Muscle fiber type disproportion (FTD) in a family with mutations in the LMNA gene (366 views)
Muscle Nerve (ISSN: 0148-639x), 2015; 51(4): 604-608.
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Paper type: Journal Article,
Impact factor: 2.713, 5-year impact factor: 2.474
Url: http://www.scopus.com/inward/record.url?eid=2-s2.0-84925460051&partnerID=40&md5=e6dd7ea88fd0963058d32577cbf3dfac
Keywords: Cardiomyopathy, Ftd, Laminopathy, Lgmd, Lmna, Creatine Kinase, Prednisone, Lmna Protein, Human, Achilles Tendon, Adult, Article, Atrioventricular Conduction, Autosomal Dominant Inheritance, Biceps Brachii Muscle, Bradycardia, Case Report, Computer Assisted Tomography, Congestive Cardiomyopathy, Exon, Fatigue, Female, Fiber Type Disproportion, Flexor Muscle, Gait Disorder, Gene Mutation, Hamstring, Heart Muscle Conduction Disturbance, Heterozygosity, Histopathology, Human Tissue, Hyperlordosis, Iliopsoas Muscle, Limb Girdle Muscular Dystrophy, Middle Aged, Muscle Atrophy, Muscle Biopsy, Muscle Cell, Muscle Disease, Muscle Rigidity, Muscle Strength, Neurologic Examination, Nuclear Magnetic Resonance Imaging, Pacemaker, Phenotype, Polymyositis, Priority Journal, Sinus Bradycardia, Tendon Contracture, Tendon Reflex, Genetic Predisposition, Myopathies, Structural, Congenital, Pedigree, Skeletal Muscle, Genetic Predisposition To Disease, Lamin Type A, Muscle Fibers,
Affiliations:
*** IBB - CNR ***
Department of Neurosciences, Reproductive and Odontostomatological Sciences, University Federico II of Naples, Via Sergio Pansini 5, Naples, Italy
Neuromuscular and Molecular Medicine Unit, Department of Developmental Neuroscience, IRCCS Stella Maris, Pisa, Italy
Institute of Biostructure and Bioimaging (IBB) of the italian National Research Council, Naples, Italy
References:
Bonne, G., Disease associated with myonuclear abnormalities: defects of nuclear membrane related proteins (emerin, lamins a/c) (2002) Structural and molecular basis of skeletal muscle diseases, chapter 3, pp. 48-56. , In: Karpati G, editor. . Basel, Switzerland: ISN Neuropath Pres
Goizet, C., Yaou, R.B., Demay, L., Richard, P., Bouillot, S., Rouanet, M., A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia (2004) J Med Genet, 41, p. e29
Subramanyam, L., Simha, V., Garg, A., Overlapping syndrome with familial partial lipodystrophy, Dunnigan variety and cardiomyopathy due to amino-terminal heterozygous missense lamin A/C mutations (2010) Clin Genet, 78, pp. 66-73
Chen, L., Lee, L., Kudlow, B.A., Dos Santos, H.G., Sletvold, O., Shafeghati, Y., LMNA mutations in atypical Werner's syndrome (2003) Lancet, 362, pp. 440-445
Zirn, B., Kress, W., Grimm, T., Berthold, L.D., Neubauer, B., Kuchelmeister, K., Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy (2008) Am J Med Genet A, 146 A, pp. 1049-1054
Madej-Pilarczyk, A., Rosińska-Borkowska, D., Rekawek, J., Marchel, M., Szaluś, E., Jablońska, S., Progeroid syndrome with scleroderma-like skin changes associated with homozygous R435C LMNA mutation (2009) Am J Med Genet A, 149, pp. 2387-2392
Menezes, M.P., Waddell, L.B., Evesson, F.J., Cooper, S., Webster, R., Jones, K., Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophy (2012) Neurology, 78, pp. 1258-1263
Kajino, S., Ishihara, K., Goto, K., Ishigaki, K., Noguchi, S., Nonaka, I., Congenital fiber type disproportion myopathy caused by LMNA mutations (2014) J Neurol Sci, 340, pp. 94-98
Clarke, N.F., Congenital fiber-type disproportion Semin Pediatr Neurol, 201 (18), pp. 264-271
Clarke, N.F., Kolski, H., Dye, D.E., Lim, E., Smith, R.L., Patel, R., Fahey, M.C., Mutations in TPM3 are a common cause of congenital fiber type disproportion (2008) Ann Neurol, 63, pp. 329-337
Clarke, N.F., Waddell, L.B., Cooper, S.T., Perry, M., Smith, R.L., Kornberg, A.J., Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion (2010) Hum Mutat, 31, pp. 544-550
Laing, N.G., Clarke, N.F., Dye, D.E., Liyanage, K., Walker, K.R., Kobayashi, Y., Actin mutations are one cause of congenital fiber type disproportion (2004) Ann Neurol, 56, pp. 689-694
Ortolano, S., Tarrío, R., Blanco-Arias, P., Teijeira, S., Rodríguez-Trelles, F., García-Murias, M., A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy (2011) Neuromuscul Disord, 21, pp. 254-262
Brandis, A., Aronica, E., Goebel, H.H., TPM2 mutation (2008) Neuromuscul Disord, 18, p. 1005
Bove, K.E., Iannaccone, S.T., Vogler, C., Intramuscular hematopoiesis in hypotonic infants with type 1 muscle fiber dysmaturation (1986) Arch Pathol Lab Med, 110, pp. 207-211
