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A catalog of hemizygous variation in 127 22q11 deletion patients.

Human genome variation

Hestand MS, Nowakowska BA, Vergaelen E, Van Houdt J, Dehaspe L, Suhl JA, Del-Favero J, Mortier G, Zackai E, Swillen A, Devriendt K, Gur RE, McDonald-McGinn DM, Warren ST, Emanuel BS, Vermeesch JR.
PMID: 27274857
Hum Genome Var. 2016 Jan 14;3:15065. doi: 10.1038/hgv.2015.65. eCollection 2016.

The 22q11.2 deletion syndrome is the most common microdeletion disorder, with wide phenotypic variability. To investigate variation within the non-deleted allele we performed targeted resequencing of the 22q11.2 region for 127 patients, identifying multiple deletion sizes, including two deletions...

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Hestand MS, Nowakowska BA, Vergaelen E, et al. A catalog of hemizygous variation in 127 22q11 deletion patients. Hum Genome Var. 2016;3:15065doi: 10.1038/hgv.2015.65.
Hestand, M. S., Nowakowska, B. A., Vergaelen, E., Van Houdt, J., Dehaspe, L., Suhl, J. A., Del-Favero, J., Mortier, G., Zackai, E., Swillen, A., Devriendt, K., Gur, R. E., McDonald-McGinn, D. M., Warren, S. T., Emanuel, B. S., & Vermeesch, J. R. (2016). A catalog of hemizygous variation in 127 22q11 deletion patients. Human genome variation, 315065. https://doi.org/10.1038/hgv.2015.65
Hestand, Matthew S, et al. "A catalog of hemizygous variation in 127 22q11 deletion patients." Human genome variation vol. 3 (2016): 15065. doi: https://doi.org/10.1038/hgv.2015.65
Hestand MS, Nowakowska BA, Vergaelen E, Van Houdt J, Dehaspe L, Suhl JA, Del-Favero J, Mortier G, Zackai E, Swillen A, Devriendt K, Gur RE, McDonald-McGinn DM, Warren ST, Emanuel BS, Vermeesch JR. A catalog of hemizygous variation in 127 22q11 deletion patients. Hum Genome Var. 2016 Jan 14;3:15065. doi: 10.1038/hgv.2015.65. eCollection 2016. PMID: 27274857; PMCID: PMC4892188.
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Molecular typing of fluoroquinolone-resistant and fluoroquinolone-susceptible Escherichia coli isolated from blood of neutropenic cancer patients in a single center.

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases

Tascini C, Menichetti F, Bozza S, Fedele M, Preziosi R, Allegrucci M, Del Favero A, Micozzi A, Martino P, Bistoni F.
PMID: 11856289
Clin Microbiol Infect. 1999 Aug;5(8):457-461. doi: 10.1111/j.1469-0691.1999.tb00175.x.

OBJECTIVE: To investigate the molecular epidemiology of fluoroquinolone-resistant (FQ-R) and fluoroquinolone-susceptible (FQ-S) bacteremic Escherichia coli isolates from neutropenic patients by pulsed-field gel electrophoresis (PFGE) and random amplified polymorphic DNA (RAPD) analysis. METHODS: Nineteen FQ-R and 27 FQ-S isolates of...

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Tascini C, Menichetti F, Bozza S, et al. Molecular typing of fluoroquinolone-resistant and fluoroquinolone-susceptible Escherichia coli isolated from blood of neutropenic cancer patients in a single center. Clin Microbiol Infect. 1999;5(8):457-461doi: 10.1111/j.1469-0691.1999.tb00175.x.
Tascini, C., Menichetti, F., Bozza, S., Fedele, M., Preziosi, R., Allegrucci, M., Del Favero, A., Micozzi, A., Martino, P., & Bistoni, F. (1999). Molecular typing of fluoroquinolone-resistant and fluoroquinolone-susceptible Escherichia coli isolated from blood of neutropenic cancer patients in a single center. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, 5(8), 457-461. https://doi.org/10.1111/j.1469-0691.1999.tb00175.x
Tascini, Carlo, et al. "Molecular typing of fluoroquinolone-resistant and fluoroquinolone-susceptible Escherichia coli isolated from blood of neutropenic cancer patients in a single center." Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases vol. 5,8 (1999): 457-461. doi: https://doi.org/10.1111/j.1469-0691.1999.tb00175.x
Tascini C, Menichetti F, Bozza S, Fedele M, Preziosi R, Allegrucci M, Del Favero A, Micozzi A, Martino P, Bistoni F. Molecular typing of fluoroquinolone-resistant and fluoroquinolone-susceptible Escherichia coli isolated from blood of neutropenic cancer patients in a single center. Clin Microbiol Infect. 1999 Aug;5(8):457-461. doi: 10.1111/j.1469-0691.1999.tb00175.x. PMID: 11856289.
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Construction and characterisation of a yeast artificial chromosome library containing five haploid sugarbeet (Beta vulgaris L.) genome equivalents.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik

