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Girls4STEM: Gender diversity in STEM for a sustainable future

STEM education

Benavent X, Botella-Mascarell C, de E, Forte A.
GSID: nfLGoxlvmSQJ
X Benavent, E de Ves, A Forte, C Botella-Mascarell… - Sustainability, 2020 - mdpi.com

Science, Technology, Engineering, and Mathematics (STEM) are key disciplines towards tackling the challenges related to the Sustainable Development Goals. However, evidence …

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Benavent, X., de Ves, E., Forte, A., Botella-Mascarell, C., López-Iñesta, E., Rueda, S., ... & Marzal, P. (2020). Girls4STEM: Gender diversity in STEM for a sustainable future. Sustainability, 12(15), 6051.
Benavent, Xaro, et al. "Girls4STEM: Gender diversity in STEM for a sustainable future." Sustainability 12.15 (2020): 6051.
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Students' and instructors' perceptions of five different active learning strategies used to teach software modeling

science instructors

Silva W, Steinmacher I, Conte T.
GSID: 54hR_oGu4xUJ
W Silva, I Steinmacher, T Conte - IEEE Access, 2019 - ieeexplore.ieee.org

… Additionally, we identified four challenges that instructors may face when employing active learning … instructors conduct a teachercentered learning environment to present theoretical concepts to students. The complex nature of Computer Science courses prevents instructors …

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Silva, W., Steinmacher, I., & Conte, T. (2019). Students’ and instructors’ perceptions of five different active learning strategies used to teach software modeling. IEEE Access, 7, 184063-184077.
Silva, Williamson, Igor Steinmacher, and Tayana Conte. "Students’ and instructors’ perceptions of five different active learning strategies used to teach software modeling." IEEE Access 7 (2019): 184063-184077.
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Two simultaneous autoimmune processes in a patient presenting with respiratory insufficiency.

Respirology case reports

Troy L, Hamor P, Bleasel J, Corte T.
PMID: 25473554
Respirol Case Rep. 2014 Mar;2(1):21-3. doi: 10.1002/rcr2.36. Epub 2013 Dec 20.

The idiopathic inflammatory myopathies, including dermatomyositis, are uncommon acquired autoimmune diseases, sometimes associated with interstitial lung disease. Myasthenia gravis, a separate autoimmune disorder involving the neuromuscular junction, has some overlapping clinical features but has only rarely been reported to...

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Troy L, Hamor P, Bleasel J, et al. Two simultaneous autoimmune processes in a patient presenting with respiratory insufficiency. Respirol Case Rep. 2013;2(1):21-3doi: 10.1002/rcr2.36.
Troy, L., Hamor, P., Bleasel, J., & Corte, T. (2014). Two simultaneous autoimmune processes in a patient presenting with respiratory insufficiency. Respirology case reports, 2(1), 21-3. https://doi.org/10.1002/rcr2.36
Troy, Lauren, et al. "Two simultaneous autoimmune processes in a patient presenting with respiratory insufficiency." Respirology case reports vol. 2,1 (2014): 21-3. doi: https://doi.org/10.1002/rcr2.36
Troy L, Hamor P, Bleasel J, Corte T. Two simultaneous autoimmune processes in a patient presenting with respiratory insufficiency. Respirol Case Rep. 2014 Mar;2(1):21-3. doi: 10.1002/rcr2.36. Epub 2013 Dec 20. PMID: 25473554; PMCID: PMC4184724.
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Escape Extinction and Negative Reinforcement in the Treatment of Pediatric Feeding Disorders: a Single Case Analysis.

Behavior analysis in practice

Voulgarakis H, Forte S.
PMID: 27703921
Behav Anal Pract. 2015 Sep 03;8(2):212-214. doi: 10.1007/s40617-015-0086-8. eCollection 2015 Oct.

Pediatric feeding disorders are common among children with developmental disabilities and can have detrimental effects on growth and development. An escape extinction and negative reinforcement-based approach to treating food refusal was examined in a child with cerebral palsy. A...