Iannaccone, S.T., Bove, K.E., Vogler, C.A., Buchino, J.J., Type 1 fiber size disproportion: morphometric data from 37 children with myopathic, neuropathic, or idiopathic hypotonia (1987) Pediatr Pathol, 7, pp. 395-419
Schessl, J., Goemans, N.M., Magold, A.I., Zou, Y., Hu, Y., Kirschner, J., Predominant fiber atrophy and fiber type disproportion in early Ullrich disease (2008) Muscle Nerve, 38, pp. 1184-1191
Simón, R., Mateos, F., Seijo, M., Balseiro, J., Madero, S., Cabello, A., Congenital fiber-type disproportion: analysis of a series of 11 cases [in Spanish] (1991) Neurologia, 6, pp. 281-286
Dubowitz, V., (1985) Muscle biopsy. A practical approach, , London: BaillieÁre Tindall
Mercuri, E., An integrated approach to the diagnosis of muscle disorders: what is the role of muscle imaging? (2010) Dev Med Child Neurol, 52, p. 693
Lattanzi, G., Benedetti, S., Bertini, E., Boriani, G., Mazzanti, L., Novelli, G., Laminopathies: many diseases, one gene. Report of the first italian Meeting Course on Laminopathies (2011) Acta Myol, 30, pp. 138-143
Mercuri, E., Poppe, M., Quinlivan, R., Messina, S., Kinali, M., Demay, L., Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene (2004) Arch Neurol, 61, pp. 690-694
Nzwalo, H., Conceição, I., Pereira, P., Santos, R., Evangelista, T., A family with 2 different hereditary diseases leading to early cardiac involvement (2013) J Clin Neuromuscul Dis, 14, pp. 204-208
Van Tintelen, J.P., High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics (2007) Am Heart J, 154, pp. 1130-1139
Muscle Nerve (ISSN: 0148-639x), 2015; 51(4): 604-608.
Export to BibTeX Export to EndNote
Paper type: Journal Article,
Impact factor: 2.713, 5-year impact factor: 2.474
Url: http://www.scopus.com/inward/record.url?eid=2-s2.0-84925460051&partnerID=40&md5=e6dd7ea88fd0963058d32577cbf3dfac
Keywords: Cardiomyopathy, Ftd, Laminopathy, Lgmd, Lmna, Creatine Kinase, Prednisone, Lmna Protein, Human, Achilles Tendon, Adult, Article, Atrioventricular Conduction, Autosomal Dominant Inheritance, Biceps Brachii Muscle, Bradycardia, Case Report, Computer Assisted Tomography, Congestive Cardiomyopathy, Exon, Fatigue, Female, Fiber Type Disproportion, Flexor Muscle, Gait Disorder, Gene Mutation, Hamstring, Heart Muscle Conduction Disturbance, Heterozygosity, Histopathology, Human Tissue, Hyperlordosis, Iliopsoas Muscle, Limb Girdle Muscular Dystrophy, Middle Aged, Muscle Atrophy, Muscle Biopsy, Muscle Cell, Muscle Disease, Muscle Rigidity, Muscle Strength, Neurologic Examination, Nuclear Magnetic Resonance Imaging, Pacemaker, Phenotype, Polymyositis, Priority Journal, Sinus Bradycardia, Tendon Contracture, Tendon Reflex, Genetic Predisposition, Myopathies, Structural, Congenital, Pedigree, Skeletal Muscle, Genetic Predisposition To Disease, Lamin Type A, Muscle Fibers,
Affiliations:
*** IBB - CNR ***
Department of Neurosciences, Reproductive and Odontostomatological Sciences, University Federico II of Naples, Via Sergio Pansini 5, Naples, Italy
Neuromuscular and Molecular Medicine Unit, Department of Developmental Neuroscience, IRCCS Stella Maris, Pisa, Italy
Institute of Biostructure and Bioimaging (IBB) of the italian National Research Council, Naples, Italy
References:
Bonne, G., Disease associated with myonuclear abnormalities: defects of nuclear membrane related proteins (emerin, lamins a/c) (2002) Structural and molecular basis of skeletal muscle diseases, chapter 3, pp. 48-56. , In: Karpati G, editor. . Basel, Switzerland: ISN Neuropath Pres
Goizet, C., Yaou, R.B., Demay, L., Richard, P., Bouillot, S., Rouanet, M., A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia (2004) J Med Genet, 41, p. e29
Subramanyam, L., Simha, V., Garg, A., Overlapping syndrome with familial partial lipodystrophy, Dunnigan variety and cardiomyopathy due to amino-terminal heterozygous missense lamin A/C mutations (2010) Clin Genet, 78, pp. 66-73
Chen, L., Lee, L., Kudlow, B.A., Dos Santos, H.G., Sletvold, O., Shafeghati, Y., LMNA mutations in atypical Werner's syndrome (2003) Lancet, 362, pp. 440-445
Zirn, B., Kress, W., Grimm, T., Berthold, L.D., Neubauer, B., Kuchelmeister, K., Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy (2008) Am J Med Genet A, 146 A, pp. 1049-1054
