INSL3: a marker of Leydig cell function and testis-bone-skeletal muscle network
2020-01-01 Facondo, Paolo; Delbarba, Andrea; Maffezzoni, Filippo; Cappelli, Carlo; Ferlin, Alberto
Hypogonadism and bone health in men with HIV
2020-01-01 Maffezzoni, F.; Porcelli, T.; Delbarba, A.; Pezzaioli, L. C.; Properzi, M.; Cappelli, C.; Castelli, F.; Quiros-Roldan, M. E.; Ferlin, A.
Personalized Medicine in prostate cancer: future perspectives for tailored treatments
2015-01-01 Alitto, Ar; Gatta, R; Meldolesi, E; Masciocchi, C; Damiani, A; Lanzotti, V; Valentini, V; Mantini, G
Magnetic Resonance, Vendor-independent, Intensity Histogram Analysis Predicting Pathologic Complete Response After Radiochemotherapy of Rectal Cancer
2018-01-01 Dinapoli, N; Barbaro, B; Gatta, R; Chiloiro, G; Casa, C; Masciocchi, C; Damiani, A; Boldrini, L; Gambacorta, A; Dezio, M; Mattiucci, C; Balducci, M; van Soest, J; Dekker, A; Lambin, P; Fiorino, C; Sini, C; De Cobelli, F; Di Muzio, N; Gumina, C; Passoni, P; Manfredi, R; Valentini, V
Towards a modular decision support system for radiomics: a case study on rectal cancer
2019-01-01 Gatta, R; Vallati, M; Dinapoli, N; Masciocchi, C; Lenkowicz, J; Cusumano, D; Casá, C; Farchione, A; Damiani, A; van Soest, J; Dekker, A; Valentini, V
The molecular species responsible for α1 -antitrypsin deficiency are suppressed by a small molecule chaperone
2020-01-01 Ronzoni, Riccardo; Heyer-Chauhan, Nina; Fra, Annamaria; Pearce, Andrew C; Rüdiger, Martin; Miranda, Elena; Irving, James A; Lomas, David A
T-cell anti-apoptotic mechanisms in inflammatory myopathies
2000-01-01 Vattemi, G.; Tonin, P.; Filosto, M.; Spagnolo, M.; Rizzuto, N.; Tomelleri, G.
A new mutation in the mitochondrial tRNAAla gene in a patient with ophthalmoplegia and dysphagia
2001-01-01 Spagnolo, M.; Tomelleri, G.; Vattemi, G.; Filosto, M.; Rizzuto, N.; Tonin, P.
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy
2001-01-01 Zanusso, G.; Vattemi, G.; Ferrari, S.; Tabaton, M.; Pecini, E.; Cavallaro, T.; Tomelleri, G.; Filosto, M.; Tonin, P.; Nardelli, E.; Rizzuto, N.; Monaco, S.
Dermatomyositis and retroperitoneal germ cell cancer
2001-01-01 Vattemi, G.; Tonin, P.; Martignoni, G.; Filosto, M.; Marchioretto, F.; Rizzuto, N.; Tomelleri, G.
Axillary injection of botulinum A toxin in a patient with muscle cramps associated with severe axillary hyperhidrosis
2001-01-01 Filosto, M.; Bertolasi, L.; Fincati, E.; Priori, A.; Tomelleri, G.; Chieregato, G.; Rizzuto, N.
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: A case report
2001-01-01 Filosto, M.; Tonin, P.; Vattemi, G.; Bongiovanni, L. G.; Rizzuto, N.; Tomelleri, G.
Spinal muscular atrophy and mitochondrial DNA depletion. Response to Berber et al. (2003) Acta Neuropathol 105:245-251
2003-01-01 Mancuso, M.; Filosto, M.; Hirano, M.; Dimauro, S.
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases
2002-01-01 Filosto, M.; Tonin, P.; Vattemi, G.; Spagnolo, M.; Rizzuto, N.; Tomelleri, G.
A screening for superoxide dismutase-1 D90A mutation in Italian patients with sporadic amyotrophic lateral sclerosis
2002-01-01 Mancuso, M.; Filosto, M.; Naini, A.; Rocchi, A.; Del Corona, A.; Sartucci, F.; Siciliano, G.; Murri, L.
Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene
2003-01-01 Mancuso, M.; Filosto, M.; Bonilla, E.; Hirano, M.; Shanske, S.; Vu, T. H.; Dimauro, S.
Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase γ
2003-01-01 Filosto, M.; Mancuso, M.; Nishigaki, Y.; Pancrudo, J.; Harati, Y.; Gooch, C.; Mankodi, A.; Bayne, L.; Bonilla, E.; Shanske, S.; Hirano, M.; Dimauro, S.
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease
2003-01-01 Simonati, A.; Filosto, M.; Tomelleri, G.; Savio, C.; Tonin, P.; Polo, A.; Rizzuto, N.
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease)
2003-01-01 Simonati, A.; Filosto, M.; Savio, C.; Tomelleri, G.; Tonin, P.; Dalla Bernardina, B.; Rizzuto, N.
