Isam Naom

Mapping of a susceptibility locus for Crohn's disease on chromosome 16

Jean‐Pierre Hugot, Pierre Laurent‐Puig, Corinne Gower‐Rousseau et al. · Nature · 1996 · 952 citations

Disease Susceptibility, Disease Mechanism, Genetics +9

Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy

Caroline A. Sewry, J. Philpot, Leigh Wilson et al. · The Lancet · 1996 · 83 citations

Rare Diseases, Medicine, Degenerative Disease +5

Assignment of a Form of Congenital Muscular Dystrophy with Secondary Merosin Deficiency to Chromosome 1q42

Martin Brockington, Caroline A. Sewry, R. Herrmann et al. · The American Journal of Human Genetics · 2000 · 80 citations · Full text

Rare Diseases, Developmental Biology, Mendelian Disorder +9

Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency

Ersin Tan, Haluk Topaloğlu, Caroline A. Sewry et al. · Neuromuscular Disorders · 1997 · 79 citations

Neurological Disorder, Corticobasal Degeneration, White Matter +10

Laminin α2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy

Isam Naom, Mariella D’Alessandro, Caroline A. Sewry et al. · Neuromuscular Disorders · 1998 · 50 citations

Mendelian Disorder, Genetic Disorder, Medicine +8