Madej-Pilarczyk, A., Rosińska-Borkowska, D., Rekawek, J., Marchel, M., Szaluś, E., Jablońska, S., Progeroid syndrome with scleroderma-like skin changes associated with homozygous R435C LMNA mutation (2009) Am J Med Genet A, 149, pp. 2387-2392
Menezes, M.P., Waddell, L.B., Evesson, F.J., Cooper, S., Webster, R., Jones, K., Importance and challenge of making an early diagnosis in LMNA-related muscular dystrophy (2012) Neurology, 78, pp. 1258-1263
Kajino, S., Ishihara, K., Goto, K., Ishigaki, K., Noguchi, S., Nonaka, I., Congenital fiber type disproportion myopathy caused by LMNA mutations (2014) J Neurol Sci, 340, pp. 94-98
Clarke, N.F., Congenital fiber-type disproportion Semin Pediatr Neurol, 201 (18), pp. 264-271
Clarke, N.F., Kolski, H., Dye, D.E., Lim, E., Smith, R.L., Patel, R., Fahey, M.C., Mutations in TPM3 are a common cause of congenital fiber type disproportion (2008) Ann Neurol, 63, pp. 329-337
Clarke, N.F., Waddell, L.B., Cooper, S.T., Perry, M., Smith, R.L., Kornberg, A.J., Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion (2010) Hum Mutat, 31, pp. 544-550
Laing, N.G., Clarke, N.F., Dye, D.E., Liyanage, K., Walker, K.R., Kobayashi, Y., Actin mutations are one cause of congenital fiber type disproportion (2004) Ann Neurol, 56, pp. 689-694
Ortolano, S., Tarrío, R., Blanco-Arias, P., Teijeira, S., Rodríguez-Trelles, F., García-Murias, M., A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy (2011) Neuromuscul Disord, 21, pp. 254-262
Brandis, A., Aronica, E., Goebel, H.H., TPM2 mutation (2008) Neuromuscul Disord, 18, p. 1005
Bove, K.E., Iannaccone, S.T., Vogler, C., Intramuscular hematopoiesis in hypotonic infants with type 1 muscle fiber dysmaturation (1986) Arch Pathol Lab Med, 110, pp. 207-211
Iannaccone, S.T., Bove, K.E., Vogler, C.A., Buchino, J.J., Type 1 fiber size disproportion: morphometric data from 37 children with myopathic, neuropathic, or idiopathic hypotonia (1987) Pediatr Pathol, 7, pp. 395-419
Schessl, J., Goemans, N.M., Magold, A.I., Zou, Y., Hu, Y., Kirschner, J., Predominant fiber atrophy and fiber type disproportion in early Ullrich disease (2008) Muscle Nerve, 38, pp. 1184-1191
Simón, R., Mateos, F., Seijo, M., Balseiro, J., Madero, S., Cabello, A., Congenital fiber-type disproportion: analysis of a series of 11 cases [in Spanish] (1991) Neurologia, 6, pp. 281-286
Dubowitz, V., (1985) Muscle biopsy. A practical approach, , London: BaillieÁre Tindall
Mercuri, E., An integrated approach to the diagnosis of muscle disorders: what is the role of muscle imaging? (2010) Dev Med Child Neurol, 52, p. 693
Lattanzi, G., Benedetti, S., Bertini, E., Boriani, G., Mazzanti, L., Novelli, G., Laminopathies: many diseases, one gene. Report of the first italian Meeting Course on Laminopathies (2011) Acta Myol, 30, pp. 138-143
Mercuri, E., Poppe, M., Quinlivan, R., Messina, S., Kinali, M., Demay, L., Extreme variability of phenotype in patients with an identical missense mutation in the lamin A/C gene (2004) Arch Neurol, 61, pp. 690-694
Nzwalo, H., Conceição, I., Pereira, P., Santos, R., Evangelista, T., A family with 2 different hereditary diseases leading to early cardiac involvement (2013) J Clin Neuromuscul Dis, 14, pp. 204-208
Van Tintelen, J.P., High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics (2007) Am Heart J, 154, pp. 1130-1139
Muscle fiber type disproportion (FTD) in a family with mutations in the LMNA gene
Introduction: Mutations in the lamin A/C protein cause laminopathies, a heterogeneous group of disorders that include recessive axonal neuropathy (CMT2B1), Emery-Dreifuss muscular dystrophy (EDMD), limb-girdle muscular dystrophy (LGMD), dilated cardiomyopathy with conduction defect, and different forms of lipodystrophy and progeria. Methods: We provide clinical, histopathological, muscle imaging, and cardiac features of a family with heterozygous mutation in the LMNA gene. Results: We identified heterozygous mutations (c.80C> T; pT27I) in the LMNA gene in 3 family members who had the LGMD phenotype with onset in their early thirties and cardiac conduction defects or dilated cardiomyopathy. Interestingly, muscle biopsies showed changes consistent with fiber type disproportion (FTD). Conclusions: Fiber type disproportion has been reported only anecdotally in muscle biopsies of patients with LMNA mutations. Our report further supports this association and suggests inclusion of molecular testing for LMNA in the differential diagnosis of myopathies with FTD due to the risk for life threatening events. © 2014 Wiley Periodicals, Inc..
