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RELATION OF BODY MASS INDEX WITH IgE LEVELS, ALLERGIC SENSITIZATION AND LUNG FUNCTION IN ASTHMATIC CHILDREN: OUR EXPERIENCE AND REVISION OF LITERATURE.

Journal of biological regulators and homeostatic agents

Garozzo MT, Cuppari C, Filippelli M, Arrigo T, Attardo D, Capizzi A, Lanzafame A, Leonardi S.
PMID: 26634594
J Biol Regul Homeost Agents. 2015 Apr-Jun;29(2):89-95.

In recent decades, there has been an increase in the prevalence of asthma and obesity in pediatric age. In this regard several studies have provided controversial data to demonstrate the link between Body Mass Index (BMI) and asthma, both...

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Garozzo MT, Cuppari C, Filippelli M, et al. RELATION OF BODY MASS INDEX WITH IgE LEVELS, ALLERGIC SENSITIZATION AND LUNG FUNCTION IN ASTHMATIC CHILDREN: OUR EXPERIENCE AND REVISION OF LITERATURE. J Biol Regul Homeost Agents. 2015;29(2):89-95
Garozzo, M. T., Cuppari, C., Filippelli, M., Arrigo, T., Attardo, D., Capizzi, A., Lanzafame, A., & Leonardi, S. (2015). RELATION OF BODY MASS INDEX WITH IgE LEVELS, ALLERGIC SENSITIZATION AND LUNG FUNCTION IN ASTHMATIC CHILDREN: OUR EXPERIENCE AND REVISION OF LITERATURE. Journal of biological regulators and homeostatic agents, 29(2), 89-95.
Garozzo, M T, et al. "RELATION OF BODY MASS INDEX WITH IgE LEVELS, ALLERGIC SENSITIZATION AND LUNG FUNCTION IN ASTHMATIC CHILDREN: OUR EXPERIENCE AND REVISION OF LITERATURE." Journal of biological regulators and homeostatic agents vol. 29,2 (2015): 89-95.
Garozzo MT, Cuppari C, Filippelli M, Arrigo T, Attardo D, Capizzi A, Lanzafame A, Leonardi S. RELATION OF BODY MASS INDEX WITH IgE LEVELS, ALLERGIC SENSITIZATION AND LUNG FUNCTION IN ASTHMATIC CHILDREN: OUR EXPERIENCE AND REVISION OF LITERATURE. J Biol Regul Homeost Agents. 2015 Apr-Jun;29(2):89-95. PMID: 26634594.
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C-5'-Triazolyl-2'-oxa-3'-aza-4'a-carbanucleosides: Synthesis and biological evaluation.

Beilstein journal of organic chemistry

Romeo R, Carnovale C, Giofrè SV, Chiacchio MA, Garozzo A, Amata E, Romeo G, Chiacchio U.
PMID: 25815087
Beilstein J Org Chem. 2015 Mar 09;11:328-34. doi: 10.3762/bjoc.11.38. eCollection 2015.

A novel series of 2'-oxa-3'-aza-4'a-carbanucleosides, featured with a triazole linker at the 5'-position, has been developed by exploiting a click chemistry reaction of 5'-azido-2'-oxa-3'-aza-4'a-carbanucleosides with substituted alkynes. Biological tests indicate an antitumor activity for the synthesized compounds: most of...

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Romeo R, Carnovale C, Giofrè SV, et al. C-5'-Triazolyl-2'-oxa-3'-aza-4'a-carbanucleosides: Synthesis and biological evaluation. Beilstein J Org Chem. 2015;11:328-34doi: 10.3762/bjoc.11.38.
Romeo, R., Carnovale, C., Giofrè, S. V., Chiacchio, M. A., Garozzo, A., Amata, E., Romeo, G., & Chiacchio, U. (2015). C-5'-Triazolyl-2'-oxa-3'-aza-4'a-carbanucleosides: Synthesis and biological evaluation. Beilstein journal of organic chemistry, 11328-34. https://doi.org/10.3762/bjoc.11.38
Romeo, Roberto, et al. "C-5'-Triazolyl-2'-oxa-3'-aza-4'a-carbanucleosides: Synthesis and biological evaluation." Beilstein journal of organic chemistry vol. 11 (2015): 328-34. doi: https://doi.org/10.3762/bjoc.11.38
Romeo R, Carnovale C, Giofrè SV, Chiacchio MA, Garozzo A, Amata E, Romeo G, Chiacchio U. C-5'-Triazolyl-2'-oxa-3'-aza-4'a-carbanucleosides: Synthesis and biological evaluation. Beilstein J Org Chem. 2015 Mar 09;11:328-34. doi: 10.3762/bjoc.11.38. eCollection 2015. PMID: 25815087; PMCID: PMC4362054.
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Morphological and structural effects of excimer laser treatment of amorphous silicon.

