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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

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

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

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.

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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

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.

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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

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

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

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-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.

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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 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 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 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 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 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 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 : 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., May 31 2019, In : Italian Journal of Pediatrics. 45, 1, 67.

Research output: Contribution to journalArticle

Open Access

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 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 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 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 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 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 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, 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 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: 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 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

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

Xenodermatosis: A case of ciguatera

Schiazza, L., Bleidl, D., Occella, C. & Rampini, E., 1988, In : Giornale Italiano di Dermatologia e Venereologia. 123, 1-2, p. 41-45 5 p.

Research output: Contribution to journalArticle

XENODERMATOSI. UN CASO DI ULCERE TROPICALOIDI

Translated title of the contribution: Xenodermatosis: A case of tropicaloid ulcersRampini, E., Cannata, G., Occella, C. & Nunzi, E., 1980, In : Giornale Italiano di Dermatologia e Venereologia. 115, 11-12, p. 569-571 3 p.

Research output: Contribution to journalArticle

X chromosome replication patterns in a case of X;9 balanced translocation

Filippi, G., Pecile, V., Archidiacono, N., Baragino, E., Auber, G. & Rocchi, M., 1983, In : Journal of Medical Genetics. 20, 6, p. 467-468 2 p.

Research output: Contribution to journalArticle

X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative Group.

Moschese, V., Orlandi, P., Plebani, A., Arvanitidis, K., Fiorini, M., Speletas, M., Mella, P., Ritis, K., Sideras, P., Finocchi, A., Livadiotti, S. & Rossi, P., Feb 2000, In : Molecular medicine (Cambridge, Mass.). 6, 2, p. 104-113 10 p.

Research output: Contribution to journalArticle

X-chromosome inactivation analysis in a female carrier of FOXP3 mutation

Tommasini, A., Ferrari, S., Moratto, D., Badolato, R., Boniotto, M., Pirulli, D., Notarangelo, L. D. & Andolina, M., 2002, In : Clinical and Experimental Immunology. 130, 1, p. 127-130 4 p.

Research output: Contribution to journalArticle

Xantomatosi cerebro-tendinea

Bruno, I., May 1 2016, In : Medico e Bambino. 35, 5, p. 310-312 3 p.

Research output: Contribution to journalArticle

X/Y translocation in a family with Leri-Weill dyschondrosteosis

Calabrese, G., Fischetto, R., Stuppia, L., Capodiferro, F., Mingarelli, R., Causio, F., Rocchi, M., Rappold, G. A. & Palka, G., 1999, In : Human Genetics. 105, 4, p. 367-368 2 p.

Research output: Contribution to journalArticle

WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): Case report and literature review of the disease clinical, genetic and radiological features

Zicari, A. M., Tarani, L., Perotti, D., Papetti, L., Nicita, F., Liberati, N., Spalice, A., Salvatori, G., Guaraldi, F. & Duse, M., 2012, In : Italian Journal of Pediatrics. 38, 1, 27.

Research output: Contribution to journalArticle

WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes

Aucella, F., Bisceglia, L., Bonis, P., Gigante, M., Caridi, G., Barbano, G., Mattioli, G., Perfumo, F., Gesualdo, L. & Ghiggeri, G. M., Oct 2006, In : Pediatric Nephrology. 21, 10, p. 1393-1398 6 p.

Research output: Contribution to journalArticle

WT1-mediated repression of the proapoptotic transcription factor ZNF224 is triggered by the BCR-ABL oncogene

Montano, G., Vidovic, K., Palladino, C., Cesaro, E., Sodaro, G., Quintarelli, C., Angelis, B. D., Errichiello, S., Pane, F., Izzo, P., Grosso, M., Gullberg, U. & Costanzo, P., 2015, In : Oncotarget. 6, 29, p. 28223-28237 15 p.

Research output: Contribution to journalArticle

Writing abilities in intellectual disabilities: A comparison between Down and Williams syndrome

Varuzza, C., De Rose, P., Vicari, S. & Menghini, D., Feb 1 2015, In : Research in Developmental Disabilities. 37, p. 135-142 8 p.

Research output: Contribution to journalArticle

Wrist circumference is a biomarker of adipose tissue dysfunction and cardiovascular risk in children with obesity

Luordi, C., Maddaloni, E., Bizzarri, C., Pedicelli, S., Zampetti, S., D'Onofrio, L., Moretti, C., Cappa, M. & Buzzetti, R., Jul 25 2019, In : Journal of Endocrinological Investigation.

Research output: Contribution to journalArticle

Worth continuing doing ex situ liver graft splitting? A single-center analysis

Noujaima, H. M., Gunson, B., Mayer, D. A., Mirza, D. F., Buckels, J. A. C., Candinas, D., McMaster, P. & De Ville de Goyet, J., Mar 2003, In : American Journal of Transplantation. 3, 3, p. 318-323 6 p.

Research output: Contribution to journalArticle