Authors:
Spelbrink, JN
Li, FY
Tiranti, V
Nikali, K
Yuan, QP
Tariq, M
Wanrooij, S
Garrido, N
Comi, G
Morandi, L
Santoro, L
Toscano, A
Fabrizi, GM
Somer, H
Croxen, R
Beeson, D
Poulton, J
Suomalainen, A
Jacobs, HT
Zeviani, M
Larsson, C
Citation: Jn. Spelbrink et al., Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria (vol 28, pg 223, 2001), NAT GENET, 29(1), 2001, pp. 100-100
Authors:
Spelbrink, JN
Li, FY
Tiranti, V
Nikali, K
Yuan, QP
Tariq, M
Wanrooij, S
Garrido, N
Comi, G
Morandi, L
Santoro, L
Toscano, A
Fabrizi, GM
Somer, H
Croxen, R
Beeson, D
Poulton, L
Suomalainen, A
Jacobs, HT
Zeviani, M
Larsson, C
Citation: Jn. Spelbrink et al., Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene LF-like protein localized in mitochondria, NAT GENET, 28(3), 2001, pp. 223-231
Authors:
Gellera, C
Castellotti, B
Riggio, MC
Silani, V
Morandi, L
Testa, D
Casali, C
Taroni, F
Di Donato, S
Zeviani, M
Mariotti, C
Citation: C. Gellera et al., Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations, NEUROMUSC D, 11(4), 2001, pp. 404-410
Authors:
Di Blasi, C
He, Y
Morandi, L
Cornelio, F
Guicheney, P
Mora, M
Citation: C. Di Blasi et al., Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping, BRAIN, 124, 2001, pp. 698-704
Authors:
Villanova, M
Mercuri, E
Bertini, E
Sabatelli, P
Morandi, L
Mora, M
Sewry, C
Brockington, M
Brown, SC
Ferreiro, A
Maraldi, NM
Toda, T
Guicheney, P
Merlini, L
Muntoni, F
Citation: M. Villanova et al., Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndrome, NEUROMUSC D, 10(8), 2000, pp. 541-547
Authors:
Di Blasi, C
Morandi, L
di Barletta, MR
Bione, S
Bernasconi, P
Cerletti, M
Bono, R
Blasevich, F
Toniolo, D
Mora, M
Citation: C. Di Blasi et al., Unusual expression of emerin in a patient with X-linked Emery-Dreifuss muscular dystrophy, NEUROMUSC D, 10(8), 2000, pp. 567-571
Authors:
Di Blasi, C
Mora, M
Pareyson, D
Farina, L
Sghirlanzoni, A
Vignier, N
Blasevich, F
Cornelio, F
Guicheney, P
Morandi, L
Citation: C. Di Blasi et al., Partial laminin alpha 2 chain deficiency in a patient with myopathy resembling inclusion body myositis, ANN NEUROL, 47(6), 2000, pp. 811-816
Authors:
Barresi, R
Di Blasi, C
Negri, T
Brugnoni, R
Vitali, A
Felisari, G
Salandi, A
Daniel, S
Cornelio, F
Morandi, L
Mora, M
Citation: R. Barresi et al., Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations, J MED GENET, 37(2), 2000, pp. 102-107
Authors:
di Barletta, MR
Ricci, E
Galluzzi, G
Tonali, P
Mora, M
Morandi, L
Romorini, A
Voit, T
Orstavik, KH
Merlini, L
Trevisan, C
Biancalana, V
Housmanowa-Petrusewicz, I
Bione, S
Ricotti, R
Schwartz, K
Bonne, G
Toniolo, D
Citation: Mr. Di Barletta et al., Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy, AM J HU GEN, 66(4), 2000, pp. 1407-1412
Authors:
Russo, F
Notarnicola, M
Di Matteo, G
Leoci, C
Caruso, ML
Pirrelli, M
Caradonna, M
Morandi, L
Di Leo, A
Citation: F. Russo et al., Detection of Helicobacter pylori cagA gene by polymerase chain reaction infaecal samples, EUR J GASTR, 11(3), 1999, pp. 251-256
Authors:
Morandi, L
Di Blasi, C
Farina, L
Sorokin, L
Uziel, G
Azan, G
Pini, A
Toscano, A
Lanfossi, M
Galbiati, S
Cornelio, F
Mora, M
Citation: L. Morandi et al., Clinical correlations in 16 patients with total or partial laminin alpha 2deficiency characterized using antibodies against 2 fragments of the protein, ARCH NEUROL, 56(2), 1999, pp. 209-215
Authors:
Lanfossi, M
Cozzi, F
Bugini, D
Colombo, S
Scarpa, P
Morandi, L
Galbiati, S
Cornelio, F
Pozza, O
Mora, M
Citation: M. Lanfossi et al., Development of muscle pathology in canine X-linked muscular dystrophy. I. Delayed postnatal maturation of affected and normal muscle as revealed by myosin isoform analysis and utrophin expression, ACT NEUROP, 97(2), 1999, pp. 127-138
Authors:
Farina, L
Morandi, L
Milanesi, I
Ciceri, E
Mora, M
Moroni, I
Pantaleoni, C
Savoiardo, M
Citation: L. Farina et al., Congenital muscular dystrophy with merosin deficiency: MRI findings in five patients, NEURORADIOL, 40(12), 1998, pp. 807-811