Del-Favero J, Vauterin M, Weyens G, Edwards KE, Jacobs M.
PMID: 24186033
Theor Appl Genet. 1994 Jun;88(3):449-53. doi: 10.1007/BF00223659.

A yeast artificial chromosome (YAC) genomic library of Beta vulgaris was constructed in the pYAC4 vector. High-molecular-weight DNA was prepared from agarose-embedded leaf protoplasts from a triploid cultivar. The library was found to contain 33,500 clones in an ordered...

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Del-Favero J, Vauterin M, Weyens G, et al. Construction and characterisation of a yeast artificial chromosome library containing five haploid sugarbeet (Beta vulgaris L.) genome equivalents. Theor Appl Genet. 1994;88(3):449-53doi: 10.1007/BF00223659.
Del-Favero, J., Vauterin, M., Weyens, G., Edwards, K. E., & Jacobs, M. (1994). Construction and characterisation of a yeast artificial chromosome library containing five haploid sugarbeet (Beta vulgaris L.) genome equivalents. TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 88(3), 449-53. https://doi.org/10.1007/BF00223659
Del-Favero, J, et al. "Construction and characterisation of a yeast artificial chromosome library containing five haploid sugarbeet (Beta vulgaris L.) genome equivalents." TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik vol. 88,3 (1994): 449-53. doi: https://doi.org/10.1007/BF00223659
Del-Favero J, Vauterin M, Weyens G, Edwards KE, Jacobs M. Construction and characterisation of a yeast artificial chromosome library containing five haploid sugarbeet (Beta vulgaris L.) genome equivalents. Theor Appl Genet. 1994 Jun;88(3):449-53. doi: 10.1007/BF00223659. PMID: 24186033.
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Highly asymmetric intergeneric nuclear hybrids between Nicotiana and Petunia: evidence for recombinogenic and translocation events in somatic hybrid plants after "gamma"-fusion.

TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik

Hinnisdaels S, Bariller L, Mouras A, Sidorov V, Del-Favero J, Veuskens J, Negrutiu I, Jacobs M.
PMID: 24213341
Theor Appl Genet. 1991 Oct;82(5):609-14. doi: 10.1007/BF00226798.

Extremely asymmetric nuclear hybrids have been obtained via protoplast fusion in an intergeneric combination. Irradiated (cobalt(60),100 krad) kanamycinresistant Petunia hybrida mesophyll protoplasts were chemically fused with wild-type mesophyll protoplasts of Nicotiana plumbaginifolia. Eighty-six hybrid colonies were selected on kanamycin-containing...

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Hinnisdaels S, Bariller L, Mouras A, et al. Highly asymmetric intergeneric nuclear hybrids between Nicotiana and Petunia: evidence for recombinogenic and translocation events in somatic hybrid plants after "gamma"-fusion. Theor Appl Genet. 1991;82(5):609-14doi: 10.1007/BF00226798.
Hinnisdaels, S., Bariller, L., Mouras, A., Sidorov, V., Del-Favero, J., Veuskens, J., Negrutiu, I., & Jacobs, M. (1991). Highly asymmetric intergeneric nuclear hybrids between Nicotiana and Petunia: evidence for recombinogenic and translocation events in somatic hybrid plants after "gamma"-fusion. TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik, 82(5), 609-14. https://doi.org/10.1007/BF00226798
Hinnisdaels, S, et al. "Highly asymmetric intergeneric nuclear hybrids between Nicotiana and Petunia: evidence for recombinogenic and translocation events in somatic hybrid plants after "gamma"-fusion." TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik vol. 82,5 (1991): 609-14. doi: https://doi.org/10.1007/BF00226798
Hinnisdaels S, Bariller L, Mouras A, Sidorov V, Del-Favero J, Veuskens J, Negrutiu I, Jacobs M. Highly asymmetric intergeneric nuclear hybrids between Nicotiana and Petunia: evidence for recombinogenic and translocation events in somatic hybrid plants after "gamma"-fusion. Theor Appl Genet. 1991 Oct;82(5):609-14. doi: 10.1007/BF00226798. PMID: 24213341.
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Clinical presentation and management of primary ovarian neuroendocrine tumor in multiple endocrine neoplasia type 1.

