Performance of Distributed Optical Fiber Sensors (DOFS) and Digital Image Correlation (DIC) in the monitoring of RC structures
Bado, M F, Kaklauskas, G, Casas, J R
Published in IOP conference series. Materials Science and Engineering (01.10.2019)
Published in IOP conference series. Materials Science and Engineering (01.10.2019)
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Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV)
Bruno, C, van Diggelen, O P, Cassandrini, D, Gimpelev, M, Giuffrè, B, Donati, M A, Introvini, P, Alegria, A, Assereto, S, Morandi, L, Mora, M, Tonoli, E, Mascelli, S, Traverso, M, Pasquini, E, Bado, M, Vilarinho, L, van Noort, G, Mosca, F, DiMauro, S, Zara, F, Minetti, C
Published in Neurology (28.09.2004)
Published in Neurology (28.09.2004)
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Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy
Cordone, Giuseppe, Zara, Federico, Bricarelli, Franca Dagna, Bado, Massimo, Volonté, Daniela, Scartezzini, Paolo, Egeo, Aliana, Bruno, Claudio, Mazzocco, Michela, Lisanti, Michael P, Minetti, Carlo, Donati, Maria Alice, Galbiati, Ferruccio, Sotgia, Federica, Broda, Paolo, Masetti, Emiliana
Published in Nature genetics (01.04.1998)
Published in Nature genetics (01.04.1998)
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Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemia
Carbone, I, Bruno, C, Sotgia, F, Bado, M, Broda, P, Masetti, E, Panella, A, Zara, F, Bricarelli, F D, Cordone, G, Lisanti, M P, Minetti, C
Published in Neurology (28.03.2000)
Published in Neurology (28.03.2000)
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A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect
Di Maria, E, Gulli, R, Balestra, P, Cassandrini, D, Pigullo, S, Doria-Lamba, L, Bado, M, Schenone, A, Ajmar, F, Mandich, P, Bellone, E
Published in Journal of neurology, neurosurgery and psychiatry (01.10.2004)
Published in Journal of neurology, neurosurgery and psychiatry (01.10.2004)
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Congenital hypomyelination due to myelin protein zero Q215X mutation
Mandich, P., Mancardi, G. L., Varese, A., Soriani, S., Di Maria, E., Bellone, E., Bado, M., Gross, L., Windebank, A. J., Ajmar, F., Schenone, A.
Published in Annals of neurology (01.05.1999)
Published in Annals of neurology (01.05.1999)
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Combined defects of muscle phosphofructokinase and AMP deaminase in a child with myoglobinuria
Bruno, C, Minetti, C, Shanske, S, Morreale, G, Bado, M, Cordone, G, DiMauro, S
Published in Neurology (01.01.1998)
Published in Neurology (01.01.1998)
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Disorganization of dystrophin costameric lattice in Becker muscular dystrophy
Minetti, C., Cordone, G., Beltrame, F., Bado, M., Bonilla, E.
Published in Muscle & nerve (01.02.1998)
Published in Muscle & nerve (01.02.1998)
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A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy
Bruno, C, DiRocco, M, Doria Lamba, L, Bado, M, Marino, C, Tsujino, S, Shanske, S, Stella, G, Minetti, C, van Diggelen, O.P, DiMauro, S
Published in Neuromuscular disorders : NMD (01.10.1999)
Published in Neuromuscular disorders : NMD (01.10.1999)
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Forearm Semi-ischemic Exercise Test in Pediatric Patients
Bruno, Claudio, Bado, Massimo, Minetti, Carlo, Cordone, Giuseppe
Published in Journal of child neurology (01.06.1998)
Published in Journal of child neurology (01.06.1998)
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Tubulopathy, endocrinopathies and encephalomyopathy in a child with a novel large-scale mitochondrial DNA deletion
Bruno, C, Gandullia, P, Santorelli, FM, Biedi, C, Carbone, I, Bado, M, Gatti, R, Minetti, C
Published in Clinical genetics (01.06.2002)
Published in Clinical genetics (01.06.2002)
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Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria
Minetti, C, Garavaglia, B, Bado, M, Invernizzi, F, Bruno, C, Rimoldi, M, Pons, R, Taroni, F, Cordone, G
Published in Neuromuscular disorders : NMD (01.02.1998)
Published in Neuromuscular disorders : NMD (01.02.1998)
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Primary adrenal insufficiency in a child with a mitochondrial DNA deletion
Bruno, C., Minetti, C., Tang, Y., Magalhães, P. J., Santorelli, F. M., Shanske, S., Bado, M., Cordone, G., Gatti, R., DiMauro, S.
Published in Journal of inherited metabolic disease (01.04.1998)
Published in Journal of inherited metabolic disease (01.04.1998)
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Auriculo-condylar syndrome or new syndrome?
Divizia, M T, Cordone, A, Bado, M, Rosaia, L, Cirillo Silengo, M, Ravazzolo, R, Lerone, M
Published in Clinical dysmorphology (01.04.2002)
Published in Clinical dysmorphology (01.04.2002)
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Severe dystrophinopathy in a patient with congenital hypotonia
Cordone, G, Bado, M, Morreale, G, Pedemonte, M, Minetti, C
Published in Child's nervous system (01.08.1996)
Published in Child's nervous system (01.08.1996)
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Diagnostic problems in congenital myotonic dystrophy
DiRocco, M, Gennarelli, M, Veneselli, E, Bado, M, Romanengo, M, Celle, M E, Cordone, G, Borrone, C
Published in European journal of pediatrics (01.11.1996)
Published in European journal of pediatrics (01.11.1996)
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Impairment of Caveolae Formation and T-System Disorganization in Human Muscular Dystrophy with Caveolin-3 Deficiency
Minetti, Carlo, Bado, Massimo, Broda, Paolo, Sotgia, Federica, Bruno, Claudio, Galbiati, Ferruccio, Volonte, Daniela, Lucania, Giuseppe, Pavan, Antonio, Bonilla, Eduardo, Lisanti, Michael P., Cordone, Giuseppe
Published in The American journal of pathology (2002)
Published in The American journal of pathology (2002)
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