Maja Poppe

The phenotype of limb-girdle muscular dystrophy type 2I

Maja Poppe, Lynsey Cree, John Bourke et al. · Neurology · 2003 · 196 citations

Medicine, Genetics, Neurology +10

Cardiac and respiratory failure in limb‐girdle muscular dystrophy 2I

Maja Poppe, John Bourke, Michelle Eagle et al. · Annals of Neurology · 2004 · 135 citations

Medicine, Genetics, Neurology +11

Extreme Variability of Phenotype in Patients With an Identical Missense Mutation in the Lamin A/C Gene

Eugenio Mercuri, Maja Poppe, Rosaline C. M. Quinlivan et al. · Archives of Neurology · 2004 · 125 citations

Medicine, Genetics, Molecular Genetics +15

DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion

Oliver Bartsch, Michaela Nemecková, Eduard Kočárek et al. · American Journal of Medical Genetics Part A · 2003 · 91 citations

Life Sciences, Genetics, Molecular Genetics +17

Variable reduction of caveolin-3 in patients with LGMD2B/MM

Maggie C. Walter, Christian Braun, Matthias Vorgerd et al. · Journal of Neurology · 2003 · 44 citations

Life Sciences, Molecular Medicine, Neuroscience +8