Endocrinology, diabetes & metabolism case reports

Jhawar S, Lakhotia R, Suzuki M, Welch J, Agarwal SK, Sharretts J, Merino M, Ahlman M, Blau JE, Simonds WF, Del Rivero J.
PMID: 31480016
Endocrinol Diabetes Metab Case Rep. 2019 Aug 20;2019. doi: 10.1530/EDM-19-0040. Epub 2019 Aug 20.

SUMMARY: Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant condition characterized by parathyroid, anterior pituitary and enteropancreatic endocrine cell tumors. Neuroendocrine tumors occur in approximately in 5-15% of MEN1 patients. Very few cases of ovarian NETs have...

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Jhawar S, Lakhotia R, Suzuki M, et al. Clinical presentation and management of primary ovarian neuroendocrine tumor in multiple endocrine neoplasia type 1. Endocrinol Diabetes Metab Case Rep. 2019;2019doi: 10.1530/EDM-19-0040.
Jhawar, S., Lakhotia, R., Suzuki, M., Welch, J., Agarwal, S. K., Sharretts, J., Merino, M., Ahlman, M., Blau, J. E., Simonds, W. F., & Del Rivero, J. (2019). Clinical presentation and management of primary ovarian neuroendocrine tumor in multiple endocrine neoplasia type 1. Endocrinology, diabetes & metabolism case reports, 2019. https://doi.org/10.1530/EDM-19-0040
Jhawar, Sakshi, et al. "Clinical presentation and management of primary ovarian neuroendocrine tumor in multiple endocrine neoplasia type 1." Endocrinology, diabetes & metabolism case reports vol. 2019 (2019). doi: https://doi.org/10.1530/EDM-19-0040
Jhawar S, Lakhotia R, Suzuki M, Welch J, Agarwal SK, Sharretts J, Merino M, Ahlman M, Blau JE, Simonds WF, Del Rivero J. Clinical presentation and management of primary ovarian neuroendocrine tumor in multiple endocrine neoplasia type 1. Endocrinol Diabetes Metab Case Rep. 2019 Aug 20;2019. doi: 10.1530/EDM-19-0040. Epub 2019 Aug 20. PMID: 31480016; PMCID: PMC6709536.
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Elucidation of xenoestrogen metabolism by non-targeted, stable isotope-assisted mass spectrometry in breast cancer cells.

Environment international

Flasch M, Bueschl C, Del Favero G, Adam G, Schuhmacher R, Marko D, Warth B.
PMID: 34673318
Environ Int. 2022 Jan;158:106940. doi: 10.1016/j.envint.2021.106940. Epub 2021 Oct 18.

Environmental exposure to xenoestrogens, i.e., chemicals that imitate the hormone 17β-estradiol, has the potential to influence hormone homeostasis and action. Detailed knowledge of xenobiotic biotransformation processes in cell models is key when transferring knowledge learned from in vitro models...

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Flasch M, Bueschl C, Del Favero G, et al. Elucidation of xenoestrogen metabolism by non-targeted, stable isotope-assisted mass spectrometry in breast cancer cells. Environ Int. 2021;158:106940doi: 10.1016/j.envint.2021.106940.
Flasch, M., Bueschl, C., Del Favero, G., Adam, G., Schuhmacher, R., Marko, D., & Warth, B. (2022). Elucidation of xenoestrogen metabolism by non-targeted, stable isotope-assisted mass spectrometry in breast cancer cells. Environment international, 158106940. https://doi.org/10.1016/j.envint.2021.106940
Flasch, Mira, et al. "Elucidation of xenoestrogen metabolism by non-targeted, stable isotope-assisted mass spectrometry in breast cancer cells." Environment international vol. 158 (2022): 106940. doi: https://doi.org/10.1016/j.envint.2021.106940
Flasch M, Bueschl C, Del Favero G, Adam G, Schuhmacher R, Marko D, Warth B. Elucidation of xenoestrogen metabolism by non-targeted, stable isotope-assisted mass spectrometry in breast cancer cells. Environ Int. 2022 Jan;158:106940. doi: 10.1016/j.envint.2021.106940. Epub 2021 Oct 18. PMID: 34673318.
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The aging venous system: from varicosities to vascular cognitive impairment.

