Avemaria F - Search Results

1

Role of fructosamine-3-kinase in protecting against the onset of microvascular and macrovascular complications in patients with T2DM.

Sartore G, Ragazzi E, Burlina S, Paleari R, Chilelli NC, Mosca A, Avemaria F, Lapolla A. Sartore G, et al. Among authors: avemaria f. BMJ Open Diabetes Res Care. 2020 May;8(1):e001256. doi: 10.1136/bmjdrc-2020-001256. BMJ Open Diabetes Res Care. 2020. PMID: 32467223 Free PMC article.

2

Possible role of fructosamine 3-kinase genotyping for the management of diabetic patients.

Avemaria F, Carrera P, Lapolla A, Sartore G, Chilelli NC, Paleari R, Ambrosi A, Ferrari M, Mosca A. Avemaria F, et al. Clin Chem Lab Med. 2015 Aug;53(9):1315-20. doi: 10.1515/cclm-2015-0207. Clin Chem Lab Med. 2015. PMID: 26352355 Free article.

3

PDCD10 gene mutations in multiple cerebral cavernous malformations.

Cigoli MS, Avemaria F, De Benedetti S, Gesu GP, Accorsi LG, Parmigiani S, Corona MF, Capra V, Mosca A, Giovannini S, Notturno F, Ciccocioppo F, Volpi L, Estienne M, De Michele G, Antenora A, Bilo L, Tavoni A, Zamponi N, Alfei E, Baranello G, Riva D, Penco S. Cigoli MS, et al. Among authors: avemaria f. PLoS One. 2014 Oct 29;9(10):e110438. doi: 10.1371/journal.pone.0110438. eCollection 2014. PLoS One. 2014. PMID: 25354366 Free PMC article.

4

De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformations.

Mosca L, Pileggi S, Avemaria F, Tarlarini C, Cigoli MS, Capra V, De Marco P, Pavanello M, Marocchi A, Penco S. Mosca L, et al. Among authors: avemaria f. J Mol Neurosci. 2012 Jul;47(3):475-80. doi: 10.1007/s12031-012-9741-5. Epub 2012 Mar 14. J Mol Neurosci. 2012. PMID: 22415356

5

Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression.

Avemaria F, Lunetta C, Tarlarini C, Mosca L, Maestri E, Marocchi A, Melazzini M, Penco S, Corbo M. Avemaria F, et al. Amyotroph Lateral Scler. 2011 May;12(3):228-30. doi: 10.3109/17482968.2011.566930. Epub 2011 Mar 28. Amyotroph Lateral Scler. 2011. PMID: 21438761

6

Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject.

Mosca L, Lunetta C, Tarlarini C, Avemaria F, Maestri E, Melazzini M, Corbo M, Penco S. Mosca L, et al. Among authors: avemaria f. Neurobiol Aging. 2012 Aug;33(8):1846.e1-4. doi: 10.1016/j.neurobiolaging.2012.01.108. Epub 2012 Mar 6. Neurobiol Aging. 2012. PMID: 22398199

7

Phenotypic heterogeneity in a SOD1 G93D Italian ALS family: an example of human model to study a complex disease.

Penco S, Lunetta C, Mosca L, Maestri E, Avemaria F, Tarlarini C, Patrosso MC, Marocchi A, Corbo M. Penco S, et al. Among authors: avemaria f. J Mol Neurosci. 2011 May;44(1):25-30. doi: 10.1007/s12031-010-9480-4. Epub 2010 Dec 1. J Mol Neurosci. 2011. PMID: 21120636

8

Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort.

Ricci C, Battistini S, Avemaria F, Benigni M, Tarlarini C, Giannini F, Corbo M, Lunetta C, Penco S. Ricci C, et al. Among authors: avemaria f. Gene. 2015 Sep 1;568(2):186-9. doi: 10.1016/j.gene.2015.05.040. Epub 2015 May 19. Gene. 2015. PMID: 26003296

9

Novel FUS mutations identified through molecular screening in a large cohort of familial and sporadic amyotrophic lateral sclerosis.

Tarlarini C, Lunetta C, Mosca L, Avemaria F, Riva N, Mantero V, Maestri E, Quattrini A, Corbo M, Melazzini MG, Penco S. Tarlarini C, et al. Among authors: avemaria f. Eur J Neurol. 2015 Nov;22(11):1474-81. doi: 10.1111/ene.12772. Epub 2015 Jul 15. Eur J Neurol. 2015. PMID: 26176978

10

Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotype.

Lunetta C, Sansone VA, Penco S, Mosca L, Tarlarini C, Avemaria F, Maestri E, Melazzini MG, Meola G, Corbo M. Lunetta C, et al. Among authors: avemaria f. Eur J Neurol. 2014 Apr;21(4):594-8. doi: 10.1111/ene.12345. Epub 2014 Jan 28. Eur J Neurol. 2014. PMID: 24471417

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