Research Output

XK-aprosencephaly and related entities

Renzetti, G., Villani, A., Bizzarri, C., Chessa, L., Vignati, E., Gianotti, A., Cappa, M., Szakacs, J., Townsend, J. J., Miller, M. E., Opitz, J. M., Kennedy, A. M. & Byrne, J. L., Nov 1 2005, In : American Journal of Medical Genetics. 138 A, 4, p. 401-410 10 p.

Research output: Contribution to journalArticle

X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism: Report on new mutation of the DAX-1 gene in two siblings

Calvari, V., Alpigiani, M. G., Poggi, E., Podesta, B., Camerino, G. & Lorini, R., Jan 2006, In : Journal of Endocrinological Investigation. 29, 1, p. 41-47 7 p.

Research output: Contribution to journalArticle

X-linked adrenoleukodystrophy: First report of the Italian Study Group

Di Biase, A., Salvati, S., Avellino, C., Cappa, M., Bertini, E., Moroni, I., Rimoldi, M. & Uziel, G., 1998, In : Neurological Sciences. 19, 5, p. 315-319 5 p.

Research output: Contribution to journalArticle

X-linked adrenoleukodystrophy: Prenatal diagnosis by DHPLC analysis

Montagna, G., Cappa, M., Cannelli, N., Fattori, F. & Santorelli, F. M., Dec 2005, In : Italian Journal of Pediatrics. 31, 6, p. 399-401 3 p.

Research output: Contribution to journalArticle

X-Linked adrenoleukodystrophy (X-ALD)

Severino, M., Jan 1 2010, Brain Imaging with MRI and CT: An Image Pattern Approach. Cambridge University Press, p. 61-62 2 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty

Buzi, F., Notarangelo, L. D., Plebani, A., Duse, M., Parolini, O., Monteleone, M. & Ugazio, A. G., 1994, In : Acta Paediatrica, International Journal of Paediatrics. 83, 1, p. 99-102 4 p.

Research output: Contribution to journalArticle

X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world

El-Sayed, Z. A., Abramova, I., Aldave, J. C., Al-Herz, W., Bezrodnik, L., Boukari, R., Bousfiha, A. A., Cancrini, C., Condino-Neto, A., Dbaibo, G., Derfalvi, B., Dogu, F., Edgar, J. D. M., Eley, B., El-Owaidy, R. H., Espinosa-Padilla, S. E., Galal, N., Haerynck, F., Hanna-Wakim, R., Hossny, E. & 31 others, Ikinciogullari, A., Kamal, E., Kanegane, H., Kechout, N., Lau, Y. L., Morio, T., Moschese, V., Neves, J. F., Ouederni, M., Paganelli, R., Paris, K., Pignata, C., Plebani, A., Qamar, F. N., Qureshi, S., Radhakrishnan, N., Rezaei, N., Rosario, N., Routes, J., Sanchez, B., Sediva, A., Seppanen, M. R., Serrano, E. G., Shcherbina, A., Singh, S., Siniah, S., Spadaro, G., Tang, M., Vinet, A. M., Volokha, A. & Sullivan, K. E., 2019, In : World Allergy Organization Journal. 12, 3, p. 100018

Research output: Contribution to journalArticle

X-linked agammaglobulinemia and isolated growth hormone deficiency

Monafo, V., Maghnie, M., Terracciano, L., Valtorta, A., Massa, M. & Severi, F., 1991, In : Acta Paediatrica Scandinavica. 80, 5, p. 563-566 4 p.

Research output: Contribution to journalArticle

X-linked Alport syndrome: An SSCP-based mutation survey over all 51 exons of the COL4A5 gene

Renieri, A., Bruttini, M., Galli, L., Zanelli, P., Neri, T., Rossetti, S., Turco, A., Heiskari, N., Zhou, J., Gusmano, R., Massella, L., Banfi, G., Scolari, F., Sessa, A., Rizzoni, G., Tryggvason, K., Pignatti, P. F., Savi, M., Ballabio, A. & De Marchi, M., 1996, In : American Journal of Human Genetics. 58, 6, p. 1192-1204 13 p.

