Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ujwal Kariholu"'
Autor:
Omer F. Eker, Edoardo Boccardi, Ulrich Sure, Maneesh C. Patel, Saverio Alicante, Ali Alsafi, Nicola Coote, Freya Droege, Olivier Dupuis, Annette Dam Fialla, Bryony Jones, Ujwal Kariholu, Anette D. Kjeldsen, David Lefroy, Gennaro M. Lenato, Hans Jurgen Mager, Guido Manfredi, Troels H. Nielsen, Fabio Pagella, Marco C. Post, Catherine Rennie, Carlo Sabbà, Patrizia Suppressa, Pernille M. Toerring, Sara Ugolini, Elisabetta Buscarini, Sophie Dupuis-Girod, Claire L. Shovlin
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Abstract Hereditary haemorrhagic telangiectasia (HHT) is a multisystemic vascular dysplasia inherited as an autosomal dominant trait. Approximately 10 % of patients have cerebral vascular malformations, a proportion being cerebral arteriovenous malfo
Externí odkaz:
https://doaj.org/article/a9d04b977e8b45be8e4d3ae5ea739381
Autor:
Fabio Pagella, Annette Dam Fialla, E. Boccardi, Sara Ugolini, Saverio Alicante, Claire L. Shovlin, David C. Lefroy, Bryony A Jones, Freya Droege, O Dupuis, Pernille Mathiesen Toerring, Ujwal Kariholu, Maneesh C. Patel, Ali Alsafi, Catherine Rennie, Sophie Dupuis-Girod, Anette Drøhse Kjeldsen, Ulrich Sure, Carlo Sabbà, G Manfredi, Gennaro M. Lenato, T H Nielsen, N. Coote, Hans Jurgen Mager, Marco C. Post, E. Buscarini, O F Eker, Patrizia Suppressa
Publikováno v:
Shovlin, C L, Buscarini, E, Sabbà, C, Mager, H J, Kjeldsen, A D, Pagella, F, Sure, U, Ugolini, S, Torring, P M, Suppressa, P, Rennie, C, Post, M C, Patel, M C, Nielsen, T H, Manfredi, G, Lenato, G M, Lefroy, D, Kariholu, U, Jones, B, Fialla, A D, Eker, O F, Dupuis, O, Droege, F, Coote, N, Boccardi, E, Alsafi, A, Alicante, S & Dupuis-Girod, S 2022, ' The European Rare Disease Network for HHT Frameworks for management of hereditary haemorrhagic telangiectasia in general and speciality care ', European Journal of Medical Genetics, vol. 65, no. 1, 104370 . https://doi.org/10.1016/j.ejmg.2021.104370
Hereditary haemorrhagic telangiectasia (HHT) is a complex, multisystemic vascular dysplasia affecting approximately 85,000 European Citizens. In 2016, eight founding centres operating within 6 countries, set up a working group dedicated to HHT within
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b55e3ae4507a240bfd0ea2895fe43ef
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85120636967
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85120636967
Autor:
Niha Peshimam, Hani Farah, Richard Caswell, Sian Ellard, Wajanat Jan, Alistair D. Calder, Jan Cobben, Ujwal Kariholu, Harry G. Leitch
Publikováno v:
European journal of medical genetics. 65(8)
Sedaghatian type spondylometaphyseal dysplasia (SSMD) is a rare skeletal dysplasia with only 24 reported cases to date. Despite the limited literature available, evidence suggests this is a multi-system disorder, with neurological and cardiovascular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e89856ec3f6fcfb5becc4a5ae1ad3152
https://pubmed.ncbi.nlm.nih.gov/35718083
https://pubmed.ncbi.nlm.nih.gov/35718083
Autor:
Seetha Shankaran, Natasha Liow, Russell Pryce, Paolo Montaldo, Aung Soe, Justinas Teiserskas, Theodora Markati, Vânia Oliveira, Ujwal Kariholu, Sudhin Thayyil, Peter J Lally
Publikováno v:
Archives of Disease in Childhood - Fetal and Neonatal Edition. 105:225-228
ObjectivesTo examine if therapeutic hypothermia reduces the composite outcome of death, moderate or severe disability at 18 months or more after mild neonatal encephalopathy (NE).Data sourceMEDLINE, Cochrane database, Scopus and ISI Web of Knowledge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee96cd27232509a0719ea2c5948d4f70
https://doi.org/10.1136/archdischild-2018-315711
https://doi.org/10.1136/archdischild-2018-315711
Autor:
Catherine Rennie, Olivier Dupuis, Maneesh C. Patel, Ali Alsafi, Sophie Dupuis-Girod, Pernille Mathiesen Toerring, Troels Halfeld Nielsen, Sara Ugolini, Marco C. Post, Edoardo Boccardi, Nicola Coote, Ulrich Sure, Omer Eker, Hans Jurgen Mager, Elisabetta Buscarini, Patrizia Suppressa, Anette Drøhse Kjeldsen, Ujwal Kariholu, David C. Lefroy, Carlo Sabbà, Guido Manfredi, Bryony A Jones, Claire L. Shovlin, Gennaro M. Lenato, Saverio Alicante, Fabio Pagella, Annette Dam Fialla, Freya Droege
