Publications

Found 4 results

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1994
Identification and characterization of three calmodulin binding sites of the skeletal muscle ryanodine receptor., Menegazzi, P., Larini F., Treves S., Guerrini R., Quadroni M., and Zorzato F. , Biochemistry, 1994 Aug 9, Volume 33, Issue 31, p.9078-84, (1994) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/8049209?dopt=Abstract

1996
Sequential occurrence of benign partial epilepsy and childhood absence epilepsy in three patients., Gambardella, A., Aguglia U., Guerrini R., Morelli F., Zappia M., and Quattrone A. , Brain & development, 1996 May-Jun, Volume 18, Issue 3, p.212-5, (1996) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/8836503?dopt=Abstract

1998
Angelman syndrome: correlations between epilepsy phenotypes and genotypes., Minassian, B. A., DeLorey T. M., Olsen R. W., Philippart M., Bronstein Y., Zhang Q., Guerrini R., Van Ness P., Livet M. O., and Delgado-Escueta A. V. , Annals of neurology, 1998 Apr, Volume 43, Issue 4, p.485-93, (1998) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/9546330?dopt=Abstract

2014
Periventricular nodular heterotopia in Smith-Magenis syndrome., Capra, Valeria, Biancheri Roberta, Morana Giovanni, Striano Pasquale, Novara Francesca, Ferrero Giovanni Battista, Boeri Luca, Celle Maria Elena, Mancardi Maria Margherita, Zuffardi Orsetta, et al. , American journal of medical genetics. Part A, 2014 Dec, Volume 164A, Issue 12, p.3142-7, (2014) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/25257626?dopt=Abstract