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Items: 10

1.

Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.

Piovani G, Borsani G, Bertini V, Kalscheuer VM, Viertel P, Bellotti D, Valseriati D, Barlati S.

Eur J Med Genet. 2006 May-Jun;49(3):215-23. Epub 2005 Aug 25.

PMID:
16762823
2.

Width of the fetal lateral ventricular atrium between 10 and 12 mm: a simple variation of the norm?

Signorelli M, Tiberti A, Valseriati D, Molin E, Cerri V, Groli C, Bianchi UA.

Ultrasound Obstet Gynecol. 2004 Jan;23(1):14-8.

3.

Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.

Nabbout R, Gennaro E, Dalla Bernardina B, Dulac O, Madia F, Bertini E, Capovilla G, Chiron C, Cristofori G, Elia M, Fontana E, Gaggero R, Granata T, Guerrini R, Loi M, La Selva L, Lispi ML, Matricardi A, Romeo A, Tzolas V, Valseriati D, Veggiotti P, Vigevano F, Vallée L, Dagna Bricarelli F, Bianchi A, Zara F.

Neurology. 2003 Jun 24;60(12):1961-7.

PMID:
12821740
4.

Peripheral markers of the gamma-aminobutyric acid (GABA)ergic system in Angelman's syndrome.

Borgatti R, Piccinelli P, Passoni D, Romeo A, Viri M, Musumeci SA, Elia M, Cogliati T, Valseriati D, Grasso R, Raggi ME, Ferrarese C.

J Child Neurol. 2003 Jan;18(1):21-5.

PMID:
12661934
5.

Another case of reversibility of visual-field defect induced by vigabatrin monotherapy: is young age a favorable factor?

Giordano L, Valseriati D, Vignoli A, Morescalchi F, Gandolfo E.

Neurol Sci. 2000 Jun;21(3):185-6. No abstract available.

PMID:
11076009
6.

Benign infantile familial convulsions: natural history of a case and clinical characteristics of a large Italian family.

Giordano L, Accorsi P, Valseriati D, Tiberti A, Menegati E, Zara F, Vignoli A, Vigevano F.

Neuropediatrics. 1999 Apr;30(2):99-101.

PMID:
10401694
7.

Prospective study of first-line vigabatrin monotherapy in childhood partial epilepsies.

Gobbi G, Pini A, Bertani G, Menegati E, Tiberti A, Valseriati D, Besana D, Rasmini P, Guerrini R, Belmonte A, Veggiotti P, Resi C, Lanzi G, Capovilla G, Galeone D, Milani S.

Epilepsy Res. 1999 May;35(1):29-37.

PMID:
10232792
8.

Benign partial epilepsy in infancy with complex partial seizures (Watanabe's syndrome): 12 non-Japanese new cases.

Capovilla G, Giordano L, Tiberti S, Valseriati D, Menegati E.

Brain Dev. 1998 Mar;20(2):105-11.

PMID:
9545181
9.

Early-onset benign occipital seizure susceptibility syndrome.

Ferrie CD, Beaumanoir A, Guerrini R, Kivity S, Vigevano F, Takaishi Y, Watanabe K, Mira L, Capizzi G, Costa P, Valseriati D, Grioni D, Lerman P, Ricci S, Vigliano P, Goumas-Kartalas A, Hashimoto K, Robinson RO, Panayiotopoulos CP.

Epilepsia. 1997 Mar;38(3):285-93.

10.

[EEG anomalies in the prodromic phase of Rasmussen's syndrome. Report of two cases].

Beaumanoir A, Grioni D, Kullmann G, Tiberti A, Valseriati D.

Neurophysiol Clin. 1997;27(1):25-32. French.

PMID:
9206756

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