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Cancer Research|May 29, 2000
Estradiol induces functional inactivation of p53 by intracellular redistributionA M Molinari, P Bontempo, E M Schiavone, et al.Neuromuscular Disorders : NMD|March 21, 2001
Evaluation of cardiac and respiratory involvement in sarcoglycanopathiesL Politano, V Nigro, L Passamano, et al.Human Molecular Genetics|August 1, 1996
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoproteinV Nigro, G Piluso, A Belsito, et al.Annals of Neurology|August 1, 1997
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sampleM Mora, L Cartegni, C Di Blasi, et al.Human Molecular Genetics|December 1, 1996
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophiesM Vainzof, M R Passos-Bueno, M Canovas, et al.Clinical Genetics|March 5, 2016
Expanding the phenotype of RTTN variations: a new family with primary microcephaly, severe growth failure, brain malformations and dermatitisA Grandone, A Torella, C Santoro, et al.Human Heredity|August 7, 1998
Exclusion of identified LGMD1 loci from four dominant limb-girdle muscular dystrophy familiesM C Speer, J M Vance, F Lennon-Graham, et al.Journal of Physics. Condensed Matter : an Institute of Physics Journal|February 8, 2024
Advanced spectroscopic investigation of colour centres in LiF crystals irradiated with monochromatic hard x-raysM A Vincenti, R M Montereali, F Bonfigli, et al.Journal of Medical Genetics|September 6, 2005
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypesG Piluso, L Politano, S Aurino, et al.Orphanet Journal of Rare Diseases|July 9, 2016
MYH7-related myopathies: clinical, histopathological and imaging findings in a cohort of Italian patientsC Fiorillo, G Astrea, M Savarese, et al.Pageof 7