Introduction: Mutations in the lamin A/C protein cause laminopathies, a heterogeneous group of disorders that include recessive axonal neuropathy (CMT2B1), Emery-Dreifuss muscular dystrophy (EDMD), limb-girdle muscular dystrophy (LGMD), dilated cardiomyopathy with conduction defect, and different forms of lipodystrophy and progeria. Methods: We provide clinical, histopathological, muscle imaging, and cardiac features of a family with heterozygous mutation in the LMNA gene. Results: We identified heterozygous mutations (c.80C> T; pT27I) in the LMNA gene in 3 family members who had the LGMD phenotype with onset in their early thirties and cardiac conduction defects or dilated cardiomyopathy. Interestingly, muscle biopsies showed changes consistent with fiber type disproportion (FTD). Conclusions: Fiber type disproportion has been reported only anecdotally in muscle biopsies of patients with LMNA mutations. Our report further supports this association and suggests inclusion of molecular testing for LMNA in the differential diagnosis of myopathies with FTD due to the risk for life threatening events. © 2014 Wiley Periodicals, Inc..
Muscle fiber type disproportion (FTD) in a family with mutations in the LMNA gene
| ▼ Targeting Of Protein-Protein Interactions For Therapeutic Purposes |
Muscle fiber type disproportion (FTD) in a family with mutations in the LMNA gene
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Clin Endocrinol (ISSN: 0300-0664, 1365-2265, 1365-2265electronic), 2003 Feb; 58(2): 169-176.
Impact Factor: 2.767
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Petretta M, Vicario ML, Spinelli L, Ferro A, Cuocolo A, Condorelli M, Bonaduce D
* Combined effect of the force-frequency and length-tension mechanisms on left ventricular function in patients with dilated cardiomyopathy (325 views)
Eur J Heart Fail European Journal Of Heart Failure (ISSN: 1388-9842), 2002 Dec; 4(6): 727-735.
Impact Factor: 2.134
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Acampa W, Petretta M, Cuocolo A
* Nuclear medicine procedures in cardiovascular diseases: An evidence based approach (468 views)
Q J Nucl Med (ISSN: 1124-3937, 1125-0135), 2002 Dec; 46(4): 323-330.
Impact Factor: 1.903
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Ciampi Q, Betocchi S, Lombardi R, Losi M, Manganelli F, Storto G, Aversa M, Miranda M, Cuocolo A, Tocchetti CG, Chiariello M
* The diastolic function in hypertrophic cardiomyopathy (208 views)
Cardiologia, 2002 Nov 5; 33(8): 741-746.
Impact Factor: 0
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Ciampi Q, Betocchi S, Lombardi R, Manganelli F, Storto G, Losi MA, Pezzella E, Finizio F, Cuocolo A, Chiariello M
* Hemodynamic determinants of exercise-induced abnormal blood pressure response in hypertrophic cardiomyopathy (289 views)
Journal Of The American College Of Cardiology (ISSN: 0735-1097), 2002 Jul 17; 40(2): 278-284.
Impact Factor: 6.278
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Colao A, Spinelli L, Cuocolo A, Spiezia S, Pivonello R, Di Somma C, Bonaduce D, Salvatore M, Lombardi G
* Cardiovascular consequences of early-onset growth hormone excess (422 views)
J Clin Endocrinol Metab (ISSN: 0021-972x), 2002 Jul; 87(7): 3097-3104.
Impact Factor: 5.199
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Manganelli F, Betocchi S, Ciampi Q, Storto G, Losi MA, Violante A, Briguori C, Tocchetti CG, Lombardi R, Cuocolo A, Chiariello M
* Myopia and IOP (417 views)
Ann Ottalmol Clin Ocul, 2002 Jun 15; 115(10): 1053-1058.
