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Prognosis of Acute Kidney Injury and Hepatorenal Syndrome in Patients with Cirrhosis: A Prospective Cohort Study.

International journal of nephrology

Allegretti AS, Ortiz G, Wenger J, Deferio JJ, Wibecan J, Kalim S, Tamez H, Chung RT, Karumanchi SA, Thadhani RI.
PMID: 26266048
Int J Nephrol. 2015;2015:108139. doi: 10.1155/2015/108139. Epub 2015 Jul 22.

Background/Aims. Acute kidney injury is a common problem for patients with cirrhosis and is associated with poor survival. We aimed to examine the association between type of acute kidney injury and 90-day mortality. Methods. Prospective cohort study at a...

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Allegretti AS, Ortiz G, Wenger J, et al. Prognosis of Acute Kidney Injury and Hepatorenal Syndrome in Patients with Cirrhosis: A Prospective Cohort Study. Int J Nephrol. 2015;2015:108139doi: 10.1155/2015/108139.
Allegretti, A. S., Ortiz, G., Wenger, J., Deferio, J. J., Wibecan, J., Kalim, S., Tamez, H., Chung, R. T., Karumanchi, S. A., & Thadhani, R. I. (2015). Prognosis of Acute Kidney Injury and Hepatorenal Syndrome in Patients with Cirrhosis: A Prospective Cohort Study. International journal of nephrology, 2015108139. https://doi.org/10.1155/2015/108139
Allegretti, Andrew S, et al. "Prognosis of Acute Kidney Injury and Hepatorenal Syndrome in Patients with Cirrhosis: A Prospective Cohort Study." International journal of nephrology vol. 2015 (2015): 108139. doi: https://doi.org/10.1155/2015/108139
Allegretti AS, Ortiz G, Wenger J, Deferio JJ, Wibecan J, Kalim S, Tamez H, Chung RT, Karumanchi SA, Thadhani RI. Prognosis of Acute Kidney Injury and Hepatorenal Syndrome in Patients with Cirrhosis: A Prospective Cohort Study. Int J Nephrol. 2015;2015:108139. doi: 10.1155/2015/108139. Epub 2015 Jul 22. PMID: 26266048; PMCID: PMC4525763.
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Synthesis of Pyrene-Fused Pyrazaacenes on Metal Surfaces: Toward One-Dimensional Conjugated Nanostructures.

ACS nano

Jiang L, Papageorgiou AC, Oh SC, Sağlam Ö, Reichert J, Duncan DA, Zhang YQ, Klappenberger F, Guo Y, Allegretti F, More S, Bhosale R, Mateo-Alonso A, Barth JV.
PMID: 26651905
ACS Nano. 2016 Jan 26;10(1):1033-41. doi: 10.1021/acsnano.5b06340. Epub 2015 Dec 14.

We investigated the synthesis of one-dimensional nanostructures via Schiff base (imine) formation on three close-packed coinage metal (Au, Ag, and Cu) surfaces under ultrahigh vacuum conditions. We demonstrate the feasibility of forming pyrene-fused pyrazaacene-based oligomers on the Ag(111) surface...

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Jiang L, Papageorgiou AC, Oh SC, et al. Synthesis of Pyrene-Fused Pyrazaacenes on Metal Surfaces: Toward One-Dimensional Conjugated Nanostructures. ACS Nano. 2015;10(1):1033-41doi: 10.1021/acsnano.5b06340.
Jiang, L., Papageorgiou, A. C., Oh, S. C., Sağlam, �. �., Reichert, J., Duncan, D. A., Zhang, Y. Q., Klappenberger, F., Guo, Y., Allegretti, F., More, S., Bhosale, R., Mateo-Alonso, A., & Barth, J. V. (2016). Synthesis of Pyrene-Fused Pyrazaacenes on Metal Surfaces: Toward One-Dimensional Conjugated Nanostructures. ACS nano, 10(1), 1033-41. https://doi.org/10.1021/acsnano.5b06340
Jiang, Li, et al. "Synthesis of Pyrene-Fused Pyrazaacenes on Metal Surfaces: Toward One-Dimensional Conjugated Nanostructures." ACS nano vol. 10,1 (2016): 1033-41. doi: https://doi.org/10.1021/acsnano.5b06340
Jiang L, Papageorgiou AC, Oh SC, Sağlam Ö, Reichert J, Duncan DA, Zhang YQ, Klappenberger F, Guo Y, Allegretti F, More S, Bhosale R, Mateo-Alonso A, Barth JV. Synthesis of Pyrene-Fused Pyrazaacenes on Metal Surfaces: Toward One-Dimensional Conjugated Nanostructures. ACS Nano. 2016 Jan 26;10(1):1033-41. doi: 10.1021/acsnano.5b06340. Epub 2015 Dec 14. PMID: 26651905.
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Allosteric Modulation of Chemoattractant Receptors.