Research output: Contribution to journalArticle

X-linked congenital ataxia: A clinical and genetic study

Bertini, E., Des Portes, V., Zanni, G., Santorelli, F., Dionisi-Vici, C., Vicari, S., Fariello, G. & Chelly, J., May 1 2000, In : American Journal of Medical Genetics. 92, 1, p. 53-56 4 p.

Research output: Contribution to journalArticle

X-linked congenital ataxia: A new locus maps to Xq25-q27.1

Zanni, G., Bertini, E., Bellcross, C., Nedelec, B., Froyen, G., Neuhäuser, G., Opitz, J. M. & Chelly, J., Mar 1 2008, In : American Journal of Medical Genetics, Part A. 146, 5, p. 593-600 8 p.

Research output: Contribution to journalArticle

X-linked creatine transporter deficiency: Clinical description of a patient with a novel SLC6A8 gene mutation

Schiaffino, M. C., Bellini, C., Costabello, L., Caruso, U., Jakobs, C., Salomons, G. S. & Bonioli, E., Sep 2005, In : Neurogenetics. 6, 3, p. 165-168 4 p.

Research output: Contribution to journalArticle

X-linked disorders with cerebellar dysgenesis

Zanni, G. & Bertini, E. S., 2011, In : Orphanet Journal of Rare Diseases. 6, 1, 24.

Research output: Contribution to journalArticle

X-linked hypophosphatemic rickets: An Italian experts' opinion survey

Emma, F., Cappa, M., Antoniazzi, F., Bianchi, M. L., Chiodini, I., Eller Vainicher, C., Di Iorgi, N., Maghnie, M., Cassio, A., Balsamo, A., Baronio, F., De Sanctis, L., Tessaris, D., Baroncelli, G. I., Mora, S., Brandi, M. L., Weber, G., D'Ausilio, A. & Lanati, E. P., May 31 2019, In : Italian Journal of Pediatrics. 45, 1, 67.

Research output: Contribution to journalArticle

Open Access

X-linked hypophosphatemic rickets: an Italian experts' opinion survey

Emma, F., Cappa, M., Antoniazzi, F., Bianchi, M. L., Chiodini, I., Eller Vainicher, C., Di Iorgi, N., Maghnie, M., Cassio, A., Balsamo, A., Baronio, F., de Sanctis, L., Tessaris, D., Baroncelli, G. I., Mora, S., Brandi, M. L., Weber, G., D'Ausilio, A. & Lanati, E. P., May 31 2019, In : Italian Journal of Pediatrics. 45, 1, p. 67

Research output: Contribution to journalArticle

X-linked hypophosphatemic rickets: An Italian experts' opinion survey

Emma, F., Cappa, M., Antoniazzi, F., Bianchi, M. L., Chiodini, I., Eller Vainicher, C., Di Iorgi, N., Maghnie, M., Cassio, A., Balsamo, A., Baronio, F., De Sanctis, L., Tessaris, D., Baroncelli, G. I., Mora, S., Brandi, M. L., Weber, G., D'Ausilio, A. & Lanati, E. P., 2019, In : Italian Journal of Pediatrics. 45, 1

Research output: Contribution to journalArticle

X-linked hypophosphatemic rickets: An Italian experts' opinion survey

Emma, F., Cappa, M., Antoniazzi, F., Bianchi, M. L., Chiodini, I., Eller Vainicher, C., Di Iorgi, N., Maghnie, M., Cassio, A., Balsamo, A., Baronio, F., De Sanctis, L., Tessaris, D., Baroncelli, G. I., Mora, S., Brandi, M. L., Weber, G., D'Ausilio, A. & Lanati, E. P., May 31 2019, In : Ital. J. Pediatr.. 45, 1

