Fatma Tuba Eminoğlu

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 13

Top Topics

Replacement Therapy

Respiratory Syndrome Coronavirus

Genome Wide Identification

Cerebral Ischemia

Top Venues

Journal of pediatric endocrinology & metabolism : JPEM

Turkish archives of pediatrics

Telemedicine journal and e-health : the official journal of the American Telemedicine Association

Turkish journal of medical sciences

This page only lists publications with an associated author ORCID identifier.

Publications

İlknur Sürücü Kara, Engin Köse, Busranur Erozan Cavdarli, Fatma Tuba Eminoğlu
Neuronal ceroid lipofuscinosis type 11 diagnosed patient with bi-allelic variants in GRN gene: case report and review of literature. Journal of pediatric endocrinology & metabolism : JPEM 37 (3) (2024)
Gülreyhan Sonuç Kartal, Merve Koç Yekedüz, Engin Köse, Fatma Tuba Eminoğlu
Two Turkish patients with Primary Coenzyme Q10 Deficiency-7: case report and literature review. Journal of pediatric endocrinology & metabolism : JPEM 37 (3) (2024)
Gülreyhan Sonuç Kartal, Merve Koç Yekedüz, Engin Köse, Fatma Tuba Eminoğlu
Two Turkish patients with Primary Coenzyme Q10 Deficiency-7: case report and literature review. Journal of pediatric endocrinology & metabolism : JPEM 37 (3) (2024)
İlknur Sürücü Kara, Engin Köse, Busranur Erozan Cavdarli, Fatma Tuba Eminoğlu
Neuronal ceroid lipofuscinosis type 11 diagnosed patient with bi-allelic variants in GRN gene: case report and review of literature. Journal of pediatric endocrinology & metabolism : JPEM 37 (3) (2024)
Gülreyhan Sonuç Kartal, Merve Koç Yekedüz, Engin Köse, Fatma Tuba Eminoğlu
Two Turkish patients with Primary Coenzyme Q10 Deficiency-7: case report and literature review. Journal of pediatric endocrinology & metabolism : JPEM 37 (3) (2024)
İlknur Sürücü Kara, Engin Köse, Busranur Erozan Cavdarli, Fatma Tuba Eminoğlu
Neuronal ceroid lipofuscinosis type 11 diagnosed patient with bi-allelic variants in GNR gene: case report and review of literature. Journal of pediatric endocrinology & metabolism : JPEM (2024)
Gülreyhan Sonuç Kartal, Merve Koç Yekedüz, Engin Köse, Fatma Tuba Eminoğlu
Two Turkish patients with Primary Coenzyme Q10 Deficiency-7: case report and literature review. Journal of pediatric endocrinology & metabolism : JPEM (2024)
İlknur Sürücü Kara, Engin Köse, Busranur Erozan Cavdarli, Fatma Tuba Eminoğlu
Neuronal ceroid lipofuscinosis type 11 diagnosed patient with bi-allelic variants in GRN gene: case report and review of literature. Journal of pediatric endocrinology & metabolism : JPEM 37 (3) (2024)
İlknur Sürücü Kara, Engin Köse, Merve Koç Yekedüz, Fatma Tuba Eminoğlu
A different approach to the evaluation of the genotype-phenotype relationship in biotinidase deficiency: repeated measurement of biotinidase enzyme activity. Journal of pediatric endocrinology & metabolism : JPEM (2023)
Merve Koç Yekedüz, Neslihan Doğulu, İlknur Sürücü Kara, Ümmühan Öncül, Batuhan Bakirarar, Pinar Kullu, Yilmaz Ar, Engin Köse, Fatma Tuba Eminoğlu
Pros and Cons of Telemedicine for Inherited Metabolic Disorders in a Developing Country During the COVID-19 Pandemic. Telemedicine journal and e-health : the official journal of the American Telemedicine Association (2022)
Merve Koç Yekedüz, Engin Köse, Fatma Tuba Eminoğlu
A case with Gaucher disease unable to reach enzyme replacement therapy because of COVID-19 quarantine: The first case from Turkey. Turkish archives of pediatrics 56 (3) (2021)
Fatma Tuba Eminoğlu, Ümmühan Öncül, Fevzi Kahveci, Emel Okulu, Elvis Kraja, Engin Köse, Tanıl Kendirli
Characteristics of continuous venovenous hemodiafiltration in the acute treatment of inherited metabolic disorders. Pediatric nephrology (Berlin, Germany) (2021)
Hasan Akduman, Emel Okulu, Fatma Tuba Eminoğlu, Tanıl Kendirli, Gaffari Tunc, Ebru Azapağası, Oktay Perk, Ömer Erdeve, Begüm Atasay, Saadet Arsan
Continuous venovenous hemodiafiltration in the treatment of newborns with an inborn metabolic disease: a single center experience Turkish journal of medical sciences 50 (1) (2020)