Yayınlar & Eserler

Yayın Ağı
Makaleler 73
Tümü (73)
SCI-E, SSCI, AHCI (58)
SCI-E, SSCI, AHCI, ESCI (69)
ESCI (6)
Scopus (68)
TRDizin (13)

1. Is mild citrullinemia type I truly benign? a study of long-term clinical outcomes.

İşler-Soylu E., Aras-Çöl T., Babazade Aghakishili H., Çalışgan K., Zubarioglu T., Kıykım E., et al.
Journal of pediatric endocrinology & metabolism : JPEM , 2026 (SCI-Expanded, Scopus)

2. Early laboratory indicators of acute metabolic decompensation during emergency presentations in pediatric maple syrup urine disease.

Oral-Cebeci S., Aktuğlu-Zeybek Ç., Aslan B., Uysal Ö. Y., Cansever M. Ş., Kıykım E., et al.
European journal of pediatrics , cilt.185, sa.6, 2026 (SCI-Expanded, Scopus)

3. Acute hepatic porphyria masquerading as familial Mediterranean fever: results of a cross-sectional porphobilinogen screening.

Musayeva G., İşat E., Yıldız M., Cansever M. Ş., Uğurlu S., Alkaya D. U., et al.
Orphanet journal of rare diseases , 2026 (SCI-Expanded, Scopus)

4. Plasma sterol profiling in autism spectrum disorder: insights from cerebrotendinous xanthomatosis screening and beyond

Calisgan K., Zubarioglu T., İsat E., Babazade H., Akca-Yesil S., Akbulut S., et al.
METABOLIC BRAIN DISEASE , cilt.41, sa.1, 2026 (SCI-Expanded, Scopus)

5. Revealing BCKDK Deficiency Under Autism: A Case Report, Therapeutic Outcomes, and Literature Review

Babazade H., Günal B., Çalışgan K., Uygur E., Durcan G., Kılıç H., et al.
TURKISH ARCHIVES OF PEDIATRICS , cilt.61, sa.1, ss.1-6, 2025 (ESCI, Scopus, TRDizin)

6. Early prediction of retinopathy of prematurity using targeted metabolomic profiling of 6-hydroxymethylpterin in preterm infants

Alp Ünkar Z., Demir H., Batu Oto B., Cansever M. Ş., Aliyeva L., Demirel A., et al.
BMC OPHTHALMOLOGY , cilt.25, sa.1, 2025 (SCI-Expanded, Scopus) Creative Commons License

7. Determination of Biotinidase Enzyme Levels in Umbilical Cord Blood and Comparisons with Dried Blood Spot Testing in Newborns

Uzunyayla G., Zübarioğlu T., İşat E., Cansever M. Ş., Dinçer E., Zübarioğlu A. U., et al.
JOURNAL OF PEDIATRIC RESEARCH , cilt.1, ss.1-6, 2025 (ESCI, TRDizin)

8. Impact of individualized and supervised strength training on muscle physiology, metabolic control and quality of life in metabolic myopathies.

Zubarioglu T., Yakal S., Yegin F., Uygur E., Şahinkaya T., Dinçer Ş., et al.
Scientific reports , cilt.15, sa.1, ss.26125, 2025 (SCI-Expanded, Scopus)

9. The clinical utility of short-term protein substitute use during intercurrent illness in BH4-responsive phenylketonuria.

Akbulut S., Uygur E., Zubarioglu T., Cansever M. Ş., Kiykim E., Zeybek Ç. A.
Molecular genetics and metabolism , cilt.145, sa.4, ss.109187, 2025 (SCI-Expanded, Scopus)

10. Evaluating the Humoral Immune Response to Sinovac-Coronavac in a Pediatric Patient with Propionic Acidemia: A Case Study.

