Sfoglia per Autore
CONGENITAL CYSTIC LUNG DISEASE: PRENATAL ULTRASOUND AND POSTNATAL MULTIDETECTOR COMPUTER TOMOGRAPHY EVALUATION. CORRELATION WITH SURGICAL AND PATHOLOGICAL DATA
2014-01-01 Bondioni, Maria Pia; Diego, Gatta; Lougaris, Vassilios; Nicoletta, Palai; Marino, Signorelli; Silvia, Michelini; Giuseppe Di, Gaetano; Paola, Tessitore; Lorella, Mascaro; Andrea, Tironi; Giovanni, Boroni; Maroldi, Roberto; Alberti, Daniele
Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype
2015-01-01 Lougaris, Vassilios; Faletra, Flavio; Lanzi, Gaetana; Vozzi, Diego; Marcuzzi, Annalisa; Valencic, Erica; Piscianz, Elisa; Bianco, Annamonica; Girardelli, Martina; Baronio, Manuela; Loganes, Claudia; Fasth, Anders; Salvini, Filippo; Trizzino, Antonino; Moratto, Daniele; Facchetti, Fabio; Giliani, Silvia Clara; Plebani, Alessandro; Tommasini, Alberto
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency
2015-01-01 Gualdi, G; Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Moratto, D; Tanghetti, P; Monari, P; CALZAVARA PINTON, Piergiacomo; Plebani, Alessandro
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency
2015-01-01 Engelhardt, Karin R.; Gertz, Michael E.; Keles, Sevgi; Schäffer, Alejandro A.; Sigmund, Elena C.; Glocker, Cristina; Saghafi, Shiva; Pourpak, Zahra; Ceja, Ruben; Sassi, Atfa; Graham, Laura E.; Massaad, Michel J.; Mellouli, Fethi; Ben Mustapha, Imen; Khemiri, Monia; Kilic, Sara Sebnem; Etzioni, Amos; Freeman, Alexandra F.; Thiel, Jens; Schulze, Ilka; Al Herz, Waleed; Metin, Ayse; Sanal, Özden; Tezcan, Ilhan; Yeganeh, Mehdi; Niehues, Tim; Dueckers, Gregor; Weinspach, Sebastian; Patiroglu, Turkan; Unal, Ekrem; Dasouki, Majed; Yilmaz, Mustafa; Genel, Ferah; Aytekin, Caner; Kutukculer, Necil; Somer, Ayper; Kilic, Mehmet; Reisli, Ismail; Camcioglu, Yildiz; Gennery, Andrew R.; Cant, Andrew J.; Jones, Alison; Gaspar, Bobby H.; Arkwright, Peter D.; Pietrogrande, Maria C.; Baz, Zeina; Al Tamemi, Salem; Lougaris, Vassilios; Lefranc, Gerard; Megarbane, Andre; Boutros, Jeannette; Galal, Nermeen; Bejaoui, Mohamed; Barbouche, Mohamed Ridha; Geha, Raif S.; Chatila, Talal A.; Grimbacher, Bodo
Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients
2015-01-01 Lougaris, Vassilios; Baronio, Manuela; Masneri, Stefania; Lorenzini, Tiziana; Cattivelli, Kim; Tampella, Giacomo; Soresina, Annarosa; Moratto, Daniele; Plebani, Alessandro
Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease
2015-01-01 Lougaris, Vassilios; Tabellini, Giovanna; Vitali, Massimiliano; Baronio, Manuela; Patrizi, Ornella; Tampella, Giacomo; Biasini, Augusto; Moratto, Daniele; Parolini, Silvia; Plebani, Alessandro
Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency
2015-01-01 Lougaris, Vassilios; Ravelli, Alberto; Villanacci, Vincenzo; Salemme, Marianna; Soresina, Annarosa; Fuoti, Maurizio Giuseppe; Lanzarotto, Francesco; Lanzini, Alberto; Plebani, Alessandro; Bassotti, Gabrio
Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study
