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M Zappella

Showing results (31-40 of 48) with videos related to

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European Journal of Neurology|November 28, 2002
Septo-optic dysplasia with digital anomalies associated with maternal multidrug abuse during pregnancyA Orrico, L Galli, M Zappella, et al.
Nuclear Medicine Communications|June 1, 1997
Brain perfusion abnormalities in Rett syndrome: a qualitative and quantitative SPET study with 99Tc(m)-ECDL Burroni, A M Aucone, D Volterrani, et al.
The Journal of Pediatrics|December 26, 2006
Rett syndrome and plasma leptin levelsP Blardi, A de Lalla, T D'Ambrogio, et al.
Brain & Development|December 29, 1998
Ultrastructural study of enteric ganglia in three patients with Rett syndromeA Malandrini, G Hayek, M Villanova, et al.
Clinical Genetics|February 28, 2004
Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like featuresC Pescucci, I Meloni, M Bruttini, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Preserved speech variant is allelic of classic Rett syndromeC De Bona, M Zappella, G Hayek, et al.
Brain & Development|June 20, 2008
Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant)A Renieri, F Mari, M A Mencarelli, et al.
FEBS Letters|September 29, 2000
MECP2 mutation in male patients with non-specific X-linked mental retardationA Orrico, C Lam, L Galli, et al.
Calcified Tissue International|January 5, 2002
Dual X-ray absorptiometry and bone ultrasonography in patients with Rett syndromeC Cepollaro, S Gonnelli, D Bruni, et al.
European Journal of Neurology|August 2, 2006
Neurocutaneous syndrome with mental delay, autism, blockage in intracellular vescicular trafficking and melanosome defectsS Buoni, R Zannolli, M de Santi, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
European Journal of Neurology|November 28, 2002
Septo-optic dysplasia with digital anomalies associated with maternal multidrug abuse during pregnancyA Orrico, L Galli, M Zappella, et al.
Nuclear Medicine Communications|June 1, 1997
Brain perfusion abnormalities in Rett syndrome: a qualitative and quantitative SPET study with 99Tc(m)-ECDL Burroni, A M Aucone, D Volterrani, et al.
The Journal of Pediatrics|December 26, 2006
Rett syndrome and plasma leptin levelsP Blardi, A de Lalla, T D'Ambrogio, et al.
Brain & Development|December 29, 1998
Ultrastructural study of enteric ganglia in three patients with Rett syndromeA Malandrini, G Hayek, M Villanova, et al.
Clinical Genetics|February 28, 2004
Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like featuresC Pescucci, I Meloni, M Bruttini, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Preserved speech variant is allelic of classic Rett syndromeC De Bona, M Zappella, G Hayek, et al.
Brain & Development|June 20, 2008
Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant)A Renieri, F Mari, M A Mencarelli, et al.
FEBS Letters|September 29, 2000
MECP2 mutation in male patients with non-specific X-linked mental retardationA Orrico, C Lam, L Galli, et al.
Calcified Tissue International|January 5, 2002
Dual X-ray absorptiometry and bone ultrasonography in patients with Rett syndromeC Cepollaro, S Gonnelli, D Bruni, et al.
European Journal of Neurology|August 2, 2006
Neurocutaneous syndrome with mental delay, autism, blockage in intracellular vescicular trafficking and melanosome defectsS Buoni, R Zannolli, M de Santi, et al.
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