Ergün İ., Dinç H. Ö., Burtecene N., Kıykım E., Aktuğlu-Zeybek Ç., Cansever M. Ş., et al.
Turkish archives of pediatrics , cilt.60, sa.4, ss.440-442, 2025 (ESCI, Scopus, TRDizin)

11. Carglumic acid as a treatment for persistent hyperammonemia in carnitine-acylcarnitine translocase deficiency: A case study

Babazade H., Zubarioglu T., Uygur E., Cansever M. S., KIYKIM E., Zeybek c. A.
MOLECULAR GENETICS AND METABOLISM REPORTS , cilt.42, 2025 (SCI-Expanded, Scopus)

12. Amino Acid Metabolism and Immune Dysfunction in Urea Cycle Disorders: T and B Cell Perspectives.

Gemici Karaaslan B., Kiykim A., Burtecene N., Gokden M., Cansever M. Ş., Hopurcuoglu D., et al.
Journal of inherited metabolic disease , cilt.48, sa.2, 2025 (SCI-Expanded, Scopus)

13. Primary systemic carnitine deficiency: Phenotypic variability, diagnostic challenges, and long-term outcomes.

Pınar E., Zubarioglu T., Babazade H., Çalışgan K., Cansever M. Ş., Kıykım E., et al.
Pediatrics international : official journal of the Japan Pediatric Society , cilt.67, sa.1, 2025 (SCI-Expanded, Scopus)

14. Symptomatic Benefit of Acetyl-DL-Leucine for Cerebellar Ataxia in Juvenile Tay-Sachs Disease: A Pediatric Case and Literature Review.

Calisgan K., Aghakıshılı H. B., Soylu E. I., Col T. A., Cansever M. Ş., Zubarioglu T., et al.
Molecular syndromology , ss.1-7, 2025 (SCI-Expanded, Scopus)

15. Pteridine and tryptophan pathways in children with type 1 diabetes: Isoxanthopterin as an indicator of endothelial dysfunction.

Özer Y., Cansever M. Ş., Turan H., Bayramoğlu E., Bingöl Aydın D., İşat E., et al.
Journal of pharmaceutical and biomedical analysis , cilt.243, ss.116072, 2024 (SCI-Expanded, Scopus)

16. Comparison of Cost Analysis in Patients with Tetrahydrobiopterin-Responsive and Non-Responsive Phenylketonuria in Turkey.

Karaca Sahin M., Aktuglu Zeybek A. Ç., Zubarioglu T., Cansever M. Ş., Kıykım E.
Nutrients , cilt.16, sa.10, 2024 (SCI-Expanded, Scopus) Creative Commons License

17. Comparison of Cost Analysis in Patients with Tetrahydrobiopterin-Responsive and Non-Responsive Phenylketonuria

Sahin M. K., Aktuğlu Zeybek A. Ç., Zubarioglu T., Cansever M. Ş., Kıykım E.
NUTRIENTS , cilt.16, sa.10, ss.1444-1454, 2024 (SCI-Expanded, Scopus)

18. Serum Neopterin, Biopterin, Tryptophan, and Kynurenine Levels in Patients with Fabry Disease.

Uçar T., Cansever M. Ş., Isat E., Zubarioğlu T., Aktuğlu Zeybek A. Ç., Topçu B., et al.
Balkan medical journal , cilt.41, sa.2, ss.113-120, 2024 (SCI-Expanded, Scopus) Creative Commons License

19. A Novel Homozygous ACBD5 Variant in an Emerging Peroxisomal Disorder Presenting with Retinal Dystrophy and a Review of the Literature

HASTÜRK B. A., ÇINAR Ç., ZÜBARİOĞLU T., Tiryaki-Demir S., CANSEVER M. Ş., KIYKIM E., et al.
MOLECULAR SYNDROMOLOGY , cilt.15, sa.3, ss.232-239, 2024 (SCI-Expanded, Scopus)

20. Highly sensitive rapid determination of orotic acid in urine samples using a field-amplified sample stacking approach in capillary electrophoresis coupled with contactless conductivity detection

Adımcılar V., Saygili M. T., CANSEVER M. Ş., Öztekin N.
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS , cilt.238, 2024 (SCI-Expanded, Scopus)

21. Urinary neopterin and biopterin indicate that inflammation has a role in autism spectrum disorder.

Oge-Enver E., Isat E., Cansever M. Ş., Zubarioglu T., Yilmaz G., Cebi M. N., et al.
Metabolic brain disease , cilt.38, sa.8, ss.2645-2651, 2023 (SCI-Expanded, Scopus)

22. Analysis of Biotinidase Activity in Serum by Digital Imaging Colorimetry Detection.

Destanoğlu O., Cansever M. Ş., İşat E., Zübarioğlu T., Aktuğlu Zeybek A. Ç., Kıykım E.
ACS omega , cilt.8, sa.42, ss.39796-39806, 2023 (SCI-Expanded, Scopus)

23. Neopterin and tryptophan pathways in children with type 1 diabetes: isoxanthopteridine as a marker of endothelial dysfunction

EVLİYAOĞLU S. O., Ozer Y., KIYKIM E., CANSEVER M. Ş., TURAN H., BAYRAMOĞLU E., et al.
HORMONE RESEARCH IN PAEDIATRICS , ss.184-185, 2023 (SCI-Expanded, Scopus)

24. Separation and quantification of the urinary enantiomers of 2-hydroxyglutaric acid by capillary electrophoresis with capacitively coupled contactless conductivity detection: Application to the diagnosis of D- and L-2-hydroxyglutaric aciduria.

