Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Giuseppe A. Latino"'
Autor:
Alexandra Kilian, Giuseppe A. Latino, Andrew J. White, Felix Ratjen, Jamie McDonald, Kevin J. Whitehead, James R. Gossage, Timo Krings, Michael T. Lawton, Helen Kim, Marie E. Faughnan, The Brain Vascular Malformation Consortium HHT Investigator Group
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 23, p 7462 (2023)
We are grateful to Eker et al. for their thoughtful analysis and response to our publication titled Comparing Characteristics and Treatment of Brain Vascular Malformations in Children and Adults with HHT [...]
Externí odkaz:
https://doaj.org/article/b20126dd449b44a389714c9e399fb60a
Autor:
Alexandra Kilian, Giuseppe A. Latino, Andrew J. White, Felix Ratjen, Jamie McDonald, Kevin J. Whitehead, James R. Gossage, Timo Krings, Michael T. Lawton, Helen Kim, Marie E. Faughnan, The Brain Vascular Malformation Consortium HHT Investigator Group
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 7, p 2704 (2023)
Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant disease characterized by the development of vascular malformations (VMs) in organs such as the brain and lungs, as well as telangiectases on mucosal surfaces. Prophylactic treat
Externí odkaz:
https://doaj.org/article/d2f458cc6dda4b458980b047e2794bd0
Autor:
Alexandra Kilian, Giuseppe A. Latino, Andrew J. White, Dewi Clark, Murali M. Chakinala, Felix Ratjen, Jamie McDonald, Kevin J. Whitehead, James R. Gossage, Doris Lin, Katharine Henderson, Jeffrey Pollak, Justin P. McWilliams, Helen Kim, Michael T. Lawton, Marie E. Faughnan, the Brain Vascular Malformation Consortium HHT Investigator Group
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 9, p 2714 (2020)
Hereditary hemorrhagic telangiectasia (HHT), a rare autosomal dominant disease mostly caused by mutations in three known genes (ENG, ACVRL1, and SMAD4), is characterized by the development of vascular malformations (VMs). Patients with HHT may presen
Externí odkaz:
https://doaj.org/article/dabf32e373b84789909bd081fbf8fe9d
Autor:
Group, Alexandra Kilian, Giuseppe A. Latino, Andrew J. White, Felix Ratjen, Jamie McDonald, Kevin J. Whitehead, James R. Gossage, Timo Krings, Michael T. Lawton, Helen Kim, Marie E. Faughnan, The Brain Vascular Malformation Consortium HHT Investigator Group The Brain Vascular Malformation Consortium HHT Investigator
Publikováno v:
Journal of Clinical Medicine; Volume 12; Issue 7; Pages: 2704
Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant disease characterized by the development of vascular malformations (VMs) in organs such as the brain and lungs, as well as telangiectases on mucosal surfaces. Prophylactic treat
Autor:
Dinesh R. Apala, Vivek N. Iyer, Vikram Prabhudesai, Carl Chartrand-Lefebvre, Véronique Cyr, Marie E. Faughnan, Giuseppe A. Latino, Vitor Nagai Yamaki, Rose Pantalone, Ahmad Parvinian, Waleed Brinjikji, Andreanne Gauthier
Publikováno v:
Journal of Vascular and Interventional Radiology. 30:1982-1987
Purpose To determine the yield of rescreening adult hereditary hemorrhagic telangiectasia (HHT) patients with initial negative screening CT for pulmonary arteriovenous malformations (PAVMs). Materials and Methods Patients with a definite diagnosis of
Publikováno v:
Paediatr Child Health
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa5baf8fd205cdcf5fd140cbe745e3d5
https://europepmc.org/articles/PMC8448499/
https://europepmc.org/articles/PMC8448499/
Autor:
Jeffrey Pollak, Felix Ratjen, Alexandra Kilian, Marie E. Faughnan, Doris D. M. Lin, Jamie McDonald, James R. Gossage, Giuseppe A. Latino, Murali M. Chakinala, Dewi Clark, Kevin J. Whitehead, Justin P. McWilliams, Katharine J. Henderson, Michael T. Lawton, Helen Kim, Andrew J. White
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 2714, p 2714 (2020)
Journal of Clinical Medicine
Volume 9
Issue 9
Journal of Clinical Medicine
Volume 9
Issue 9
Hereditary hemorrhagic telangiectasia (HHT), a rare autosomal dominant disease mostly caused by mutations in three known genes (ENG, ACVRL1, and SMAD4), is characterized by the development of vascular malformations (VMs). Patients with HHT may presen
Publikováno v:
Pediatric Neurology. 49:445-450
Background Hereditary hemorrhagic telangiectasia is an autosomal dominant genetic disease with a wide array of vascular malformations involving multiple organs. Brain arteriovenous malformations can lead to intracranial hemorrhage and are often diagn
Autor:
Giuseppe A. Latino, Nita Chahal, Mallory L. Downie, Cedric Manlhiot, Tanveer H. Collins, Rae S. M. Yeung, Brian W. McCrindle
Publikováno v:
The Journal of pediatrics. 179
To characterize the pattern of temperature response to intravenous immunoglobulin (IVIG) infusion in patients with Kawasaki disease (KD).Patients nonresponsive to IVIG (axillary temperature ≥37.5°C24 hours after end of IVIG) were identified. Each
Publikováno v:
The Journal of Pediatrics. 165:197-199
The diagnostic yield of rescreening children with hereditary hemorrhagic telangiectasia at regular intervals for arteriovenous malformations is unclear. Here, we show that when children with initially negative screening were reassessed after 5 years,