Zobrazeno 1 - 10
of 36
pro vyhledávání: '"L. Gaetaniello"'
Autor:
Mariacarolina Salerno, Claudio Pignata, L. Gaetaniello, E. Matrecano, Alfonso junior Apicella, Matilde Valeria Ursini, Raffaele Ambrosio
Publikováno v:
Clinical and Experimental Immunology. 129:502-509
SUMMARY Severe combined immunodeficiency (SCID) is a heterogeneous group of disorders characterized by defect of T- and B-cell immunity. In many cases of autosomal recessive SCID, thus far described, the molecular alteration involves genes encoding f
Autor:
G. Arrigo, Luigi Racioppi, Matilde Valeria Ursini, Eliana Matrecano, L. Gaetaniello, E. Del Giudice, Claudio Pignata, E. Cosentini
Publikováno v:
Neuropediatrics. 31:265-268
In this study we report on a patient affected by a brain migration disorder and a T-cell activation deficiency presumably inherited as an autosomal recessive trait. The immunological evaluation revealed that the mitogen stimulation failed to induce a
Autor:
Raffaele Iorio, Claudio Pignata, L. Gaetaniello, Michele Fiore, G Palmese, C De Felice, Rosario Ammendola, M. Sommantico, Angela Vegnente, Barbara Balestrieri
Publikováno v:
Journal of Clinical Gastroenterology. 26:187-192
Liver disease may be found in patients with primary immunodeficiency syndromes because of the high risk of infection with hepatotropic viruses related to the treatment with blood derivatives. The prevalence of liver disease in these patients and its
Autor:
Anna Maria Masci, Eliana Matrecano, Luigi Racioppi, L. Gaetaniello, Claudio Pignata, Angela M. Christiano, Jorge Frank
Publikováno v:
Blood. 97(4)
Human Nude/SCID (severe combined immunodeficiency) is the first severe combined immunodeficiency caused by mutation of the winged–helix–nude (WHN) gene, which is expressed in the thymus but not in the hematopoietic lineage. The disease is charact
Autor:
Donatella Mattia, E. Cosentini, Jonathan S. Duke-Cohan, Claudio Pignata, Stuart F. Schlossman, Baldassarre Martire, L. Gaetaniello, Barbara Balestrieri, N. Pozzi
SUMMARYThe proliferative responses of T lymphocytes of a subset of patients with CVID are abnormally low. This may be due to abnormalities in extracellular interactions or signalling defects downstream from membrane-associated receptors. Demonstratin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7df71e88d36eacf425ee6be56b55b4bd
http://hdl.handle.net/11588/459469
http://hdl.handle.net/11588/459469
Autor:
Ennio Toscano, R. Della Casa, Claudio Pignata, Sek Mardy, L. Gaetaniello, Yasuhiro Indo, Generoso Andria, F. Sadile
Congenital insensitivity to pain with anhidrosis (CIPA), a rare autosomal recessive disorder, is characterized by insensitivity to pain, self-mutilating behaviour, anhidrosis and recurrent hyperpyrexia. It is a hereditary sensory and autonomic neurop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2141288f45ce30d4f799ece8ce54375
http://hdl.handle.net/11588/332711
http://hdl.handle.net/11588/332711
Publikováno v:
Hepatology (Baltimore, Md.). 27(4)
Dipeptidyl peptidase IV (CD26/DPP-IV) is an ectoenzyme expressed on different cell types. Signaling properties and functional consequences of the CD26 triggering have been elucidated mostly on T cells, where the molecule delivers a costimulatory sign
Autor:
Immacolata Scotese, Angela Vegnente, Raffaele Iorio, Claudio Pignata, Michele Fiore, L. Gaetaniello, S Guida
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 24(3)
Chronic hepatitis B (CHB) virus infection is associated with functional abnormalities of cell-mediated immunity, defective interferons alpha and gamma synthesis, and interleukin-2 receptor expression. In this study, interleukin-2 (IL-2) production an
Autor:
L Gaetaniello
Publikováno v:
Molecular Immunology. 35:754