Cansever M. Ş., Öztekin N., Kıykım E., Zübarioğlu T., Aktuğlu Zeybek A. Ç.
Journal of separation science , cilt.46, sa.16, 2023 (SCI-Expanded, Scopus) Creative Commons License

25. Maternal Inborn Errors of Metabolism Detected in Expanded Newborn Metabolic Screening.

Tin O., Zübarioğlu T., Cansever M. Ş., Kıykım E., Aktuğlu-Zeybek Ç.
Turkish archives of pediatrics , cilt.58, sa.4, ss.382-387, 2023 (ESCI, Scopus, TRDizin)

26. A Methionine-Portioning-Based Medical Nutrition Therapy with Relaxed Fruit and Vegetable Consumption in Patients with Pyridoxine-Nonresponsive Cystathionine-β-Synthase Deficiency

Uygur E., Aktuğlu Zeybek A. Ç., Aghalarov M., Cansever M. Ş., Kıykım E., Zübarioğlu T.
NUTRIENTS , cilt.15, ss.3105-3115, 2023 (SCI-Expanded, Scopus)

27. Evaluation of dynamic thiol/disulfide homeostasis in hereditary tyrosinemia type 1 patients

Aktuglu Zeybek A. Ç., Kiykim E., Neselioglu S., Iscan H. Z., Zubarioglu T., Cansever M. Ş., et al.
PEDIATRIC RESEARCH , cilt.92, sa.2, ss.474-479, 2022 (SCI-Expanded, Scopus)

28. The Impact of Telemedicine for Monitoring and Treatment of Phenylketonuria Patients on Metabolic Outcome During Coronavirus Disease-19 Outbreak

Zubarioglu T., Hopurcuoglu D., Uygur E., Ahmadzada S., Oge-Enver E., Isat E., et al.
TELEMEDICINE AND E-HEALTH , cilt.28, sa.2, ss.258-265, 2022 (SCI-Expanded, Scopus) Creative Commons License

29. Inborn errors of metabolism and COVID-19: Evaluation of the metabolic outcome.

Zubarioglu T., Hopurcuoglu D., Ahmadzada S., Uzunyayla-Inci G., Cansever M. Ş., Kiykim E., et al.
Pediatrics international : official journal of the Japan Pediatric Society , cilt.64, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

30. Evaluation of plasma carnitine status in patients diagnosed with juvenile idiopathic arthritis

Aktuglu Zeybek A. Ç., Kiykim E., Barut K., Zubarioglu T., Cansever M. Ş., Kasapcopur Ö.
TURKISH JOURNAL OF MEDICAL SCIENCES , cilt.52, sa.3, ss.724-729, 2022 (SCI-Expanded, Scopus, TRDizin) Creative Commons License

31. Altered immune response in organic acidemia.

Altun İ., Kiykim A., Zubarioglu T., Burtecene N., Hopurcuoglu D., Topcu B., et al.
Pediatrics international : official journal of the Japan Pediatric Society , cilt.64, sa.1, 2022 (SCI-Expanded, Scopus)

32. Long-term N-carbamylglutamate treatment of hyperammonemia in patients with classic organic acidemias

Kıykım E., Oguz O., Duman Ç., Zübarioğlu T., Cansever M. Ş., Aktuğlu Zeybek A. Ç.
MOLECULAR GENETICS AND METABOLISM REPORTS , cilt.26, 2021 (SCI-Expanded)

33. Impact of sodium phenylbutyrate treatment in acute management of maple syrup urine disease attacks: A single-center experience

Zubarioglu T., Dede E., Cigdem H., Kiykim E., Cansever M. Ş., Aktuglu-Zeybek C.
Journal of Pediatric Endocrinology and Metabolism , cilt.34, ss.121-126, 2021 (SCI-Expanded)