Micron (Oxford, England : 1993)

Loreti S, della Sala D, Garozzo M.
PMID: 10702980
Micron. 2000 Jun;31(3):299-307. doi: 10.1016/s0968-4328(99)00097-9.

The excimer laser irradiation of thin film amorphous silicon (a-Si) precursors on glass is a suitable method for obtaining high-performance polycrystalline silicon (p-Si) active layers for devices and circuits. By changing the experimental conditions, the recrystallization method generates a...

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Loreti S, della Sala D, Garozzo M. Morphological and structural effects of excimer laser treatment of amorphous silicon. Micron. 2000;31(3):299-307doi: 10.1016/s0968-4328(99)00097-9.
Loreti, S., della Sala D, & Garozzo, M. (2000). Morphological and structural effects of excimer laser treatment of amorphous silicon. Micron (Oxford, England : 1993), 31(3), 299-307. https://doi.org/10.1016/s0968-4328(99)00097-9
Loreti, et al. "Morphological and structural effects of excimer laser treatment of amorphous silicon." Micron (Oxford, England : 1993) vol. 31,3 (2000): 299-307. doi: https://doi.org/10.1016/s0968-4328(99)00097-9
Loreti S, della Sala D, Garozzo M. Morphological and structural effects of excimer laser treatment of amorphous silicon. Micron. 2000 Jun;31(3):299-307. doi: 10.1016/s0968-4328(99)00097-9. PMID: 10702980.
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A comparison of two automated methods for the detection and identification of red blood cell alloantibodies.

Blood transfusion = Trasfusione del sangue

Garozzo G, Licitra V, Criscione R, Comitini N, Noto C, Lomagno R, Ruta D, Spadola G, Zago V, Bonomo P.
PMID: 19204749
Blood Transfus. 2007 Jan;5(1):33-40. doi: 10.2450/2007.0022-06.

BACKGROUND: The aim of this study was to compare the routine use of two automated systems (OrthoAutoVue Innova, microcolumn, and Immucor Galileo, solid phase) for the screening and identification of irregular red blood cell alloantibodies in samples, analysed in...

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Garozzo G, Licitra V, Criscione R, et al. A comparison of two automated methods for the detection and identification of red blood cell alloantibodies. Blood Transfus. 2007;5(1):33-40doi: 10.2450/2007.0022-06.
Garozzo, G., Licitra, V., Criscione, R., Comitini, N., Noto, C., Lomagno, R., Ruta, D., Spadola, G., Zago, V., & Bonomo, P. (2007). A comparison of two automated methods for the detection and identification of red blood cell alloantibodies. Blood transfusion = Trasfusione del sangue, 5(1), 33-40. https://doi.org/10.2450/2007.0022-06
Garozzo, Giovanni, et al. "A comparison of two automated methods for the detection and identification of red blood cell alloantibodies." Blood transfusion = Trasfusione del sangue vol. 5,1 (2007): 33-40. doi: https://doi.org/10.2450/2007.0022-06
Garozzo G, Licitra V, Criscione R, Comitini N, Noto C, Lomagno R, Ruta D, Spadola G, Zago V, Bonomo P. A comparison of two automated methods for the detection and identification of red blood cell alloantibodies. Blood Transfus. 2007 Jan;5(1):33-40. doi: 10.2450/2007.0022-06. PMID: 19204749; PMCID: PMC2535873.
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Routine Digital Pathology Workflow: The Catania Experience.