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Voulgarakis H, Forte S. Escape Extinction and Negative Reinforcement in the Treatment of Pediatric Feeding Disorders: a Single Case Analysis. Behav Anal Pract. 2015;8(2):212-214doi: 10.1007/s40617-015-0086-8.
Voulgarakis, H., & Forte, S. (2015). Escape Extinction and Negative Reinforcement in the Treatment of Pediatric Feeding Disorders: a Single Case Analysis. Behavior analysis in practice, 8(2), 212-214. https://doi.org/10.1007/s40617-015-0086-8
Voulgarakis, Harry, and Forte, Solandy. "Escape Extinction and Negative Reinforcement in the Treatment of Pediatric Feeding Disorders: a Single Case Analysis." Behavior analysis in practice vol. 8,2 (2015): 212-214. doi: https://doi.org/10.1007/s40617-015-0086-8
Voulgarakis H, Forte S. Escape Extinction and Negative Reinforcement in the Treatment of Pediatric Feeding Disorders: a Single Case Analysis. Behav Anal Pract. 2015 Sep 03;8(2):212-214. doi: 10.1007/s40617-015-0086-8. eCollection 2015 Oct. PMID: 27703921; PMCID: PMC5048282.
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Potential Role of Activating Transcription Factor 5 during Osteogenesis.

Stem cells international

Vicari L, Calabrese G, Forte S, Giuffrida R, Colarossi C, Parrinello NL, Memeo L.
PMID: 26770207
Stem Cells Int. 2016;2016:5282185. doi: 10.1155/2016/5282185. Epub 2015 Dec 06.

Human adipose-derived stem cells are an abundant population of stem cells readily isolated from human adipose tissue that can differentiate into connective tissue lineages including bone, cartilage, fat, and muscle. Activating transcription factor 5 is a transcription factor of...

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Vicari L, Calabrese G, Forte S, et al. Potential Role of Activating Transcription Factor 5 during Osteogenesis. Stem Cells Int. 2015;2016:5282185doi: 10.1155/2016/5282185.
Vicari, L., Calabrese, G., Forte, S., Giuffrida, R., Colarossi, C., Parrinello, N. L., & Memeo, L. (2016). Potential Role of Activating Transcription Factor 5 during Osteogenesis. Stem cells international, 20165282185. https://doi.org/10.1155/2016/5282185
Vicari, Luisa, et al. "Potential Role of Activating Transcription Factor 5 during Osteogenesis." Stem cells international vol. 2016 (2016): 5282185. doi: https://doi.org/10.1155/2016/5282185
Vicari L, Calabrese G, Forte S, Giuffrida R, Colarossi C, Parrinello NL, Memeo L. Potential Role of Activating Transcription Factor 5 during Osteogenesis. Stem Cells Int. 2016;2016:5282185. doi: 10.1155/2016/5282185. Epub 2015 Dec 06. PMID: 26770207; PMCID: PMC4684884.
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Nasal Lobular Capillary Hemangioma as a Complication after an Endoscopic Transsphenoidal Gonadotrophin-Producing Pituitary Adenoma Resection.

Journal of neurological surgery reports

Forte D, Irañeta AS, Nabais A, Figueiredo A, Mafra M, Gonçalves V.
PMID: 28326242
J Neurol Surg Rep. 2017 Jan;78(1):e59-e61. doi: 10.1055/s-0037-1600913.

No abstract available.