2015-01-01 Dellepiane, Rosa Maria; Dell’Era, Laura; Beilis, Lorena Vanesa; Pavesi, Paola; Raimondi, Micol; Soresina, Annarosa; Lougaris, Vassilios; Carrabba, Maria; Martire, Baldassarre; Martino, Silvana; Russo, Giovanna; Patuzzo, Giuseppe; Pignata, Claudio; Spadaro, Giuseppe; Gallizzi, Romina; Duse, Marzia; Specchia, Fernando Giuseppe; Moschese, Viviana; Marseglia, Gian Luigi; Pietrogrande, Maria Cristina; Bedogni, Giorgio; Agostoni, Carlo
Reduced germinal center follicular helper T cells but normal follicular regulatory T cells in the tonsils of a patient with a mutation in the PI3KR1 gene
2016-01-01 Di Fonte, Roberta; Baronio, Manuela; Plebani, Alessandro; Lougaris, Vassilios; Fousteri, Georgia
Diagnostics of primary immunodeficiencies through next-generation sequencing
2016-01-01 Gallo, Vera; Dotta, Laura; Giardino, Giuliana; Cirillo, Emilia; Lougaris, Vassilios; D'Assante, Roberta; Prandini, Alberto; Consolini, Rita; Farrow, Emily G.; Thiffault, Isabelle; Saunders, Carol J.; Leonardi, Antonio; Plebani, Alessandro; Badolato, Raffaele; Pignata, Claudio
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions
2016-01-01 Giacomelli, Mauro Simone; Kumar, Rajesh; Soresina, Annarosa; Tamassia, Nicola; Lorenzini, Tiziana; Moratto, Daniele; Gasperini, Sara; Cassatella, Marco; Plebani, Alessandro; Lougaris, Vassilios; Badolato, Raffaele
Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies
2016-01-01 Lougaris, Vassilios; Baronio, Manuela; Moratto, Daniele; Cardinale, Fabio; Plebani, Alessandro
Proteus syndrome: evaluation of the immunological profile
2016-01-01 Lougaris, Vassilios; Salpietro, Vincenzo; Cutrupi, Maricia; Baronio, Manuela; Moratto, Daniele; Pizzino, M. R; Mankad, Kshitij; Briuglia, Silvana; Salpietro, Carmelo; Plebani, Alessandro
Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome
2016-01-01 Lougaris, Vassilios; Facchini, Elena; Baronio, Manuela; Lorenzini, Tiziana; Moratto, Daniele; Specchia, Fernando; Plebani, Alessandro
P85α is an intrinsic regulator of human natural killer cell effector functions
2016-01-01 Lougaris, Vassilios; Patrizi, Ornella; Baronio, Manuela; Tabellini, Giovanna; Tampella, Giacomo; Lanzi, Gaetana; Salvini, Filippo; Trizzino, Antonino; Parolini, Silvia; Plebani, Alessandro
Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study
2016-01-01 Elkaim, Elodie; Neven, Benedicte; Bruneau, Julie; Mitsui Sekinaka, Kanako; Stanislas, Aurelie; Heurtier, Lucie; Lucas, Carrie L.; Matthews, Helen; Deau, Marie Céline; Sharapova, Svetlana; Curtis, James; Reichenbach, Janine; Glastre, Catherine; Parry, David A.; Arumugakani, Gururaj; Mcdermott, Elizabeth; Kilic, Sara Sebnem; Yamashita, Motoi; Moshous, Despina; Lamrini, Hicham; Otremba, Burkhard; Gennery, Andrew; Coulter, Tanya; Quinti, Isabella; Stephan, Jean Louis; Lougaris, Vassilios; Brodszki, Nicholas; Barlogis, Vincent; Asano, Takaki; Galicier, Lionel; Boutboul, David; Nonoyama, Shigeaki; Cant, Andrew; Imai, Kohsuke; Picard, Capucine; Nejentsev, Sergey; Molina, Thierry Jo; Lenardo, Michael; Savic, Sinisa; Cavazzana, Marina; Fischer, Alain; Durandy, Anne; Kracker, Sven
