Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Anna-Irma Croce"'
Autor:
Margaglione, Maria d’Apolito, Caterina Ceccarini, Rosa Savino, Iolanda Adipietro, Ighli di Bari, Rosa Santacroce, Maria Curcetti, Giovanna D’Andrea, Anna-Irma Croce, Carla Cesarano, Anna Nunzia Polito, Maurizio
Publikováno v:
Genes; Volume 14; Issue 7; Pages: 1380
Background: Essential tremor (ET) is one of the more common movement disorders. Current diagnosis is solely based on clinical findings. ET appears to be inherited in an autosomal dominant pattern. Several loci on specific chromosomes have been studie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::c5376d1ffc8782de669abf54d9f6447c
Autor:
Natascia Malerba, Patrizia Benzoni, Gabriella Maria Squeo, Raffaella Milanesi, Federica Giannetti, Lynette G. Sadleir, Gemma Poke, Bartolomeo Augello, Anna Irma Croce, Andrea Barbuti, Giuseppe Merla
Publikováno v:
Stem Cell Research, Vol 40, Iss , Pp - (2019)
GNB5 loss-of-function pathogenic variants cause IDDCA, a rare autosomal recessive human genetic disease characterized by infantile onset of intellectual disability, sinus bradycardia, hypotonia, visual abnormalities, and epilepsy. We generated human
Externí odkaz:
https://doaj.org/article/7e6ca3fb95ff4982867323666b32b676
Autor:
Anna Irma Croce, Vincenzo Giambra, Pietro Pucci, Maria Chiara Monti, Giuseppe Merla, Lucia Micale, Flora Cozzolino, Tommaso Mazza, Santina Venuto, Carmela Fusco, Diana Canetti, Paolo Malatesta, Patrizio Panelli, Gabriella Maria Squeo, Silvia Soddu, Laura Monteonofrio, Irene Appolloni
Publikováno v:
Cancer letters. 473
The faithful inheritance of chromosomes is essential for the propagation of organisms. In eukaryotes, central to this process is the mitotic spindle. Recently, we have identified TRIM8 as a gene aberrantly expressed in gliomas whose expression reduce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::166a9f8e5fc37ec939e2c65ca26efdcc
https://pubmed.ncbi.nlm.nih.gov/31904480
https://pubmed.ncbi.nlm.nih.gov/31904480
Autor:
Raffaella Milanesi, Bartolomeo Augello, Lynette G. Sadleir, Giuseppe Merla, Patrizia Benzoni, Natascia Malerba, Gabriella Maria Squeo, Andrea Barbuti, Federica Giannetti, Gemma Poke, Anna Irma Croce
Publikováno v:
Stem Cell Research, Vol 40, Iss, Pp-(2019)
GNB5 loss-of-function pathogenic variants cause IDDCA, a rare autosomal recessive human genetic disease characterized by infantile onset of intellectual disability, sinus bradycardia, hypotonia, visual abnormalities, and epilepsy. We generated human
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b95b19c76b4dc48eadfdf237c9c8d426
https://doi.org/10.1016/j.scr.2019.101547
https://doi.org/10.1016/j.scr.2019.101547
Autor:
Elvira Grandone, Anna Irma Croce, Maurizio Margaglione, Donatella Colaizzo, Gennaro Vecchione, Natale Sciannamè, Angelo Notarangelo
Publikováno v:
Thrombosis and haemostasis. 95(4)
SummaryHyperhomocysteinemia could playa similar role in the placenta to that played in adults at risk of thrombosis. Moreover, hyperhomocysteinemia in women is described to be associated with the birth of small for gestational age (SGA) newborns, alt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1be2b6ecc82ebc86eae3331ebe71057a
https://pubmed.ncbi.nlm.nih.gov/16601832
https://pubmed.ncbi.nlm.nih.gov/16601832
Publikováno v:
Prenatal Diagnosis; Mar2004, Vol. 24 Issue 3, p229-230, 2p
Publikováno v:
Prenatal diagnosis [Prenat Diagn] 2004 Mar; Vol. 24 (3), pp. 229-30.