Carla Gliubizzi

Author PubWeight™ 10.05^‹?›

Top papers

Rank	Title	Journal	Year	PubWeight™‹?›
1	Novel GNE mutations in Italian families with autosomal recessive hereditary inclusion-body myopathy.	Hum Mutat	2004	1.14
2	MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle.	Proc Natl Acad Sci U S A	2006	1.11
3	Isolation and characterization of mesoangioblasts from facioscapulohumeral muscular dystrophy muscle biopsies.	Stem Cells	2007	1.02
4	Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle.	J Neurochem	2007	0.93
5	Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis.	J Neurochem	2006	0.91
6	alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy.	Neuromuscul Disord	2004	0.87
7	TWEAK in inclusion-body myositis muscle: possible pathogenic role of a cytokine inhibiting myogenesis.	Am J Pathol	2012	0.86
8	Increased aging in primary muscle cultures of sporadic inclusion-body myositis.	Neurobiol Aging	2008	0.84
9	Insulin-like growth factor I in inclusion-body myositis and human muscle cultures.	J Neuropathol Exp Neurol	2004	0.83
10	Mesoangioblasts from facioscapulohumeral muscular dystrophy display in vivo a variable myogenic ability predictable by their in vitro behavior.	Cell Transplant	2010	0.80
11	Vessel-associated stem cells from skeletal muscle: From biology to future uses in cell therapy.	World J Stem Cells	2010	0.79