Frontiers in immunology

Allegretti M, Cesta MC, Locati M.
PMID: 27199992
Front Immunol. 2016 May 02;7:170. doi: 10.3389/fimmu.2016.00170. eCollection 2016.

Chemoattractants control selective leukocyte homing via interactions with a dedicated family of related G protein-coupled receptor (GPCR). Emerging evidence indicates that the signaling activity of these receptors, as for other GPCR, is influenced by allosteric modulators, which interact with...

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Allegretti M, Cesta MC, Locati M. Allosteric Modulation of Chemoattractant Receptors. Front Immunol. 2016;7:170doi: 10.3389/fimmu.2016.00170.
Allegretti, M., Cesta, M. C., & Locati, M. (2016). Allosteric Modulation of Chemoattractant Receptors. Frontiers in immunology, 7170. https://doi.org/10.3389/fimmu.2016.00170
Allegretti, Marcello, et al. "Allosteric Modulation of Chemoattractant Receptors." Frontiers in immunology vol. 7 (2016): 170. doi: https://doi.org/10.3389/fimmu.2016.00170
Allegretti M, Cesta MC, Locati M. Allosteric Modulation of Chemoattractant Receptors. Front Immunol. 2016 May 02;7:170. doi: 10.3389/fimmu.2016.00170. eCollection 2016. PMID: 27199992; PMCID: PMC4852175.
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Conformational Change in the Mechanism of Inclusion of Ketoprofen in β-Cyclodextrin: NMR Spectroscopy, Ab Initio Calculations, Molecular Dynamics Simulations, and Photoreactivity.

The journal of physical chemistry. B

Guzzo T, Mandaliti W, Nepravishta R, Aramini A, Bodo E, Daidone I, Allegretti M, Topai A, Paci M.
PMID: 27689813
J Phys Chem B. 2016 Oct 20;120(41):10668-10678. doi: 10.1021/acs.jpcb.6b07913. Epub 2016 Oct 11.

Inclusion of drugs in cyclodextrins (CDs) is a recognized tool for modifying several properties such as solubility, stability, bioavailability, and so on. The photoreactive behavior of the β-CD/ketoprofen (KP) complex upon UV exposure showed a significant increase in photodecarboxylation,...

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Guzzo T, Mandaliti W, Nepravishta R, et al. Conformational Change in the Mechanism of Inclusion of Ketoprofen in β-Cyclodextrin: NMR Spectroscopy, Ab Initio Calculations, Molecular Dynamics Simulations, and Photoreactivity. J Phys Chem B. 2016;120(41):10668-10678doi: 10.1021/acs.jpcb.6b07913.
Guzzo, T., Mandaliti, W., Nepravishta, R., Aramini, A., Bodo, E., Daidone, I., Allegretti, M., Topai, A., & Paci, M. (2016). Conformational Change in the Mechanism of Inclusion of Ketoprofen in β-Cyclodextrin: NMR Spectroscopy, Ab Initio Calculations, Molecular Dynamics Simulations, and Photoreactivity. The journal of physical chemistry. B, 120(41), 10668-10678. https://doi.org/10.1021/acs.jpcb.6b07913
Guzzo, T, et al. "Conformational Change in the Mechanism of Inclusion of Ketoprofen in β-Cyclodextrin: NMR Spectroscopy, Ab Initio Calculations, Molecular Dynamics Simulations, and Photoreactivity." The journal of physical chemistry. B vol. 120,41 (2016): 10668-10678. doi: https://doi.org/10.1021/acs.jpcb.6b07913
Guzzo T, Mandaliti W, Nepravishta R, Aramini A, Bodo E, Daidone I, Allegretti M, Topai A, Paci M. Conformational Change in the Mechanism of Inclusion of Ketoprofen in β-Cyclodextrin: NMR Spectroscopy, Ab Initio Calculations, Molecular Dynamics Simulations, and Photoreactivity. J Phys Chem B. 2016 Oct 20;120(41):10668-10678. doi: 10.1021/acs.jpcb.6b07913. Epub 2016 Oct 11. PMID: 27689813.
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Adsorption bond length for H2O on TiO2(110): a key parameter for theoretical understanding.