Research output: Contribution to journalArticle

X-linked hypophosphatemic rickets: An Italian experts' opinion survey

Emma, F., Cappa, M., Antoniazzi, F., Bianchi, M. L., Chiodini, I., Eller Vainicher, C., Di Iorgi, N., Maghnie, M., Cassio, A., Balsamo, A., Baronio, F., De Sanctis, L., Tessaris, D., Baroncelli, G. I., Mora, S., Brandi, M. L., Weber, G., D'Ausilio, A. & Lanati, E. P., 2019, In : Italian Journal of Pediatrics. 45, 1

Research output: Contribution to journalArticle

X-linked lymphoproliferative disease: The dark side of 2b4 function

Bottino, C., Parolini, S., Biassoni, R., Falco, M., Notarangelo, L. & Moretta, A., 2001, In : Advances in Experimental Medicine and Biology. 495, p. 63-67 5 p.

Research output: Contribution to journalArticle

X-linked lymphoproliferative disease: 2B4 molecules displaying inhibitory rather than activating function are responsible for the inability of natural killer cells to kill Epstein-Barr virus-infected cells

Parolini, S., Bottino, C., Falco, M., Augugliaro, R., Giliani, S., Franceschini, R., Ochs, H. D., Wolf, H., Bonnefoy, J. Y., Biassoni, R., Moretta, L., Notarangelo, L. D. & Moretta, A., Aug 7 2000, In : Journal of Experimental Medicine. 192, 3, p. 337-346 10 p.

Research output: Contribution to journalArticle

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: A multicenter study on the manifestations, management and outcome of the disease

Booth, C., Gilmour, K. C., Veys, P., Gennery, A. R., Slatter, M. A., Chapel, H., Heath, P. T., Steward, C. G., Smith, O., O'Meara, A., Kerrigan, H., Mahlaoui, N., Cavazzana-Calvo, M., Fischer, A., Moshous, D., Blanche, S., Pachlopnick-Schmid, J., Latour, S., De Saint-Basile, G., Albert, M. & 28 others, Notheis, G., Rieber, N., Strahm, B., Ritterbusch, H., Lankester, A., Hartwig, N. G., Meyts, I., Plebani, A., Soresina, A., Finocchi, A., Pignata, C., Cirillo, E., Bonanomi, S., Peters, C., Kalwak, K., Pasic, S., Sedlacek, P., Jazbec, J., Kanegane, H., Nichols, K. E., Hanson, I. C., Kapoor, N., Haddad, E., Cowan, M., Choo, S., Smart, J., Arkwright, P. D. & Gaspar, H. B., Jan 6 2011, In : Blood. 117, 1, p. 53-62 10 p.

Research output: Contribution to journalArticle

X-linked mental retardation, short stature, microcephaly and hypogonadism maps to Xp22.1-p21.3 in a Belgian family

Van Esch, H., Zanni, G., Holvoet, M., Borghgraef, M., Chelly, J., Fryns, J. P. & Devriendt, K., Apr 2005, In : European Journal of Medical Genetics. 48, 2, p. 145-152 8 p.

Research output: Contribution to journalArticle

X-linked myotubular myopathy: A prospective international natural history study

Annoussamy, M., Lilien, C., Gidaro, T., Gargaun, E., Chê, V., Schara, U., Gangfuß, A., D'Amico, A., Dowling, J. J., Darras, B. T., Daron, A., Hernandez, A., de Lattre, C., Arnal, J-M., Mayer, M., Cuisset, J-M., Vuillerot, C., Fontaine, S., Bellance, R., Biancalana, V. & 4 others, Buj-Bello, A., Hogrel, J-Y., Landy, H. & Servais, L., Apr 16 2019, In : Neurology. 92, 16, p. e1852-e1867

Research output: Contribution to journalArticle

X-linked neurodegenerative syndrome with congenital ataxia, late-onset progressive myoclonic encephalopathy and selective macular degeneration, linked to Xp22.33-pter

Des Portes, V., Bachner, L., Brüls, T., Beldjord, C., Billuart, P., Soufir, N., Bienvenu, T., Vinet, M. C., Malaspina, E., Marchiani, V., Bertini, E., Kahn, A., Franzoni, E. & Chelly, J., Jul 12 1996, In : American Journal of Medical Genetics. 64, 1, p. 69-72 4 p.

