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Bukola A Olarewaju

Showing results (1-10 of 14) with videos related to

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Clinical Medicine Insights. Endocrinology and Diabetes|May 14, 2026
Cornea Arcus and Dyslipidemia in Unrelated Adults With Monoallelic Germline Variants in the <i>Glucokinase Regulator</i> GeneBukola A Olarewaju, Ileana Trujillo, Mayowa A Osundiji
Journal of Surgical Case Reports|October 8, 2024
Follow-up report on pulmonary mucosa-associated lymphoma in a patient with von Hippel-Lindau diseaseBukola A Olarewaju, Judy B Tejon, Mayowa A Osundiji
Genetics in Medicine Open|December 13, 2024
ACMG/AMP variant classification framework in arginase 1 deficiency: Implications for birth prevalence estimates and diagnosticsJessie M Cameron, Mayowa Azeez Osundiji, Rory J Olson, et al.
Neuroradiology|July 1, 2026
Frontotemporal lobar degeneration in a patient carrying a pathogenic PABPN1 expansionEhab Y Harahsheh, Bukola A Olarewaju, Misha B Asif, et al.
Annals of Internal Medicine. Clinical Cases|January 30, 2026
Congenital Coarctation of the Aorta in a Patient With <i>ROBO4</i> c.695C>T (p.Thr232Met) Germline VariantMohammad Karam Chaaban, George Bcharah, Bukola A Olarewaju, et al.
Kidney & Blood Pressure Research|March 18, 2026
Composite Phenotype: Recurrent Nephrolithiasis and Chronic Kidney Disease in an Adult with Biallelic SLC34A3 and Monoallelic SLC3A1 Pathogenic Variants: Who is 'The Culprit'?Bukola A Olarewaju, Sonia Sabrowsky, Shaymaa Shurrab, et al.
American Journal of Medical Genetics. Part A|December 16, 2024
COL4A2 -Related Disorder Presenting in Adulthood With RhabdomyolysisBukola A Olarewaju, Judy Tejon, Shaymaa Shurrab, et al.
Skeletal Radiology|December 5, 2024
COL9A1-related disorder with pectus carinatum, without epiphyseal dysplasia: case report and review of literatureBukola A Olarewaju, Erin R Alexander, Monica M Crowe, et al.
Neurogenetics|November 5, 2025
CADASIL-like cerebral vasculopathy in a patient with a heterozygous MYBPC3 likely pathogenic splice site variantEhab Harahsheh, Bukola A Olarewaju, Deanna M Weaver, et al.
Annals of Internal Medicine. Clinical Cases|May 28, 2026
Concurrent Phenylalanine Hydroxylase-Related Disorder and Celiac: A Rare Co-occurrence With Implications for Clinical ManagementJade Jensen, Erin Merritt, Bukola A Olarewaju, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Clinical Medicine Insights. Endocrinology and Diabetes|May 14, 2026
Cornea Arcus and Dyslipidemia in Unrelated Adults With Monoallelic Germline Variants in the <i>Glucokinase Regulator</i> GeneBukola A Olarewaju, Ileana Trujillo, Mayowa A Osundiji
Journal of Surgical Case Reports|October 8, 2024
Follow-up report on pulmonary mucosa-associated lymphoma in a patient with von Hippel-Lindau diseaseBukola A Olarewaju, Judy B Tejon, Mayowa A Osundiji
Genetics in Medicine Open|December 13, 2024
ACMG/AMP variant classification framework in arginase 1 deficiency: Implications for birth prevalence estimates and diagnosticsJessie M Cameron, Mayowa Azeez Osundiji, Rory J Olson, et al.
Neuroradiology|July 1, 2026
Frontotemporal lobar degeneration in a patient carrying a pathogenic PABPN1 expansionEhab Y Harahsheh, Bukola A Olarewaju, Misha B Asif, et al.
Annals of Internal Medicine. Clinical Cases|January 30, 2026
Congenital Coarctation of the Aorta in a Patient With <i>ROBO4</i> c.695C>T (p.Thr232Met) Germline VariantMohammad Karam Chaaban, George Bcharah, Bukola A Olarewaju, et al.
Kidney & Blood Pressure Research|March 18, 2026
Composite Phenotype: Recurrent Nephrolithiasis and Chronic Kidney Disease in an Adult with Biallelic SLC34A3 and Monoallelic SLC3A1 Pathogenic Variants: Who is 'The Culprit'?Bukola A Olarewaju, Sonia Sabrowsky, Shaymaa Shurrab, et al.
American Journal of Medical Genetics. Part A|December 16, 2024
COL4A2 -Related Disorder Presenting in Adulthood With RhabdomyolysisBukola A Olarewaju, Judy Tejon, Shaymaa Shurrab, et al.
Skeletal Radiology|December 5, 2024
COL9A1-related disorder with pectus carinatum, without epiphyseal dysplasia: case report and review of literatureBukola A Olarewaju, Erin R Alexander, Monica M Crowe, et al.
Neurogenetics|November 5, 2025
CADASIL-like cerebral vasculopathy in a patient with a heterozygous MYBPC3 likely pathogenic splice site variantEhab Harahsheh, Bukola A Olarewaju, Deanna M Weaver, et al.
Annals of Internal Medicine. Clinical Cases|May 28, 2026
Concurrent Phenylalanine Hydroxylase-Related Disorder and Celiac: A Rare Co-occurrence With Implications for Clinical ManagementJade Jensen, Erin Merritt, Bukola A Olarewaju, et al.
Pageof 2