34. İdrarda Orotik Asit’in Temassız İletkenlik Dedektörü Kullanılarak Kapiler Elektroforez Yöntemi İle Hızlı Tayini

CANSEVER M. Ş., ÖZTEKİN N., ADIMCILAR V., ZÜBARİOĞLU T., KIYKIM E., AKTUĞLU ZEYBEK A. Ç.
SÜLEYMAN DEMIREL ÜNIVERSITESI FEN EDEBIYAT FAKÜLTESI FEN DERGISI = SÜLEYMAN DEMIREL UNIVERSITY FACULTY OF ARTS AND SCIENCE JOURNAL OF SCIENCE , cilt.15, sa.2, ss.194-202, 2020 (TRDizin) Creative Commons License

35. Evaluation of clinical, neuroradiologic, and genotypic features of patients with L-2-hydroxyglutaric aciduria

Zübarioğlu T., Yalçınkaya C., Oruç Ç., Kıykım E., Cansever M. Ş., Gezdirici A., et al.
TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS , cilt.55, sa.3, ss.290-298, 2020 (Hakemli Dergi)

36. Rapid determination of L-2-hydoxyglutaric acid in urine samples by capillary electrophoresis with indirect UV detection

CANSEVER M. Ş., KALAYCIOĞLU Z., ZÜBARİOĞLU T., KIYKIM E., AKTUĞLU ZEYBEK A. Ç., BERKER F. B.
Namık Kemal Tıp Dergisi , cilt.8, sa.2, ss.264-270, 2020 (TRDizin) Creative Commons License

37. Capillary electrophoresis with capacitively coupled contactless conductivity detection for the determination of urinary ethylmalonic acid for the diagnosis of ethylmalonic aciduria

Ozcelik S., Öztekin N., Kiykim E., Cansever M. Ş., Aktuglu-Zeybek A. Ç.
JOURNAL OF SEPARATION SCIENCE , cilt.43, sa.7, ss.1365-1371, 2020 (SCI-Expanded)

38. Screening for Fabry Disease in Patients With Juvenile Systemic Lupus Erythematosus

Kiykim E., Sahin S., Zubarioglu T., Barut K., Adrovic A., Cansever M. Ş., et al.
ARCHIVES OF RHEUMATOLOGY , cilt.35, sa.1, ss.7-12, 2020 (SCI-Expanded)

39. A New Mutation in Diagnosis of Wolman Disease: Case Report

Cansever M. S., Aslan M., Zubarioglu T.
JOURNAL OF ACADEMIC RESEARCH IN MEDICINE-JAREM , cilt.9, sa.3, ss.150-152, 2019 (ESCI, TRDizin) Sürdürülebilir Kalkınma

40. Early diagnosed cerebrotendinous xanthomatosis patients: clinical, neuroradiological characteristics and therapy results of a single center from Turkey

Zubarioglu T., Kiykim E., YEŞİL G., Demircioglu D., Cansever M. S., Yalcinkaya C., et al.
ACTA NEUROLOGICA BELGICA , cilt.119, sa.3, ss.343-350, 2019 (SCI-Expanded, Scopus)

41. Evaluation of the effect of chenodeoxycholic acid treatment on skeletal system findings in patients with cerebrotendinous xanthomatosis.

Zubarioglu T., Bilen I. P., Kiykim E., Dogan B. B., Enver E. O., Cansever M. S., et al.
Turk pediatri arsivi , cilt.54, sa.2, ss.113-118, 2019 (Scopus, TRDizin) Creative Commons License

42. Oxidative stress among L-2-hydroxyglutaric aciduria disease patients: evaluation of dynamic thiol/disulfide homeostasis

Cansever M. S., Zubarioglu T., Oruc C., Kiykim E., Gezdirici A., Neşelioğlu S., et al.
METABOLIC BRAIN DISEASE , cilt.34, sa.1, ss.283-288, 2019 (SCI-Expanded)

43. Early Diagnosis of Fanconi-Bickel Syndrome and a Novel Mutation in SLC2A2 Gene Erken Dönemde Tanı Alan Bir Fanconi-Bickel Sendromu Olgusu ve SLC2A2 Geninde Yeni Bir Mutasyon

Celikboya E., Cansever M. Ş., Zubarioglu T., Yesil G., Akinci N.
Haseki Tip Bulteni , cilt.57, sa.3, ss.328-331, 2019 (Scopus, TRDizin)

