The direct health care costs of obesity in the United States
Allison, D B, Zannolli, R, Narayan, K M
Published in American journal of public health (1971) (01.08.1999)
Published in American journal of public health (1971) (01.08.1999)
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Neurological outcome following isolated 10–12 mm fetal ventriculomegaly
Melchiorre, K, Liberati, M, Celentano, C, Domizio, S, Puglielli, C, Buoni, S, Strambi, M, Zannolli, R
Published in Archives of disease in childhood. Fetal and neonatal edition (01.07.2009)
Published in Archives of disease in childhood. Fetal and neonatal edition (01.07.2009)
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Weight loss increases and fat loss decreases all-cause mortality rate : results from two independent cohort studies
ALLISON, D. B, ZANNOLLI, R, FAITH, M. S, HEO, M, PIETROBELLI, A, VANITALLIE, T. B, PI-SUNYER, F. X, HEYMSFIELD, S. B
Published in International Journal of Obesity (1999)
Published in International Journal of Obesity (1999)
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SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy
Buoni, S, Orrico, A, Galli, L, Zannolli, R, Burroni, L, Hayek, J, Fois, A, Sorrentino, V
Published in Neurology (28.02.2006)
Published in Neurology (28.02.2006)
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Delayed response of seizures with vagus nerve stimulation in Lennox-Gastaut syndrome
Buoni, S, Zannolli, R, Macucci, F, Pieri, S, Galluzzi, P, Mariottini, A, Fois, A
Published in Neurology (26.10.2004)
Published in Neurology (26.10.2004)
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The FBN1 (R2726W) mutation is not fully penetrant
Buoni, S., Zannolli, R., Macucci, F., Ansaldi, S., Grasso, M., Arbustini, E., Fois, A.
Published in Annals of human genetics (01.11.2004)
Published in Annals of human genetics (01.11.2004)
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Neurocutaneous syndrome with mental delay, autism, blockage in intracellular vescicular trafficking and melanosome defects
Buoni, S., Zannolli, R., De Santi, M., Macucci, F., Hayek, J., Orsi, A., Scarinci, R., Buscalferri, A., Cuccia, A., Zappella, M., Miracco, C.
Published in European journal of neurology (01.08.2006)
Published in European journal of neurology (01.08.2006)
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Occipital intermittent rhythmic delta activity only following eye closure in atypical CNS Salmonellosis
Buoni, S., Zannolli, R., Di Bartolo, R.M., Macucci, F., Migliorini, L., Sansoni, R., Cellesi, C.
Published in Clinical neurophysiology (01.08.2005)
Published in Clinical neurophysiology (01.08.2005)
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Hereditary xanthinuria type II associated with mental delay, autism, cortical renal cysts, nephrocalcinosis, osteopenia, and hair and teeth defects
Zannolli, R, Micheli, V, Mazzei, M A, Sacco, P, Piomboni, P, Bruni, E, Miracco, C, de Santi, M M, Terrosi Vagnoli, P, Volterrani, L, Pellegrini, L, Livi, W, Lucani, B, Gonnelli, S, Burlina, A B, Jacomelli, G, Macucci, F, Pucci, L, Fimiani, M, Swift, J A, Zappella, M, Morgese, G
Published in Journal of medical genetics (01.11.2003)
Published in Journal of medical genetics (01.11.2003)
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Atypical BECTS and homocystinuria
Buoni, S, Di Bartolo, R M, Molinelli, M, Palmeri, S, Zannolli, R
Published in Neurology (28.10.2003)
Published in Neurology (28.10.2003)
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Hypertelorism, ptosis, and myopia associated with drug-resistant epilepsy, mental delay, growth deficiency, ectodermal defects, and osteopenia
Zannolli, R., Buoni, S., Macucci, F., Miracco, C., de Santi, M.M., Piomboni, P., Bruni, E., Malandrini, A., Galluzzi, P., Hadjistilianou, T., Medaglini, S., Mazzei, M.A., Sacco, P., Terrosi-Vagnoli, P., Volterrani, L., Molinelli, M., Burlina, A.B., Swift, J.A., Fimiani, M.
Published in American journal of medical genetics. Part A (01.06.2004)
Published in American journal of medical genetics. Part A (01.06.2004)
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Posterior knee pain: primary symptom of a small non-occlusive venous clot
Zannolli, R, Mazzei, M A, Sacco, P, Turchetti, V, Amato, T, Battistini, S, Berardi, R, Volterrani, L, De Stefano, V, Morgese, G
Published in Archives of disease in childhood (01.08.2003)
Published in Archives of disease in childhood (01.08.2003)
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18q‐ syndrome and ectodermal dysplasia syndrome: Description of a child and his family
Zannolli, R., Pierluigi, M., Pucci, L., Lagrasta, N., Gasparre, O., Matera, M.R., Di Bartolo, R.M., Mazzei, M.A., Sacco, P., Miracco, C., de Santi, M.M., Aitiani, P., Cavani, S., Pellegrini, L., Fimiani, M., Alessandrini, C., Galluzzi, P., Livi, W., Gonnelli, S., Terrosi‐Vagnoli, P., Zappella, M., Morgese, G.
Published in American journal of medical genetics. Part A (15.01.2003)
Published in American journal of medical genetics. Part A (15.01.2003)
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Novel CNS syndrome and ectodermal dysplasia
Zannolli, R., Macucci, F., Di Bartolo, R.M., Serracca, L., Miracco, C., de Santi, M.M., Giannini, F., Malandrini, A., Galluzzi, P., De Robertis, S., Hadjistilianou, T., Perotti, R., Fimiani, M., Doldo, T., Giorgetti, R., Cavani, S., Pierluigi, M.
Published in American journal of medical genetics. Part A (15.01.2003)
Published in American journal of medical genetics. Part A (15.01.2003)
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Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B
Halgren, C, Kjaergaard, S, Bak, M, Hansen, C, El-Schich, Z, Anderson, CM, Henriksen, KF, Hjalgrim, H, Kirchhoff, M, Bijlsma, EK, Nielsen, M, den Hollander, NS, Ruivenkamp, CAL, Isidor, B, Le Caignec, C, Zannolli, R, Mucciolo, M, Renieri, A, Mari, F, Anderlid, B-M, Andrieux, J, Dieux, A, Tommerup, N, Bache, I
Published in Clinical genetics (01.09.2012)
Published in Clinical genetics (01.09.2012)
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