Physical review letters

Allegretti F, O'Brien S, Polcik M, Sayago DI, Woodruff DP.
PMID: 16384241
Phys Rev Lett. 2005 Nov 25;95(22):226104. doi: 10.1103/PhysRevLett.95.226104. Epub 2005 Nov 22.

Scanned-energy mode photoelectron diffraction results show the adsorption site of molecular water on TiO2(110) to be atop under-coordinated surface Ti atoms, confirming the results of total energy calculations and STM imaging. However, the Ti-O(water) bond length is 2.21 +/-...

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Allegretti F, O'Brien S, Polcik M, et al. Adsorption bond length for H2O on TiO2(110): a key parameter for theoretical understanding. Phys Rev Lett. 2005;95(22):226104doi: 10.1103/PhysRevLett.95.226104.
Allegretti, F., O'Brien, S., Polcik, M., Sayago, D. I., & Woodruff, D. P. (2005). Adsorption bond length for H2O on TiO2(110): a key parameter for theoretical understanding. Physical review letters, 95(22), 226104. https://doi.org/10.1103/PhysRevLett.95.226104
Allegretti, F, et al. "Adsorption bond length for H2O on TiO2(110): a key parameter for theoretical understanding." Physical review letters vol. 95,22 (2005): 226104. doi: https://doi.org/10.1103/PhysRevLett.95.226104
Allegretti F, O'Brien S, Polcik M, Sayago DI, Woodruff DP. Adsorption bond length for H2O on TiO2(110): a key parameter for theoretical understanding. Phys Rev Lett. 2005 Nov 25;95(22):226104. doi: 10.1103/PhysRevLett.95.226104. Epub 2005 Nov 22. PMID: 16384241.
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Investigating the molecule-substrate interaction of prototypic tetrapyrrole compounds: adsorption and self-metalation of porphine on Cu(111).

The Journal of chemical physics

Diller K, Klappenberger F, Allegretti F, Papageorgiou AC, Fischer S, Wiengarten A, Joshi S, Seufert K, Écija D, Auwärter W, Barth JV.
PMID: 23614439
J Chem Phys. 2013 Apr 21;138(15):154710. doi: 10.1063/1.4800771.

We report on the adsorption and self-metalation of a prototypic tetrapyrrole compound, the free-base porphine (2H-P), on the Cu(111) surface. Our multitechnique study combines scanning tunneling microscopy (STM) results with near-edge X-ray absorption fine-structure (NEXAFS) and X-ray photoelectron spectroscopy...

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Diller K, Klappenberger F, Allegretti F, et al. Investigating the molecule-substrate interaction of prototypic tetrapyrrole compounds: adsorption and self-metalation of porphine on Cu(111). J Chem Phys. 2013;138(15):154710doi: 10.1063/1.4800771.
Diller, K., Klappenberger, F., Allegretti, F., Papageorgiou, A. C., Fischer, S., Wiengarten, A., Joshi, S., Seufert, K., Écija, D., Auwärter, W., & Barth, J. V. (2013). Investigating the molecule-substrate interaction of prototypic tetrapyrrole compounds: adsorption and self-metalation of porphine on Cu(111). The Journal of chemical physics, 138(15), 154710. https://doi.org/10.1063/1.4800771
Diller, K, et al. "Investigating the molecule-substrate interaction of prototypic tetrapyrrole compounds: adsorption and self-metalation of porphine on Cu(111)." The Journal of chemical physics vol. 138,15 (2013): 154710. doi: https://doi.org/10.1063/1.4800771
Diller K, Klappenberger F, Allegretti F, Papageorgiou AC, Fischer S, Wiengarten A, Joshi S, Seufert K, Écija D, Auwärter W, Barth JV. Investigating the molecule-substrate interaction of prototypic tetrapyrrole compounds: adsorption and self-metalation of porphine on Cu(111). J Chem Phys. 2013 Apr 21;138(15):154710. doi: 10.1063/1.4800771. PMID: 23614439.
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The influence of D-.