Journal of pathology informatics

Fraggetta F, Garozzo S, Zannoni GF, Pantanowitz L, Rossi ED.
PMID: 29416914
J Pathol Inform. 2017 Dec 19;8:51. doi: 10.4103/jpi.jpi_58_17. eCollection 2017.

INTRODUCTION: Successful implementation of whole slide imaging (WSI) for routine clinical practice has been accomplished in only a few pathology laboratories worldwide. We report the transition to an effective and complete digital surgical pathology workflow in the pathology laboratory...

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Fraggetta F, Garozzo S, Zannoni GF, et al. Routine Digital Pathology Workflow: The Catania Experience. J Pathol Inform. 2017;8:51doi: 10.4103/jpi.jpi_58_17.
Fraggetta, F., Garozzo, S., Zannoni, G. F., Pantanowitz, L., & Rossi, E. D. (2017). Routine Digital Pathology Workflow: The Catania Experience. Journal of pathology informatics, 851. https://doi.org/10.4103/jpi.jpi_58_17
Fraggetta, Filippo, et al. "Routine Digital Pathology Workflow: The Catania Experience." Journal of pathology informatics vol. 8 (2017): 51. doi: https://doi.org/10.4103/jpi.jpi_58_17
Fraggetta F, Garozzo S, Zannoni GF, Pantanowitz L, Rossi ED. Routine Digital Pathology Workflow: The Catania Experience. J Pathol Inform. 2017 Dec 19;8:51. doi: 10.4103/jpi.jpi_58_17. eCollection 2017. PMID: 29416914; PMCID: PMC5760840.
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Structure of the Lipopolysaccharide from the .

ChemistryOpen

Di Lorenzo F, Palmigiano A, Duda KA, Pallach M, Busset N, Sturiale L, Giraud E, Garozzo D, Molinaro A, Silipo A.
PMID: 28794950
ChemistryOpen. 2017 Jun 12;6(4):541-553. doi: 10.1002/open.201700074. eCollection 2017 Aug.

The importance of the outer membrane and of its main constituent, lipopolysaccharide, in the symbiosis between rhizobia and leguminous host plants has been well studied. Here, the first complete structural characterization of the entire lipopolysaccharide from an O-chain-deficient

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Di Lorenzo F, Palmigiano A, Duda KA, et al. Structure of the Lipopolysaccharide from the . ChemistryOpen. 2017;6(4):541-553doi: 10.1002/open.201700074.
Di Lorenzo, F., Palmigiano, A., Duda, K. A., Pallach, M., Busset, N., Sturiale, L., Giraud, E., Garozzo, D., Molinaro, A., & Silipo, A. (2017). Structure of the Lipopolysaccharide from the . ChemistryOpen, 6(4), 541-553. https://doi.org/10.1002/open.201700074
Di Lorenzo, Flaviana, et al. "Structure of the Lipopolysaccharide from the ." ChemistryOpen vol. 6,4 (2017): 541-553. doi: https://doi.org/10.1002/open.201700074
Di Lorenzo F, Palmigiano A, Duda KA, Pallach M, Busset N, Sturiale L, Giraud E, Garozzo D, Molinaro A, Silipo A. Structure of the Lipopolysaccharide from the . ChemistryOpen. 2017 Jun 12;6(4):541-553. doi: 10.1002/open.201700074. eCollection 2017 Aug. PMID: 28794950; PMCID: PMC5542761.
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An Unexplained Congenital Disorder of Glycosylation-II in a Child with Neurohepatic Involvement, Hypercholesterolemia and Hypoceruloplasminemia.

JIMD reports

Calvo PL, Spada M, Rabbone I, Pinon M, Porta F, Cisarò F, Reggiani S, Cefalù AB, Sturiale L, Garozzo D, Lefeber DJ, Jaeken J.
PMID: 28643274
JIMD Rep. 2018;38:97-100. doi: 10.1007/8904_2017_35. Epub 2017 Jun 23.