Impact Factor: 0
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Colao A, Cuocolo A, Marzullo P, Nicolai E, Ferone D, Morte A, Pivonello R, Salvatore M, Lombardi G
* Is the acromegalic cardiomyopathy reversible? Effect of 5-year normalization of growth hormone and insulin-like growth factor I levels on cardiac performance (347 views)
J Clin Endocrinol Metab (ISSN: 0021-972x), 2001 Apr; 86(4): 1551-1557.
Impact Factor: 5.16
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Clampi Q, Losi M, Violante A, Manganelli F, Pezzella E, Storto G, Tocchetti C, Finizio F, Lombardi R, Briguori C, Cuocolo A, Betocchi S
Effects of isometric exercise in obstructive hypertrophic cardiomyopathy (253 views)
Circulationcirculation (ISSN: 0009-7322), 1999 Nov 2; 100(18SUPPL.): N/D-N/D.
Impact Factor: 9.903
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Manganelli F, Betocchi S, Ciampi Q, Losi MA, Tocchetti GC, Cuocolo A, Storto G, Violante A, Lombardi R, Chiariello M
Haemodynamic determinants of syncope in hypertrophic cardiomyopathy (243 views)
European Heart Journal (ISSN: 0195-668x), 1999 Sep; 20(ABSTR.SUPPL.): N/D-N/D.
Impact Factor: 3.21
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Lombardi G, Colao A, Cuocolo A, Longobardi S, Di Somma C, Orio F, Merola B, Nicolai E, Salvatore M
Cardiological aspects of growth hormone and insulin-like growth factor- (798 views)
J Pediatr Endocrinol Metab (ISSN: 0334-018x), 1997 Nov; 10(6): 553-560.
Impact Factor: 0.481
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Nappi A, Cuocolo A, Nicolai E, Imbriaco M, Pace L, Salvatore M
Ambulatory monitoring of left ventricular function with a radionuclide detector system (297 views)
Radiol Med (ISSN: 0033-8362, 1826-6983, 1826-6983electronic), 1992; 84(1-2): 132-139.
Impact Factor: 0.967
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Manna R, Salvatore M, Pantoli D, Vecchio FM, Greco AV, Carosella L, Schiavino D, Ghirlanda G
Malignant histiocytosis: Report of three cases (360 views)
Br J Clin Pract (ISSN: 0007-0947), 1988 Feb; 42(2): 82-86.
Impact Factor: 0.351
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* Exercise triggers CAPN1-mediated AIF truncation, inducing myocyte cell death in arrhythmogenic cardiomyopathy (170 views)
Sci Transl Med (ISSN: 1946-6234linking), 2021 Feb 17; 13(581): N/D-N/D.
Impact Factor: 17.956
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Perrino C, Imbriaco M, Magliulo F, Ponsiglione A, Puglia M, Stabile E, Avvedimento M, Esposito G, Perrone Filardi P, Cuocolo A, Galderisi M, Trimarco B
* Tako-tsubo syndrome and myocarditis: Two sides of the same coin or same side for two different coins? (202 views)
Int J Cardiol (ISSN: 0167-5273, 1874-1754electronic), 2016 Jan 15; 203: 40-42.
Impact Factor: 6.189
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Cella L, Oh JH, Deasy JO, Palma G, Liuzzi R, D'Avino V, Conson M, Picardi M, Salvatore M, Pacelli R
* Predicting radiation-induced valvular heart damage (334 views)
Acta Oncol (ISSN: 0284-186x, 0284-186xlinking), 2015 Mar 24; 54(10): 1796-1804.
Impact Factor: 3.73
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Gallicchio R, Mansueto G, Simeon V, Nardelli A, Guariglia R, Capacchione D, Soscia E, Pedicini P, Gattozzi D, Musto P, Storto G
* F-18 FDG PET/CT quantization parameters as predictors of outcome in patients with diffuse large B-cell lymphoma (546 views)
Eur J Haematol (ISSN: 0902-4441), 2014 May; 92(5): 382-389.
Impact Factor: 2.066
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Cella L, Liuzzi R, D'Avino V, Conson M, Di Biase A, Picardi M, Pugliese N, Solla R, Salvatore M, Pacelli R
* Pulmonary damage in Hodgkin's lymphoma patients treated with sequential chemo-radiotherapy: Predictors of radiation-induced lung injury (379 views)
Acta Oncol (ISSN: 0284-186x), 2014 May; 53(5): 613-619.
Impact Factor: 2.997
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Petretta M, Pellegrino T, Cuocolo A
* The "gray Zone" For The Heart To Mediastinum Mibg Uptake Ratio (314 views)
J Nucl Cardiol (ISSN: 1071-3581, 1532-6551, 1532-6551electronic), 2014; 21(5): 921-924.