Breastfeeding and IL-10 levels in children affected by cow's milk protein allergy: A restrospective study
2016-01-01 Manti, Sara; Lougaris, Vassilios; Cuppari, Caterina; Tardino, Lucia; Dipasquale, Valeria; Arrigo, Teresa; Salpietro, Carmelo; Leonardi, Salvatore
Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects
2016-01-01 Abolhassani, Hassan; Vitali, Massimiliano; Lougaris, Vassilios; Giliani, Silvia Clara; Parvaneh, Nima; Parvaneh, Leila; Mirminachi, Babak; Cheraghi, Taher; Khazaei, Hosseinali; Mahdaviani, Seyed Alireza; Kiaei, Fatemeh; Tavakolinia, Naiimeh; Mohammadi, Javad; Negahdari, Babak; Rezaei, Nima; Hammarstrom, Lennart; Plebani, Alessandro; Aghamohammadi, Asghar
Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease
2016-01-01 Lougaris, Vassilios; Moratto, Daniele; Baronio, Manuela; Tampella, Giacomo; van der Meer, Jos W. M; Badolato, Raffaele; Fliegauf, Manfred; Plebani, Alessandro
The nested graft acts by inducing the process of de-senescence of the fibroblasts in chronic venous ulcers
2016-01-01 Gualdi, Giulio; Crotti, Silvia; Monari, Paola; CALZAVARA PINTON, Piergiacomo; Vitali, Massimiliano; Baronio, Manuela; Lougaris, Vassilios
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| CONGENITAL CYSTIC LUNG DISEASE: PRENATAL ULTRASOUND AND POSTNATAL MULTIDETECTOR COMPUTER TOMOGRAPHY EVALUATION. CORRELATION WITH SURGICAL AND PATHOLOGICAL DATA | 1-gen-2014 | Bondioni, Maria Pia; Diego, Gatta; Lougaris, Vassilios; Nicoletta, Palai; Marino, Signorelli; Silvia, Michelini; Giuseppe Di, Gaetano; Paola, Tessitore; Lorella, Mascaro; Andrea, Tironi; Giovanni, Boroni; Maroldi, Roberto; Alberti, Daniele | |
| Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype | 1-gen-2015 | Lougaris, Vassilios; Faletra, Flavio; Lanzi, Gaetana; Vozzi, Diego; Marcuzzi, Annalisa; Valencic, Erica; Piscianz, Elisa; Bianco, Annamonica; Girardelli, Martina; Baronio, Manuela; Loganes, Claudia; Fasth, Anders; Salvini, Filippo; Trizzino, Antonino; Moratto, Daniele; Facchetti, Fabio; Giliani, Silvia Clara; Plebani, Alessandro; Tommasini, Alberto | |
| Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency | 1-gen-2015 | Gualdi, G; Lougaris, Vassilios; Baronio, Manuela; Vitali, Massimiliano; Tampella, Giacomo; Moratto, D; Tanghetti, P; Monari, P; CALZAVARA PINTON, Piergiacomo; Plebani, Alessandro | |
| The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency | 1-gen-2015 | Engelhardt, Karin R.; Gertz, Michael E.; Keles, Sevgi; Schäffer, Alejandro A.; Sigmund, Elena C.; Glocker, Cristina; Saghafi, Shiva; Pourpak, Zahra; Ceja, Ruben; Sassi, Atfa; Graham, Laura E.; Massaad, Michel J.; Mellouli, Fethi; Ben Mustapha, Imen; Khemiri, Monia; Kilic, Sara Sebnem; Etzioni, Amos; Freeman, Alexandra F.; Thiel, Jens; Schulze, Ilka; Al Herz, Waleed; Metin, Ayse; Sanal, Özden; Tezcan, Ilhan; Yeganeh, Mehdi; Niehues, Tim; Dueckers, Gregor; Weinspach, Sebastian; Patiroglu, Turkan; Unal, Ekrem; Dasouki, Majed; Yilmaz, Mustafa; Genel, Ferah; Aytekin, Caner; Kutukculer, Necil; Somer, Ayper; Kilic, Mehmet; Reisli, Ismail; Camcioglu, Yildiz; Gennery, Andrew R.; Cant, Andrew J.; Jones, Alison; Gaspar, Bobby H.; Arkwright, Peter D.; Pietrogrande, Maria C.; Baz, Zeina; Al Tamemi, Salem; Lougaris, Vassilios; Lefranc, Gerard; Megarbane, Andre; Boutros, Jeannette; Galal, Nermeen; Bejaoui, Mohamed; Barbouche, Mohamed Ridha; Geha, Raif S.; Chatila, Talal A.; Grimbacher, Bodo | |
