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Neurology
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March 27, 2015
Author response
Andrea Cortese, Arianna Tucci
The New England Journal of Medicine
|
May 24, 2023
Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia
Zhongbo Chen, Arianna Tucci, Mina Ryten
Neurology
|
February 11, 2015
Novel CLN3 mutation causing autophagic vacuolar myopathy
Peter E Taschner, Andrea Cortese, Arianna Tucci
Molecular Cytogenetics
|
November 9, 2016
<i>MIR137</i> is the key gene mediator of the syndromic obesity phenotype of patients with 1p21.3 microdeletions
Arianna Tucci, Claudia Ciaccio, Giulietta Scuvera, et al.
BMC Medical Genetics
|
March 13, 2016
The p.Phe174Ser mutation is associated with mild forms of Smith Lemli Opitz Syndrome
Arianna Tucci, Luisa Ronzoni, Carlo Arduino, et al.
American Journal of Medical Genetics. Part A
|
January 13, 2016
Interstitial 6q25 microdeletion syndrome: ARID1B is the key gene
Luisa Ronzoni, Francesco Tagliaferri, Arianna Tucci, et al.
The Prostate
|
January 15, 2008
2-chloroadenosine modulates PAR-1 and IL-23 expression and enhances docetaxel effects on PC3 cells
Alba Minelli, Ilaria Bellezza, Arianna Tucci, et al.
European Journal of Medical Genetics
|
December 24, 2016
16p13 microduplication without CREBBP involvement: Moving toward a phenotype delineation
Claudia Ciaccio, Arianna Tucci, Giulietta Scuvera, et al.
Journal of the Neurological Sciences
|
June 8, 2015
A novel ABCD1 mutation detected by next generation sequencing in presumed hereditary spastic paraplegia: A 30-year diagnostic delay caused by misleading biochemical findings
Georgios Koutsis, David S Lynch, Arianna Tucci, et al.
The Prostate
|
December 25, 2008
Differential involvement of reactive oxygen species and nucleoside transporters in cytotoxicity induced by two adenosine analogues in human prostate cancer cells
Alba Minelli, Ilaria Bellezza, Arianna Tucci, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 75) with videos related to
Sort By:
Page
of 8
Neurology
|
March 27, 2015
Author response
Andrea Cortese, Arianna Tucci
The New England Journal of Medicine
|
May 24, 2023
Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia
Zhongbo Chen, Arianna Tucci, Mina Ryten
Neurology
|
February 11, 2015
Novel CLN3 mutation causing autophagic vacuolar myopathy
Peter E Taschner, Andrea Cortese, Arianna Tucci
Molecular Cytogenetics
|
November 9, 2016
<i>MIR137</i> is the key gene mediator of the syndromic obesity phenotype of patients with 1p21.3 microdeletions
Arianna Tucci, Claudia Ciaccio, Giulietta Scuvera, et al.
BMC Medical Genetics
|
March 13, 2016
The p.Phe174Ser mutation is associated with mild forms of Smith Lemli Opitz Syndrome
Arianna Tucci, Luisa Ronzoni, Carlo Arduino, et al.
American Journal of Medical Genetics. Part A
|
January 13, 2016
Interstitial 6q25 microdeletion syndrome: ARID1B is the key gene
Luisa Ronzoni, Francesco Tagliaferri, Arianna Tucci, et al.
The Prostate
|
January 15, 2008
2-chloroadenosine modulates PAR-1 and IL-23 expression and enhances docetaxel effects on PC3 cells
Alba Minelli, Ilaria Bellezza, Arianna Tucci, et al.
European Journal of Medical Genetics
|
December 24, 2016
16p13 microduplication without CREBBP involvement: Moving toward a phenotype delineation
Claudia Ciaccio, Arianna Tucci, Giulietta Scuvera, et al.
Journal of the Neurological Sciences
|
June 8, 2015
A novel ABCD1 mutation detected by next generation sequencing in presumed hereditary spastic paraplegia: A 30-year diagnostic delay caused by misleading biochemical findings
Georgios Koutsis, David S Lynch, Arianna Tucci, et al.
The Prostate
|
December 25, 2008
Differential involvement of reactive oxygen species and nucleoside transporters in cytotoxicity induced by two adenosine analogues in human prostate cancer cells
Alba Minelli, Ilaria Bellezza, Arianna Tucci, et al.
Page
of 8