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Journal of Lipid Research
|
August 12, 2010
Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian population
Ilaria Guella, Rosanna Asselta, Diego Ardissino, et al.
The FEBS Journal
|
November 1, 2007
A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency
Cristina Bozzao, Valeria Rimoldi, Rosanna Asselta, et al.
Epilepsia
|
April 16, 2002
Mutational analysis of nicotinic acetylcholine receptor beta2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsy
Stefano Duga, Rosanna Asselta, Maria Teresa Bonati, et al.
Thoracic Cancer
|
March 11, 2021
Mutation profile and immunoscore signature in thymic carcinomas: An exploratory study and review of the literature
Rosanna Asselta, Luca Di Tommaso, Matteo Perrino, et al.
Thrombosis and Haemostasis
|
November 28, 2014
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency
Rosanna Asselta, Manuela Platè, Michela Robusto, et al.
Brain : a Journal of Neurology
|
August 15, 2020
Saposin D variants are not a common cause of familial Parkinson's disease among Italians
Daniele Facchi, Valeria Rimoldi, Letizia Straniero, et al.
Journal of Neurology
|
August 27, 2002
Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated families
Maria Teresa Bonati, Romina Combi, Rosanna Asselta, et al.
Scientific Reports
|
October 7, 2017
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p
Letizia Straniero, Valeria Rimoldi, Maura Samarani, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 9, 2025
Genetics Influences Telomere Length in Parkinson's Disease: A Study in Monozygotic Discordant Twins
Letizia Straniero, Valeria Rimoldi, Emanuele Cereda, et al.
Neurology. Genetics
|
August 18, 2020
Late-onset leukoencephalopathy in a patient with recessive <i>EARS2</i> mutations
Edoardo Monfrini, Dario Ronchi, Giulia Franco, et al.
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of 15
Search research articles
Search
Showing results (61-70 of 141) with videos related to
Sort By:
Page
of 15
Journal of Lipid Research
|
August 12, 2010
Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian population
Ilaria Guella, Rosanna Asselta, Diego Ardissino, et al.
The FEBS Journal
|
November 1, 2007
A novel factor XI missense mutation (Val371Ile) in the activation loop is responsible for a case of mild type II factor XI deficiency
Cristina Bozzao, Valeria Rimoldi, Rosanna Asselta, et al.
Epilepsia
|
April 16, 2002
Mutational analysis of nicotinic acetylcholine receptor beta2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsy
Stefano Duga, Rosanna Asselta, Maria Teresa Bonati, et al.
Thoracic Cancer
|
March 11, 2021
Mutation profile and immunoscore signature in thymic carcinomas: An exploratory study and review of the literature
Rosanna Asselta, Luca Di Tommaso, Matteo Perrino, et al.
Thrombosis and Haemostasis
|
November 28, 2014
Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency
Rosanna Asselta, Manuela Platè, Michela Robusto, et al.
Brain : a Journal of Neurology
|
August 15, 2020
Saposin D variants are not a common cause of familial Parkinson's disease among Italians
Daniele Facchi, Valeria Rimoldi, Letizia Straniero, et al.
Journal of Neurology
|
August 27, 2002
Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated families
Maria Teresa Bonati, Romina Combi, Rosanna Asselta, et al.
Scientific Reports
|
October 7, 2017
The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p
Letizia Straniero, Valeria Rimoldi, Maura Samarani, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 9, 2025
Genetics Influences Telomere Length in Parkinson's Disease: A Study in Monozygotic Discordant Twins
Letizia Straniero, Valeria Rimoldi, Emanuele Cereda, et al.
Neurology. Genetics
|
August 18, 2020
Late-onset leukoencephalopathy in a patient with recessive <i>EARS2</i> mutations
Edoardo Monfrini, Dario Ronchi, Giulia Franco, et al.
Page
of 15