We report on a 12-year-old adopted boy with psychomotor disability, absence seizures, and normal brain MRI. He showed increased (but initially, at 5 months, normal) serum cholesterol, increased alkaline phosphatases, transiently increased transaminases and hypoceruloplasminemia with normal serum and...

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Calvo PL, Spada M, Rabbone I, et al. An Unexplained Congenital Disorder of Glycosylation-II in a Child with Neurohepatic Involvement, Hypercholesterolemia and Hypoceruloplasminemia. JIMD Rep. 2017;38:97-100doi: 10.1007/8904_2017_35.
Calvo, P. L., Spada, M., Rabbone, I., Pinon, M., Porta, F., Cisarò, F., Reggiani, S., Cefalù, A. B., Sturiale, L., Garozzo, D., Lefeber, D. J., & Jaeken, J. (2018). An Unexplained Congenital Disorder of Glycosylation-II in a Child with Neurohepatic Involvement, Hypercholesterolemia and Hypoceruloplasminemia. JIMD reports, 3897-100. https://doi.org/10.1007/8904_2017_35
Calvo, Pier Luigi, et al. "An Unexplained Congenital Disorder of Glycosylation-II in a Child with Neurohepatic Involvement, Hypercholesterolemia and Hypoceruloplasminemia." JIMD reports vol. 38 (2018): 97-100. doi: https://doi.org/10.1007/8904_2017_35
Calvo PL, Spada M, Rabbone I, Pinon M, Porta F, Cisarò F, Reggiani S, Cefalù AB, Sturiale L, Garozzo D, Lefeber DJ, Jaeken J. An Unexplained Congenital Disorder of Glycosylation-II in a Child with Neurohepatic Involvement, Hypercholesterolemia and Hypoceruloplasminemia. JIMD Rep. 2018;38:97-100. doi: 10.1007/8904_2017_35. Epub 2017 Jun 23. PMID: 28643274; PMCID: PMC5874206.
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Cerebral small vessel disease due to a unique heterozygous .

Neurology. Genetics

Oluwole OJ, Ibrahim H, Garozzo D, Ben Hamouda K, Ismail Mostafa Hassan S, Hegazy AM, Msaddi AK.
PMID: 32042911
Neurol Genet. 2019 Dec 26;6(1):e382. doi: 10.1212/NXG.0000000000000382. eCollection 2020 Feb.

OBJECTIVE: To describe the case of an African patient who was diagnosed with cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL).METHODS: Case report and literature review.RESULTS: We present a 39-year-old Gabonese man who developed progressive gait difficulty...

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Oluwole OJ, Ibrahim H, Garozzo D, et al. Cerebral small vessel disease due to a unique heterozygous . Neurol Genet. 2019;6(1):e382doi: 10.1212/NXG.0000000000000382.
Oluwole, O. J., Ibrahim, H., Garozzo, D., Ben Hamouda, K., Ismail Mostafa Hassan, S., Hegazy, A. M., & Msaddi, A. K. (2020). Cerebral small vessel disease due to a unique heterozygous . Neurology. Genetics, 6(1), e382. https://doi.org/10.1212/NXG.0000000000000382
Oluwole, Olusegun John, et al. "Cerebral small vessel disease due to a unique heterozygous ." Neurology. Genetics vol. 6,1 (2020): e382. doi: https://doi.org/10.1212/NXG.0000000000000382
Oluwole OJ, Ibrahim H, Garozzo D, Ben Hamouda K, Ismail Mostafa Hassan S, Hegazy AM, Msaddi AK. Cerebral small vessel disease due to a unique heterozygous . Neurol Genet. 2019 Dec 26;6(1):e382. doi: 10.1212/NXG.0000000000000382. eCollection 2020 Feb. PMID: 32042911; PMCID: PMC6936311.
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Antimicrobial, Antioxidant, and Cytotoxic Activities of .

Antibiotics (Basel, Switzerland)

D'Angeli F, Malfa GA, Garozzo A, Li Volti G, Genovese C, Stivala A, Nicolosi D, Attanasio F, Bellia F, Ronsisvalle S, Acquaviva R.
PMID: 33557378
Antibiotics (Basel). 2021 Feb 04;10(2). doi: 10.3390/antibiotics10020159.

