Zara F - Search Results

1

White matter involvement in a family with a novel PDGFB mutation.

Biancheri R, Severino M, Robbiano A, Iacomino M, Del Sette M, Minetti C, Cervasio M, Del Basso De Caro M, Striano P, Zara F. Biancheri R, et al. Among authors: zara f. Neurol Genet. 2016 May 5;2(3):e77. doi: 10.1212/NXG.0000000000000077. eCollection 2016 Jun. Neurol Genet. 2016. PMID: 27227165 Free PMC article.

2

Chemokine receptor CCR7 is expressed in muscle fibers in juvenile dermatomyositis.

Minetti C, Gattorno M, Repetto S, Gregorio A, Pedemonte M, Assereto S, Zara F, Bruno C, Martini A. Minetti C, et al. Among authors: zara f. Biochem Biophys Res Commun. 2005 Jul 29;333(2):540-3. doi: 10.1016/j.bbrc.2005.05.146. Biochem Biophys Res Commun. 2005. PMID: 15950936

3

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.

4

Pharmacological rescue of the dystrophin-glycoprotein complex in Duchenne and Becker skeletal muscle explants by proteasome inhibitor treatment.

Assereto S, Stringara S, Sotgia F, Bonuccelli G, Broccolini A, Pedemonte M, Traverso M, Biancheri R, Zara F, Bruno C, Lisanti MP, Minetti C. Assereto S, et al. Among authors: zara f. Am J Physiol Cell Physiol. 2006 Feb;290(2):C577-82. doi: 10.1152/ajpcell.00434.2005. Epub 2005 Sep 28. Am J Physiol Cell Physiol. 2006. PMID: 16192300 Free article.

5

Multiplex real-time PCR for detection of deletions and duplications in dystrophin gene.

Traverso M, Malnati M, Minetti C, Regis S, Tedeschi S, Pedemonte M, Bruno C, Biassoni R, Zara F. Traverso M, et al. Among authors: zara f. Biochem Biophys Res Commun. 2006 Jan 6;339(1):145-50. doi: 10.1016/j.bbrc.2005.11.006. Epub 2005 Nov 9. Biochem Biophys Res Commun. 2006. PMID: 16297882

6

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.

7

A novel SCN2A mutation in family with benign familial infantile seizures.

Striano P, Bordo L, Lispi ML, Specchio N, Minetti C, Vigevano F, Zara F. Striano P, et al. Among authors: zara f. Epilepsia. 2006 Jan;47(1):218-20. doi: 10.1111/j.1528-1167.2006.00392.x. Epilepsia. 2006. PMID: 16417554 Free article.

8

Somatic and germline mosaicisms in severe myoclonic epilepsy of infancy.

Gennaro E, Santorelli FM, Bertini E, Buti D, Gaggero R, Gobbi G, Lini M, Granata T, Freri E, Parmeggiani A, Striano P, Veggiotti P, Cardinali S, Bricarelli FD, Minetti C, Zara F. Gennaro E, et al. Among authors: zara f. Biochem Biophys Res Commun. 2006 Mar 10;341(2):489-93. doi: 10.1016/j.bbrc.2005.12.209. Epub 2006 Jan 13. Biochem Biophys Res Commun. 2006. PMID: 16430863

9

A new method for analysis of mitochondrial DNA point mutations and assess levels of heteroplasmy.

Cassandrini D, Calevo MG, Tessa A, Manfredi G, Fattori F, Meschini MC, Carrozzo R, Tonoli E, Pedemonte M, Minetti C, Zara F, Santorelli FM, Bruno C. Cassandrini D, et al. Among authors: zara f. Biochem Biophys Res Commun. 2006 Apr 7;342(2):387-93. doi: 10.1016/j.bbrc.2006.01.152. Epub 2006 Feb 8. Biochem Biophys Res Commun. 2006. PMID: 16483543

10

Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the Mediterranean.

Cannelli N, Cassandrini D, Bertini E, Striano P, Fusco L, Gaggero R, Specchio N, Biancheri R, Vigevano F, Bruno C, Simonati A, Zara F, Santorelli FM. Cannelli N, et al. Among authors: zara f. Neurogenetics. 2006 May;7(2):111-7. doi: 10.1007/s10048-005-0024-y. Epub 2006 Mar 29. Neurogenetics. 2006. PMID: 16570191

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