44. Ion chromatographic method for the determination of orotic acid in urine

Destanoglu O., Zeydanli D., Cansever M. Ş., Yilmaz G. G.
Analytical Biochemistry , cilt.563, ss.9-14, 2018 (SCI-Expanded, Scopus)

45. Determination of homogentisic acid in urine for diagnosis of alcaptonuria: Capillary electrophoretic method optimization using experimental design

Öztekin N., Balta G. S., Cansever M. Ş.
BIOMEDICAL CHROMATOGRAPHY , cilt.32, sa.7, 2018 (SCI-Expanded, Scopus)

46. Coagulation Disturbances in Patients with Argininemia

Kiykim E., Zubarioglu T., Cansever M. S., Celkan T., Haberle J., Zeybek A. C. A.
ACTA HAEMATOLOGICA , cilt.140, sa.4, ss.221-225, 2018 (SCI-Expanded) Sürdürülebilir Kalkınma

47. Evaluation of dynamic thiol/disulphide homeostasis as a novel indicator of oxidative stress in maple syrup urine disease patients under treatment

Zubarioglu T., Kiykim E., Cansever M. Ş., Neşelioğlu S., Aktuglu-Zeybek C., Erel Ö.
Metabolic Brain Disease , cilt.32, sa.1, ss.179-184, 2017 (SCI-Expanded)

48. Hereditary Tyrosinemia Type 1 in Turkey.

Aktuglu-Zeybek A. Ç., Kıykım E., Cansever M. Ş.
Advances in experimental medicine and biology , cilt.959, ss.157-172, 2017 (SCI-Expanded)

49. Neonatal nonketotic hyperglycinemia: diffusion-weighted magnetic resonance imaging and diagnostic clues

Zubarioglu T., Kiykim E., Cansever M. Ş., Zeybek C. A., Yalcinkaya C.
Acta Neurologica Belgica , cilt.116, sa.4, ss.671-673, 2016 (SCI-Expanded, Scopus)

50. Ornithine Aminotransferase Deficiency in Differential Diagnosis of Neonatal Hyperammonemia: A Case with a Novel OAT Gene Mutation

Zubarioglu T., Kiykim E., Cansever M. Ş., Zeybek C. A.
Indian Journal of Pediatrics , cilt.83, sa.7, ss.754-755, 2016 (SCI-Expanded, Scopus)

51. Inherited metabolic disorders in Turkish patients with autism spectrum disorders

Kiykim E., Zeybek C. A., Zubarioglu T., Cansever S., Yalcinkaya C., Soyucen E., et al.
Autism Research , cilt.9, sa.2, ss.217-223, 2016 (SCI-Expanded, SSCI, Scopus)

52. Plazmada çok uzun zincirli yağ asidi düzeyleri normal olan bir X’e bağlı adrenolökodistrofi hastasında daha önce tanımlanmamış bir ABCD1 gen mutasyonu

ZÜBARİOĞLU T., KIYKIM E., CANSEVER M. Ş., AKTUĞLU ZEYBEK A. Ç.
MARMARA MEDICAL JOURNAL , cilt.29, sa.1, ss.45-47, 2016 (Scopus, TRDizin)

53. Screening of free carnitine and acylcarnitine status in children with familial mediterranean fever

Kiykim E., Aktuglu Zeybek A. C., Barut K., Zubarioglu T., Cansever M. Ş., ALSANCAK S., et al.
Archives of Rheumatology , cilt.31, sa.2, ss.133-138, 2016 (SCI-Expanded, Scopus, TRDizin) Creative Commons License

54. A novel ABCD1 gene mutation in a patient with X-linked adrenoleukodystrophy with atypically normal plasma levels of very long chain fatty acids Plazmada çok uzun zincirli yağ asidi düzeyleri normal olan bir X’e bağlı adrenolökodistrofi hastasında daha önce tanımlanmamış bir ABCD1 gen mutasyonu

Zubarioglu T., Kiykim E., Cansever M. Ş., Aktuglu Zeybek C.
Marmara Medical Journal , cilt.29, sa.1, ss.45-47, 2016 (Scopus, TRDizin) Creative Commons License

55. Screening Mucopolysaccharidosis Type IX in Patients with Juvenile Idiopathic Arthritis.

KIYKIM E., BARUT K., CANSEVER M. Ş., Zeybek C., ZUBARIOGLU T., AYDIN A., et al.
JIMD reports , cilt.25, ss.21-24, 2016 (SCI-Expanded, Scopus) Creative Commons License