The difficulty to treat resistant strains-related hospital-acquired infections (HAIs) promoted the study of phytoextracts, known sources of bioactive molecules. Accordingly, in the present study, the pharmacological activities of

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D'Angeli F, Malfa GA, Garozzo A, et al. Antimicrobial, Antioxidant, and Cytotoxic Activities of . Antibiotics (Basel). 2021;10(2)doi: 10.3390/antibiotics10020159.
D'Angeli, F., Malfa, G. A., Garozzo, A., Li Volti, G., Genovese, C., Stivala, A., Nicolosi, D., Attanasio, F., Bellia, F., Ronsisvalle, S., & Acquaviva, R. (2021). Antimicrobial, Antioxidant, and Cytotoxic Activities of . Antibiotics (Basel, Switzerland), 10(2), . https://doi.org/10.3390/antibiotics10020159
D'Angeli, Floriana, et al. "Antimicrobial, Antioxidant, and Cytotoxic Activities of ." Antibiotics (Basel, Switzerland) vol. 10,2 (2021). doi: https://doi.org/10.3390/antibiotics10020159
D'Angeli F, Malfa GA, Garozzo A, Li Volti G, Genovese C, Stivala A, Nicolosi D, Attanasio F, Bellia F, Ronsisvalle S, Acquaviva R. Antimicrobial, Antioxidant, and Cytotoxic Activities of . Antibiotics (Basel). 2021 Feb 04;10(2). doi: 10.3390/antibiotics10020159. PMID: 33557378; PMCID: PMC7915249.
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VI Conferenza Nazionale dei Servizi Trasfusionali, Rimini, 9-11 maggio 2019.

Blood transfusion = Trasfusione del sangue

Berti P, Aprili G, Bennardello F, Coluzzi S, Curciarello G, Di Gregorio P, Facco G, Fiorin F, Gandini G, Garozzo G, Nocera C, Velati C, Visceglie D.
PMID: 31009593
Blood Transfus. 2019 Apr 10;17:s29-s200. doi: 10.2450/2019.S2. Epub 2019 Apr 10.

No abstract available.

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Berti P, Aprili G, Bennardello F, et al. VI Conferenza Nazionale dei Servizi Trasfusionali, Rimini, 9-11 maggio 2019. Blood Transfus. 2019;17:s29-s200doi: 10.2450/2019.S2.
Berti, P., Aprili, G., Bennardello, F., Coluzzi, S., Curciarello, G., Di Gregorio, P., Facco, G., Fiorin, F., Gandini, G., Garozzo, G., Nocera, C., Velati, C., & Visceglie, D. (2019). VI Conferenza Nazionale dei Servizi Trasfusionali, Rimini, 9-11 maggio 2019. Blood transfusion = Trasfusione del sangue, 17s29-s200. https://doi.org/10.2450/2019.S2
Berti, Pierluigi, et al. "VI Conferenza Nazionale dei Servizi Trasfusionali, Rimini, 9-11 maggio 2019." Blood transfusion = Trasfusione del sangue vol. 17 (2019): s29-s200. doi: https://doi.org/10.2450/2019.S2
Berti P, Aprili G, Bennardello F, Coluzzi S, Curciarello G, Di Gregorio P, Facco G, Fiorin F, Gandini G, Garozzo G, Nocera C, Velati C, Visceglie D. VI Conferenza Nazionale dei Servizi Trasfusionali, Rimini, 9-11 maggio 2019. Blood Transfus. 2019 Apr 10;17:s29-s200. doi: 10.2450/2019.S2. Epub 2019 Apr 10. PMID: 31009593.
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Notch4 and mhc class II polymorphisms are associated with hcv-related benign and malignant lymphoproliferative diseases.

Oncotarget

Gragnani L, Fognani E, De Re V, Libra M, Garozzo A, Caini P, Cerretelli G, Giovannelli A, Lorini S, Monti M, Bagnoli S, Piaceri I, Zignego AL.
PMID: 29069725
Oncotarget. 2017 May 06;8(42):71528-71535. doi: 10.18632/oncotarget.17655. eCollection 2017 Sep 22.