Research output: Contribution to journalArticle

X-linked reticulate pigmentary disorder with systemic manifestations: A new family and review of the literature

Pezzani, L., Brena, M., Callea, M., Colombi, M. & Tadini, G., Jun 2013, In : American Journal of Medical Genetics, Part A. 161, 6, p. 1414-1420 7 p.

Research output: Contribution to journalArticle

X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene

Villa, A., Notarangelo, L., Macchi, P., Mantuano, E., Cavagni, G., Brugnoni, D., Strina, D., Patrosso, M. C., Ramenghi, U., Sacco, M. G., Ugazio, A. & Vezzoni, P., 1995, In : Nature Genetics. 9, 4, p. 414-417 4 p.

Research output: Contribution to journalArticle

X LONG-ARM DELETION WITH FEATURES OF TURNER'S SYNDROME

Forabosco, A. & Dallapiccola, B., Aug 17 1974, In : Lancet. 304, 7877, p. 403-404 2 p.

Research output: Contribution to journalArticle

XLP1 inhibitory effect by 2B4 does not affect DNAM-1 and NKG2D activating pathways in NK cells

Meazza, R., Tuberosa, C., Cetica, V., Falco, M., Loiacono, F., Parolini, S., Micalizzi, C., Moretta, A., Mingari, M. C., Moretta, L., Bottino, C., Aricò, M. & Pende, D., 2014, In : European Journal of Immunology. 44, 5, p. 1526-1534 9 p.

Research output: Contribution to journalArticle

Xp11.22 Microduplications Including HUWE1: Case Report and Literature Review

Orivoli, S., Pavlidis, E., Cantalupo, G., Pezzella, M., Zara, F., Garavelli, L., Pisani, F. & Piccolo, B., Jan 2016, In : Neuropediatrics. 47, 1, p. 51-6 6 p.

Research output: Contribution to journalArticle

Xp1122 Microduplications Including HUWE1: Case Report and Literature Review

Orivoli, S., Pavlidis, E., Cantalupo, G., Pezzella, M., Zara, F., Garavelli, L., Pisani, F. & Piccolo, B., Nov 20 2015, In : Neuropediatrics. 47, 1, p. 51-56 6 p.

Research output: Contribution to journalArticle

X-ray fluorescence elemental mapping and microscopy to follow hepatic disposition of a Gd-based magnetic resonance imaging contrast agent

Delfino, R., Altissimo, M., Menk, R. H., Alberti, R., Klatka, T., Frizzi, T., Longoni, A., Salomè, M., Tromba, G., Arfelli, F., Clai, M., Vaccari, L., Lorusso, V., Tiribelli, C. & Pascolo, L., Dec 2011, In : Clinical and Experimental Pharmacology and Physiology. 38, 12, p. 834-845 12 p.

Research output: Contribution to journalArticle

XRF analyses reveal that capacitation procedures produce changes in magnesium and copper levels in human sperm

Pascolo, L., Zupin, L., Gianoncelli, A., Giolo, E., Luppi, S., Martinelli, M., De Rocco, D., Sala, S., Crovella, S. & Ricci, G., Nov 15 2019, In : Nuclear Instruments and Methods in Physics Research, Section B: Beam Interactions with Materials and Atoms. 459, p. 120-124 5 p.

Research output: Contribution to journalArticle

XRF mapping and TEM analysis of coated and uncoated silica nanoparticles in A549 cells and human monocytes

Rio-Echevarria, I. M., Ponti, J., Bogni, A., Gilliland, D., Altissimo, M., Pascolo, L., Ceccone, G. & Gianoncelli, A., Jan 1 2019, (Accepted/In press) In : X-Ray Spectrometry.