GeroScience

Molnár AÁ, Nádasy GL, Dörnyei G, Patai BB, Delfavero J, Fülöp GÁ, Kirkpatrick AC, Ungvári Z, Merkely B.
PMID: 34762274
Geroscience. 2021 Dec;43(6):2761-2784. doi: 10.1007/s11357-021-00475-2. Epub 2021 Nov 11.

Aging-induced pathological alterations of the circulatory system play a critical role in morbidity and mortality of older adults. While the importance of cellular and molecular mechanisms of arterial aging for increased cardiovascular risk in older adults is increasingly appreciated,...

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Molnár AÁ, Nádasy GL, Dörnyei G, et al. The aging venous system: from varicosities to vascular cognitive impairment. Geroscience. 2021;43(6):2761-2784doi: 10.1007/s11357-021-00475-2.
Molnár, A. �. �., Nádasy, G. L., Dörnyei, G., Patai, B. B., Delfavero, J., Fülöp, G. �. �., Kirkpatrick, A. C., Ungvári, Z., & Merkely, B. (2021). The aging venous system: from varicosities to vascular cognitive impairment. GeroScience, 43(6), 2761-2784. https://doi.org/10.1007/s11357-021-00475-2
Molnár, Andrea Ágnes, et al. "The aging venous system: from varicosities to vascular cognitive impairment." GeroScience vol. 43,6 (2021): 2761-2784. doi: https://doi.org/10.1007/s11357-021-00475-2
Molnár AÁ, Nádasy GL, Dörnyei G, Patai BB, Delfavero J, Fülöp GÁ, Kirkpatrick AC, Ungvári Z, Merkely B. The aging venous system: from varicosities to vascular cognitive impairment. Geroscience. 2021 Dec;43(6):2761-2784. doi: 10.1007/s11357-021-00475-2. Epub 2021 Nov 11. PMID: 34762274; PMCID: PMC8602591.
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Laparoscopic assisted mini-ECIRS for ectopic kidney lithiasis: A case report and literature review.

CEN case reports

Amato M, Piazza P, Deruyver Y, Del Favero L, Van den Broeck T, Sarchi L, Scarcella S, Bravi CA, Puliatti S, Micali S, Van Haute C, Van Cleynenbreugel B.
PMID: 34982417
CEN Case Rep. 2022 Jan 04; doi: 10.1007/s13730-021-00683-x. Epub 2022 Jan 04.

INTRODUCTION: Ectopic kidney is a rare anatomic variant with an incidence of about 1 in 900. Renal stones can pose a challenge when a standard approach is not possible. Laparoscopic-assisted endourologic procedure can be a feasible and safe choice.CASE...

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Amato M, Piazza P, Deruyver Y, et al. Laparoscopic assisted mini-ECIRS for ectopic kidney lithiasis: A case report and literature review. CEN Case Rep. 2022;doi: 10.1007/s13730-021-00683-x.
Amato, M., Piazza, P., Deruyver, Y., Del Favero, L., Van den Broeck, T., Sarchi, L., Scarcella, S., Bravi, C. A., Puliatti, S., Micali, S., Van Haute, C., & Van Cleynenbreugel, B. (2022). Laparoscopic assisted mini-ECIRS for ectopic kidney lithiasis: A case report and literature review. CEN case reports, . https://doi.org/10.1007/s13730-021-00683-x
Amato, Marco, et al. "Laparoscopic assisted mini-ECIRS for ectopic kidney lithiasis: A case report and literature review." CEN case reports vol. (2022). doi: https://doi.org/10.1007/s13730-021-00683-x
Amato M, Piazza P, Deruyver Y, Del Favero L, Van den Broeck T, Sarchi L, Scarcella S, Bravi CA, Puliatti S, Micali S, Van Haute C, Van Cleynenbreugel B. Laparoscopic assisted mini-ECIRS for ectopic kidney lithiasis: A case report and literature review. CEN Case Rep. 2022 Jan 04; doi: 10.1007/s13730-021-00683-x. Epub 2022 Jan 04. PMID: 34982417.
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Smart Device for Biologically Enhanced Functional Regeneration of Osteo-Tendon Interface.

