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Susan Akbaroghli

Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica
2017 · Ariana Kariminejad, Fariba Afroozan, et al. · International Journal of Molecular Sciences · 35
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Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypes
2018 · Ivan Ivanovski, Susan Akbaroghli, et al. · American Journal of Medical Genetics Part A · 31
Factors Associated with Surgery and Imaging Characteristics in Severe Orbital Infections
2022 · Peter J. Gill, Olivier Drouin, et al. · The Journal of Pediatrics · 17
Variation in the Management of Hospitalized Children With Orbital Cellulitis Over 10 Years
2023 · Emily Lan-Vy Nguyen, Leo Hersi, et al. · Hospital Pediatrics · 14
A Case Series: Congenital Hyperinsulinism
2016 · Mohammad Reza Alaei, Susan Akbaroghli, et al. · Intern J Endocrinol Metab · 14
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Identifying serious underlying diagnoses among patients with brief resolved unexplained events (BRUEs): a Canadian cohort study
2024 · Nassr Nama, Zerlyn Lee, et al. · BMJ Paediatrics Open · 13
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Abscess volume as a predictor of surgical intervention in children hospitalized with orbital cellulitis: A multicentre cohort study
2023 · Morgyn F. McKerlie, Nikolaus E. Wolter, et al. · International Journal of Pediatric Otorhinolaryngology · 12
Profile of Iranian GJB2 Mutations in Young Population with Novel Mutation
2011 · Masoumeh Falah, Massoud Houshmand, et al. · DOAJ (DOAJ: Directory of Open Access Journals) · 11
External Validation of Brief Resolved Unexplained Events Prediction Rules for Serious Underlying Diagnosis
2024 · Nassr Nama, Ye Shen, et al. · Archives of Pediatrics and Adolescent Medicine · 10
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Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies.
2019 · Akbar Mohammadzadeh, Susan Akbaroghli, et al. · PubMed Central · 8
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De-novo interstitial 2.33 Mb deletion in 8q24.3: new insights on a very rare partial monosomy syndrome
2018 · Susan Akbaroghli, Seyed H. Tonekaboni, et al. · Clinical Dysmorphology · 3
Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous families.
2022 · Susan Akbaroghli, Daniz Kooshavar, et al. · Iranian journal of child neurology. · 2
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Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas
2016 · Susan Akbaroghli, Maryam Balali, et al. · Therapeutics and Clinical Risk Management · 2
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45 Variation in the Management of Hospitalized Children with Orbital Cellulitis over Ten Years
2023 · Emily Nguyen, Sanjay Mahant, et al. · Paediatrics & Child Health
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Hereditary Angioedema: A Family with Several Affected Members
2019 · Zahra Daneshmandi, Sepideh Darougar, et al. · Immunology and Genetics Journal
Works count: 15
Citation count: 172
H-index: 9
I10-index: 9
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