Santorelli FM - Search Results

1

Pharmacogenomics of episodic migraine: time has come for a step forward.

Viana M, Terrazzino S, Genazzani AA, Grieco GS, Cargnin S, Santorelli FM, Pierelli F, Tassorelli C, Nappi G, Di Lorenzo C. Viana M, et al. Among authors: santorelli fm. Pharmacogenomics. 2014 Mar;15(4):541-9. doi: 10.2217/pgs.14.20. Pharmacogenomics. 2014. PMID: 24624920 Review.

2

Chronic diarrhea associated with the A3243G mtDNA mutation.

Santorelli FM, Villanova M, Malandrini A, Grieco GS, Palmeri S, Merlini L, Casali C. Santorelli FM, et al. Neurology. 2000 Jan 11;54(1):266-7. doi: 10.1212/wnl.54.1.266. Neurology. 2000. PMID: 10636171 No abstract available.

3

mtDNA A3243G MELAS mutation is not associated with multigenerational female migraine.

Buzzi MG, Di Gennaro G, D'Onofrio M, Ciccarelli O, Santorelli FM, Fortini D, Nappi G, Nicoletti F, Casali C. Buzzi MG, et al. Among authors: santorelli fm. Neurology. 2000 Feb 22;54(4):1005-7. doi: 10.1212/wnl.54.4.1005. Neurology. 2000. PMID: 10691007

4

Migraine as a complex disease: heterogeneity, comorbidity and genotype-phenotype interactions.

Nappi G, Costa A, Tassorelli C, Santorelli FM. Nappi G, et al. Among authors: santorelli fm. Funct Neurol. 2000 Apr-Jun;15(2):87-93. Funct Neurol. 2000. PMID: 10916720 Review.

5

Assessing the relative incidence of mitochondrial DNA A3243G in migraine without aura with maternal inheritance.

Di Gennaro G, Buzzi MG, Ciccarelli O, Santorelli FM, Pierelli F, Fortini D, D'Onofrio M, Costa A, Nappi G, Casali C. Di Gennaro G, et al. Among authors: santorelli fm. Headache. 2000 Jul-Aug;40(7):568-71. doi: 10.1046/j.1526-4610.2000.00088.x. Headache. 2000. PMID: 10940095

6

Family-based association study of 5-HTTLPR, TPH, MAO-A, and DRD4 polymorphisms in mood disorders.

Serretti A, Cristina S, Lilli R, Cusin C, Lattuada E, Lorenzi C, Corradi B, Grieco G, Costa A, Santorelli F, Barale F, Nappi G, Smeraldi E. Serretti A, et al. Am J Med Genet. 2002 May 8;114(4):361-9. doi: 10.1002/ajmg.10356. Am J Med Genet. 2002. PMID: 11992558

7

Heterogeneity in migraine: many genes for many phenotypes?

Martini B, Grieco GS, Fortini D, Costa A, Nappi G, Santorelli FM. Martini B, et al. Among authors: santorelli fm. Funct Neurol. 2001;16(4 Suppl):63-7. Funct Neurol. 2001. PMID: 11996532 Review. No abstract available.

8

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: santorelli fm. Neuromuscul Disord. 2003 Feb;13(2):162-5. doi: 10.1016/s0960-8966(02)00221-3. Neuromuscul Disord. 2003. PMID: 12565915

9

Current insights into familial spastic paraparesis: new advances in an old disease.

Fortini D, Cricchi F, Di Fabio R, Damiano M, Comanducci G, Benedetti L, Valoppi M, Grieco GS, D'Eugenio O, Celato A, Santorelli F, Casali C, Amabile GA, Pierelli F. Fortini D, et al. Funct Neurol. 2003 Jan-Mar;18(1):43-9. Funct Neurol. 2003. PMID: 12760414 Review.

10

Multicentre Italian family-based association study on tyrosine hydroxylase, catechol-O-methyl transferase and Wolfram syndrome 1 polymorphisms in mood disorders.

Serretti A, Cusin C, Cristina S, Lorenzi C, Lilli R, Lattuada E, Grieco G, Costa A, Santorelli F, Barale F, Smeraldi E, Nappi G. Serretti A, et al. Psychiatr Genet. 2003 Jun;13(2):121-6. doi: 10.1097/01.ypg.0000056172.32550.f9. Psychiatr Genet. 2003. PMID: 12782971

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