Heterogeneous Genetic Alterations Predict Resistance To Immunosuppressive Treatments In Sporadic Steroid-resistant Nephrotic Syndrome
2014-01-01 Giglio, S; Provenzano, A; Mazzinghi, B; Becherucci, F; Giunti, L; Sansavini, G; Ravaglia, F; Roperto, Rm; Farsetti, S; Benetti, E; Rotondi, M; Murer, ; Eazzeri, E; Lasagni, L; Materassi, M; Romagnani, P
MOLECULAR CHARACTERIZATION OF PEDIATRIC GLIONEURONAL TUMOR WITH NEUROPIL-LIKE ISLANDS: A GENOME-WIDE COPY NUMBER ANALYSIS
2016-01-01 Giunti, L; Lucchesi, M; Palazzo, Viviana; Guidi, M; Genitori, L; Giglio, Sabrina Rita; Sardi, I.
Mosaic variegated aneuploidy: two new cases including a prenatal one
2005-01-01 Arrigo, G; Gimelli, S; Illekova, Z; Giglio, S; Zuffardi, O
MICRORNAS PROFILE IN PAEDIATRIC GBMS
2017-01-01 Giunti, Laura; Da Ros, Martina; Iorio, Anna Lisa; Magi, Alberto; Mazzinghi, Benedetta; Giglio, Sabrina; Sardi, Iacopo
Inverted low copy repeats and a common 8p23 inversion polymorphism
2001-01-01 Matsumoto, N; Harada, N; Giglio, Sabrina Rita; Kuroiwa, K; Ledbetter, Dh; Niikawa, N.
URINE-DERIVED HUMAN RENAL PROGENITOR CULTURES FOR MODELING OF GENETIC KIDNEY DISORDERS
2014-01-01 Lazzeri, Elena; Ronconi, Elisa; Angelotti, Maria Lucia; Peired, Anna Julie; Mazzinghi, B; Becherucci, F; Sansavini, G; Sisti, A; Provenzano, Aldesia; Giglio, Sabrina Rita; Lasagni, Laura; Romagnani, Paola
Is the experience mutation of G-CSF truly a predictive indicator of trends in early myolodysplasia or leukemia?
2008-01-01 Tucci, F; Giunti, L; Gambineri, Eleonora; Tondo, A; Giglio, Sabrina Rita; Sainati, L; Arico, M.
Genomic architecture and chromosome rearrangements
2003-01-01 Zuffardi, O; Giglio, Sabrina Rita
Urine-derived Human Renal Progenitor Cultures For Modeling Of Genetic Kidney Disorders
2014-01-01 Lazzeri, Elena; Ronconi, Elisa; Angelotti, Maria Lucia; Peired, Anna Julie; Mazzinghi, B; Giglio, Sabrina Rita; Lasagni, Laura; Romagnani, Paola
Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation
2002-01-01 Giglio, Sabrina Rita; Calvari, V; Gregato, G; Gimelli, G; Camanini, S; Giorda, R; Ragusa, A; Guerneri, S; Selicorni, A; Stumm, M; Tonnies, H; Ventura, M; Zollino, M; Neri, G; Barber, J; Wieczorek, D; Rocchi, M; Zuffardi, O.
Olfactory receptor gene clusters mediate common chromosome rearrangements
2001-01-01 Giglio, S; Matsumoto, N; Fantes, J; Calvari, V; Broman, Kw; Weber, Jl; Ledbetter, Dh; Zuffardi, O
HOMOZYGOUS DELETION IN STXBP2 CAUSATIVE OF FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS TYPE 5 (FHL-5)
2015-01-01 Cetica, V; Sieni, E; Ciambotti, B; Coniglio, Ml; Da Ros, M; Rizzari, C; Biondi, A; Pantaleo, M; Giglio, Sabrina Rita; Grieve, S; Griffiths, G; Arico, M.
