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Neuromuscular Disorders : NMD|July 10, 1999
A novel de novo mutation in the triple helix of the COL6A3 gene in a two-generation Italian family affected by Bethlem myopathy. A diagnostic approach in the mutations' screening of type VI collagenG Pepe, E Bertini, B Giusti, et al.
Biochemical and Biophysical Research Communications|November 4, 2000
Unusual laminin alpha2 processing in myoblasts from a patient with a novel variant of congenital muscular dystrophyG Lattanzi, F Muntoni, P Sabatelli, et al.
Neuromuscular Disorders : NMD|June 3, 1998
Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery-Dreifuss muscular dystrophy patients and carriersP Sabatelli, S Squarzoni, S Petrini, et al.
Muscle & Nerve|October 1, 1994
Fetus-like dystrophin expression and other cytoskeletal protein abnormalities in centronuclear myopathiesM Mora, L Morandi, L Merlini, et al.
American Journal of Medical Genetics|January 2, 1995
Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disordersA Ferlini, M C Patrosso, D Guidetti, et al.
Breast Cancer Research and Treatment|August 10, 2000
Is salvage chemotherapy for metastatic breast cancer always effective and well tolerated? A phase II randomized trial of vinorelbine versus 5-fluorouracil plus leucovorin versus combination of mitoxantrone, 5-fluorouracil plus leucovorinA Venturino, D Comandini, C Simoni, et al.
Journal of Submicroscopic Cytology and Pathology|July 1, 1997
Immunolocalization of several laminin chains in the normal human central and peripheral nervous systemM Villanova, C Sewry, A Malandrini, et al.
European Journal of Cancer (Oxford, England : 1990)|January 1, 1991
Adjuvant cisplatin-based chemotherapy for stage I and II ovarian cancer: a 7-year experienceS Chiara, S Mammoliti, C Oliva, et al.
Cell Death and Differentiation|February 12, 2011
Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscleE Mattioli, M Columbaro, C Capanni, et al.
Biochemical and Biophysical Research Communications|May 18, 1999
A heterozygous splice site mutation in COL6A1 leading to an in-frame deletion of the alpha1(VI) collagen chain in an italian family affected by bethlem myopathyG Pepe, B Giusti, E Bertini, et al.
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