H. Barry Collin

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

Kiichiro Matsumura, F.M.S. Tomé, H. Barry Collin et al. · Nature · 1992 · 252 citations

Rare Diseases, Mendelian Disorder, Genetic Disorder +5

Juvenile limb-girdle muscular dystrophy

Michel Fardeau, Dominique Hillaire, C. Mignard et al. · Brain · 1996 · 197 citations · Full text

Rare Diseases, Kinesiology, Mendelian Disorder +15

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Fédérica Piccolo, Steven L. Roberds, Marc Jeanpierre et al. · Nature Genetics · 1995 · 190 citations

Rare Diseases, Variable Severity, Ophthalmology +6

Primary adhalinopathy (α‐sarcoglycanopathy)

B. Eymard, Norma B. Romero, France Leturcq et al. · Neurology · 1997 · 134 citations

Mendelian Disorder, Ophthalmology, Genetic Disorder +13

Gene delivery to the myocardium by intrapericardial injection

Yves Fromes, André Salmon, X Wang et al. · Gene Therapy · 1999 · 127 citations

Cardiac Muscle, Cardiomyopathy, Medicine +5