Research output: Contribution to journalArticle

XTENS - A JSON-based digital repository for biomedical data management

Izzo, M., Arnulfo, G., Piastra, M. C., Tedone, V., Varesio, L. & Fato, M. M., 2015, Bioinformatics and Biomedical Engineering - 3rd International Conference, IWBBIO 2015, Proceedings. Springer Verlag, Vol. 9044. p. 123-130 8 p. (Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics); vol. 9044).

Research output: Chapter in Book/Report/Conference proceedingConference contribution

XY female with a dysgerminoma and no mutation in the coding sequence of the SRY gene

Morerio, C., Calvari, V., Rosanda, C., Porta, S., Gambini, C. & Panarello, C., Jul 1 2002, In : Cancer Genetics and Cytogenetics. 136, 1, p. 58-61 4 p.

Research output: Contribution to journalArticle

Y3+ embedded in polymeric nanoparticles: Morphology, dimension and stability of composite colloidal system

Venditti, I., Cartoni, A., Fontana, L., Testa, G., Scaramuzzo, F. A., Faccini, R., Terracciano, C. M., Camillocci, E. S., Morganti, S., Giordano, A., Scotognella, T., Rotili, D., Dini, V., Marini, F. & Fratoddi, I., Nov 5 2017, In : Colloids and Surfaces A: Physicochemical and Engineering Aspects. 532, p. 125-131 7 p.

Research output: Contribution to journalArticle

Yalutazione funzionale al treadmill in bambini ed adolescenti dopo correzione di tetralogia di fallot

Translated title of the contribution: Functional evaluation on treadmill in children and adolescents after total correction of Tetralogy of FalletPastore, E., Turchetta, A., Giordano, U., Giannico, S., Marcelletti, C., Ragonese, P. & Calzolari, A., 1996, In : Giornale Italiano di Cardiologia. 26, 6, p. 739-745 7 p.

Research output: Contribution to journalArticle

Y chromosome duplication: A minor route evolutive pattern in CML

Alimena, G., Mandelli, F., Montuoro, A., Gastaldi, R. & Dallapiccola, B., 1979, In : Acta Haematologica. 61, 6, p. 310-316 7 p.

Research output: Contribution to journalArticle

Year in review: Critical Care 2004 - Nephrology

Ricci, Z. & Ronco, C., Oct 2005, In : Critical Care. 9, 5, p. 523-527 5 p.

Research output: Contribution to journalArticle

Year in review 2005: Critical Care - Nephrology

Ricci, Z. & Ronco, C., Aug 15 2006, In : Critical Care. 10, 4, 226.

Research output: Contribution to journalArticle

Year in review 2007: Critical care - Nephrology

Ricci, Z. & Ronco, C., Oct 14 2008, In : Critical Care. 12, 5, 230.

Research output: Contribution to journalArticle

Year in review 2008: Critical Care - nephrology

Ricci, Z. & Ronco, C., Oct 21 2009, In : Critical Care. 13, 5, 227.

Research output: Contribution to journalArticle

Year in review 2009: Critical Care - nephrology

Ricci, Z. & Ronco, C., Nov 5 2010, In : Critical Care. 14, 6, 241.

Research output: Contribution to journalArticle

Year in review 2012: Critical Care - nephrology

Ricci, Z. & Ronco, C., Nov 22 2013, In : Critical Care. 17, 6, 246.

Research output: Contribution to journalArticle

Year in review 2013: Critical Care - nephrology

Ricci, Z., Nardo, M. D. & Ronco, C., 2014, In : Critical Care. 18, 5, p. 1-7 7 p., 574.

