Santorelli FM - Search Results

1

Migraine headache: a review of the molecular genetics of a common disorder.

Di Lorenzo C, Grieco GS, Santorelli FM. Di Lorenzo C, et al. Among authors: santorelli fm. J Headache Pain. 2012 Oct;13(7):571-80. doi: 10.1007/s10194-012-0478-x. Epub 2012 Sep 1. J Headache Pain. 2012. PMID: 22940869 Free PMC article. 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

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

4

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.

5

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

6

Cyclic vomiting syndrome, migraine, and epilepsy: a common underlying disorder?

Cupini LM, Santorelli FM, Iani C, Fariello G, Calabresi P. Cupini LM, et al. Among authors: santorelli fm. Headache. 2003 Apr;43(4):407-9. doi: 10.1046/j.1526-4610.2003.03078.x. Headache. 2003. PMID: 12656714 No abstract available.

7

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.

8

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

9

Six novel mutations of the RUNX2 gene in Italian patients with cleidocranial dysplasia.

Tessa A, Salvi S, Casali C, Garavelli L, Digilio MC, Dotti MT, Di Giandomenico S, Valoppi M, Grieco GS, Comanducci G, Bianchini G, Fortini D, Federico A, Giannotti A, Santorelli FM. Tessa A, et al. Among authors: santorelli fm. Hum Mutat. 2003 Jul;22(1):104. doi: 10.1002/humu.9155. Hum Mutat. 2003. PMID: 12815605

10

Novel SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type.

Grieco GS, Malandrini A, Comanducci G, Leuzzi V, Valoppi M, Tessa A, Palmeri S, Benedetti L, Pierallini A, Gambelli S, Federico A, Pierelli F, Bertini E, Casali C, Santorelli FM. Grieco GS, et al. Among authors: santorelli fm. Neurology. 2004 Jan 13;62(1):103-6. doi: 10.1212/01.wnl.0000104491.66816.77. Neurology. 2004. PMID: 14718707

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