Severe Obesity Associated with Severe Hyperinsulinism and T2D in a Family with Mutation in SH2B1 Gene
2015-01-01 Artuso, R; Provenzano, Aldesia; Mazzinghi, B; Palazzo, Viviana; Romano, S; Stagi, Stefano; Giglio, Sabrina Rita
High throughput sequencing in sporadic forms of steroid-resistant nephrotic syndrome in children frequently identifies heterogeneous genetic alterations that predict resistance to immunosuppressive treatments
2014-01-01 Mazzinghi, B.; Giglio, Sabrina Rita; Provenzano, Aldesia; Becherucci, Francesca; Sansavini, G.; Ravaglia, F.; Romagnani, Paola
A de novo 2q interstitial deletion in a patient with a Turner phenotype
2007-01-01 Giglio, Sabrina Rita; Andreucci, Elena; Ricca, I.; Guarducci, S.; Ricci, U.; Sani, I.; Nanni, L.; Seminara, Salvatore; Genuardi, ; O. Zuffardi, M. Genuardi; O., Zuffardi
Resting-state EEG parameters reveal associations with AD plasma biomarkers in cognitive impairment.
2025-01-01 Cecchetti, G; Rugarli, G; Zanchi, L; Lanzone, J; Basaia, S; Cursi, M; Coraglia, F; Spinelli, Eg; Caso, F; Curti, Dg; Fanelli, Gf; Bellini, A; Magnani, G; Agosta, F; Filippi, M.
Cross-linguistic characterization of speech and language profiles of English, Chinese, and Italian Primary Progressive Aphasia patients: a data-driven approach
2025-01-01 Santi, Gc; Catricalà, E; Kwan, S; Wong, A; Ezzes, Z; Wauters, Ld; Esposito, V; Conca, F; Chen, Tf; Li-Ying Kwan Chen, L; Lo, Ry; Tsoh, J; Chan, Lt; Garcia, Am; Deleon, J; Miller, Z; Vonk, Jmj; Allen, Ie; Canu, E; Agosta, F; Filippi, M; Cappa, Sf; Gorno Tempini, Ml; Lead Tee, B.
Relationship between retinal thickness and plasma biomarkers in a Memory Centre population.
2025-01-01 Rugarli, G; Cecchetti, G; Santangelo, R; Napoli, G; Coraglia, F; Spinelli, Eg; Caso, F; Magnani, G; Filippi, M; Agosta, F.
Genetic and Pathological Characteristics of Frontotemporal Dementia with Right Anterior Temporal Predominance: A Multicenter Retrospective Cohort Study
2025-01-01 Ulugut, H; Younes, K; Bertoux, M; Montembeault, M; Fumagalli, Gg; Ghirelli, A; Spinelli, Eg; Jung, Ny; Samancı, B; Illán-Gala, I; Thompson, J; Kobylecki, C; Santillo, A; Englund, E; Landqvist Waldö, M; Riedl, L; Van Den Stock, J; Vandenbulcke, M; Vandenberghe, R; Laforce, Jr. R.; Ducharme, S; Pressman, Ps; Tartaglia, C; Caramelli, P; Cruz De Souza, L; Tadao Takada, L; Morin, A; Schroeter, Ml; Kim, Ej; Young Moon, S; Agosta, F; Canu, E; Filippi, M; Gurvit, H; Diehl-Schmid, J; Galimberti, D; Lebouvier, T; Miller, Bl; Sturm, Ve; Miyagawa, T; Whitwell, Jl; Boeve, Bf; Rohrer, Jd; Gorno Tempini, Ml; Josephs, Ka; Snowden, Js; Warren, Jd; Rankin, Kp; Pijnenburg, Yal
Valori dell’indice di distribuzione eritrocita ria in pazienti affetti da scompenso cardiaco acuto
2011-01-01 Pezzali, N; Vizzardi, Enrico; Lupi, L; Rocco, E; Ciccarese, C; Maiandi, C; Caretta, G; Bordonali, T; Metra, Marco; Dei Cas, Livio
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Heterogeneous Genetic Alterations Predict Resistance To Immunosuppressive Treatments In Sporadic Steroid-resistant Nephrotic Syndrome | 1-gen-2014 | Giglio, S; Provenzano, A; Mazzinghi, B; Becherucci, F; Giunti, L; Sansavini, G; Ravaglia, F; Roperto, Rm; Farsetti, S; Benetti, E; Rotondi, M; Murer, ; Eazzeri, E; Lasagni, L; Materassi, M; Romagnani, P | |