56. Screening Inherited Metabolic Disorders in Patients with Familial Mediterranean Fever

Kiykim E., Zeybek A. Ç., Barut K., Zubarioglu T., Cansever M. Ş., Kasapcopur O.
JOURNAL OF PEDIATRIC RESEARCH , cilt.2, sa.4, ss.201-205, 2015 (Hakemli Dergi) Creative Commons License

57. Clinical and neuroradiological approach to fucosidosis in a child with atypical presentation

Zubarioglu T., Kiykim E., Zeybek C. A., Cansever M. S., Benbir G., Aydin A., et al.
ANNALS OF INDIAN ACADEMY OF NEUROLOGY , cilt.18, sa.4, ss.471-474, 2015 (SCI-Expanded, Scopus)

58. DETERMINATION OF FREE CARNITINE AND ACYL-CARNITINE STATUS OF PATIENTS WITH JUVENILE IDIOPATHIC ARTHRITIS

Kiykim E., Aktuglu-Zeybek A. Ç., Barut K., Zubarioglu T., Cansever M. Ş., Aydin A., et al.
ANNALS OF THE RHEUMATIC DISEASES , cilt.74, ss.1235, 2015 (SCI-Expanded, Scopus)

59. SCREENING OF FREE CARNITINE AND ACYL-CARNITINE STATUS IN PATIENTS WITH FAMILIAL MEDITERRANEAN FEVER

Kiykim E., Barut K., Aktuglu-Zeybek A. Ç., Zubarioglu T., Cansever S., Aydin A., et al.
ANNALS OF THE RHEUMATIC DISEASES , cilt.74, ss.1236, 2015 (SCI-Expanded, Scopus)

60. Biotinidase deficiency mimicking primary immune deficiencies.

Kiykim E., Kiykim A., Cansever M. Ş., Aktuglu Zeybek C. A.
BMJ case reports , cilt.2015, 2015 (Scopus)

61. Determination of Ethylmalonic Acid in Human Urine by Ion Chromatography with Suppressed Conductivity

Destanoglu O., Cansever M. S., Yılmaz G.
ORBITAL-THE ELECTRONIC JOURNAL OF CHEMISTRY , cilt.7, sa.2, ss.131-140, 2015 (ESCI, Scopus) Sürdürülebilir Kalkınma

62. Citrin deficiency: An infant incidentally detected by phenylketonuria screening with a novel mutation in SLC25A 13 gene

Zeybek A. Ç., Kiykim E., Zubarioglu T., Cansever M. Ş., CEYLANER S., Erkan T.
Genetic Counseling , cilt.26, sa.4, ss.409-413, 2015 (SCI-Expanded, Scopus)

63. A novel aspartylglucosaminuria mutation in a patient with co-existence of Gaucher disease

Kiykim E., Zubarioglu T., GORUKMEZ O., Gunev S., Cansever M. Ş., Zeybek A. Ç.
Genetic Counseling , cilt.26, sa.4, ss.463-466, 2015 (SCI-Expanded, Scopus)

64. Hereditary tyrosinemia type 1 in Turkey: Twenty year single-center experience

Zeybek A. Ç., Kiykim E., SOYUÇEN E., Cansever S., Altay S., Zubarioglu T., et al.
Pediatrics International , cilt.57, sa.2, ss.281-289, 2015 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

65. DETERMINATION OF OROTIC ACID IN URINE BY ION CHROMATOGRAPHY

Zeydanli D., Destanoglu O., CANSEVER M. Ş., Yilmaz G. G.
JOURNAL OF INHERITED METABOLIC DISEASE , cilt.35, 2012 (SCI-Expanded, Scopus)

66. Determination of NTBC in serum samples from patients with hereditary tyrosinemia type I by capillary electrophoresis

Cansever M. Ş., Aktuglu-Zeybek A. Ç., Erim F. B.
TALANTA , cilt.80, sa.5, ss.1846-1848, 2010 (SCI-Expanded, Scopus)

67. Management of phenylketonuria in Europe: Survey results from 19 countries

Blau N., Bélanger-Quıntana A., Demırkol M. E., Feıllet F., Gıovannını M., Macdonald A., et al.
MOLECULAR GENETICS AND METABOLISM , cilt.99, sa.2, ss.109-115, 2010 (SCI-Expanded, Scopus)

