Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Susan Akbaroghli"'
Autor:
Sanjay Mahant, Nassr Nama, Ronik Kanani, Jessica Foulds, Julie Quet, Anupam Sehgal, Ran D Goldman, Jeffrey N Bone, Peter Gill, Martin Ogwuru, Parnian Hosseini, Zerlyn Lee, Kara Picco, Josée Anne Gagnon, Joanna Holland, Falla Jin, Nardin Kirolos, Susan Akbaroghli, Chris Novak, Brigitte Parisien, Matthew Donlan, Polina Kyrychenko, Ioulia Opotchanova, Émilie Harnois, Alyse Schacter, Elisa Frizon-Peresa, Praveen Rajasegaran, Melody Wyslobicky, Prathiksha Nalan, Joel Tieder, Marie-Pier Goupil, Shawn Lee, Emy Philibert, Juliette Dufresne, Raman Chawla
Publikováno v:
BMJ Paediatrics Open, Vol 8, Iss 1 (2024)
Objective To describe the demographics and clinical outcomes of infants with brief resolved unexplained events (BRUE).Design A retrospective cohort study.Setting 11 centres within the Canadian Paediatric Inpatient Research Network.Patients Patients p
Externí odkaz:
https://doaj.org/article/6a32db2c8689448fb6c422d8eb1d73c8
Autor:
Akbar Mohammadzadeh, Susan Akbaroghli, Ehsan Aghaei-Moghadam, Nejat Mahdieh, Reza Shervin Badv, Payman Jamali, Roxana Kariminejad, Zahra Chavoshzadeh, Saghar Ghasemi Firouzabadi, Roxana Mansour Ghanaie, Ahoura Nozari, Sussan Banihashemi, Fatemeh Hadipour, Zahra Hadipour, Ariana Kariminejad, Hossein Najmabadi, Yousef Shafeghati, Farkhondeh Behjati
Publikováno v:
Cell Journal, Vol 21, Iss 3, Pp 337-349 (2019)
Objective: Major birth defects are inborn structural or functional anomalies with long-term disability and adverse impacts on individuals, families, health-care systems, and societies. Approximately 20% of birth defects are due to chromosomal and g
Externí odkaz:
https://doaj.org/article/7f76be7241904573b1cdae79e809ff61
Autor:
Ariana Kariminejad, Fariba Afroozan, Bita Bozorgmehr, Alireza Ghanadan, Susan Akbaroghli, Hamid Reza Khorram Khorshid, Faezeh Mojahedi, Aria Setoodeh, Abigail Loh, Yu Xuan Tan, Nathalie Escande-Beillard, Fransiska Malfait, Bruno Reversade, Thatjana Gardeitchik, Eva Morava
Publikováno v:
International Journal of Molecular Sciences, Vol 18, Iss 3, p 635 (2017)
Cutis laxa is a heterogeneous condition characterized by redundant, sagging, inelastic, and wrinkled skin. The inherited forms of this disease are rare and can have autosomal dominant, autosomal recessive, or X-linked inheritance. Three of the autoso
Externí odkaz:
https://doaj.org/article/4c166db2fb024c9bbcbc1fe5b7799b2c
Autor:
Masoumeh Falah, Massoud Houshmand, Susan Akbaroghli, Saeid Mahmodian, Yaser Ghavami, Mohammad Farhadi
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 14, Iss 50 (2011)
AbstractObjective(s)Despite the enormous heterogeneity of genetic hearing loss, most non-syndromic hearing losses are caused by mutations in the GJB2 gene. We aimed to characterize the mutation profiles of 100 Iranian deaf patients that were under 10
Externí odkaz:
https://doaj.org/article/946f42ea073144c891b6abdd19631e87
Autor:
