MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution

Por Laccone, F, Zoll, B, Huppke, P, Hanefeld, F, Pepinski, W, Trappe, R
Publicado em 2002

BROADENED AND ELEVATED HUMORAL IMMUNE RESPONSE TO EBNA1 IN PEDIATRIC MULTIPLE SCLEROSIS

Por Lünemann, J D., Huppke, P, Roberts, S, Brück, W, Gärtner, J, Münz, C
Publicado em 2008

Very mild cases of Rett syndrome with skewed X inactivation

Por Huppke, P, Maier, E M, Warnke, A, Brendel, C, Laccone, F, Gärtner, J
Publicado em 2006

MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin

Por Trappe, R., Laccone, F., Cobilanschi, J., Meins, M., Huppke, P., Hanefeld, F., Engel, W.
Publicado em 2001

Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patients

Por Archer, H L, Whatley, S D, Evans, J C, Ravine, D, Huppke, P, Kerr, A, Bunyan, D, Kerr, B, Sweeney, E, Davies, S J, Reardon, W, Horn, J, MacDermot, K D, Smith, R A, Magee, A, Donaldson, A, Crow, Y, Hermon, G, Miedzybrodzka, Z, Cooper, D N, Lazarou, L, Butler, R, Sampson, J, Pilz, D T, Laccone, F, Clarke, A J
Publicado em 2006