Reversible upper limb muscle weakness with selective loss of thick filaments
2003-01-01 Vattemi, G.; Tonin, P.; Filosto, M.; Savio, C.; Rizzuto, N.; Tomelleri, G.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| INSL3: a marker of Leydig cell function and testis-bone-skeletal muscle network | 1-gen-2020 | Facondo, Paolo; Delbarba, Andrea; Maffezzoni, Filippo; Cappelli, Carlo; Ferlin, Alberto | |
| Hypogonadism and bone health in men with HIV | 1-gen-2020 | Maffezzoni, F.; Porcelli, T.; Delbarba, A.; Pezzaioli, L. C.; Properzi, M.; Cappelli, C.; Castelli, F.; Quiros-Roldan, M. E.; Ferlin, A. | |
| Personalized Medicine in prostate cancer: future perspectives for tailored treatments | 1-gen-2015 | Alitto, Ar; Gatta, R; Meldolesi, E; Masciocchi, C; Damiani, A; Lanzotti, V; Valentini, V; Mantini, G | |
| Magnetic Resonance, Vendor-independent, Intensity Histogram Analysis Predicting Pathologic Complete Response After Radiochemotherapy of Rectal Cancer | 1-gen-2018 | Dinapoli, N; Barbaro, B; Gatta, R; Chiloiro, G; Casa, C; Masciocchi, C; Damiani, A; Boldrini, L; Gambacorta, A; Dezio, M; Mattiucci, C; Balducci, M; van Soest, J; Dekker, A; Lambin, P; Fiorino, C; Sini, C; De Cobelli, F; Di Muzio, N; Gumina, C; Passoni, P; Manfredi, R; Valentini, V | |
| Towards a modular decision support system for radiomics: a case study on rectal cancer | 1-gen-2019 | Gatta, R; Vallati, M; Dinapoli, N; Masciocchi, C; Lenkowicz, J; Cusumano, D; Casá, C; Farchione, A; Damiani, A; van Soest, J; Dekker, A; Valentini, V | |
| The molecular species responsible for α1 -antitrypsin deficiency are suppressed by a small molecule chaperone | 1-gen-2020 | Ronzoni, Riccardo; Heyer-Chauhan, Nina; Fra, Annamaria; Pearce, Andrew C; Rüdiger, Martin; Miranda, Elena; Irving, James A; Lomas, David A | |
| T-cell anti-apoptotic mechanisms in inflammatory myopathies | 1-gen-2000 | Vattemi, G.; Tonin, P.; Filosto, M.; Spagnolo, M.; Rizzuto, N.; Tomelleri, G. | |
| A new mutation in the mitochondrial tRNAAla gene in a patient with ophthalmoplegia and dysphagia | 1-gen-2001 | Spagnolo, M.; Tomelleri, G.; Vattemi, G.; Filosto, M.; Rizzuto, N.; Tonin, P. | |
| Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy | 1-gen-2001 | Zanusso, G.; Vattemi, G.; Ferrari, S.; Tabaton, M.; Pecini, E.; Cavallaro, T.; Tomelleri, G.; Filosto, M.; Tonin, P.; Nardelli, E.; Rizzuto, N.; Monaco, S. | |
| Dermatomyositis and retroperitoneal germ cell cancer | 1-gen-2001 | Vattemi, G.; Tonin, P.; Martignoni, G.; Filosto, M.; Marchioretto, F.; Rizzuto, N.; Tomelleri, G. | |
| Axillary injection of botulinum A toxin in a patient with muscle cramps associated with severe axillary hyperhidrosis | 1-gen-2001 | Filosto, M.; Bertolasi, L.; Fincati, E.; Priori, A.; Tomelleri, G.; Chieregato, G.; Rizzuto, N. | |
| Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: A case report | 1-gen-2001 | Filosto, M.; Tonin, P.; Vattemi, G.; Bongiovanni, L. G.; Rizzuto, N.; Tomelleri, G. | |
| Spinal muscular atrophy and mitochondrial DNA depletion. Response to Berber et al. (2003) Acta Neuropathol 105:245-251 | 1-gen-2003 | Mancuso, M.; Filosto, M.; Hirano, M.; Dimauro, S. | |
| Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases | 1-gen-2002 | Filosto, M.; Tonin, P.; Vattemi, G.; Spagnolo, M.; Rizzuto, N.; Tomelleri, G. | |
| A screening for superoxide dismutase-1 D90A mutation in Italian patients with sporadic amyotrophic lateral sclerosis | 1-gen-2002 | Mancuso, M.; Filosto, M.; Naini, A.; Rocchi, A.; Del Corona, A.; Sartucci, F.; Siciliano, G.; Murri, L. | |
| Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene | 1-gen-2003 | Mancuso, M.; Filosto, M.; Bonilla, E.; Hirano, M.; Shanske, S.; Vu, T. H.; Dimauro, S. | |
| Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase γ | 1-gen-2003 | Filosto, M.; Mancuso, M.; Nishigaki, Y.; Pancrudo, J.; Harati, Y.; Gooch, C.; Mankodi, A.; Bayne, L.; Bonilla, E.; Shanske, S.; Hirano, M.; Dimauro, S. | |
| Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease | 1-gen-2003 | Simonati, A.; Filosto, M.; Tomelleri, G.; Savio, C.; Tonin, P.; Polo, A.; Rizzuto, N. | |
| Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) | 1-gen-2003 | Simonati, A.; Filosto, M.; Savio, C.; Tomelleri, G.; Tonin, P.; Dalla Bernardina, B.; Rizzuto, N. | |
| Reversible upper limb muscle weakness with selective loss of thick filaments | 1-gen-2003 | Vattemi, G.; Tonin, P.; Filosto, M.; Savio, C.; Rizzuto, N.; Tomelleri, G. |
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