Emily Lan-Vy Nguyen, Leo Hersi, Sanjay Mahant, Jessica Cichon, Olivier Drouin, Catherine Pound, Julie Quet, Gita Wahi, Ann Bayliss, Gemma Vomiero, Jessica L. Foulds, Ronik Kanani, Mahmoud Sakran, Anupam Sehgal, Cornelia M. Borkhoff, Eleanor Pullenayegum, Elysa Widjaja, Arun Reginald, Nikolaus E. Wolter, Semipe Oni, Rashid Anwar, Hossam Louriachi, Yipeng Ge, Nardin Kirolos, Ashaka Patel, Hardika Jasani, Emily Kornelsen, Ashton Chugh, Sandra Gouda, Susan Akbaroghli, Morgyn McKerlie, Patricia C. Parkin, Peter J. Gill
Publikováno v:
Hospital Pediatrics. 13:375-391
OBJECTIVES No previous study has examined the management of hospitalized children with orbital cellulitis at both children’s and community hospitals across multiple sites in Canada. We describe variation and trends over time in diagnostic testing a
Autor:
Peter J. Gill, Olivier Drouin, Catherine Pound, Julie Quet, Gita Wahi, Ann Bayliss, Gemma Vomiero, Jessica Foulds, Ronik Kanani, Mahmoud Sakran, Anupam Sehgal, Eleanor Pullenayegum, Elysa Widjaja, Arun Reginald, Nikolaus E. Wolter, Semipe Oni, Rashid Anwar, Jessica Cichon, Hossam Louriachi, Yipeng Ge, Nardin Kirolos, Ashaka Patel, Hardika Jasani, Emily Kornelsen, Ashton Chugh, Sandra Gouda, Susan Akbaroghli, Morgyn McKerlie, Patricia C. Parkin, Sanjay Mahant
Publikováno v:
The Journal of pediatrics. 248
To evaluate risk factors associated with surgical intervention and subperiosteal/orbital abscess in hospitalized children with severe orbital infections.We conducted a multicenter cohort study of children 2 months to 18 years hospitalized with perior
Autor:
Susan, Akbaroghli, Daniz, Kooshavar, Zahra, Golchehre, Arezou, Karamzade, Mohammad, Saberi, Mohammad Reza, Alaei, Masoud, Abbasi Sadegh, Mostafa, Asadollahi, Mohammad, Keramatipour
Publikováno v:
Iranian journal of child neurology. 16(1)
Bardet-Biedl syndrome (BBS) is an autosomal recessive pleiotropic ciliopathy, which includes multi-organ clinical manifestations. The known genes involved in the development of the disease account for the causality in about 80% of the examined cases.
Autor:
Ivan Ivanovski, Raoul C.M. Hennekam, Valeria Polizzi, Mahboubeh Mansouri, Livia Garavelli, Marzia Pollazzon, Marielle Alders, Zahra Chavoshzadeh, Susan Akbaroghli, Simonetta Rosato, Stefano Giuseppe Caraffi, Giancarlo Gargano, Chiara Gelmini
Publikováno v:
American journal of medical genetics. Part A, 176(5), 1166-1174. Wiley-Liss Inc.
Biallelic variants in FAT4 are associated with the two disorders, Van Maldergem syndrome (VMS) (n = 11) and Hennekam syndrome (HS) (n= 40). Both conditions are characterized by a typical facial gestalt and mild to moderate intellectual disability, bu
Autor:
Siamak Saber, Behnam Kamalidehghan, Massoud Houshmand, Goh Yong Meng, Omid Aryani, Susan Akbaroghli, Maryam Balali
Publikováno v:
Therapeutics and Clinical Risk Management
Susan Akbaroghli,1,* Maryam Balali,2,* Behnam Kamalidehghan,3,4 Siamak Saber,4 Omid Aryani,5 Goh Yong Meng,6 Massoud Houshmand4 1Mofid Children’s Hospital, Shahid Beheshti University of Medical Sciences, 2ENT and Head & Neck Research Center and Dep
Publikováno v:
Clinical dysmorphology. 27(3)