Tessa A - Search Results

1

Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitation.

Siciliano G, Tessa A, Renna M, Manca ML, Mancuso M, Murri L. Siciliano G, et al. Among authors: tessa a. Clin Genet. 1999 Jul;56(1):51-8. doi: 10.1034/j.1399-0004.1999.560107.x. Clin Genet. 1999. PMID: 10466417

2

Abnormal H-Tfam in a patient harboring a single mtDNA deletion.

Tessa A, Manca ML, Mancuso M, Renna MR, Murri L, Martini B, Santorelli FM, Siciliano G. Tessa A, et al. Funct Neurol. 2000 Oct-Dec;15(4):211-4. Funct Neurol. 2000. PMID: 11213524

3

Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathies.

Siciliano G, Mancuso M, Pasquali L, Manca ML, Tessa A, Iudice A. Siciliano G, et al. Among authors: tessa a. Neurol Sci. 2000;21(5 Suppl):S985-7. doi: 10.1007/s100720070017. Neurol Sci. 2000. PMID: 11382203

4

Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene.

Siciliano G, Tessa A, Petrini S, Mancuso M, Bruno C, Grieco GS, Malandrini A, DeFlorio L, Martini B, Federico A, Nappi G, Santorelli FM, Murri L. Siciliano G, et al. Among authors: tessa a. Neuromuscul Disord. 2003 Feb;13(2):162-5. doi: 10.1016/s0960-8966(02)00221-3. Neuromuscul Disord. 2003. PMID: 12565915

5

Residual muscle cytochrome c oxidase activity accounts for submaximal exercise lactate threshold in chronic progressive external ophthalmoplegia.

Siciliano G, Rossi B, Manca L, Angelini C, Tessa A, Vergani L, Martinuzzi A, Muratorio A. Siciliano G, et al. Among authors: tessa a. Muscle Nerve. 1996 Mar;19(3):342-9. doi: 10.1002/(SICI)1097-4598(199603)19:3<342::AID-MUS10>3.0.CO;2-U. Muscle Nerve. 1996. PMID: 8606699

6

Encephalomyopathy with multiple mitochondrial DNA deletions and multiple symmetric lipomatosis: further evidence of a possible association.

Mancuso M, Bianchi MC, Santorelli FM, Tessa A, Casali C, Murri L, Siciliano G. Mancuso M, et al. Among authors: tessa a. J Neurol. 1999 Dec;246(12):1197-8. doi: 10.1007/s004150050543. J Neurol. 1999. PMID: 10653316 No abstract available.

7

Multiple mtDNA deletions: clinical and molecular correlations.

Santorelli FM, De Joanna G, Casali C, Tessa A, Siciliano G, Amabile GA, Pierelli F, Vilarinho L, Santoro L. Santorelli FM, et al. Among authors: tessa a. J Inherit Metab Dis. 2000 Mar;23(2):155-61. doi: 10.1023/a:1005617916260. J Inherit Metab Dis. 2000. PMID: 10801057

8

Respiratory chain defects in hereditary spastic paraplegias.

Piemonte F, Casali C, Carrozzo R, Schägger H, Patrono C, Tessa A, Tozzi G, Cricchi F, Di Capua M, Siciliano G, Amabile GA, Morocutti C, Bertini E, Santorelli FM. Piemonte F, et al. Among authors: tessa a. Neuromuscul Disord. 2001 Sep;11(6-7):565-9. doi: 10.1016/s0960-8966(01)00214-0. Neuromuscul Disord. 2001. PMID: 11525886

9

'When atlastin meets spastin'.

Di Fabio R, Tessa A, Marcotulli C, Leonardi L, Pierelli F, Santorelli FM, Casali C. Di Fabio R, et al. Among authors: tessa a. Clin Genet. 2014 Nov;86(5):504-5. doi: 10.1111/cge.12331. Epub 2014 Jan 13. Clin Genet. 2014. PMID: 24417445 No abstract available.

10

Do not jump to easy conclusions! Lessons from pitfall in the molecular diagnosis of ARSACS.

Masciullo M, Silvestri G, Modoni A, Tessa A, Bianchi ML, Santorelli FM. Masciullo M, et al. Among authors: tessa a. Clin Genet. 2014 Oct;86(4):396-7. doi: 10.1111/cge.12295. Epub 2013 Oct 25. Clin Genet. 2014. PMID: 24164681 No abstract available.

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