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Forte D, Irañeta AS, Nabais A, et al. Nasal Lobular Capillary Hemangioma as a Complication after an Endoscopic Transsphenoidal Gonadotrophin-Producing Pituitary Adenoma Resection. J Neurol Surg Rep. 2017;78(1):e59-e61doi: 10.1055/s-0037-1600913.
Forte, D., Irañeta, A. S., Nabais, A., Figueiredo, A., Mafra, M., & Gonçalves, V. (2017). Nasal Lobular Capillary Hemangioma as a Complication after an Endoscopic Transsphenoidal Gonadotrophin-Producing Pituitary Adenoma Resection. Journal of neurological surgery reports, 78(1), e59-e61. https://doi.org/10.1055/s-0037-1600913
Forte, Dalila, et al. "Nasal Lobular Capillary Hemangioma as a Complication after an Endoscopic Transsphenoidal Gonadotrophin-Producing Pituitary Adenoma Resection." Journal of neurological surgery reports vol. 78,1 (2017): e59-e61. doi: https://doi.org/10.1055/s-0037-1600913
Forte D, Irañeta AS, Nabais A, Figueiredo A, Mafra M, Gonçalves V. Nasal Lobular Capillary Hemangioma as a Complication after an Endoscopic Transsphenoidal Gonadotrophin-Producing Pituitary Adenoma Resection. J Neurol Surg Rep. 2017 Jan;78(1):e59-e61. doi: 10.1055/s-0037-1600913. PMID: 28326242; PMCID: PMC5359141.
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Premalignant Gastric Lesions in Patients Included in National Colorectal Cancer Screening.

Radiology and oncology

Tepes B, Seruga M, Vujasinovic M, Urlep D, Ljepovic L, Brglez JN, Forte A, Anita Kek L, Skvarc M.
PMID: 29520200
Radiol Oncol. 2017 Dec 07;52(1):7-13. doi: 10.1515/raon-2017-0054. eCollection 2018 Mar.

BACKGROUND: Gastric cancer is the fifth most common malignancy in the world with almost one million new cases annually. Helicobacter pylori infection causes 89% of all gastric cancers. Premalignant lesions (atrophy and intestinal metaplasia) develop after several decades of...

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Tepes B, Seruga M, Vujasinovic M, et al. Premalignant Gastric Lesions in Patients Included in National Colorectal Cancer Screening. Radiol Oncol. 2017;52(1):7-13doi: 10.1515/raon-2017-0054.
Tepes, B., Seruga, M., Vujasinovic, M., Urlep, D., Ljepovic, L., Brglez, J. N., Forte, A., Anita Kek, L., & Skvarc, M. (2018). Premalignant Gastric Lesions in Patients Included in National Colorectal Cancer Screening. Radiology and oncology, 52(1), 7-13. https://doi.org/10.1515/raon-2017-0054
Tepes, Bojan, et al. "Premalignant Gastric Lesions in Patients Included in National Colorectal Cancer Screening." Radiology and oncology vol. 52,1 (2018): 7-13. doi: https://doi.org/10.1515/raon-2017-0054
Tepes B, Seruga M, Vujasinovic M, Urlep D, Ljepovic L, Brglez JN, Forte A, Anita Kek L, Skvarc M. Premalignant Gastric Lesions in Patients Included in National Colorectal Cancer Screening. Radiol Oncol. 2017 Dec 07;52(1):7-13. doi: 10.1515/raon-2017-0054. eCollection 2018 Mar. PMID: 29520200; PMCID: PMC5839076.
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Aggregates of Defined Stereochemical Scaffolds: A Study in Solution of a Zinc(II) Schiff Base Complex Derived from the Enantiopure trans-1,2-Cyclopentanediamine.

Inorganic chemistry

Oliveri IP, Forte G, Consiglio G, Failla S, Di Bella S.
PMID: 29112387
Inorg Chem. 2017 Nov 20;56(22):14206-14213. doi: 10.1021/acs.inorgchem.7b02341. Epub 2017 Nov 07.