Biomedical reports

Dell'Edera D, Sarlo F, Allegretti A, Simone F, Lupo MG, Epifania AA.
PMID: 28804631
Biomed Rep. 2017 Aug;7(2):169-172. doi: 10.3892/br.2017.939. Epub 2017 Jul 04.

The aim of the present study was to demonstrate that the use of inositol and folic acid from the first trimester of pregnancy, counteracts the onset of gestational diabetes mellitus (GDM) in women at risk, preserving the infants from...

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Dell'Edera D, Sarlo F, Allegretti A, et al. The influence of D-. Biomed Rep. 2017;7(2):169-172doi: 10.3892/br.2017.939.
Dell'Edera, D., Sarlo, F., Allegretti, A., Simone, F., Lupo, M. G., & Epifania, A. A. (2017). The influence of D-. Biomedical reports, 7(2), 169-172. https://doi.org/10.3892/br.2017.939
Dell'Edera, Domenico, et al. "The influence of D-." Biomedical reports vol. 7,2 (2017): 169-172. doi: https://doi.org/10.3892/br.2017.939
Dell'Edera D, Sarlo F, Allegretti A, Simone F, Lupo MG, Epifania AA. The influence of D-. Biomed Rep. 2017 Aug;7(2):169-172. doi: 10.3892/br.2017.939. Epub 2017 Jul 04. PMID: 28804631; PMCID: PMC5526159.
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Case report: Percutaneous treatment of multiple honeycomb-like liver hydatid cysts (type III CE2, according to WHO classification).

The Indian journal of radiology & imaging

Corona M, Cannavale A, Bruni A, Boatta E, Allegritti M, Lucatelli P, Fanelli F, Pucci A, Paciotti C, Salvatori FM.
PMID: 22623811
Indian J Radiol Imaging. 2012 Jan;22(1):23-6. doi: 10.4103/0971-3026.95399.

Percutaneous treatment has been developing as a reliable and effective alternative to surgery in the treatment of liver hydatid cysts. However, percutaneous treatment is strongly recommended only for some types of hydatid cysts (types I and II). We report...

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Corona M, Cannavale A, Bruni A, et al. Case report: Percutaneous treatment of multiple honeycomb-like liver hydatid cysts (type III CE2, according to WHO classification). Indian J Radiol Imaging. 2012;22(1):23-6doi: 10.4103/0971-3026.95399.
Corona, M., Cannavale, A., Bruni, A., Boatta, E., Allegritti, M., Lucatelli, P., Fanelli, F., Pucci, A., Paciotti, C., & Salvatori, F. M. (2012). Case report: Percutaneous treatment of multiple honeycomb-like liver hydatid cysts (type III CE2, according to WHO classification). The Indian journal of radiology & imaging, 22(1), 23-6. https://doi.org/10.4103/0971-3026.95399
Corona, Mario, et al. "Case report: Percutaneous treatment of multiple honeycomb-like liver hydatid cysts (type III CE2, according to WHO classification)." The Indian journal of radiology & imaging vol. 22,1 (2012): 23-6. doi: https://doi.org/10.4103/0971-3026.95399
Corona M, Cannavale A, Bruni A, Boatta E, Allegritti M, Lucatelli P, Fanelli F, Pucci A, Paciotti C, Salvatori FM. Case report: Percutaneous treatment of multiple honeycomb-like liver hydatid cysts (type III CE2, according to WHO classification). Indian J Radiol Imaging. 2012 Jan;22(1):23-6. doi: 10.4103/0971-3026.95399. PMID: 22623811; PMCID: PMC3354352.
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Unraveling the Oxidation and Spin State of Mn-Corrole through X-ray Spectroscopy and Quantum Chemical Analysis.

The journal of physical chemistry letters

Paszkiewicz M, Biktagirov T, Aldahhak H, Allegretti F, Rauls E, Schöfberger W, Schmidt WG, Barth JV, Gerstmann U, Klappenberger F.
PMID: 30362761
J Phys Chem Lett. 2018 Nov 15;9(22):6412-6420. doi: 10.1021/acs.jpclett.8b02525. Epub 2018 Oct 26.

The interplay between Mn ions and corrole ligands gives rise to complex scenarios regarding the metal centers' electronic properties expressing a range of high oxidation states and spin configurations. The resulting potential of Mn-corroles for applications such as catalysts...