| Correlation of bone marrow abnormalities, peripheral lymphocyte subsets and clinical features in uncomplicated common variable immunodeficiency (CVID) patients | 1-gen-2015 | Lougaris, Vassilios; Baronio, Manuela; Masneri, Stefania; Lorenzini, Tiziana; Cattivelli, Kim; Tampella, Giacomo; Soresina, Annarosa; Moratto, Daniele; Plebani, Alessandro | |
| Defective natural killer-cell cytotoxic activity in NFKB2-mutated CVID-like disease | 1-gen-2015 | Lougaris, Vassilios; Tabellini, Giovanna; Vitali, Massimiliano; Baronio, Manuela; Patrizi, Ornella; Tampella, Giacomo; Biasini, Augusto; Moratto, Daniele; Parolini, Silvia; Plebani, Alessandro | |
| Gastrointestinal Pathologic Abnormalities in Pediatric- and Adult-Onset Common Variable Immunodeficiency | 1-gen-2015 | Lougaris, Vassilios; Ravelli, Alberto; Villanacci, Vincenzo; Salemme, Marianna; Soresina, Annarosa; Fuoti, Maurizio Giuseppe; Lanzarotto, Francesco; Lanzini, Alberto; Plebani, Alessandro; Bassotti, Gabrio | |
| Nutritional Status in Agammaglobulinemia: An Italian Multicenter Study | 1-gen-2015 | Dellepiane, Rosa Maria; Dell’Era, Laura; Beilis, Lorena Vanesa; Pavesi, Paola; Raimondi, Micol; Soresina, Annarosa; Lougaris, Vassilios; Carrabba, Maria; Martire, Baldassarre; Martino, Silvana; Russo, Giovanna; Patuzzo, Giuseppe; Pignata, Claudio; Spadaro, Giuseppe; Gallizzi, Romina; Duse, Marzia; Specchia, Fernando Giuseppe; Moschese, Viviana; Marseglia, Gian Luigi; Pietrogrande, Maria Cristina; Bedogni, Giorgio; Agostoni, Carlo | |
| Reduced germinal center follicular helper T cells but normal follicular regulatory T cells in the tonsils of a patient with a mutation in the PI3KR1 gene | 1-gen-2016 | Di Fonte, Roberta; Baronio, Manuela; Plebani, Alessandro; Lougaris, Vassilios; Fousteri, Georgia | |
| Diagnostics of primary immunodeficiencies through next-generation sequencing | 1-gen-2016 | Gallo, Vera; Dotta, Laura; Giardino, Giuliana; Cirillo, Emilia; Lougaris, Vassilios; D'Assante, Roberta; Prandini, Alberto; Consolini, Rita; Farrow, Emily G.; Thiffault, Isabelle; Saunders, Carol J.; Leonardi, Antonio; Plebani, Alessandro; Badolato, Raffaele; Pignata, Claudio | |
| Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions | 1-gen-2016 | Giacomelli, Mauro Simone; Kumar, Rajesh; Soresina, Annarosa; Tamassia, Nicola; Lorenzini, Tiziana; Moratto, Daniele; Gasperini, Sara; Cassatella, Marco; Plebani, Alessandro; Lougaris, Vassilios; Badolato, Raffaele | |
| Monoallelic BAFFR P21R/H159Y Mutations and Familiar Primary Antibody Deficiencies | 1-gen-2016 | Lougaris, Vassilios; Baronio, Manuela; Moratto, Daniele; Cardinale, Fabio; Plebani, Alessandro | |