Molecular aggregation of bis(salicylaldiminato) Zn

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Oliveri IP, Forte G, Consiglio G, et al. Aggregates of Defined Stereochemical Scaffolds: A Study in Solution of a Zinc(II) Schiff Base Complex Derived from the Enantiopure trans-1,2-Cyclopentanediamine. Inorg Chem. 2017;56(22):14206-14213doi: 10.1021/acs.inorgchem.7b02341.
Oliveri, I. P., Forte, G., Consiglio, G., Failla, S., & Di Bella, S. (2017). Aggregates of Defined Stereochemical Scaffolds: A Study in Solution of a Zinc(II) Schiff Base Complex Derived from the Enantiopure trans-1,2-Cyclopentanediamine. Inorganic chemistry, 56(22), 14206-14213. https://doi.org/10.1021/acs.inorgchem.7b02341
Oliveri, Ivan Pietro, et al. "Aggregates of Defined Stereochemical Scaffolds: A Study in Solution of a Zinc(II) Schiff Base Complex Derived from the Enantiopure trans-1,2-Cyclopentanediamine." Inorganic chemistry vol. 56,22 (2017): 14206-14213. doi: https://doi.org/10.1021/acs.inorgchem.7b02341
Oliveri IP, Forte G, Consiglio G, Failla S, Di Bella S. Aggregates of Defined Stereochemical Scaffolds: A Study in Solution of a Zinc(II) Schiff Base Complex Derived from the Enantiopure trans-1,2-Cyclopentanediamine. Inorg Chem. 2017 Nov 20;56(22):14206-14213. doi: 10.1021/acs.inorgchem.7b02341. Epub 2017 Nov 07. PMID: 29112387.
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The More, The Better: "Do the Right Thing" For Natural Killer Immunotherapy in Acute Myeloid Leukemia.

Frontiers in immunology

Parisi S, Lecciso M, Ocadlikova D, Salvestrini V, Ciciarello M, Forte D, Corradi G, Cavo M, Curti A.
PMID: 29097997
Front Immunol. 2017 Oct 19;8:1330. doi: 10.3389/fimmu.2017.01330. eCollection 2017.

Natural killer (NK) cells are circulating CD3

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Parisi S, Lecciso M, Ocadlikova D, et al. The More, The Better: "Do the Right Thing" For Natural Killer Immunotherapy in Acute Myeloid Leukemia. Front Immunol. 2017;8:1330doi: 10.3389/fimmu.2017.01330.
Parisi, S., Lecciso, M., Ocadlikova, D., Salvestrini, V., Ciciarello, M., Forte, D., Corradi, G., Cavo, M., & Curti, A. (2017). The More, The Better: "Do the Right Thing" For Natural Killer Immunotherapy in Acute Myeloid Leukemia. Frontiers in immunology, 81330. https://doi.org/10.3389/fimmu.2017.01330
Parisi, Sarah, et al. "The More, The Better: "Do the Right Thing" For Natural Killer Immunotherapy in Acute Myeloid Leukemia." Frontiers in immunology vol. 8 (2017): 1330. doi: https://doi.org/10.3389/fimmu.2017.01330
Parisi S, Lecciso M, Ocadlikova D, Salvestrini V, Ciciarello M, Forte D, Corradi G, Cavo M, Curti A. The More, The Better: "Do the Right Thing" For Natural Killer Immunotherapy in Acute Myeloid Leukemia. Front Immunol. 2017 Oct 19;8:1330. doi: 10.3389/fimmu.2017.01330. eCollection 2017. PMID: 29097997; PMCID: PMC5653691.
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Obesity hypoventilation syndrome: A different beast.

Paediatrics & child health

Folman R, Grenier D, Birken C, Campisi P, Do MT, Forte V, Maclusky I, McCrindle BW, Narang I, Witmans M.
PMID: 24381492
Paediatr Child Health. 2013 Jan;18(1):36.

No abstract available.

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Folman R, Grenier D, Birken C, et al. Obesity hypoventilation syndrome: A different beast. Paediatr Child Health. 2013;18(1):36
Folman, R., Grenier, D., Birken, C., Campisi, P., Do, M. T., Forte, V., Maclusky, I., McCrindle, B. W., Narang, I., & Witmans, M. (2013). Obesity hypoventilation syndrome: A different beast. Paediatrics & child health, 18(1), 36.
Folman, Ralph, et al. "Obesity hypoventilation syndrome: A different beast." Paediatrics & child health vol. 18,1 (2013): 36.
Folman R, Grenier D, Birken C, Campisi P, Do MT, Forte V, Maclusky I, McCrindle BW, Narang I, Witmans M. Obesity hypoventilation syndrome: A different beast. Paediatr Child Health. 2013 Jan;18(1):36. PMID: 24381492; PMCID: PMC3680272.
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Correction: A Comparison of Experimental and Analytical Procedures to Measure Passive Drag in Human Swimming.

