Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Laura, Banov"'
Autor:
Erika Alboreto, Federico Pezzotta, Francesco Vinci, Andrea Calandrino, Laura Banov, Federica Mongelli, Paolo Massirio, Silvia Buratti, Andrea Moscatelli, Luca Antonio Ramenghi
Publikováno v:
Children, Vol 11, Iss 11, p 1352 (2024)
Introduction: We report the case of a neonate diagnosed with severe hemophilia A (HA) and conduct a literature review of cases of severe HA presenting at the neonatal age to help define the clinical diagnostic findings and existing differences betwee
Externí odkaz:
https://doaj.org/article/8939986b101a46409f69798383b6ec97
Autor:
Giulia MILANO, Laura Banov, Johanna Svahn, Marco Gucciardo, Fernando Marotta, Angelo Claudio Molinari
Publikováno v:
Acta Haematologica.
Successful management of surgery in severe coagulation disorders depends on adequate replacement of the deficient factors from intervention until wound healing. Extended half-life (EHL) recombinant factor IX (rFIX) has been increasingly used in hemop
Autor:
Marco Pavanello, Alessia Aiello, Maria Stella Vari, Alessandro Rimini, Paolo Moretti, Valeria Capra, Antonella Palmieri, Alice Grossi, Sara Uccella, Pasquale Striano, Silvia Pederzoli, Maja Di Rocco, Luca A. Ramenghi, Isabella Ceccherini, Thea Giacomini, Giulia Prato, Domenico Tortora, Andrea Moscatelli, Carlo Gandolfo, Paolo Picco, Francesca Minoia, Marta Bertamino, Clara Malattia, Mariasavina Severino, Laura Banov, Paola Lanteri, Marta Rusmini, Angelo Claudio Molinari, Andrea Rossi
Publikováno v:
European Journal of Paediatric Neurology. 22:725-728
Pseudoxanthoma elasticum (PXE) is a rare genetic disorder characterized by fragmented and mineralized elastic fibers in the mid-dermis of the skin, eye, digestive tract and cardiovascular system. Clinical presentation includes typical skin lesions, o
Autor:
Laura Banov, Antonella Palmieri, Marta Bertamino, Capra, Sara Uccella, Lino Nobili, Andrea Rossi, Anna Bruna Ronchetti, Alice Grossi, Luca A. Ramenghi, Mariasavina Severino, Marco Pavanello, G. Prato, Roberta Caorsi, Angelo Claudio Molinari, Andrea Moscatelli, Domenico Tortora, Giulia Amico, Francesco Caroli, Carlo Gandolfo, Maja Di Rocco, Isabella Ceccherini, Thea Giacomini, Paolo Moretti, Armando Cama, Sara Signa, Alessandro Rimini, Marta Rusmini
Publikováno v:
European Journal of Medical Genetics. 63:104030
Pediatric and perinatal stroke can present as an early symptom in undiagnosed syndromes characterized by simple Mendelian inheritance. In order to diagnose those patients affected with a monogenic disorder in which an arterial cerebrovascular event o
Autor:
Michaela Calvillo, Concetta Micalizzi, Johanna Svahn, Laura Banov, Tiziana Lanza, Elena Palmisani, Maria Scalzone, Francesca Fioredda, Maurizio Miano, Paola Terranova, Ilaria Caviglia, Carlo Dufour, Katia Perri
Publikováno v:
British Journal of Haematology. 171:247-253
Summary The management of refractory autoimmune cytopenias in childhood is challenging due to the lack of established evidence on escalating treatments. The long-term efficacy of immunosuppressive drugs was evaluated in children with refractory autoi
Publikováno v:
European Journal of Haematology. 93:21-25
Haemophilia is an X-linked recessive genetic disease of haemostasis. Women carriers may present with a bleeding tendency similar to milder forms of the disease. Haemophilic newborns present risk factors and patterns of bleeding that are challenging.
Autor:
Concetta Micalizzi, Michaela Calvillo, Rosanna Parasole, Laura Banov, Federica Gallicola, Vincenzo Poggi, Maurizio Miano, Francesca Fioredda, Alain Fischer, Angelo Claudio Molinari, Fara Petruzziello, Carlo Dufour, Giovanni Montobbio, Johanna Svahn
Publikováno v:
Journal of Pediatric Hematology/Oncology. 36:e145-e148
A 9-month-old boy with life-threatening multiresistant pure red cell anemia/autoimmune hemolytic anemia within the frame of a possible, undiagnosed immune-mediated disease was initially treated with prednisone. Further-line therapies of the following
Autor:
Laura Banov, Margherita Mancardi, Giovanni Morana, Antonella Palmieri, Salvatore Renna, Martina Finetti, Marta Bertamino
Publikováno v:
Open Journal of Emergency Medicine. :62-66
To analyze how the multidisciplinary clinical, biohumoral, instrumental approach to ALTE (Apparent Life Threatening Event) episode may discover cardiovascular disease in the newborn. Introduction: In the first year of life ALTEs concern 0.8% of acces
Publikováno v:
SickKids Handbook of Pediatric Thrombosis and Hemostasis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6b43aae7520fe6940c182b6ba896d8f
https://doi.org/10.1159/000446741
https://doi.org/10.1159/000446741
Autor:
Maura Faraci, Patrizia Comoli, Laura Banov, Edoardo Lanino, Annarosa Soresina, Daniela Di Martino, Franco Locatelli, Giuseppe Morreale, Alessandro Plebani, Concetta Micalizzi
Publikováno v:
Pediatric Transplantation. 13:785-789
Cernunnos-XLF deficiency is a rare CI characterized by a defective DNA DSB repair mechanism. Its clinical manifestations are growth retardation, dysmorphic features, malformations, and severe B- and T-cell lymphopenia. BM failure may complicate the c