Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Ebru Canda

Showing results (21-30 of 55) with videos related to

Pageof 6
Sort By:
ACS Omega|January 5, 2026
Simultaneous Determination of Lyso-Gb1 and Lyso-Gb3 in Plasma Using Salt-Assisted Liquid-Liquid Extraction Combined with LC-MS/MSErhan Canbay, Çetin Uzun, Yasemin Akçay, et al.
Pediatric Nephrology (Berlin, Germany)|January 20, 2010
Co-existence of chronic renal failure, renal clear cell carcinoma, and Blau syndromeIpek Akil, Aykan Ozguven, Ebru Canda, et al.
Cytokine|November 4, 2023
Glycosaminoglycan-induced proinflammatory cytokine levels as disease marker in mucopolysaccharidosisOznur Çopur, Havva Yazıcı, Erhan Canbay, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 7, 2022
Long-term follow-up of alkaptonuria patients: single center experienceAyse Ergul Bozaci, Havva Yazici, Ebru Canda, et al.
Metabolic Brain Disease|March 11, 2017
A treatable cause of myelopathy and vision loss mimicking neuromyelitis optica spectrum disorder: late-onset biotinidase deficiencySanem Yilmaz, Mine Serin, Ebru Canda, et al.
Turkish Archives of Pediatrics|May 5, 2023
COVID-19 and Vaccination Status in Lysosomal Storage Diseases: A Single-Center ExperienceMerve Yoldaş Çelik, Ebru Canda, Havva Yazıcı, et al.
JIMD Reports|September 14, 2022
Clinical spectrum of early onset "Mediterranean" (homozygous p.P131L mutation) mitochondrial neurogastrointestinal encephalomyopathySema Kalkan Uçar, Havva Yazıcı, Ebru Canda, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 12, 2018
Single center experience of biotinidase deficiency: 259 patients and six novel mutationsEbru Canda, Havva Yazici, Esra Er, et al.
Blood Cells, Molecules & Diseases|November 27, 2018
Coexistence of Gaucher Disease and severe congenital neutropeniaMelis Demir Kose, Ebru Canda, Mehtap Kağnıcı, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 4, 2023
Mild Aromatic L-Amino Acid Decarboxylase Deficiency Causing Hypoketotic Hypoglycemia in a 4-year-old GirlMerve Yoldaş Çelik, Ebru Canda, Havva Yazıcı, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
ACS Omega|January 5, 2026
Simultaneous Determination of Lyso-Gb1 and Lyso-Gb3 in Plasma Using Salt-Assisted Liquid-Liquid Extraction Combined with LC-MS/MSErhan Canbay, Çetin Uzun, Yasemin Akçay, et al.
Pediatric Nephrology (Berlin, Germany)|January 20, 2010
Co-existence of chronic renal failure, renal clear cell carcinoma, and Blau syndromeIpek Akil, Aykan Ozguven, Ebru Canda, et al.
Cytokine|November 4, 2023
Glycosaminoglycan-induced proinflammatory cytokine levels as disease marker in mucopolysaccharidosisOznur Çopur, Havva Yazıcı, Erhan Canbay, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|June 7, 2022
Long-term follow-up of alkaptonuria patients: single center experienceAyse Ergul Bozaci, Havva Yazici, Ebru Canda, et al.
Metabolic Brain Disease|March 11, 2017
A treatable cause of myelopathy and vision loss mimicking neuromyelitis optica spectrum disorder: late-onset biotinidase deficiencySanem Yilmaz, Mine Serin, Ebru Canda, et al.
Turkish Archives of Pediatrics|May 5, 2023
COVID-19 and Vaccination Status in Lysosomal Storage Diseases: A Single-Center ExperienceMerve Yoldaş Çelik, Ebru Canda, Havva Yazıcı, et al.
JIMD Reports|September 14, 2022
Clinical spectrum of early onset "Mediterranean" (homozygous p.P131L mutation) mitochondrial neurogastrointestinal encephalomyopathySema Kalkan Uçar, Havva Yazıcı, Ebru Canda, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 12, 2018
Single center experience of biotinidase deficiency: 259 patients and six novel mutationsEbru Canda, Havva Yazici, Esra Er, et al.
Blood Cells, Molecules & Diseases|November 27, 2018
Coexistence of Gaucher Disease and severe congenital neutropeniaMelis Demir Kose, Ebru Canda, Mehtap Kağnıcı, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 4, 2023
Mild Aromatic L-Amino Acid Decarboxylase Deficiency Causing Hypoketotic Hypoglycemia in a 4-year-old GirlMerve Yoldaş Çelik, Ebru Canda, Havva Yazıcı, et al.
Pageof 6