Jimenez C.   Brockington M.   Yuva Y.   Sewry C.A.   Muntoni F.  

Neuromuscular Disorders, Vol. 13, Iss. 7, 2003-09 ,pp. : 554-558

Elsevier

Access to resources Recommend Favorite

Congenital muscular dystrophy in Sweden. A preliminary report from a national survey

By Eeg-Olofsson K.E.   Eeg-Olofsson O.   Olsson Y.   Dahl N.  

Electroencephalography and Clinical Neurophysiology/ Electromyography and Motor Control, Vol. 97, Iss. 4, 1995-09 ,pp. : 128-128

Elsevier

Access to resources Recommend Favorite

Thymus acetylcholinesterase activity is reduced in mice with congenital muscular dystrophy

By Nieto-Cerón Susana   Sánchez del Campo Luis   Delgado Encarnación   Vidal Cecilio   Campoy Francisco  

Journal of Molecular Neuroscience, Vol. 30, Iss. 1-2, 2006-02 ,pp. : 49-50

Humana Press, Inc

Access to resources Recommend Favorite

A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21

By Tétreault M.   Duquette A.   Thiffault I.   Bherer C.   Jarry J.   Loisel L.   Banwell B.   D'Anjou G.   Mathieu J.   Robitaille Y.   Vanasse M.   Brais B.  

Brain, Vol. 129, Iss. 8, 2006-08 ,pp. : 2077-2084

Oxford University Press

Access to resources Recommend Favorite

Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue

By Hicks D.  

Brain, Vol. 132, Iss. 1, 2009-01 ,pp. : 147-155

Oxford University Press

Access to resources Recommend Favorite