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Ebru Canda

Showing results (1-10 of 55) with videos related to

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Pediatric Health, Medicine and Therapeutics|May 23, 2020
Biotinidase Deficiency: Prevalence, Impact And Management StrategiesEbru Canda, Sema Kalkan Uçar, Mahmut Çoker
Archivos Argentinos De Pediatria|January 24, 2022
Severe perinatal hypophosphatasia case with a novel mutationHavva Yazici, Ebru Canda, Sema Kalkan Ucar, et al.
Pediatric Nephrology (Berlin, Germany)|September 28, 2007
An evaluation of quality of life of mothers of children with enuresis nocturnaAyten Egemen, Ipek Akil, Ebru Canda, et al.
Journal of Clinical Lipidology|November 12, 2024
Rapid lipid-lowering response in two cases of autosomal recessive hypercholesterolemiaHavva Yazıcı, Fehime Erdem, Ebru Canda, et al.
Case Reports in Pediatrics|June 8, 2017
A Patient with MSUD: Acute Management with Sodium Phenylacetate/Sodium Benzoate and Sodium PhenylbutyrateMelis Köse, Ebru Canda, Mehtap Kagnici, et al.
JIMD Reports|January 14, 2022
Two siblings with galactose mutarotase deficiency: Clinical differencesHavva Yazici, Ebru Canda, Yasemin Atik Altınok, et al.
The Turkish Journal of Pediatrics|October 28, 2022
Persistent moderate methylmalonic aciduria in a patient with methylmalonyl CoA epimerase deficiencyHavva Yazıcı, Ebru Canda, Hüseyin Onay, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 27, 2019
Two siblings with Gaucher type 3c: different clinical presentationsMiray Karakoyun, Ebru Canda, Ezgi Kiran Tasci, et al.
Molecular Genetics and Metabolism Reports|March 31, 2025
A novel <i>SLC44A</i> gene variant in a patient with neonatal cholestasis and liver failureDogan Barut, Emine Burçe Dörtkardeşler, Miray Karakoyun, et al.
European Journal of Medical Genetics|July 19, 2019
Clinical utility of a targeted next generation sequencing panel in severe and pediatric onset Mendelian diseasesEsra Isik, Huseyin Onay, Tahir Atik, et al.
Pageof 6

Showing results (1-10 of 55) with videos related to

Sort By:
Pageof 6
Pediatric Health, Medicine and Therapeutics|May 23, 2020
Biotinidase Deficiency: Prevalence, Impact And Management StrategiesEbru Canda, Sema Kalkan Uçar, Mahmut Çoker
Archivos Argentinos De Pediatria|January 24, 2022
Severe perinatal hypophosphatasia case with a novel mutationHavva Yazici, Ebru Canda, Sema Kalkan Ucar, et al.
Pediatric Nephrology (Berlin, Germany)|September 28, 2007
An evaluation of quality of life of mothers of children with enuresis nocturnaAyten Egemen, Ipek Akil, Ebru Canda, et al.
Journal of Clinical Lipidology|November 12, 2024
Rapid lipid-lowering response in two cases of autosomal recessive hypercholesterolemiaHavva Yazıcı, Fehime Erdem, Ebru Canda, et al.
Case Reports in Pediatrics|June 8, 2017
A Patient with MSUD: Acute Management with Sodium Phenylacetate/Sodium Benzoate and Sodium PhenylbutyrateMelis Köse, Ebru Canda, Mehtap Kagnici, et al.
JIMD Reports|January 14, 2022
Two siblings with galactose mutarotase deficiency: Clinical differencesHavva Yazici, Ebru Canda, Yasemin Atik Altınok, et al.
The Turkish Journal of Pediatrics|October 28, 2022
Persistent moderate methylmalonic aciduria in a patient with methylmalonyl CoA epimerase deficiencyHavva Yazıcı, Ebru Canda, Hüseyin Onay, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 27, 2019
Two siblings with Gaucher type 3c: different clinical presentationsMiray Karakoyun, Ebru Canda, Ezgi Kiran Tasci, et al.
Molecular Genetics and Metabolism Reports|March 31, 2025
A novel <i>SLC44A</i> gene variant in a patient with neonatal cholestasis and liver failureDogan Barut, Emine Burçe Dörtkardeşler, Miray Karakoyun, et al.
European Journal of Medical Genetics|July 19, 2019
Clinical utility of a targeted next generation sequencing panel in severe and pediatric onset Mendelian diseasesEsra Isik, Huseyin Onay, Tahir Atik, et al.
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