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Paszkiewicz M, Biktagirov T, Aldahhak H, et al. Unraveling the Oxidation and Spin State of Mn-Corrole through X-ray Spectroscopy and Quantum Chemical Analysis. J Phys Chem Lett. 2018;9(22):6412-6420doi: 10.1021/acs.jpclett.8b02525.
Paszkiewicz, M., Biktagirov, T., Aldahhak, H., Allegretti, F., Rauls, E., Schöfberger, W., Schmidt, W. G., Barth, J. V., Gerstmann, U., & Klappenberger, F. (2018). Unraveling the Oxidation and Spin State of Mn-Corrole through X-ray Spectroscopy and Quantum Chemical Analysis. The journal of physical chemistry letters, 9(22), 6412-6420. https://doi.org/10.1021/acs.jpclett.8b02525
Paszkiewicz, Mateusz, et al. "Unraveling the Oxidation and Spin State of Mn-Corrole through X-ray Spectroscopy and Quantum Chemical Analysis." The journal of physical chemistry letters vol. 9,22 (2018): 6412-6420. doi: https://doi.org/10.1021/acs.jpclett.8b02525
Paszkiewicz M, Biktagirov T, Aldahhak H, Allegretti F, Rauls E, Schöfberger W, Schmidt WG, Barth JV, Gerstmann U, Klappenberger F. Unraveling the Oxidation and Spin State of Mn-Corrole through X-ray Spectroscopy and Quantum Chemical Analysis. J Phys Chem Lett. 2018 Nov 15;9(22):6412-6420. doi: 10.1021/acs.jpclett.8b02525. Epub 2018 Oct 26. PMID: 30362761.
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Quantum Tunneling Mediated Interfacial Synthesis of a Benzofuran Derivative.

Angewandte Chemie (International ed. in English)

Paintner T, Björk J, Du P, Klyatskaya S, Paszkiewicz M, Hellwig R, Uphoff M, Öner MA, Cuniberto E, Deimel PS, Zhang YQ, Palma CA, Allegretti F, Ruben M, Barth JV, Klappenberger F.
PMID: 31120567
Angew Chem Int Ed Engl. 2019 Aug 12;58(33):11285-11290. doi: 10.1002/anie.201904030. Epub 2019 Jul 04.

Reaction pathways involving quantum tunneling of protons are fundamental to chemistry and biology. They are responsible for essential aspects of interstellar synthesis, the degradation and isomerization of compounds, enzymatic activity, and protein dynamics. On-surface conditions have been demonstrated to...

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Paintner T, Björk J, Du P, et al. Quantum Tunneling Mediated Interfacial Synthesis of a Benzofuran Derivative. Angew Chem Int Ed Engl. 2019;58(33):11285-11290doi: 10.1002/anie.201904030.
Paintner, T., Björk, J., Du, P., Klyatskaya, S., Paszkiewicz, M., Hellwig, R., Uphoff, M., Öner, M. A., Cuniberto, E., Deimel, P. S., Zhang, Y. Q., Palma, C. A., Allegretti, F., Ruben, M., Barth, J. V., & Klappenberger, F. (2019). Quantum Tunneling Mediated Interfacial Synthesis of a Benzofuran Derivative. Angewandte Chemie (International ed. in English), 58(33), 11285-11290. https://doi.org/10.1002/anie.201904030
Paintner, Tobias, et al. "Quantum Tunneling Mediated Interfacial Synthesis of a Benzofuran Derivative." Angewandte Chemie (International ed. in English) vol. 58,33 (2019): 11285-11290. doi: https://doi.org/10.1002/anie.201904030
Paintner T, Björk J, Du P, Klyatskaya S, Paszkiewicz M, Hellwig R, Uphoff M, Öner MA, Cuniberto E, Deimel PS, Zhang YQ, Palma CA, Allegretti F, Ruben M, Barth JV, Klappenberger F. Quantum Tunneling Mediated Interfacial Synthesis of a Benzofuran Derivative. Angew Chem Int Ed Engl. 2019 Aug 12;58(33):11285-11290. doi: 10.1002/anie.201904030. Epub 2019 Jul 04. PMID: 31120567.
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Spatial decoupling of macrocyclic metal-organic complexes from a metal support: a 4-fluorothiophenol self-assembled monolayer as a thermally removable spacer.