Impact Factor: 2.942
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Ferro A, Petretta M, Acampa W, Fiumara G, Daniele S, Petretta MP, Cantoni V, Cuocolo A
* Post-stress left ventricular ejection fraction drop in patients with diabetes: A gated myocardial perfusion imaging study (395 views)
Bmc Cardiovasc Disor (ISSN: 1471-2261), 2013 Nov 14; 13: 99-99.
Impact Factor: 1.5
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Pellegrino T, Petretta M, Paolillo S, Boemio A, Carotenuto R, Petretta MP, Di Nuzzo C, Perrone-filardi P, Cuocolo A
* Observer reproducibility of results from a low-dose 123I-metaiodobenzylguanidine cardiac imaging protocol in patients with heart failure (521 views)
Eur J Nucl Med (ISSN: 1619-7089, 1619-7070, 0340-6997), 2013 Oct; 40(10): 1549-1557.
Impact Factor: 5.217
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Ferraro F, Marano E, Petruzzi J, Tedeschi E, Santulli L, Elefante A
* Spontaneous intracranial hypotension and epidural blood patch: A report involving seven cases (350 views)
Anaesth Intensive Care (ISSN: 0310-057x), 2013 May; 41(3): 393-396.
Impact Factor: 1.47
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Cella L, Conson M, Caterino M, De Rosa N, Liuzzi R, Picardi M, Grimaldi F, Solla R, Farella A, Salvatore M, Pacelli R
* Thyroid V30 predicts radiation-induced hypothyroidism in patients treated with sequential chemo-radiotherapy for Hodgkin's lymphoma (493 views) (PDF 236 views)
Int J Radiat Oncol (ISSN: 0360-3016, 1879-355x, 1879-355xelectronic), 2012 Apr 1; 82(5): 1802-1808.
Impact Factor: 4.524
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Perrone-Filardi P, Paolillo S, Dellegrottaglie S, Gargiulo P, Savarese G, Marciano C, Casaretti L, Cecere M, Musella F, Pirozzi E, Parente A, Cuocolo A
* Assessment of cardiac sympathetic activity by MIBG imaging in patients with heart failure: a clinical appraisal (320 views)
Heart (ISSN: 1468-201x, 1355-6037), 2011 Nov; 97(22): 1828-1833.
Impact Factor: 4.223
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Cella L, Liuzzi R, Conson M, Torre G, Caterino M, De Rosa N, Picardi M, Camera L, Solla R, Farella A, Salvatore M, Pacelli R
* Dosimetric predictors of asymptomatic heart valvular dysfunction following mediastinal irradiation for Hodgkin's lymphoma (470 views)
Radiother Oncol (ISSN: 0167-8140, 1879-0887, 1879-0887electronic), 2011 Nov; 101(2): 316-321.
Impact Factor: 5.58
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Imbriaco M, Messalli G, Avitabile G, Cuocolo A, Maurea S, Soscia F, Pisani A
* Cardiac magnetic resonance imaging illustrating Anderson-Fabry disease progression (283 views)
Br J Radiol (ISSN: 0007-1285, 1748-880xelectronic, 0007-1285linking), 2010 Dec; 83(996): e249-e249.
Impact Factor: 2.062
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Strianese D, Tranfa F, Finelli M, De Renzo A, Staibano S, Schiemer R, Cardone D, Pacelli R, Perna F, Mascolo M, De Rosa G, Bonavolonta G
* Hepatitis C virus infection in ocular adnexal lymphomas (369 views)
Arch Ophthalmol (ISSN: 1538-3601, 0003-9950), 2010 Oct; 128(10): 1295-1299.
Impact Factor: 3.516
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Del Vecchio S, Zannetti A, Fonti R, Iommelli F, Pizzuti LM, Lettieri A, Salvatore M
* PET/CT in cancer research: From preclinical to clinical applications (621 views)
Contrast Media Mol Imaging (ISSN: 1555-4309, 1555-4309linking), 2010 Jul; 5(4): 190-200.
Impact Factor: 4.02
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Lanzillo R, Orefice G, Quarantelli M, Rinaldi C, Prinster A, Ventrella G, Spitaleri D, Lus G, Vacca G, Carotenuto B, Salvatore E, Brunetti A, Tedeschi G, Brescia Morra V
* Atorvastatin combined to interferon to verify the efficacy (ACTIVE) in relapsing-remitting active multiple sclerosis patients: A longitudinal controlled trial of combination therapy (561 views)
Mult Scler (ISSN: 1352-4585, 1477-0970, 1352-4585linking), 2010 Apr; 16(4): 450-454.
Impact Factor: 4.23
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Storto G, De Renzo A, Pellegrino T, Perna F, De Falco T, Erra P, Nardelli A, Speranza A, Klain M, Rotoli B, Pace L
* Assessment of Metabolic Response to Radioimmunotherapy with (90)Y-Ibritumomab Tiuxetan in Patients with Relapsed or Refractory B-Cell Non-Hodgkin Lymphoma (399 views)
Radiology (ISSN: 0033-8419, 1527-1315, 0033-8419linking), 2010 Jan; 254(1): 245-252.
