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Anna Cecchele

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Citations 27
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Recent Articles
1.
Filippi F, Reschini M, Polledri E, Cecchele A, Guarneri C, Vigano P, et al.
PLoS One . 2023 Mar; 18(3):e0280238. PMID: 36976781
Background: In women scheduled for cancer treatment, oocytes cryopreservation is a well-established procedure. Random start protocols have been a substantial improvement in this setting, allowing to prevent delay in the...
2.
Balli M, Cecchele A, Pisaturo V, Makieva S, Carullo G, Somigliana E, et al.
J Clin Med . 2022 Oct; 11(19). PMID: 36233589
Conventional IVF (c-IVF) is one of the most practiced assisted reproductive technology (ART) approaches used worldwide. However, in the last years, the number of c-IVF procedures has dropped dramatically in...
3.
Cermisoni G, Reschini M, Piccinni M, Lombardelli L, Logiodice F, Sarais V, et al.
Hum Reprod Open . 2022 Apr; 2022(2):hoac017. PMID: 35475146
Study Question: Is oral Vitamin D supplementation able to modify the intrauterine milieu in terms of cytokine/chemokine pattern? Summary Answer: No significant differences were detected in cytokine and chemokine levels...
4.
Alteri A, Bosco L, Chamayou S, Casciani V, Cervi M, Cecchele A, et al.
Hum Fertil (Camb) . 2022 Mar; 26(5):1380-1384. PMID: 35255778
Clinical embryologists are highly trained laboratory professionals with multiple roles, including laboratory, clinical, biobanking and quality system management. In most European countries, clinical embryologists are trained to work in Medically...
5.
Cecchele A, Cermisoni G, Giacomini E, Pinna M, Vigano P
Int J Mol Sci . 2022 Feb; 23(3). PMID: 35163271
Embryo fragmentation represents a phenomenon generally characterized by the presence of membrane-bound extracellular cytoplasm into the perivitelline space. Recent evidence supports the cellular and molecular heterogeneity of embryo fragments. In...
6.
Mangiameli E, Cecchele A, Morena F, Sanvito F, Matafora V, Cattaneo A, et al.
Stem Cell Reports . 2021 May; 16(6):1478-1495. PMID: 33989519
Globoid cell leukodystrophy (GLD) is a rare neurodegenerative lysosomal storage disease caused by an inherited deficiency of β-galactocerebrosidase (GALC). GLD pathogenesis and therapeutic correction have been poorly studied in patient...