Physical chemistry chemical physics : PCCP

Deimel PS, Feulner P, Barth JV, Allegretti F.
PMID: 31106802
Phys Chem Chem Phys. 2019 Jun 07;21(21):10992-11003. doi: 10.1039/c9cp01583c. Epub 2019 May 20.

The precise control over the electronic properties and function of metal centres in metal-organic complexes such as metallo-porphyrins (MPs) and metallo-phthalocyanines (MPcs) holds promise for their targeted application in, e.g., nanoscale chemical conversion devices and molecular sensors. However, when...

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Deimel PS, Feulner P, Barth JV, et al. Spatial decoupling of macrocyclic metal-organic complexes from a metal support: a 4-fluorothiophenol self-assembled monolayer as a thermally removable spacer. Phys Chem Chem Phys. 2019;21(21):10992-11003doi: 10.1039/c9cp01583c.
Deimel, P. S., Feulner, P., Barth, J. V., & Allegretti, F. (2019). Spatial decoupling of macrocyclic metal-organic complexes from a metal support: a 4-fluorothiophenol self-assembled monolayer as a thermally removable spacer. Physical chemistry chemical physics : PCCP, 21(21), 10992-11003. https://doi.org/10.1039/c9cp01583c
Deimel, Peter S, et al. "Spatial decoupling of macrocyclic metal-organic complexes from a metal support: a 4-fluorothiophenol self-assembled monolayer as a thermally removable spacer." Physical chemistry chemical physics : PCCP vol. 21,21 (2019): 10992-11003. doi: https://doi.org/10.1039/c9cp01583c
Deimel PS, Feulner P, Barth JV, Allegretti F. Spatial decoupling of macrocyclic metal-organic complexes from a metal support: a 4-fluorothiophenol self-assembled monolayer as a thermally removable spacer. Phys Chem Chem Phys. 2019 Jun 07;21(21):10992-11003. doi: 10.1039/c9cp01583c. Epub 2019 May 20. PMID: 31106802.
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Validation of the inverted adsorption structure for free-base tetraphenyl porphyrin on Cu(111).

Chemical communications (Cambridge, England)

Ryan PTP, Lalaguna PL, Haag F, Braim MM, Ding P, Payne DJ, Barth JV, Lee TL, Woodruff DP, Allegretti F, Duncan DA.
PMID: 32118210
Chem Commun (Camb). 2020 Mar 28;56(25):3681-3684. doi: 10.1039/c9cc09638h. Epub 2020 Mar 02.

Utilising normal incidence X-ray standing waves we rigourously scrutinise the "inverted model" as the adsorption structure of free-base tetraphenyl porphyrin on Cu(111). We demonstrate that the iminic N atoms are anchored at near-bridge adsorption sites on the surface displaced...

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Ryan PTP, Lalaguna PL, Haag F, et al. Validation of the inverted adsorption structure for free-base tetraphenyl porphyrin on Cu(111). Chem Commun (Camb). 2020;56(25):3681-3684doi: 10.1039/c9cc09638h.
Ryan, P. T. P., Lalaguna, P. L., Haag, F., Braim, M. M., Ding, P., Payne, D. J., Barth, J. V., Lee, T. L., Woodruff, D. P., Allegretti, F., & Duncan, D. A. (2020). Validation of the inverted adsorption structure for free-base tetraphenyl porphyrin on Cu(111). Chemical communications (Cambridge, England), 56(25), 3681-3684. https://doi.org/10.1039/c9cc09638h
Ryan, P T P, et al. "Validation of the inverted adsorption structure for free-base tetraphenyl porphyrin on Cu(111)." Chemical communications (Cambridge, England) vol. 56,25 (2020): 3681-3684. doi: https://doi.org/10.1039/c9cc09638h
Ryan PTP, Lalaguna PL, Haag F, Braim MM, Ding P, Payne DJ, Barth JV, Lee TL, Woodruff DP, Allegretti F, Duncan DA. Validation of the inverted adsorption structure for free-base tetraphenyl porphyrin on Cu(111). Chem Commun (Camb). 2020 Mar 28;56(25):3681-3684. doi: 10.1039/c9cc09638h. Epub 2020 Mar 02. PMID: 32118210.
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Showing 1 to 12 of 203 entries