Zara F - Search Results

1

Structural mapping of GABRB3 variants reveals genotype-phenotype correlations.

Johannesen KM, Iqbal S, Guazzi M, Mohammadi NA, Pérez-Palma E, Schaefer E, De Saint Martin A, Abiwarde MT, McTague A, Pons R, Piton A, Kurian MA, Ambegaonkar G, Firth H, Sanchis-Juan A, Deprez M, Jansen K, De Waele L, Briltra EH, Verbeek NE, van Kempen M, Fazeli W, Striano P, Zara F, Visser G, Braakman HMH, Haeusler M, Elbracht M, Vaher U, Smol T, Lemke JR, Platzer K, Kennedy J, Klein KM, Au PYB, Smyth K, Kaplan J, Thomas M, Dewenter MK, Dinopoulos A, Campbell AJ, Lal D, Lederer D, Liao VWY, Ahring PK, Møller RS, Gardella E. Johannesen KM, et al. Among authors: zara f. Genet Med. 2022 Mar;24(3):681-693. doi: 10.1016/j.gim.2021.11.004. Epub 2021 Dec 7. Genet Med. 2022. PMID: 34906499 Free article.

2

Late-onset and slow-progressing Lafora disease in four siblings with EPM2B mutation.

Baykan B, Striano P, Gianotti S, Bebek N, Gennaro E, Gurses C, Zara F. Baykan B, et al. Among authors: zara f. Epilepsia. 2005 Oct;46(10):1695-7. doi: 10.1111/j.1528-1167.2005.00272.x. Epilepsia. 2005. PMID: 16190947 Free article.

3

Electroclinical and genetic findings in a family with cortical tremor, myoclonus, and epilepsy.

Striano P, Madia F, Minetti C, Striano S, Zara F. Striano P, et al. Among authors: zara f. Epilepsia. 2005 Dec;46(12):1993-5. doi: 10.1111/j.1528-1167.2005.00346.x. Epilepsia. 2005. PMID: 16393167 Free article.

4

Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases.

Striano P, Malacarne M, Cavani S, Pierluigi M, Rinaldi R, Cavaliere ML, Rinaldi MM, De Bernardo C, Coppola A, Pintaudi M, Gaggero R, Grammatico P, Striano S, Dallapiccola B, Zara F, Faravelli F. Striano P, et al. Among authors: zara f. Am J Med Genet A. 2006 Sep 15;140(18):1944-9. doi: 10.1002/ajmg.a.31435. Am J Med Genet A. 2006. PMID: 16906558

5

Comment to: overlap cases of eyelid myoclonia with absences and juvenile myoclonic epilepsy.

Striano S, Zara F, Striano P. Striano S, et al. Among authors: zara f. Seizure. 2007 Sep;16(6):557-8. doi: 10.1016/j.seizure.2007.04.002. Epub 2007 May 15. Seizure. 2007. PMID: 17507253 Free article. No abstract available.

6

Life-threatening status epilepticus following gabapentin administration in a patient with benign adult familial myoclonic epilepsy.

Striano P, Coppola A, Madia F, Pezzella M, Ciampa C, Zara F, Striano S. Striano P, et al. Among authors: zara f. Epilepsia. 2007 Oct;48(10):1995-8. doi: 10.1111/j.1528-1167.2007.01198.x. Epub 2007 Jul 21. Epilepsia. 2007. PMID: 17645541 Free article.

7

Transient epileptic amnesia: a new epileptic syndrome in development?

Striano P, Zara F, Striano S. Striano P, et al. Among authors: zara f. Ann Neurol. 2010 Mar;67(3):416. doi: 10.1002/ana.21286. Ann Neurol. 2010. PMID: 18041088 No abstract available.

8

Re: Fame 3: a novel form of progressive myoclonus and epilepsy.

Striano P, Striano S, Zara F. Striano P, et al. Among authors: zara f. Neurology. 2008 Jan 1;70(1):85; author reply 85-6. doi: 10.1212/01.wnl.0000295707.90283.e6. Neurology. 2008. PMID: 18166714 No abstract available.

9

Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families.

Madia F, Striano P, Di Bonaventura C, de Falco A, de Falco FA, Manfredi M, Casari G, Striano S, Minetti C, Zara F. Madia F, et al. Among authors: zara f. Neurogenetics. 2008 May;9(2):139-42. doi: 10.1007/s10048-008-0118-4. Epub 2008 Jan 30. Neurogenetics. 2008. PMID: 18231815

10

Refractory, life-threatening status epilepticus in a 3-year-old girl.

Striano P, Striano S, Minetti C, Zara F. Striano P, et al. Among authors: zara f. Lancet Neurol. 2008 Mar;7(3):278-84. doi: 10.1016/S1474-4422(08)70043-7. Lancet Neurol. 2008. PMID: 18275929 No abstract available.

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