Mixed cryoglobulinemia (MC), is a HCV-related, clinically benign, lymphoproliferative disorder (LPD) that may evolve into a non Hodgkin's lymphoma (NHL). Significant associations were found between two single nucleotide polymorphisms near NOTCH4 (rs2071286) and the HLA class II (rs9461776) genes...

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Gragnani L, Fognani E, De Re V, et al. Notch4 and mhc class II polymorphisms are associated with hcv-related benign and malignant lymphoproliferative diseases. Oncotarget. 2017;8(42):71528-71535doi: 10.18632/oncotarget.17655.
Gragnani, L., Fognani, E., De Re, V., Libra, M., Garozzo, A., Caini, P., Cerretelli, G., Giovannelli, A., Lorini, S., Monti, M., Bagnoli, S., Piaceri, I., & Zignego, A. L. (2017). Notch4 and mhc class II polymorphisms are associated with hcv-related benign and malignant lymphoproliferative diseases. Oncotarget, 8(42), 71528-71535. https://doi.org/10.18632/oncotarget.17655
Gragnani, Laura, et al. "Notch4 and mhc class II polymorphisms are associated with hcv-related benign and malignant lymphoproliferative diseases." Oncotarget vol. 8,42 (2017): 71528-71535. doi: https://doi.org/10.18632/oncotarget.17655
Gragnani L, Fognani E, De Re V, Libra M, Garozzo A, Caini P, Cerretelli G, Giovannelli A, Lorini S, Monti M, Bagnoli S, Piaceri I, Zignego AL. Notch4 and mhc class II polymorphisms are associated with hcv-related benign and malignant lymphoproliferative diseases. Oncotarget. 2017 May 06;8(42):71528-71535. doi: 10.18632/oncotarget.17655. eCollection 2017 Sep 22. PMID: 29069725; PMCID: PMC5641068.
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Two Argentinean Siblings with CDG-Ix: A Novel Type of Congenital Disorder of Glycosylation?.

JIMD reports

Millón MB, Delgado MA, Azar NB, Guelbert N, Sturiale L, Garozzo D, Matthijs G, Jaeken J, de Kremer RD, Asteggiano CG.
PMID: 23430830
JIMD Rep. 2011;1:65-72. doi: 10.1007/8904_2011_18. Epub 2011 Jun 22.

Congenital disorders of glycosylation (CDG) are genetic diseases caused by abnormal protein and lipid glycosylation. In this chapter, we report the clinical, biochemical, and molecular findings in two siblings with an unidentified CDG (CDG-Ix). They are the first and...

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Millón MB, Delgado MA, Azar NB, et al. Two Argentinean Siblings with CDG-Ix: A Novel Type of Congenital Disorder of Glycosylation?. JIMD Rep. 2011;1:65-72doi: 10.1007/8904_2011_18.
Millón, M. B., Delgado, M. A., Azar, N. B., Guelbert, N., Sturiale, L., Garozzo, D., Matthijs, G., Jaeken, J., de Kremer, R. D., & Asteggiano, C. G. (2011). Two Argentinean Siblings with CDG-Ix: A Novel Type of Congenital Disorder of Glycosylation?. JIMD reports, 165-72. https://doi.org/10.1007/8904_2011_18
Millón, M B Bistué, et al. "Two Argentinean Siblings with CDG-Ix: A Novel Type of Congenital Disorder of Glycosylation?." JIMD reports vol. 1 (2011): 65-72. doi: https://doi.org/10.1007/8904_2011_18
Millón MB, Delgado MA, Azar NB, Guelbert N, Sturiale L, Garozzo D, Matthijs G, Jaeken J, de Kremer RD, Asteggiano CG. Two Argentinean Siblings with CDG-Ix: A Novel Type of Congenital Disorder of Glycosylation?. JIMD Rep. 2011;1:65-72. doi: 10.1007/8904_2011_18. Epub 2011 Jun 22. PMID: 23430830; PMCID: PMC3509812.
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