Impact Factor: 6.069
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Storto G, Nicolai E, Petretta M, Spinelli L, Acampa W, Evangelista L, Daniele S, Trimarco B, Cuocolo A
* Cardiac performance during exercise in hypertensive patients without ventricular hypertrophy (493 views)
Eur J Clin Invest (ISSN: 0014-2972, 1365-2362, 0014-2972linking), 2009 Sep; 39(8): 664-670.
Impact Factor: 2.643
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Spinelli L, Nicolai E, Acampa W, Imbriaco M, Pisani A, Rao MA, Scopacasa F, Cianciaruso B, De Luca N, Cuocolo A
* Cardiac performance during exercise in patients with Fabry's disease (371 views)
Eur J Clin Invest (ISSN: 0014-2972, 1365-2362, 0014-2972linking), 2008 Dec; 38(12): 910-917.
Impact Factor: 2.784
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Gallotta G, Palmieri V, Piedimonte V, Rendina D, De Bonis S, Russo V, Celentano A, Di Minno M, Postiglione A, Di Minno G
* Increased troponin I predicts in-hospital occurrence of hemodynamic instability in patients with sub-massive or non-massive pulmonary embolism independent to clinical, echocardiographic and laboratory information (332 views)
Int J Cardiol (ISSN: 0167-5273, 1874-1754electronic, 0167-5273linking), 2008 Mar 14; 124(3): 351-357.
Impact Factor: 3.121
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Migliore T, Parrella LS, Caputi A, Silvestri N, Romano R, Pace L, Imbriaco M, Losi MA, Betocchi S
* Pathogenesis of hypertrophic cardiomyopathy. Impact of growth factors on left ventricular anatomy (368 views)
Minerva Cardioangiol (ISSN: 0026-4725), 2008 Feb; 56(1): 13-20.
Impact Factor: 0.481
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Ciampi Q, Betocchi S, Losi MA, Ferro A, Cuocolo A, Lombardi R, Villari B, Chiariello M
* Abnormal blood-pressure response to exercise and oxygen consumption in patients with hypertrophic cardiomyopathy (398 views)
J Nucl Cardiol (ISSN: 1532-6551, 1071-3581, 1532-6551electronic), 2007 Nov; 14(6): 869-875.
Impact Factor: 2.359
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De Renzo A, Perna F, Persico M, Mainolfi C, Pace L
* 18F-fluorodeoxyglucose positron emission tomography/computed tomography in the evaluation of early response in a primary hepatic lymphoma (233 views)
Br J Haematol (ISSN: 0007-1048, 0007-1048linking, 1365-2141electronic), 2006 Jun; 133(6): 580-580.
Impact Factor: 4.498
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Santomauro M, Pace L, Duilio C, Ottaviano L, Borrelli A, Ferro A, Monteforte N, Cuocolo A, Salvatore M, Chiariello M
* Left ventricular pacing in patients with heart failure: Evaluation study with Fourier analysis of radionuclide ventriculography (283 views)
Ital Heart J (ISSN: 1129-471x), 2004 Dec; 5(12): 906-911.
Impact Factor: 6.023
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Ciampi Q, Betocchi S, Violante A, Lombardi R, Losi M, Storto G, Manganelli F, Tocchetti C, Aversa M, Pezzella E, Finizio F, Cuocolo A, Chiariello M
* Hemodynamic effects of isometric exercise in hypertrophic cardiomyopathy: Comparison with normal subjects (459 views)
J Nucl Cardiol (ISSN: 1071-3581, 1532-6551, 1532-6551electronic), 2003 Mar; 10(2): 154-160.
Impact Factor: 1.629
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Colao A, Marzullo P, Cuocolo A, Spinelli L, Pivonello R, Bonaduce D, Salvatore M, Lombardi G
* Reversal of acromegalic cardiomyopathy in young but not in middle-aged patients after 12 months of treatment with the depot long-acting somatostatin analogue octreotide (475 views)
Clin Endocrinol (ISSN: 0300-0664, 1365-2265, 1365-2265electronic), 2003 Feb; 58(2): 169-176.
Impact Factor: 2.767
View Export to BibTeX Export to EndNote
Petretta M, Vicario ML, Spinelli L, Ferro A, Cuocolo A, Condorelli M, Bonaduce D
* Combined effect of the force-frequency and length-tension mechanisms on left ventricular function in patients with dilated cardiomyopathy (325 views)
Eur J Heart Fail European Journal Of Heart Failure (ISSN: 1388-9842), 2002 Dec; 4(6): 727-735.
Impact Factor: 2.134
View Export to BibTeX Export to EndNote
Acampa W, Petretta M, Cuocolo A
* Nuclear medicine procedures in cardiovascular diseases: An evidence based approach (468 views)
Q J Nucl Med (ISSN: 1124-3937, 1125-0135), 2002 Dec; 46(4): 323-330.