PloS one

Barbosa TM, Morais JE, Forte P, Neiva H, Garrido ND, Marinho DA.
PMID: 28459852
PLoS One. 2017 May 01;12(5):e0177038. doi: 10.1371/journal.pone.0177038. eCollection 2017.

[This corrects the article DOI: 10.1371/journal.pone.0130868.].

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Barbosa TM, Morais JE, Forte P, et al. Correction: A Comparison of Experimental and Analytical Procedures to Measure Passive Drag in Human Swimming. PLoS One. 2017;12(5):e0177038doi: 10.1371/journal.pone.0177038.
Barbosa, T. M., Morais, J. E., Forte, P., Neiva, H., Garrido, N. D., & Marinho, D. A. (2017). Correction: A Comparison of Experimental and Analytical Procedures to Measure Passive Drag in Human Swimming. PloS one, 12(5), e0177038. https://doi.org/10.1371/journal.pone.0177038
Barbosa, Tiago M, et al. "Correction: A Comparison of Experimental and Analytical Procedures to Measure Passive Drag in Human Swimming." PloS one vol. 12,5 (2017): e0177038. doi: https://doi.org/10.1371/journal.pone.0177038
Barbosa TM, Morais JE, Forte P, Neiva H, Garrido ND, Marinho DA. Correction: A Comparison of Experimental and Analytical Procedures to Measure Passive Drag in Human Swimming. PLoS One. 2017 May 01;12(5):e0177038. doi: 10.1371/journal.pone.0177038. eCollection 2017. PMID: 28459852; PMCID: PMC5411041.
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Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss.

Molecular cytogenetics

Iossa S, Costa V, Corvino V, Auletta G, Barruffo L, Cappellani S, Ceglia C, Cennamo G, D'Adamo AP, D'Amico A, Di Paolo N, Forte R, Gasparini P, Laria C, Lombardo B, Malesci R, Vitale A, Marciano E, Franzè A.
PMID: 25821518
Mol Cytogenet. 2015 Mar 20;8:18. doi: 10.1186/s13039-015-0120-0. eCollection 2015.

BACKGROUND: Sensorineural hearing impairment is a common pathological manifestation in patients affected by X-linked intellectual disability. A few cases of interstitial deletions at Xq21 with several different phenotypic characteristics have been described, but to date, a complete molecular characterization...

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Iossa S, Costa V, Corvino V, et al. Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss. Mol Cytogenet. 2015;8:18doi: 10.1186/s13039-015-0120-0.
Iossa, S., Costa, V., Corvino, V., Auletta, G., Barruffo, L., Cappellani, S., Ceglia, C., Cennamo, G., D'Adamo, A. P., D'Amico, A., Di Paolo, N., Forte, R., Gasparini, P., Laria, C., Lombardo, B., Malesci, R., Vitale, A., Marciano, E., & Franzè, A. (2015). Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss. Molecular cytogenetics, 818. https://doi.org/10.1186/s13039-015-0120-0
Iossa, Sandra, et al. "Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss." Molecular cytogenetics vol. 8 (2015): 18. doi: https://doi.org/10.1186/s13039-015-0120-0
Iossa S, Costa V, Corvino V, Auletta G, Barruffo L, Cappellani S, Ceglia C, Cennamo G, D'Adamo AP, D'Amico A, Di Paolo N, Forte R, Gasparini P, Laria C, Lombardo B, Malesci R, Vitale A, Marciano E, Franzè A. Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss. Mol Cytogenet. 2015 Mar 20;8:18. doi: 10.1186/s13039-015-0120-0. eCollection 2015. PMID: 25821518; PMCID: PMC4376344.
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