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Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle

Cell death and differentiation, 2011-08, Vol.18 (8), p.1305-1315

2011

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Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment

Cellular and molecular life sciences : CMLS, 2005-11, Vol.62 (22), p.2669-2678, Article 2669

2005

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Autosomal recessive myosclerosis myopathy is a collagen VI disorder

Neurology, 2008-10, Vol.71 (16), p.1245-1253

2008

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Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria

European journal of histochemistry, 2011-10, Vol.55 (4), p.e36-e36

2011

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Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies

Biochimica et biophysica acta, 2014-09, Vol.1842 (9), p.1604-1612

2014

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A recently developed bifacial platelet-rich fibrin matrix

European Cells and Materials, 2010-07, Vol.20, p.13-23

2010

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Autosomal recessive Bethlem myopathy

Neurology, 2009-12, Vol.73 (22), p.1883-1891

2009

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Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathies

Journal of cellular physiology, 2012-07, Vol.227 (7), p.2927-2935

2012

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Ceramic wear debris in hip prosthesis perimplant environment. Correlation between synovial fluid and neocapsule

Bone (New York, N.Y.), 2012-05, Vol.50, p.S188-S188

2012

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Monocyte chemoattractant protein-1 is strongly expressed during the process of wearing of metal on metal hip prosthesis

Bone (New York, N.Y.), 2011-05, Vol.48, p.S264-S264

2011

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Erratum - Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria

European journal of histochemistry, 2013-12, Vol.57 (4), p.42-e42

2013

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Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery–Dreifuss muscular dystrophy

Journal of medical genetics, 2005-03, Vol.42 (3), p.214-220

2005

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Ceramic wear debris in synovial fluid allow early diagnosis of hip prosthesis failure

Bone (New York, N.Y.), 2009-06, Vol.44, p.S289-S289

2009

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Lamin A involvement in ageing processes

Ageing research reviews, 2020-09, Vol.62, p.101073-101073, Article 101073

2020

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Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophy

Muscle & nerve, 1999-07, Vol.22 (7), p.864-869

1999

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P2.7 Collagen VI alpha5 and alpha6 chains expression in human muscle

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.662-663

2011

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All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype

Oncotarget, 2015-10, Vol.6 (30), p.29914-29928

2015

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G.P.15.04 Collagen VI deficiency in skin fibroblasts from progeroid laminopathies

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.648-648

2009

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A case report of fracture of ceramic head in total hip arthroplasty: histological and biochemical features of perimplant tissues

International journal of artificial organs, 2006-08, Vol.29 (8), p.800-808

2006

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The effect of gentamicin sulphate on the fracture properties of a manually mixed bone cement

Fatigue & fracture of engineering materials & structures, 2007-06, Vol.30 (6), p.479-488

2007

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EM.P.5.08 Novel collagen VI alpha chains distribution in murine skeletal muscle: Possible implications for neuromuscular disorders

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.632-632

2009

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EM.P.4.07 Autosomal recessive Bethlem myopathy

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.608-609

2009

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EM.P.5.06 Collagen VI alpha5 chain exhibits a restricted localization at junctions in human skeletal muscle and skin

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.631-631

2009

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EM.P.4.09 Immunofluorescence and morphological alterations of capillary wall in skeletal muscle of two myosclerosis myopathy patients

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.609-609

2009

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Determination of Crystallinity and Crystal Structure of Hylamer™ Polyethylene after in vivo Wear

Journal of biomaterials applications, 2006-10, Vol.21 (2), p.131-145

2006

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Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle

Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment

Autosomal recessive myosclerosis myopathy is a collagen VI disorder

Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria

Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies

A recently developed bifacial platelet-rich fibrin matrix

Autosomal recessive Bethlem myopathy

Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathies

Ceramic wear debris in hip prosthesis perimplant environment. Correlation between synovial fluid and neocapsule

Monocyte chemoattractant protein-1 is strongly expressed during the process of wearing of metal on metal hip prosthesis

Erratum - Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria

Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery–Dreifuss muscular dystrophy

Ceramic wear debris in synovial fluid allow early diagnosis of hip prosthesis failure

Lamin A involvement in ageing processes

Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophy

P2.7 Collagen VI alpha5 and alpha6 chains expression in human muscle

All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype

G.P.15.04 Collagen VI deficiency in skin fibroblasts from progeroid laminopathies

A case report of fracture of ceramic head in total hip arthroplasty: histological and biochemical features of perimplant tissues

The effect of gentamicin sulphate on the fracture properties of a manually mixed bone cement

EM.P.5.08 Novel collagen VI alpha chains distribution in murine skeletal muscle: Possible implications for neuromuscular disorders

EM.P.4.07 Autosomal recessive Bethlem myopathy

EM.P.5.06 Collagen VI alpha5 chain exhibits a restricted localization at junctions in human skeletal muscle and skin

EM.P.4.09 Immunofluorescence and morphological alterations of capillary wall in skeletal muscle of two myosclerosis myopathy patients

Determination of Crystallinity and Crystal Structure of Hylamer™ Polyethylene after in vivo Wear

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