Impact Factor: 1.903
View Export to BibTeX Export to EndNote
Ciampi Q, Betocchi S, Lombardi R, Losi M, Manganelli F, Storto G, Aversa M, Miranda M, Cuocolo A, Tocchetti CG, Chiariello M
* The diastolic function in hypertrophic cardiomyopathy (208 views)
Cardiologia, 2002 Nov 5; 33(8): 741-746.
Impact Factor: 0
View Export to BibTeX Export to EndNote
Ciampi Q, Betocchi S, Lombardi R, Manganelli F, Storto G, Losi MA, Pezzella E, Finizio F, Cuocolo A, Chiariello M
* Hemodynamic determinants of exercise-induced abnormal blood pressure response in hypertrophic cardiomyopathy (289 views)
Journal Of The American College Of Cardiology (ISSN: 0735-1097), 2002 Jul 17; 40(2): 278-284.
Impact Factor: 6.278
View Export to BibTeX Export to EndNote
Colao A, Spinelli L, Cuocolo A, Spiezia S, Pivonello R, Di Somma C, Bonaduce D, Salvatore M, Lombardi G
* Cardiovascular consequences of early-onset growth hormone excess (422 views)
J Clin Endocrinol Metab (ISSN: 0021-972x), 2002 Jul; 87(7): 3097-3104.
Impact Factor: 5.199
View Export to BibTeX Export to EndNote
Manganelli F, Betocchi S, Ciampi Q, Storto G, Losi MA, Violante A, Briguori C, Tocchetti CG, Lombardi R, Cuocolo A, Chiariello M
* Myopia and IOP (417 views)
Ann Ottalmol Clin Ocul, 2002 Jun 15; 115(10): 1053-1058.
Impact Factor: 0
View Export to BibTeX Export to EndNote
Colao A, Cuocolo A, Marzullo P, Nicolai E, Ferone D, Morte A, Pivonello R, Salvatore M, Lombardi G
* Is the acromegalic cardiomyopathy reversible? Effect of 5-year normalization of growth hormone and insulin-like growth factor I levels on cardiac performance (347 views)
J Clin Endocrinol Metab (ISSN: 0021-972x), 2001 Apr; 86(4): 1551-1557.
Impact Factor: 5.16
View Export to BibTeX Export to EndNote
Clampi Q, Losi M, Violante A, Manganelli F, Pezzella E, Storto G, Tocchetti C, Finizio F, Lombardi R, Briguori C, Cuocolo A, Betocchi S
Effects of isometric exercise in obstructive hypertrophic cardiomyopathy (253 views)
Circulationcirculation (ISSN: 0009-7322), 1999 Nov 2; 100(18SUPPL.): N/D-N/D.
Impact Factor: 9.903
View Export to BibTeX Export to EndNote
Manganelli F, Betocchi S, Ciampi Q, Losi MA, Tocchetti GC, Cuocolo A, Storto G, Violante A, Lombardi R, Chiariello M
Haemodynamic determinants of syncope in hypertrophic cardiomyopathy (243 views)
European Heart Journal (ISSN: 0195-668x), 1999 Sep; 20(ABSTR.SUPPL.): N/D-N/D.
Impact Factor: 3.21
View Export to BibTeX Export to EndNote
Lombardi G, Colao A, Cuocolo A, Longobardi S, Di Somma C, Orio F, Merola B, Nicolai E, Salvatore M
Cardiological aspects of growth hormone and insulin-like growth factor- (798 views)
J Pediatr Endocrinol Metab (ISSN: 0334-018x), 1997 Nov; 10(6): 553-560.
Impact Factor: 0.481
View Export to BibTeX Export to EndNote
Nappi A, Cuocolo A, Nicolai E, Imbriaco M, Pace L, Salvatore M
Ambulatory monitoring of left ventricular function with a radionuclide detector system (297 views)
Radiol Med (ISSN: 0033-8362, 1826-6983, 1826-6983electronic), 1992; 84(1-2): 132-139.
Impact Factor: 0.967
View Export to BibTeX Export to EndNote
Manna R, Salvatore M, Pantoli D, Vecchio FM, Greco AV, Carosella L, Schiavino D, Ghirlanda G
Malignant histiocytosis: Report of three cases (360 views)
Br J Clin Pract (ISSN: 0007-0947), 1988 Feb; 42(2): 82-86.
Impact Factor: 0.351
View Export to BibTeX Export to EndNote
38 Records (33 excluding Abstracts).
Total impact factor: 140.182 (119.009 excluding Abstracts).
Total 5 year impact factor: 133.819 (103.654 excluding Abstracts).
Total impact factor: 140.182 (119.009 excluding Abstracts).
Total 5 year impact factor: 133.819 (103.654 excluding Abstracts).
366 views. Last view on Friday 05 May 2023, 20:07:44
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