Search filters

List of works by Roberta Morosetti

Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy

scientific article published on 01 July 2010

Dysphagia and Obstructive Sleep Apnea in Acute, First-Ever, Ischemic Stroke.

scientific article

Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity

scientific article published on 06 March 2017

Expression of cyclin-dependent kinase inhibitor p15(INK4B) during normal and leukemic myeloid differentiation

scientific article

Granulocyte colony-stimulating factor perturbs lymphocyte mitochondrial function and inhibits cell cycle progression

scientific article published on 01 June 2000

High cyclin-dependent kinase inhibitors in Bcl-2 and Bcl-xL-expressing CD34+-proliferating haematopoietic progenitors

scientific article published on 01 September 2000

Increased aging in primary muscle cultures of sporadic inclusion-body myositis.

scientific article published on 26 September 2008

Integrity of the 1,25-dihydroxyvitamin D3 receptor in bone, lung, and other cancers

scientific article published on August 1, 1997

Isolation and characterization of mesoangioblasts from facioscapulohumeral muscular dystrophy muscle biopsies

scientific article published on 30 August 2007

Mesoangioblasts from facioscapulohumeral muscular dystrophy display in vivo a variable myogenic ability predictable by their in vitro behavior

scientific article published on 22 December 2010

MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle.

scholarly article

NCAM is hyposialylated in hereditary inclusion body myopathy due to GNE mutations

scientific article published on 01 March 2006

Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis.

scientific article published on 9 January 2006

Neurofibromatosis type 1 associated with vertebrobasilar dolichoectasia and pontine ischemic stroke

scientific article published on 18 September 2014

Novel SEC61G-EGFR Fusion Gene in Pediatric Ependymomas Discovered by Clonal Expansion of Stem Cells in Absence of Exogenous Mitogens.

scientific article published in November 2017

Progression of myelodysplastic syndrome: allelic loss on chromosomal arm 1p

scientific article published on 01 July 2003

Sleep disordered breathing in a cohort of patients with sporadic inclusion body myositis.

scientific article published on 11 April 2013

Spontaneous sternocleidomastoid muscle hematoma following thrombolysis for acute ischemic stroke

scientific article published on 13 April 2014

TWEAK in inclusion-body myositis muscle: possible pathogenic role of a cytokine inhibiting myogenesis

scientific article published on 04 February 2012

Teaching NeuroImages: A cutaneous vascular malformation hides giant cerebral aneurysms

scientific article published on 01 April 2018

Thalamic Amnesia Mimicking Transient Global Amnesia.

scientific article published in June 2015

The ER-bound RING finger protein 5 (RNF5/RMA1) causes degenerative myopathy in transgenic mice and is deregulated in inclusion body myositis

scientific article (publication date: 2008)

The effect of disease activity on leptin, leptin receptor and suppressor of cytokine signalling-3 expression in relapsing-remitting multiple sclerosis

scientific article published on 29 September 2007

The recovery of platelet cyclooxygenase activity explains interindividual variability in responsiveness to low-dose aspirin in patients with and without diabetes

scientific article published on 01 July 2012

Therapy related leukemias: susceptibility, prevention and treatment.

scientific article published in April 2001

Thrombus in Transit: A Potentially Life-threatening Complication of Cerebral Sinus Thrombosis

scientific article published on 01 January 2017

Vertebral Artery Dissection Presenting With Isolated Occipital Headache

scientific article published on 05 August 2010

alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy

scientific article published on 10 December 2004