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

Journal of thrombosis and haemostasis, 2012-07, Vol.10 (7), p.1220-1230

2012

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

Neurology, 2010-07, Vol.75 (3), p.265-272

2010

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

Neurology, 2006-03, Vol.66 (5), p.755-758

2006

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P368: Association between dysphagia and OSAS in acute stroke patients

Clinical neurophysiology, 2014-06, Vol.125, p.S145-S145

2014

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Therapy Related Leukemias: Susceptibility, Prevention and Treatment

Leukemia & lymphoma, 2001, Vol.41 (3-4), p.255-276

2001

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P2.64 Muscle imaging in hereditary inclusion-body myopathy

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.679-679

2011

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P10.20 Modifications of cortical hippocampal connectivity in transient global amnesia: an EEG coherence study

Clinical neurophysiology, 2011, Vol.122, p.S109-S109

2011

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Validation study of the Richard’s Campbell Sleep Questionnaire in patients with acute stroke

Sleep medicine, 2022-12, Vol.100, p.S175-S176

2022

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Hereditary inclusion-body myopathy with sparing of the quadriceps: the many tiles of an incomplete puzzle

Acta myologica, 2011-10, Vol.30 (2), p.91-95

2011

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Mesoangioblasts of inclusion-body myositis: a twofold tool to study pathogenic mechanisms and enhance defective muscle regeneration

Acta myologica, 2011-06, Vol.30 (1), p.24-28

2011

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Cyclooxygenase-1, but not -2, is upregulated in NB4 leukemic cells and human primary promyelocytic blasts during differentiation

Leukemia, 2004-08, Vol.18 (8), p.1373-1379

2004

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G.P.5.05 Transient overexpression of the Rho family exchange factor GEFT stimulates myogenic differentiation of inclusion-body myositis (IBM) mesoangioblasts

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.770-770

2008

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G.P.13.13 Age-related abnormalities and reduced expression of the Notch ligand Delta in IBM primary muscle cultures. A clue for diminished regenerative potential of satellite cells in IBM muscle?

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.852-852

2007

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G.P.13.14 Ex vivo treatment with TSA and IGF-1 induces myogenic differentiation of inclusion-body myositis mesoangioblasts

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.852-853

2007

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G.P.17.05 Predictive role of NCAM in the identification of patients with HIBM due to GNE mutations with atypical clinical phenotype

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.885-885

2007

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

Journal of neuroimmunology, 2007-12, Vol.192 (1), p.174-183

2007

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Differentiation therapy in myelodysplastic syndromes

Seminars in hematology, 1996-07, Vol.33 (3), p.236-245

1996

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

Molecular carcinogenesis, 1997-08, Vol.19 (4), p.254-257

1997

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

Journal of neurochemistry, 2006-02, Vol.96 (3), p.777-789

2006

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Characterization of a second human cyclin A that is highly expressed in testis and in several leukemic cell lines

Cancer research (Chicago, Ill.), 1997-03, Vol.57 (5), p.913-920

1997

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

British journal of haematology, 2003-07, Vol.122 (2), p.226-230

2003

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Molecular analysis of the cyclin-dependent kinase inhibitor gene p27/Kip1 in human malignancies

Cancer research (Chicago, Ill.), 1995-06, Vol.55 (11), p.2266-2269

1995

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A Novel, Myeloid Transcription Factor, C/EBPε, Is Upregulated During Granulocytic, But Not Monocytic, Differentiation

Blood, 1997-10, Vol.90 (7), p.2591-2600

1997

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Pseudoperipheral tongue weakness

Journal of neurology, neurosurgery and psychiatry, 2010-09, Vol.81 (9), p.1024-1025

2010

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Alterations of the cyclin-dependent kinase inhibitor p19 (INK4D) is rare in hematopoietic malignancies

Leukemia, 1996-12, Vol.10 (12), p.1897-1900

1996

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

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

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

P368: Association between dysphagia and OSAS in acute stroke patients

Therapy Related Leukemias: Susceptibility, Prevention and Treatment

P2.64 Muscle imaging in hereditary inclusion-body myopathy

P10.20 Modifications of cortical hippocampal connectivity in transient global amnesia: an EEG coherence study

Validation study of the Richard’s Campbell Sleep Questionnaire in patients with acute stroke

Hereditary inclusion-body myopathy with sparing of the quadriceps: the many tiles of an incomplete puzzle

Mesoangioblasts of inclusion-body myositis: a twofold tool to study pathogenic mechanisms and enhance defective muscle regeneration

Cyclooxygenase-1, but not -2, is upregulated in NB4 leukemic cells and human primary promyelocytic blasts during differentiation

G.P.5.05 Transient overexpression of the Rho family exchange factor GEFT stimulates myogenic differentiation of inclusion-body myositis (IBM) mesoangioblasts

G.P.13.13 Age-related abnormalities and reduced expression of the Notch ligand Delta in IBM primary muscle cultures. A clue for diminished regenerative potential of satellite cells in IBM muscle?

G.P.13.14 Ex vivo treatment with TSA and IGF-1 induces myogenic differentiation of inclusion-body myositis mesoangioblasts

G.P.17.05 Predictive role of NCAM in the identification of patients with HIBM due to GNE mutations with atypical clinical phenotype

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

Differentiation therapy in myelodysplastic syndromes

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

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

Characterization of a second human cyclin A that is highly expressed in testis and in several leukemic cell lines

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

Molecular analysis of the cyclin-dependent kinase inhibitor gene p27/Kip1 in human malignancies

A Novel, Myeloid Transcription Factor, C/EBPε, Is Upregulated During Granulocytic, But Not Monocytic, Differentiation

Pseudoperipheral tongue weakness

Alterations of the cyclin-dependent kinase inhibitor p19 (INK4D) is rare in hematopoietic malignancies

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