| MOLECULAR CHARACTERIZATION OF PEDIATRIC GLIONEURONAL TUMOR WITH NEUROPIL-LIKE ISLANDS: A GENOME-WIDE COPY NUMBER ANALYSIS | 1-gen-2016 | Giunti, L; Lucchesi, M; Palazzo, Viviana; Guidi, M; Genitori, L; Giglio, Sabrina Rita; Sardi, I. | |
| Mosaic variegated aneuploidy: two new cases including a prenatal one | 1-gen-2005 | Arrigo, G; Gimelli, S; Illekova, Z; Giglio, S; Zuffardi, O | |
| MICRORNAS PROFILE IN PAEDIATRIC GBMS | 1-gen-2017 | Giunti, Laura; Da Ros, Martina; Iorio, Anna Lisa; Magi, Alberto; Mazzinghi, Benedetta; Giglio, Sabrina; Sardi, Iacopo | |
| Inverted low copy repeats and a common 8p23 inversion polymorphism | 1-gen-2001 | Matsumoto, N; Harada, N; Giglio, Sabrina Rita; Kuroiwa, K; Ledbetter, Dh; Niikawa, N. | |
| URINE-DERIVED HUMAN RENAL PROGENITOR CULTURES FOR MODELING OF GENETIC KIDNEY DISORDERS | 1-gen-2014 | Lazzeri, Elena; Ronconi, Elisa; Angelotti, Maria Lucia; Peired, Anna Julie; Mazzinghi, B; Becherucci, F; Sansavini, G; Sisti, A; Provenzano, Aldesia; Giglio, Sabrina Rita; Lasagni, Laura; Romagnani, Paola | |
| Is the experience mutation of G-CSF truly a predictive indicator of trends in early myolodysplasia or leukemia? | 1-gen-2008 | Tucci, F; Giunti, L; Gambineri, Eleonora; Tondo, A; Giglio, Sabrina Rita; Sainati, L; Arico, M. | |
| Genomic architecture and chromosome rearrangements | 1-gen-2003 | Zuffardi, O; Giglio, Sabrina Rita | |
| Urine-derived Human Renal Progenitor Cultures For Modeling Of Genetic Kidney Disorders | 1-gen-2014 | Lazzeri, Elena; Ronconi, Elisa; Angelotti, Maria Lucia; Peired, Anna Julie; Mazzinghi, B; Giglio, Sabrina Rita; Lasagni, Laura; Romagnani, Paola | |
| Heterozygous submicroscopic inversions involving olfactory receptor-gene clusters mediate the recurrent t(4;8)(p16;p23) translocation | 1-gen-2002 | Giglio, Sabrina Rita; Calvari, V; Gregato, G; Gimelli, G; Camanini, S; Giorda, R; Ragusa, A; Guerneri, S; Selicorni, A; Stumm, M; Tonnies, H; Ventura, M; Zollino, M; Neri, G; Barber, J; Wieczorek, D; Rocchi, M; Zuffardi, O. | |
| Olfactory receptor gene clusters mediate common chromosome rearrangements | 1-gen-2001 | Giglio, S; Matsumoto, N; Fantes, J; Calvari, V; Broman, Kw; Weber, Jl; Ledbetter, Dh; Zuffardi, O | |
| HOMOZYGOUS DELETION IN STXBP2 CAUSATIVE OF FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS TYPE 5 (FHL-5) | 1-gen-2015 | Cetica, V; Sieni, E; Ciambotti, B; Coniglio, Ml; Da Ros, M; Rizzari, C; Biondi, A; Pantaleo, M; Giglio, Sabrina Rita; Grieve, S; Griffiths, G; Arico, M. | |
| Severe Obesity Associated with Severe Hyperinsulinism and T2D in a Family with Mutation in SH2B1 Gene | 1-gen-2015 | Artuso, R; Provenzano, Aldesia; Mazzinghi, B; Palazzo, Viviana; Romano, S; Stagi, Stefano; Giglio, Sabrina Rita | |
| High throughput sequencing in sporadic forms of steroid-resistant nephrotic syndrome in children frequently identifies heterogeneous genetic alterations that predict resistance to immunosuppressive treatments | 1-gen-2014 | Mazzinghi, B.; Giglio, Sabrina Rita; Provenzano, Aldesia; Becherucci, Francesca; Sansavini, G.; Ravaglia, F.; Romagnani, Paola | |