Pharmaceutics

Faccendini A, Bianchi E, Ruggeri M, Vigani B, Perotti C, Pavesi FC, Caliogna L, Natali F, Del Favero E, Cantu' L, Ferrari F, Rossi S, Sandri G.
PMID: 34959280
Pharmaceutics. 2021 Nov 24;13(12). doi: 10.3390/pharmaceutics13121996.

The spontaneous healing of a tendon laceration results in the formation of scar tissue, which has lower functionality than the original tissue. Moreover, chronic non-healing tendon injuries frequently require surgical treatment. Several types of scaffolds have been developed using...

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Faccendini A, Bianchi E, Ruggeri M, et al. Smart Device for Biologically Enhanced Functional Regeneration of Osteo-Tendon Interface. Pharmaceutics. 2021;13(12)doi: 10.3390/pharmaceutics13121996.
Faccendini, A., Bianchi, E., Ruggeri, M., Vigani, B., Perotti, C., Pavesi, F. C., Caliogna, L., Natali, F., Del Favero, E., Cantu', L., Ferrari, F., Rossi, S., & Sandri, G. (2021). Smart Device for Biologically Enhanced Functional Regeneration of Osteo-Tendon Interface. Pharmaceutics, 13(12), . https://doi.org/10.3390/pharmaceutics13121996
Faccendini, Angela, et al. "Smart Device for Biologically Enhanced Functional Regeneration of Osteo-Tendon Interface." Pharmaceutics vol. 13,12 (2021). doi: https://doi.org/10.3390/pharmaceutics13121996
Faccendini A, Bianchi E, Ruggeri M, Vigani B, Perotti C, Pavesi FC, Caliogna L, Natali F, Del Favero E, Cantu' L, Ferrari F, Rossi S, Sandri G. Smart Device for Biologically Enhanced Functional Regeneration of Osteo-Tendon Interface. Pharmaceutics. 2021 Nov 24;13(12). doi: 10.3390/pharmaceutics13121996. PMID: 34959280; PMCID: PMC8707843.
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Decoration of Nanovesicles with pH (Low) Insertion Peptide (pHLIP) for Targeted Delivery.

Nanoscale research letters

Rinaldi F, Hanieh PN, Del Favero E, Rondelli V, Brocca P, Pereira MC, Andreev OA, Reshetnyak YK, Marianecci C, Carafa M.
PMID: 30515583
Nanoscale Res Lett. 2018 Dec 04;13(1):391. doi: 10.1186/s11671-018-2807-8.

Acidity at surface of cancer cells is a hallmark of tumor microenvironments, which does not depend on tumor perfusion, thus it may serve as a general biomarker for targeting tumor cells. We used the pH (low) insertion peptide (pHLIP)...

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Rinaldi F, Hanieh PN, Del Favero E, et al. Decoration of Nanovesicles with pH (Low) Insertion Peptide (pHLIP) for Targeted Delivery. Nanoscale Res Lett. 2018;13(1):391doi: 10.1186/s11671-018-2807-8.
Rinaldi, F., Hanieh, P. N., Del Favero, E., Rondelli, V., Brocca, P., Pereira, M. C., Andreev, O. A., Reshetnyak, Y. K., Marianecci, C., & Carafa, M. (2018). Decoration of Nanovesicles with pH (Low) Insertion Peptide (pHLIP) for Targeted Delivery. Nanoscale research letters, 13(1), 391. https://doi.org/10.1186/s11671-018-2807-8
Rinaldi, Federica, et al. "Decoration of Nanovesicles with pH (Low) Insertion Peptide (pHLIP) for Targeted Delivery." Nanoscale research letters vol. 13,1 (2018): 391. doi: https://doi.org/10.1186/s11671-018-2807-8
Rinaldi F, Hanieh PN, Del Favero E, Rondelli V, Brocca P, Pereira MC, Andreev OA, Reshetnyak YK, Marianecci C, Carafa M. Decoration of Nanovesicles with pH (Low) Insertion Peptide (pHLIP) for Targeted Delivery. Nanoscale Res Lett. 2018 Dec 04;13(1):391. doi: 10.1186/s11671-018-2807-8. PMID: 30515583; PMCID: PMC6279677.
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Tumor Doubling Time Using CT Volumetric Segmentation in Metastatic Adrenocortical Carcinoma.

Current oncology (Toronto, Ont.)

