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Massimo Carella

Showing results (191-200 of 207) with videos related to

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Cellular Oncology (Dordrecht, Netherlands)|September 19, 2012
CDC73 mutations and parafibromin immunohistochemistry in parathyroid tumors: clinical correlations in a single-centre patient cohortVito Guarnieri, Claudia Battista, Lucia Anna Muscarella, et al.
Journal of Human Genetics|April 30, 2025
Variant sub-tiering, disease-gene associations and strictness of clinical criteria improves the interpretation of variants of uncertain significance in hereditary cardiomyopathies and rhythm disordersMarco Castori, Sandra Mastroianno, Andrea Fontana, et al.
Diagnostics (Basel, Switzerland)|March 6, 2021
Diagnosis of COVID-19 in Patients with Negative Nasopharyngeal Swabs: Reliability of Radiological and Clinical Diagnosis and Accuracy Versus SerologyAntonio Mirijello, Michele Zarrelli, Giuseppe Miscio, et al.
Haematologica|April 16, 2017
Epigenetically induced ectopic expression of UNCX impairs the proliferation and differentiation of myeloid cellsGiulia Daniele, Giorgia Simonetti, Caterina Fusilli, et al.
Communications Medicine|April 4, 2024
Human leukocyte antigen variants associate with BNT162b2 mRNA vaccine responseMartina Esposito, Francesca Minnai, Massimiliano Copetti, et al.
Clinical Epigenetics|June 1, 2022
Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbancesLaura Pignata, Francesco Cecere, Ankit Verma, et al.
European Journal of Human Genetics : EJHG|October 30, 2014
Testis development in the absence of SRY: chromosomal rearrangements at SOX9 and SOX3Annalisa Vetro, Mohammad Reza Dehghani, Lilia Kraoua, et al.
The Journal of Clinical Endocrinology and Metabolism|October 31, 2021
Gain of Function of Malate Dehydrogenase 2 and Familial HyperglycemiaPrapaporn Jungtrakoon Thamtarana, Antonella Marucci, Luca Pannone, et al.
Breast Cancer Research : BCR|September 30, 2025
Development of a microRNA-based prognostic model for accurate prediction of distant metastasis in breast cancer patientsAndrea Fontana, Raffaela Barbano, Barbara Pasculli, et al.
Clinical Genetics|May 14, 2021
Copy number variation analysis implicates novel pathways in patients with oculo-auriculo-vertebral-spectrum and congenital heart defectsValentina Guida, Francesca Piceci Sparascio, Laura Bernardini, et al.
Pageof 21

Showing results (191-200 of 207) with videos related to

Sort By:
Pageof 21
Cellular Oncology (Dordrecht, Netherlands)|September 19, 2012
CDC73 mutations and parafibromin immunohistochemistry in parathyroid tumors: clinical correlations in a single-centre patient cohortVito Guarnieri, Claudia Battista, Lucia Anna Muscarella, et al.
Journal of Human Genetics|April 30, 2025
Variant sub-tiering, disease-gene associations and strictness of clinical criteria improves the interpretation of variants of uncertain significance in hereditary cardiomyopathies and rhythm disordersMarco Castori, Sandra Mastroianno, Andrea Fontana, et al.
Diagnostics (Basel, Switzerland)|March 6, 2021
Diagnosis of COVID-19 in Patients with Negative Nasopharyngeal Swabs: Reliability of Radiological and Clinical Diagnosis and Accuracy Versus SerologyAntonio Mirijello, Michele Zarrelli, Giuseppe Miscio, et al.
Haematologica|April 16, 2017
Epigenetically induced ectopic expression of UNCX impairs the proliferation and differentiation of myeloid cellsGiulia Daniele, Giorgia Simonetti, Caterina Fusilli, et al.
Communications Medicine|April 4, 2024
Human leukocyte antigen variants associate with BNT162b2 mRNA vaccine responseMartina Esposito, Francesca Minnai, Massimiliano Copetti, et al.
Clinical Epigenetics|June 1, 2022
Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbancesLaura Pignata, Francesco Cecere, Ankit Verma, et al.
European Journal of Human Genetics : EJHG|October 30, 2014
Testis development in the absence of SRY: chromosomal rearrangements at SOX9 and SOX3Annalisa Vetro, Mohammad Reza Dehghani, Lilia Kraoua, et al.
The Journal of Clinical Endocrinology and Metabolism|October 31, 2021
Gain of Function of Malate Dehydrogenase 2 and Familial HyperglycemiaPrapaporn Jungtrakoon Thamtarana, Antonella Marucci, Luca Pannone, et al.
Breast Cancer Research : BCR|September 30, 2025
Development of a microRNA-based prognostic model for accurate prediction of distant metastasis in breast cancer patientsAndrea Fontana, Raffaela Barbano, Barbara Pasculli, et al.
Clinical Genetics|May 14, 2021
Copy number variation analysis implicates novel pathways in patients with oculo-auriculo-vertebral-spectrum and congenital heart defectsValentina Guida, Francesca Piceci Sparascio, Laura Bernardini, et al.
Pageof 21