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Susan Akbaroghli

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International Journal of Endocrinology and Metabolism|January 27, 2017
A Case Series: Congenital HyperinsulinismMohammad Reza Alaei, Susan Akbaroghli, Mohammad Keramatipour, et al.
Therapeutics and Clinical Risk Management|January 6, 2017
Identification of a new mutation in an Iranian family with hereditary multiple osteochondromasSusan Akbaroghli, Maryam Balali, Behnam Kamalidehghan, et al.
Iranian Journal of Child Neurology|February 28, 2022
Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous familiesSusan Akbaroghli, Daniz Kooshavar, Zahra Golchehre, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypesIvan Ivanovski, Susan Akbaroghli, Marzia Pollazzon, et al.
International Journal of Molecular Sciences|March 16, 2017
Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma OsteoplasticaAriana Kariminejad, Fariba Afroozan, Bita Bozorgmehr, et al.
Cell Journal|June 19, 2019
Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital AnomaliesAkbar Mohammadzadeh, Susan Akbaroghli, Ehsan Aghaei-Moghadam, et al.
The Journal of Pediatrics|May 14, 2022
Factors Associated with Surgery and Imaging Characteristics in Severe Orbital InfectionsPeter J Gill, Olivier Drouin, Catherine Pound, et al.
BMJ Paediatrics Open|September 24, 2024
Identifying serious underlying diagnoses among patients with brief resolved unexplained events (BRUEs): a Canadian cohort studyNassr Nama, Zerlyn Lee, Kara Picco, et al.
Hospital Pediatrics|April 30, 2023
Variation in the Management of Hospitalized Children With Orbital Cellulitis Over 10 YearsEmily Lan-Vy Nguyen, Leo Hersi, Sanjay Mahant, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
International Journal of Endocrinology and Metabolism|January 27, 2017
A Case Series: Congenital HyperinsulinismMohammad Reza Alaei, Susan Akbaroghli, Mohammad Keramatipour, et al.
Therapeutics and Clinical Risk Management|January 6, 2017
Identification of a new mutation in an Iranian family with hereditary multiple osteochondromasSusan Akbaroghli, Maryam Balali, Behnam Kamalidehghan, et al.
Iranian Journal of Child Neurology|February 28, 2022
Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous familiesSusan Akbaroghli, Daniz Kooshavar, Zahra Golchehre, et al.
American Journal of Medical Genetics. Part A|April 23, 2018
Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypesIvan Ivanovski, Susan Akbaroghli, Marzia Pollazzon, et al.
International Journal of Molecular Sciences|March 16, 2017
Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma OsteoplasticaAriana Kariminejad, Fariba Afroozan, Bita Bozorgmehr, et al.
Cell Journal|June 19, 2019
Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital AnomaliesAkbar Mohammadzadeh, Susan Akbaroghli, Ehsan Aghaei-Moghadam, et al.
The Journal of Pediatrics|May 14, 2022
Factors Associated with Surgery and Imaging Characteristics in Severe Orbital InfectionsPeter J Gill, Olivier Drouin, Catherine Pound, et al.
BMJ Paediatrics Open|September 24, 2024
Identifying serious underlying diagnoses among patients with brief resolved unexplained events (BRUEs): a Canadian cohort studyNassr Nama, Zerlyn Lee, Kara Picco, et al.
Hospital Pediatrics|April 30, 2023
Variation in the Management of Hospitalized Children With Orbital Cellulitis Over 10 YearsEmily Lan-Vy Nguyen, Leo Hersi, Sanjay Mahant, et al.
Pageof 1