Fuller SN, Shafiei A, Venzon DJ, Liewehr DJ, Mauda Havanuk M, Ilanchezhian MG, Edgerly M, Anderson VL, Levy EB, Hoang CD, Jones EC, Reilly KM, Widemann BC, Wood BJ, Bagheri H, Del Rivero J.
PMID: 34898541
Curr Oncol. 2021 Nov 01;28(6):4357-4366. doi: 10.3390/curroncol28060370.

Adrenocortical carcinoma (ACC) is a rare malignancy with an overall unfavorable prognosis. Clinicians treating patients with ACC have noted accelerated growth in metastatic liver lesions that requires rapid intervention compared to other metastatic locations. This study measured and compared...

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Fuller SN, Shafiei A, Venzon DJ, et al. Tumor Doubling Time Using CT Volumetric Segmentation in Metastatic Adrenocortical Carcinoma. Curr Oncol. 2021;28(6):4357-4366doi: 10.3390/curroncol28060370.
Fuller, S. N., Shafiei, A., Venzon, D. J., Liewehr, D. J., Mauda Havanuk, M., Ilanchezhian, M. G., Edgerly, M., Anderson, V. L., Levy, E. B., Hoang, C. D., Jones, E. C., Reilly, K. M., Widemann, B. C., Wood, B. J., Bagheri, H., & Del Rivero, J. (2021). Tumor Doubling Time Using CT Volumetric Segmentation in Metastatic Adrenocortical Carcinoma. Current oncology (Toronto, Ont.), 28(6), 4357-4366. https://doi.org/10.3390/curroncol28060370
Fuller, Sarah N, et al. "Tumor Doubling Time Using CT Volumetric Segmentation in Metastatic Adrenocortical Carcinoma." Current oncology (Toronto, Ont.) vol. 28,6 (2021): 4357-4366. doi: https://doi.org/10.3390/curroncol28060370
Fuller SN, Shafiei A, Venzon DJ, Liewehr DJ, Mauda Havanuk M, Ilanchezhian MG, Edgerly M, Anderson VL, Levy EB, Hoang CD, Jones EC, Reilly KM, Widemann BC, Wood BJ, Bagheri H, Del Rivero J. Tumor Doubling Time Using CT Volumetric Segmentation in Metastatic Adrenocortical Carcinoma. Curr Oncol. 2021 Nov 01;28(6):4357-4366. doi: 10.3390/curroncol28060370. PMID: 34898541; PMCID: PMC8628706.
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Choosing the duration of continuous glucose monitoring for reliable assessment of time in range: A new analytical approach to overcome the limitations of correlation-based methods.

Diabetic medicine : a journal of the British Diabetic Association

Camerlingo N, Vettoretti M, Sparacino G, Facchinetti A, Mader JK, Choudhary P, Del Favero S.
PMID: 34862829
Diabet Med. 2021 Dec 04;e14758. doi: 10.1111/dme.14758. Epub 2021 Dec 04.

AIMS: Reliable estimation of the time spent in different glycaemic ranges (time-in-ranges) requires sufficiently long continuous glucose monitoring. In a 2019 paper (Battelino et al., Clinical targets for continuous glucose monitoring data interpretation: recommendations from the international consensus on...

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Camerlingo N, Vettoretti M, Sparacino G, et al. Choosing the duration of continuous glucose monitoring for reliable assessment of time in range: A new analytical approach to overcome the limitations of correlation-based methods. Diabet Med. 2021;e14758doi: 10.1111/dme.14758.
Camerlingo, N., Vettoretti, M., Sparacino, G., Facchinetti, A., Mader, J. K., Choudhary, P., Del Favero, S. (2021). Choosing the duration of continuous glucose monitoring for reliable assessment of time in range: A new analytical approach to overcome the limitations of correlation-based methods. Diabetic medicine : a journal of the British Diabetic Association, e14758. https://doi.org/10.1111/dme.14758
Camerlingo, Nunzio, et al. "Choosing the duration of continuous glucose monitoring for reliable assessment of time in range: A new analytical approach to overcome the limitations of correlation-based methods." Diabetic medicine : a journal of the British Diabetic Association vol. (2021): e14758. doi: https://doi.org/10.1111/dme.14758
Camerlingo N, Vettoretti M, Sparacino G, Facchinetti A, Mader JK, Choudhary P, Del Favero S. Choosing the duration of continuous glucose monitoring for reliable assessment of time in range: A new analytical approach to overcome the limitations of correlation-based methods. Diabet Med. 2021 Dec 04;e14758. doi: 10.1111/dme.14758. Epub 2021 Dec 04. PMID: 34862829.
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