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Eker, O F, Boccardi, E, Sure, U, Patel, M C, Alicante, S, Alsafi, A, Coote, N, Droege, F, Dupuis, O, Fialla, A D, Jones, B, Kariholu, U, Kjeldsen, A D, Lefroy, D, Lenato, G M, Mager, H J, Manfredi, G, Nielsen, T H, Pagella, F, Post, M C, Rennie, C, Sabbà, C, Suppressa, P, Toerring, P M, Ugolini, S, Buscarini, E, Dupuis-Girod, S & Shovlin, C L 2020, ' European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT) ', Orphanet Journal of Rare Diseases, vol. 15, 165 . https://doi.org/10.1186/s13023-020-01386-9
Orphanet Journal of Rare Diseases
Eker, O F, Boccardi, E, Sure, U, Patel, M C, Alicante, S, Alsafi, A, Coote, N, Droege, F, Dupuis, O, Fialla, A D, Jones, B, Kariholu, U, Kjeldsen, A D, Lefroy, D, Lenato, G M, Mager, H J, Manfredi, G, Nielsen, T H, Pagella, F, Post, M C, Rennie, C, Sabbà, C, Suppressa, P, Toerring, P M, Ugolini, S, Buscarini, E, Dupuis-Girod, S & Shovlin, C L 2020, ' European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT) ', Orphanet Journal of Rare Diseases, vol. 15, 165 . https://doi.org/10.1186/s13023-020-01386-9
Orphanet Journal of Rare Diseases
Hereditary haemorrhagic telangiectasia (HHT) is a multisystemic vascular dysplasia inherited as an autosomal dominant trait. Approximately 10 % of patients have cerebral vascular malformations, a proportion being cerebral arteriovenous malformations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aca034858370fdedd18b6da6f7744c90
http://hdl.handle.net/10044/1/78918
http://hdl.handle.net/10044/1/78918
Autor:
Paolo, Montaldo, Peter J, Lally, Vânia, Oliveira, Ravi, Swamy, Josephine, Mendoza, Gaurav, Atreja, Ujwal, Kariholu, Vijayakumar, Shivamurthappa, Natasha, Liow, Justinas, Teiserskas, Russell, Pryce, Aung, Soe, Seetha, Shankaran, Sudhin, Thayyil
Publikováno v:
Archives of Disease in Childhood. Fetal and Neonatal Edition
Objective To examine the effect of therapeutic hypothermia on MR biomarkers and neurodevelopmental outcomes in babies with mild hypoxic-ischaemic encephalopathy (HIE). Design Non-randomised cohort study. Setting Eight tertiary neonatal units in the U
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ca6c0ef659c6df8a58b03ff830dad8c3
https://pubmed.ncbi.nlm.nih.gov/30425113
https://pubmed.ncbi.nlm.nih.gov/30425113
Autor:
Ujwal Kariholu
Publikováno v:
Academic Journal of Pediatrics & Neonatology. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21cd534cf67313cdd735fd74c310d374
https://doi.org/10.19080/ajpn.2018.06.555755
https://doi.org/10.19080/ajpn.2018.06.555755
Autor:
Ujwal Kariholu
Publikováno v:
Academic Journal of Pediatrics & Neonatology. 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cad16434d4ab8008cf74bab135f1e6d
https://doi.org/10.19080/ajpn.2016.01.555574
https://doi.org/10.19080/ajpn.2016.01.555574
Autor:
Ezam Mat-Ali, Ujwal Kariholu, Merran Thomson, Michele Cruwys, Richa Ajitsaria, Nour Elhadi, Alexandra Mancini, Sunit Godambe
Publikováno v:
European Journal of Pediatrics. 171:921-926
In spite of recent advances in perinatal care and an increase in survival of extremely preterm infants over the last few years, there remains a lack of consensus about practical aspects of resuscitation of extremely preterm infants born before 27 wee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5471374955b805a0b862371d0885d88
https://doi.org/10.1007/s00431-011-1647-7
https://doi.org/10.1007/s00431-011-1647-7
Publikováno v:
Archives of disease in childhood. 94(4)
We report the case of a 12-year-old girl who was managed as an asthma patient since infancy but was later found to have a tracheal web. Born at 31 weeks by caesarean section for maternal prolonged rupture of membranes and oligohydramnios, the patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::752f3ed6c035ea72db1650c136186def
https://pubmed.ncbi.nlm.nih.gov/19307201
https://pubmed.ncbi.nlm.nih.gov/19307201