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8 results for Akbaroghli,+Susan

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ArticlesPeer ReviewedFull Text
Identifying serious underlying diagnoses among patients with brief resolved unexplained events (BRUEs): a Canadian cohort study
Author / Creator:Nama, Nassr ; Lee, Zerlyn ; Picco, Kara ; Jin, Falla ; Bone, Jeffrey N ; Quet, Julie ; Foulds, Jessica ; Gagnon, Josée Anne ; Novak, Chris ; Parisien, Brigitte ; Donlan, Matthew ; Goldman, Ran D ; Sehgal, Anupam ; Kanani, Ronik ; Holland, Joanna ; Kyrychenko, Polina ; Kirolos, Nardin ; Opotchanova, Ioulia ; Harnois, Émilie ; Schacter, Alyse ; Frizon-Peresa, Elisa ; Rajasegaran, Praveen ; Hosseini, Parnian ; Wyslobicky, Melody ; Akbaroghli, Susan ; Nalan, Prathiksha ; Mahant, Sanjay ; Tieder, Joel ; Gill, Peter ; Goupil, Marie-Pier ; Lee, Shawn ; Philibert, Emy ; Dufresne, Juliette ; Chawla, Raman ; Ogwuru, Martin
Publisher:England: BMJ Publishing Group Ltd
Journal title:BMJ paediatrics open, 2024-09, Vol.8 (1), p.e002525
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Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies
Author / Creator:Mohammadzadeh, Akbar ; Akbaroghli, Susan ; Aghaei-Moghadam, Ehsan ; Mahdieh, Nejat ; Badv, Reza Shervin ; Jamali, Payman ; Kariminejad, Roxana ; Chavoshzadeh, Zahra ; Ghasemi Firouzabadi, Saghar ; Mansour Ghanaie, Roxana ; Nozari, Ahoura ; Banihashemi, Sussan ; Hadipour, Fatemeh ; Hadipour, Zahra ; Kariminejad, Ariana ; Najmabadi, Hossein ; Shafeghati, Yousef ; Behjati, Farkhondeh
Publisher:Iran: Royan Institute of Iran
Journal title:Cell journal (Yakhteh), 2019-10, Vol.21 (3), p.337-349
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Association of empiric antibiotic selection and clinical outcomes in hospitalised children with severe orbital infections: a retrospective cohort study
Author / Creator:Krueger, Carsten ; Nguyen, Emily Lan-Vy ; Mahant, Sanjay ; Borkhoff, Cornelia M ; Cichon, Jessica ; Drouin, Olivier ; Pound, Catherine ; Quet, Julie ; Wahi, Gita ; Bayliss, Ann ; Vomiero, Gemma ; Foulds, Jessica ; Kanani, Ronik ; Sakran, Mahmoud ; Sehgal, Anupam ; Pullenayegum, Eleanor ; Widjaja, Elysa ; Reginald, Arun ; Wolter, Nikolaus ; Parkin, Patricia ; Gill, Peter J ; Oni, Semipe ; Anwar, Rashid ; Arafeh, Dana ; Chan, Carol ; Begum, Nurshad ; Louriachi, Hossam ; Bédard-Gauthier, Camille ; Ge, Yipeng ; Kirolos, Nardin ; Patel, Ashaka ; Jasani, Hardika ; Kornelsen, Emily ; Razvi, Yasmeen ; Chugh, Ashton ; Genereux, Olivia ; Sharma, Jovey ; Cooper, Jessica ; Czuczman, Natalie ; Ghadiry-Tavi, Rouzbeh ; Gouda, Sandra ; Akbaroghli, Susan ; McKerlie, Morgyn ; Warren, Jack ; Kozlowski, Natascha
Publisher:England: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health
Journal title:Archives of disease in childhood, 2024-11, Vol.109 (11), p.932-940
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Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica
Author / Creator:Kariminejad, Ariana ; Afroozan, Fariba ; Bozorgmehr, Bita ; Ghanadan, Alireza ; Akbaroghli, Susan ; Khorram Khorshid, Hamid ; Mojahedi, Faezeh ; Setoodeh, Aria ; Loh, Abigail ; Tan, Yu ; Escande-Beillard, Nathalie ; Malfait, Fransiska ; Reversade, Bruno ; Gardeitchik, Thatjana ; Morava, Eva
Publisher:Switzerland: MDPI
Journal title:International journal of molecular sciences, 2017-03, Vol.18 (3), p.635-635
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45 Variation in the Management of Hospitalized Children with Orbital Cellulitis over Ten Years
Author / Creator:Nguyen, Emily ; Mahant, Sanjay ; Cichon, Jessica ; Drouin, Olivier ; Pound, Catherine ; Quet, Julie ; Wahi, Gita ; Bayliss, Ann ; Vomiero, Gemma ; Foulds, Jessica L ; Kanani, Ronik ; Sakran, Mahmoud ; Sehgal, Anupam ; Borkhoff, Cornelia M ; Pullenayegum, Eleanor ; Widjaja, Elysa ; Reginald, Arun ; Wolter, Nikolaus E ; Oni, Semipe ; Anwar, Rashid ; Louriachi, Hossam ; Ge, Yipeng ; Kirolos, Nardin ; Patel, Ashaka ; Jasani, Hardika ; Kornelsen, Emily ; Chugh, Ashton ; Gouda, Sandra ; Akbaroghli, Susan ; McKerlie, Morgyn ; Parkin, Patricia C ; Gill, Peter J ; Hersi, Leo
Publisher:Oakville: Oxford University Press
Journal title:Paediatrics & child health, 2023-09, Vol.28 (Supplement_1), p.e20-e20
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Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas
Author / Creator:Akbaroghli, Susan ; Balali, Maryam ; Kamalidehghan, Behnam ; Saber, Siamak ; Aryani, Omid ; Yong Meng, Goh ; Houshmand, Massoud
Publisher:New Zealand: Dove Medical Press Limited
Journal title:Therapeutics and clinical risk management, 2017-01, Vol.13, p.15-19
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Profile of Iranian GJB2 Mutations in Young Population with Novel Mutation
Author / Creator:Falah, Masoumeh ; Houshmand, Massoud ; Akbaroghli, Susan ; Mahmodian, Saeid ; Ghavami, Yaser ; Farhadi, Mohammad
Publisher:Mashhad: Mashhad University of Medical Sciences
Journal title:Iranian journal of basic medical sciences, 2011-05, Vol.14 (3), p.213
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Profile of Iranian GJB2 Mutations in Young Population with Novel Mutation Profile of Iranian GJB2 Mutations in Young Population with Novel Mutation
Author / Creator:Masoumeh Falah ; Massoud Houshmand ; Susan Akbaroghli ; Saeid Mahmodian ; Yaser Ghavami ; Mohammad Farhadi
Publisher:Mashhad University of Medical Sciences
Journal title:Iranian journal of basic medical sciences, 2011-05, Vol.14 (50)
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Identifying serious underlying diagnoses among patients with brief resolved unexplained events (BRUEs): a Canadian cohort study

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Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies

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Association of empiric antibiotic selection and clinical outcomes in hospitalised children with severe orbital infections: a retrospective cohort study

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Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica

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45 Variation in the Management of Hospitalized Children with Orbital Cellulitis over Ten Years

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Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas

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Profile of Iranian GJB2 Mutations in Young Population with Novel Mutation

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Profile of Iranian GJB2 Mutations in Young Population with Novel Mutation Profile of Iranian GJB2 Mutations in Young Population with Novel Mutation

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