Research output: Contribution to journalReview article

Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990-2010: A systematic analysis for the Global Burden of Disease Study 2010

Vos, T., Flaxman, A. D., Naghavi, M., Lozano, R., Michaud, C., Ezzati, M., Shibuya, K., Salomon, J. A., Abdalla, S., Aboyans, V., Abraham, J., Ackerman, I., Aggarwal, R., Ahn, S. Y., Ali, M. K., Alvarado, M., Anderson, H. R., Anderson, L. M., Andrews, K. G., Atkinson, C. & 341 others, Baddour, L. M., Bahalim, A. N., Barker-Collo, S., Barrero, L. H., Bartels, D. H., Basáñez, M. G., Baxter, A., Bell, M. L., Benjamin, E. J., Bennett, D., Bernabé, E., Bhalla, K., Bhandari, B., Bikbov, B., Abdulhak, A. B., Birbeck, G., Black, J. A., Blencowe, H., Blore, J. D., Blyth, F., Bolliger, I., Bonaventure, A., Boufous, S., Bourne, R., Boussinesq, M., Braithwaite, T., Brayne, C., Bridgett, L., Brooker, S., Brooks, P., Brugha, T. S., Bryan-Hancock, C., Bucello, C., Buchbinder, R., Buckle, G., Budke, C. M., Burch, M., Burney, P., Burstein, R., Calabria, B., Campbell, B., Canter, C. E., Carabin, H., Carapetis, J., Carmona, L., Cella, C., Charlson, F., Chen, H., Cheng, A. T. A., Chou, D., Chugh, S. S., Coffeng, L. E., Colan, S. D., Colquhoun, S., Colson, K. E., Condon, J., Connor, M. D., Cooper, L. T., Corriere, M., Cortinovis, M., De Vaccaro, K. C., Couser, W., Cowie, B. C., Criqui, M. H., Cross, M., Dabhadkar, K. C., Dahiya, M., Dahodwala, N., Damsere-Derry, J., Danaei, G., Davis, A., De Leo, D., Degenhardt, L., Dellavalle, R., Delossantos, A., Denenberg, J., Derrett, S., Des Jarlais, D. C., Dharmaratne, S. D., Dherani, M., Diaz-Torne, C., Dolk, H., Dorsey, E. R., Driscoll, T., Duber, H., Ebel, B., Edmond, K., Elbaz, A., Ali, S. E., Erskine, H., Erwin, P. J., Espindola, P., Ewoigbokhan, S. E., Farzadfar, F., Feigin, V., Felson, D. T., Ferrari, A., Ferri, C. P., Fèvre, E. M., Finucane, M. M., Flaxman, S., Flood, L., Foreman, K., Forouzanfar, M. H., Fowkes, F. G. R., Franklin, R., Fransen, M., Freeman, M. K., Gabbe, B. J., Gabriel, S. E., Gakidou, E., Ganatra, H. A., Garcia, B., Gaspari, F., Gillum, R. F., Gmel, G., Gonzalez-Medina, D., Gosselin, R., Grainger, R., Grant, B., Groeger, J., Guillemin, F., Gunnell, D., Gupta, R., Haagsma, J., Hagan, H., Halasa, Y. A., Hall, W., Haring, D., Haro, J. M., Harrison, J. E., Havmoeller, R., Hay, R. J., Higashi, H., Hill, C., Hoen, B., Hoffman, H., Hotez, P. J., Hoy, D., Huang, J. J., Ibeanusi, S. E., Jacobsen, K. H., James, S. L., Jarvis, D., Jasrasaria, R., Jayaraman, S., Johns, N., Jonas, J. B., Karthikeyan, G., Kassebaum, N., Kawakami, N., Keren, A., Khoo, J. P., King, C. H., Knowlton, L. M., Kobusingye, O., Koranteng, A., Krishnamurthi, R., Laden, F., Lalloo, R., Laslett, L. L., Lathlean, T., Leasher, J. L., Lee, Y. Y., Leigh, J., Levinson, D., Lim, S. S., Limb, E., Lin, J. K., Lipnick, M., Lipshultz, S. E., Liu, W., Loane, M., Ohno, S. L., Lyons, R., Ma, J., Mabweijano, J., MacIntyre, M. F., Malekzadeh, R., Mallinger, L., Manivannan, S., Marcenes, W., March, L., Margolis, D. J., Marks, G. B., Marks, R., Matsumori, A., Matzopoulos, R., Mayosi, B. M., McAnulty, J. H., McDermott, M. M., McGill, N., McGrath, J., Medina-Mora, M. E., Meltzer, M., Mensah, G. A., Merriman, T. R., Meyer, A. C., Miglioli, V., Miller, M., Miller, T. R., Mitchell, P. B., Mock, C., Mocumbi, A. O., Moffitt, T. E., Mokdad, A. A., Monasta, L., Montico, M., Moran, A., Morawska, L., Mori, R., Murdoch, M. E., Mwaniki, M. K., Naidoo, K., Nair, M. N., Naldi, L., Narayan, K. M. V., Nelson, P. K., Nelson, R. G., Nevitt, M. C., Newton, C. R., Nolte, S., Norman, P., Norman, R., O'Donnell, M., O'Hanlon, S., Olives, C., Omer, S. B., Ortblad, K., Osborne, R., Ozgediz, D., Page, A., Pahari, B., Pandian, J. D., Rivero, A. P., Patten, S. B., Pearce, N., Padilla, R. P., Perez-Ruiz, F., Perico, N., Pesudovs, K., Phillips, D., Phillips, M. R., Pierce, K., Pion, S., Polanczyk, G. V., Polinder, S., Pope, C. A., Popova, S., Porrini, E., Pourmalek, F., Prince, M., Pullan, R. L., Ramaiah, K. D., Ranganathan, D., Razavi, H., Regan, M., Rehm, J. T., Rein, D. B., Remuzzi, G., Richardson, K., Rivara, F. P., Roberts, T., Robinson, C., De Leòn, F. R., Ronfani, L., Room, R., Rosenfeld, L. C., Rushton, L., Sacco, R. L., Saha, S., Sampson, U., Sanchez-Riera, L., Sanman, E., Schwebel, D. C., Scott, J. G., Segui-Gomez, M., Shahraz, S., Shepard, D. S., Shin, H., Shivakoti, R., Singh, D., Singh, G. M., Singh, J. A., Singleton, J., Sleet, D. A., Sliwa, K., Smith, E., Smith, J. L., Stapelberg, N. J. C., Steer, A., Steiner, T., Stolk, W. A., Stovner, L. J., Sudfeld, C., Syed, S., Tamburlini, G., Tavakkoli, M., Taylor, H. R., Taylor, J. A., Taylor, W. J., Thomas, B., Thomson, W. M., Thurston, G. D., Tleyjeh, I. M., Tonelli, M., Towbin, J. A., Truelsen, T., Tsilimbaris, M. K., Ubeda, C., Undurraga, E. A., Van Der Werf, M. J., Van Os, J., Vavilala, M. S., Venketasubramanian, N., Wang, M., Wang, W., Watt, K., Weatherall, D. J., Weinstock, M. A., Weintraub, R., Weisskopf, M. G., Weissman, M. M., White, R. A., Whiteford, H., Wiebe, N., Wiersma, S. T., Wilkinson, J. D., Williams, H. C., Williams, S. R. M., Witt, E., Wolfe, F., Woolf, A. D., Wulf, S., Yeh, P. H., Zaidi, A. K. M., Zheng, Z. J., Zonies, D., Lopez, A. D., Murray, C. J. L. & Moradi-Lakeh, M., 2012, In : Lancet. 380, 9859, p. 2163-2196 34 p.

Research output: Contribution to journalArticle

Yeast-like filamentous fungi: Molecular identification and in vitro susceptibility study

Esposto, M. C., Prigitano, A., Lo Cascio, G., Ossi, C., Grancini, A., Cavanna, C., Lallitto, F., Tejada, M., Bandettini, R., Mularoni, A. & Tortorano, A. M., Dec 6 2018, In : Medical Mycology.

Research output: Contribution to journalArticle

Yeast-like filamentous fungi: Molecular identification and in vitro susceptibility study

Esposto, M. C., Prigitano, A., Lo Cascio, G., Ossi, C., Grancini, A., Cavanna, C., Lallitto, F., Tejada, M., Bandettini, R., Mularoni, A. & Tortorano, A. M., Oct 1 2019, In : Medical Mycology.

Research output: Contribution to journalArticle