MUNIR, ZUNAIRA
MUNIR, ZUNAIRA
ONCOLOGIA
Alteration of iron concentration in alzheimer’s disease as a possible diagnostic biomarker unveiling ferroptosis
2021-01-01 Ficiarà E.; Munir Z.; Boschi S.; Caligiuri M.E.; Guiot C.
Evaluation of Chitosan/Curcumin loaded Nanobubbles with and without Photoactivated light for Food Preservation
2021-01-01 Zunaira Munir, Lorenza Cavallo, Francesca Menotti, Vivian Tullio, Sara Comini, Roberta Cavalli, Caterina Guiot, Anna Maria Cuffini, Giuliana Banche, Narcisa Mandras,
Exploitation of the Antibacterial Properties of Photoactivated Curcumin as ‘Green’ Tool for Food Preservation [*N. Mandras and E. Ficiarà are the corresponding authors]
2022-01-01 Munir Z.; Banche G.; Cavallo L.; Mandras N.; Roana J.; Pertusio R.; Ficiara E.; Cavalli R.; Guiot C.
New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder
2021-01-01 Faridi R.; Rea A.; Fenollar-Ferrer C.; O'Keefe R.T.; Gu S.; Munir Z.; Khan A.A.; Riazuddin S.; Hoa M.; Naz S.; Newman W.G.; Friedman T.B.
Variants of human CLDN9 cause mild to profound hearing loss
2021-01-01 Ramzan M.; Philippe C.; Belyantseva I.A.; Nakano Y.; Fenollar-Ferrer C.; Tona R.; Yousaf R.; Basheer R.; Imtiaz A.; Faridi R.; Munir Z.; Idrees H.; Salman M.; Nambot S.; Vitobello A.; Kartti S.; Zarrik O.; Witmer P.D.; Sobreria N.; Ibrahimi A.; Banfi B.; Moutton S.; Friedman T.B.; Naz S.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Alteration of iron concentration in alzheimer’s disease as a possible diagnostic biomarker unveiling ferroptosis | 2021 | Ficiarà E.; Munir Z.; Boschi S.; Caligiuri M.E.; Guiot C. | |
| Evaluation of Chitosan/Curcumin loaded Nanobubbles with and without Photoactivated light for Food Preservation | 2021 | Zunaira Munir, Lorenza Cavallo, Francesca Menotti, Vivian Tullio, Sara Comini, Roberta Cavalli, Caterina Guiot, Anna Maria Cuffini, Giuliana Banche, Narcisa Mandras, | |
| Exploitation of the Antibacterial Properties of Photoactivated Curcumin as ‘Green’ Tool for Food Preservation [*N. Mandras and E. Ficiarà are the corresponding authors] | 2022 | Munir Z.; Banche G.; Cavallo L.; Mandras N.; Roana J.; Pertusio R.; Ficiara E.; Cavalli R.; Guiot C. | |
| New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder | 2021 | Faridi R.; Rea A.; Fenollar-Ferrer C.; O'Keefe R.T.; Gu S.; Munir Z.; Khan A.A.; Riazuddin S.; Hoa M.; Naz S.; Newman W.G.; Friedman T.B. | |
| Variants of human CLDN9 cause mild to profound hearing loss | 2021 | Ramzan M.; Philippe C.; Belyantseva I.A.; Nakano Y.; Fenollar-Ferrer C.; Tona R.; Yousaf R.; Basheer R.; Imtiaz A.; Faridi R.; Munir Z.; Idrees H.; Salman M.; Nambot S.; Vitobello A.; Kartti S.; Zarrik O.; Witmer P.D.; Sobreria N.; Ibrahimi A.; Banfi B.; Moutton S.; Friedman T.B.; Naz S. |