| A de novo 2q interstitial deletion in a patient with a Turner phenotype | 1-gen-2007 | Giglio, Sabrina Rita; Andreucci, Elena; Ricca, I.; Guarducci, S.; Ricci, U.; Sani, I.; Nanni, L.; Seminara, Salvatore; Genuardi, ; O. Zuffardi, M. Genuardi; O., Zuffardi | |
| Resting-state EEG parameters reveal associations with AD plasma biomarkers in cognitive impairment. | 1-gen-2025 | Cecchetti, G; Rugarli, G; Zanchi, L; Lanzone, J; Basaia, S; Cursi, M; Coraglia, F; Spinelli, Eg; Caso, F; Curti, Dg; Fanelli, Gf; Bellini, A; Magnani, G; Agosta, F; Filippi, M. | |
| Cross-linguistic characterization of speech and language profiles of English, Chinese, and Italian Primary Progressive Aphasia patients: a data-driven approach | 1-gen-2025 | Santi, Gc; Catricalà, E; Kwan, S; Wong, A; Ezzes, Z; Wauters, Ld; Esposito, V; Conca, F; Chen, Tf; Li-Ying Kwan Chen, L; Lo, Ry; Tsoh, J; Chan, Lt; Garcia, Am; Deleon, J; Miller, Z; Vonk, Jmj; Allen, Ie; Canu, E; Agosta, F; Filippi, M; Cappa, Sf; Gorno Tempini, Ml; Lead Tee, B. | |
| Relationship between retinal thickness and plasma biomarkers in a Memory Centre population. | 1-gen-2025 | Rugarli, G; Cecchetti, G; Santangelo, R; Napoli, G; Coraglia, F; Spinelli, Eg; Caso, F; Magnani, G; Filippi, M; Agosta, F. | |
| Genetic and Pathological Characteristics of Frontotemporal Dementia with Right Anterior Temporal Predominance: A Multicenter Retrospective Cohort Study | 1-gen-2025 | Ulugut, H; Younes, K; Bertoux, M; Montembeault, M; Fumagalli, Gg; Ghirelli, A; Spinelli, Eg; Jung, Ny; Samancı, B; Illán-Gala, I; Thompson, J; Kobylecki, C; Santillo, A; Englund, E; Landqvist Waldö, M; Riedl, L; Van Den Stock, J; Vandenbulcke, M; Vandenberghe, R; Laforce, Jr. R.; Ducharme, S; Pressman, Ps; Tartaglia, C; Caramelli, P; Cruz De Souza, L; Tadao Takada, L; Morin, A; Schroeter, Ml; Kim, Ej; Young Moon, S; Agosta, F; Canu, E; Filippi, M; Gurvit, H; Diehl-Schmid, J; Galimberti, D; Lebouvier, T; Miller, Bl; Sturm, Ve; Miyagawa, T; Whitwell, Jl; Boeve, Bf; Rohrer, Jd; Gorno Tempini, Ml; Josephs, Ka; Snowden, Js; Warren, Jd; Rankin, Kp; Pijnenburg, Yal | |
| Valori dell’indice di distribuzione eritrocita ria in pazienti affetti da scompenso cardiaco acuto | 1-gen-2011 | Pezzali, N; Vizzardi, Enrico; Lupi, L; Rocco, E; Ciccarese, C; Maiandi, C; Caretta, G; Bordonali, T; Metra, Marco; Dei Cas, Livio |
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Scopri
Tipologia
- 1 Contributo su Rivista3192
Data di pubblicazione
- In corso di stampa1
- 2020 - 202596
- 2010 - 20191464
- 2000 - 20091294
- 1990 - 1999321
- 1983 - 198916
Editore
- ELSEVIER22
- LIPPINCOTT WILLIAMS & WILKINS14
- NLM (Medline)13
- URBAN & VOGEL12
- ELSEVIER SCIENCE BV11
- DR DIETRICH STEINKOPFF VERLAG10
- ELSEVIER SCIENCE INC10
- OXFORD UNIV PRESS10
- SPRINGER HEIDELBERG10
- SPRINGER9
Rivista
- EUROPEAN UROLOGY. SUPPLEMENTS174
- JOURNAL OF NEUROLOGY153
- THE JOURNAL OF UROLOGY152
- BONE MARROW TRANSPLANTATION127
- EUROPEAN NEUROPSYCHOPHARMACOLOGY126
- NEUROLOGICAL SCIENCES88
- BLOOD86
- EUROPEAN HEART JOURNAL72
- NEUROLOGY72
- GASTROENTEROLOGY71
Keyword
- systemic sclerosis12
- Children4
- fibrosis4
- JIA4
- JSLE4
- None4
- angiogenesis3
- animal model3
- Bone mass3
- IPMN3
Lingua
- eng1301
- ita202
- und13
Accesso al fulltext
- no fulltext3161
- reserved25
- open6