Missaglia S - Search Results

1

Harm avoidance moderates the influence of serotonin transporter gene variants on treatment outcome in bipolar patients.

Mandelli L, Mazza M, Martinotti G, Di Nicola M, Tavian D, Colombo E, Missaglia S, De Ronchi D, Colombo R, Janiri L, Serretti A. Mandelli L, et al. Among authors: missaglia s. J Affect Disord. 2009 Dec;119(1-3):205-9. doi: 10.1016/j.jad.2009.02.027. Epub 2009 Mar 29. J Affect Disord. 2009. PMID: 19332357

2

Further evidence supporting the influence of brain-derived neurotrophic factor on the outcome of bipolar depression: independent effect of brain-derived neurotrophic factor and harm avoidance.

Mandelli L, Mazza M, Martinotti G, Tavian D, Colombo E, Missaglia S, Di Nicola M, De Ronchi D, Negri G, Colombo R, Janiri L, Serretti A. Mandelli L, et al. Among authors: missaglia s. J Psychopharmacol. 2010 Dec;24(12):1747-54. doi: 10.1177/0269881109353463. Epub 2010 Feb 8. J Psychopharmacol. 2010. PMID: 20142305

3

Further evidence supporting the association between 5HTR2C gene and bipolar disorder.

Mazza M, Mandelli L, Martinotti G, Di Nicola M, Tavian D, Negri G, Colombo E, Missaglia S, De Ronchi D, Colombo R, Janiri L, Serretti A. Mazza M, et al. Among authors: missaglia s. Psychiatry Res. 2010 Dec 30;180(2-3):151-2. doi: 10.1016/j.psychres.2009.12.006. Epub 2010 May 21. Psychiatry Res. 2010. PMID: 20494452

4

A myopathy with unusual features caused by PNPLA2 gene mutations.

Pennisi EM, Missaglia S, Dimauro S, Bernardi C, Akman HO, Tavian D. Pennisi EM, et al. Among authors: missaglia s. Muscle Nerve. 2015 Apr;51(4):609-13. doi: 10.1002/mus.24477. Epub 2015 Feb 28. Muscle Nerve. 2015. PMID: 25287355

5

Social stress regulation in 4-month-old infants: contribution of maternal social engagement and infants' 5-HTTLPR genotype.

Montirosso R, Provenzi L, Tavian D, Morandi F, Bonanomi A, Missaglia S, Tronick E, Borgatti R. Montirosso R, et al. Among authors: missaglia s. Early Hum Dev. 2015 Mar;91(3):173-9. doi: 10.1016/j.earlhumdev.2015.01.010. Epub 2015 Feb 9. Early Hum Dev. 2015. PMID: 25676184

6

Novel missense mutations in PNPLA2 causing late onset and clinical heterogeneity of neutral lipid storage disease with myopathy in three siblings.

Missaglia S, Tasca E, Angelini C, Moro L, Tavian D. Missaglia S, et al. Mol Genet Metab. 2015 Jun-Jul;115(2-3):110-7. doi: 10.1016/j.ymgme.2015.05.001. Epub 2015 May 2. Mol Genet Metab. 2015. PMID: 25956450 Free article.

7

COMT_val158met polymorphism is associated with behavioral response and physiologic reactivity to socio-emotional stress in 4-month-old infants.

Montirosso R, Provenzi L, Tavian D, Missaglia S, Raggi ME, Borgatti R. Montirosso R, et al. Among authors: missaglia s. Infant Behav Dev. 2016 Nov;45(Pt A):71-82. doi: 10.1016/j.infbeh.2016.09.006. Epub 2016 Oct 13. Infant Behav Dev. 2016. PMID: 27744110

8

The BDNF_val66met polymorphism and individual differences in temperament in 4-month-old infants: A pilot study.

Giusti L, Provenzi L, Tavian D, Missaglia S, Butti N, Montirosso R. Giusti L, et al. Among authors: missaglia s. Infant Behav Dev. 2017 May;47:22-26. doi: 10.1016/j.infbeh.2017.01.006. Epub 2017 Mar 21. Infant Behav Dev. 2017. PMID: 28340382

9

Heterogeneous Phenotypes in Lipid Storage Myopathy Due to ETFDH Gene Mutations.

Angelini C, Tavian D, Missaglia S. Angelini C, et al. Among authors: missaglia s. JIMD Rep. 2018;38:33-40. doi: 10.1007/8904_2017_27. Epub 2017 Apr 30. JIMD Rep. 2018. PMID: 28456887 Free PMC article.

10

Clinical and genetic characterization of a Chanarin Dorfman Syndrome patient born to diseased parents.

Durdu M, Missaglia S, Moro L, Tavian D. Durdu M, et al. Among authors: missaglia s. BMC Med Genet. 2018 May 29;19(1):88. doi: 10.1186/s12881-018-0610-0. BMC Med Genet. 2018. PMID: 29843625 Free PMC article.

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