| Proteus syndrome: evaluation of the immunological profile | 1-gen-2016 | Lougaris, Vassilios; Salpietro, Vincenzo; Cutrupi, Maricia; Baronio, Manuela; Moratto, Daniele; Pizzino, M. R; Mankad, Kshitij; Briuglia, Silvana; Salpietro, Carmelo; Plebani, Alessandro | |
| Progressive severe B cell deficiency in pediatric Rubinstein-Taybi syndrome | 1-gen-2016 | Lougaris, Vassilios; Facchini, Elena; Baronio, Manuela; Lorenzini, Tiziana; Moratto, Daniele; Specchia, Fernando; Plebani, Alessandro | |
| P85α is an intrinsic regulator of human natural killer cell effector functions | 1-gen-2016 | Lougaris, Vassilios; Patrizi, Ornella; Baronio, Manuela; Tabellini, Giovanna; Tampella, Giacomo; Lanzi, Gaetana; Salvini, Filippo; Trizzino, Antonino; Parolini, Silvia; Plebani, Alessandro | |
| Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study | 1-gen-2016 | Elkaim, Elodie; Neven, Benedicte; Bruneau, Julie; Mitsui Sekinaka, Kanako; Stanislas, Aurelie; Heurtier, Lucie; Lucas, Carrie L.; Matthews, Helen; Deau, Marie Céline; Sharapova, Svetlana; Curtis, James; Reichenbach, Janine; Glastre, Catherine; Parry, David A.; Arumugakani, Gururaj; Mcdermott, Elizabeth; Kilic, Sara Sebnem; Yamashita, Motoi; Moshous, Despina; Lamrini, Hicham; Otremba, Burkhard; Gennery, Andrew; Coulter, Tanya; Quinti, Isabella; Stephan, Jean Louis; Lougaris, Vassilios; Brodszki, Nicholas; Barlogis, Vincent; Asano, Takaki; Galicier, Lionel; Boutboul, David; Nonoyama, Shigeaki; Cant, Andrew; Imai, Kohsuke; Picard, Capucine; Nejentsev, Sergey; Molina, Thierry Jo; Lenardo, Michael; Savic, Sinisa; Cavazzana, Marina; Fischer, Alain; Durandy, Anne; Kracker, Sven | |
| Breastfeeding and IL-10 levels in children affected by cow's milk protein allergy: A restrospective study | 1-gen-2016 | Manti, Sara; Lougaris, Vassilios; Cuppari, Caterina; Tardino, Lucia; Dipasquale, Valeria; Arrigo, Teresa; Salpietro, Carmelo; Leonardi, Salvatore | |
| Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects | 1-gen-2016 | Abolhassani, Hassan; Vitali, Massimiliano; Lougaris, Vassilios; Giliani, Silvia Clara; Parvaneh, Nima; Parvaneh, Leila; Mirminachi, Babak; Cheraghi, Taher; Khazaei, Hosseinali; Mahdaviani, Seyed Alireza; Kiaei, Fatemeh; Tavakolinia, Naiimeh; Mohammadi, Javad; Negahdari, Babak; Rezaei, Nima; Hammarstrom, Lennart; Plebani, Alessandro; Aghamohammadi, Asghar | |
| Early and late B-cell developmental impairment in nuclear factor kappa B, subunit 1-mutated common variable immunodeficiency disease | 1-gen-2016 | Lougaris, Vassilios; Moratto, Daniele; Baronio, Manuela; Tampella, Giacomo; van der Meer, Jos W. M; Badolato, Raffaele; Fliegauf, Manfred; Plebani, Alessandro | |
| The nested graft acts by inducing the process of de-senescence of the fibroblasts in chronic venous ulcers | 1-gen-2016 | Gualdi, Giulio; Crotti, Silvia; Monari, Paola; CALZAVARA PINTON, Piergiacomo; Vitali, Massimiliano; Baronio, Manuela; Lougaris, Vassilios |
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