68. Carbonyl ylide reactions of alpha-benzylidene-beta-dicarbonyl compounds: Competitive formation of dihydrofurans and dihydrobenzoxepines

Anac O., Sezer O., Candan O., Gungor F. S., Cansever M. Ş.
TETRAHEDRON LETTERS , cilt.49, sa.6, ss.1062-1065, 2008 (SCI-Expanded, Scopus)

69. Free plasma levels of bupivacaine and ropivacaine when used for caudal block in children

Bozkurt R., Arslan I., Bakan M., Cansever M. Ş.
EUROPEAN JOURNAL OF ANAESTHESIOLOGY , cilt.22, sa.8, ss.640-641, 2005 (SCI-Expanded, Scopus)

70. Determination of urinary succinylacetone by capillary electrophoresis for the diagnosis of tyrosinemia type I

Cansever M. Ş., Erim F.
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES , cilt.818, sa.2, ss.309-311, 2005 (SCI-Expanded, Scopus)

71. Interscalene brachial plexus block with bupivacaine and ropivacaine in patients with chronic renal failure: Diaphragmatic excursion and pulmonary function changes

Altintas F., GUMUS F., Kaya G., Mihmanli I., Kantarci F., Kaynak K., et al.
ANESTHESIA AND ANALGESIA , cilt.100, sa.4, ss.1166-1171, 2005 (SCI-Expanded, Scopus)

72. Effects of melatonin on plasma S-nitrosoglutathione and glutathione in streptozotocin-treated rats

Gorgun F., Kokoglu E., Gumustas M. K., Altug T., Cansever S., Kavunoglu G.
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES , cilt.67, sa.13, ss.979-986, 2004 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

73. Reactions of alpha,beta-enones with diazo compounds - Part 4. Reaction pathways from (Z)- and (E)-alpha,beta-enones with dimethyl diazomalonate

Anac O., Gungor F., Kahveci C., Cansever M. Ş.
HELVETICA CHIMICA ACTA , cilt.87, sa.2, ss.408-415, 2004 (SCI-Expanded, Scopus)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 17

1. AİLESEL AKDENİZ ATEŞİ HASTALARINDA PTERİDİN METABOLİTLERİNİN HASTALIĞIN AKTİVASYONU VE TEDAVİ YANITIYLA OLAN İLİŞKİSİ

Çalışgan K., Aktuğlu Zeybek A. Ç., Kıykım E., Zübarioğlu T., Cansever M. Ş., İşat E., et al.
XVII. ULUSLARARASI KATILIMLI METABOLİK HASTALIKLAR VE BESLENME KONGRESİ, Antalya, Türkiye, 28 Nisan - 02 Mayıs 2024, ss.55-56, (Tam Metin Bildiri)

2. Herediter tirozinemi tip 1 hastalarında tiyol disülfid homeostazı aracılığıyla oksidatif stresin değerlendirilmesi

Cansever M. Ş.
6. Genç pediatristler Kongresi, İstanbul, Türkiye, 5 - 07 Mart 2021, ss.83-159, (Özet Bildiri)

3. Multipl Açil-Koa Dehidrogenaz Eksikliği Hastalarının Klinik Özellikleri ve Tedavi Yanıtları: Tek Merkez Deneyimi

AKTUĞLU ZEYBEK A. Ç., BABAZADA K., CANSEVER M. Ş., ÖGE ENVER E., ZÜBARİOĞLU T., KIYKIM E., et al.
TPK 2020 Buluşması Pediatride Güncellemeler, Türkiye, 25 - 29 Ekim 2020, cilt.52, ss.18, (Özet Bildiri)

4. Chemometric optimization of Malonic Acid Biomarkers in Urine by Capillary Electrophoresis

Özçelik S., ÖZTEKİN N., KIYKIM E., CANSEVER M. Ş., AKTUĞLU ZEYBEK A. Ç.
4th International Conference on New Trends in Chemometrics and Applications, 1 - 03 Mayıs 2019, (Tam Metin Bildiri) Creative Commons License

5. With or Without A Diet? Ten Years Experience of a Tertiary Center on Bh4 Responsive Phenylketonuria Patients

ÖGE ENVER E., BELDE DOĞAN B., KIYKIM E., ZÜBARİOĞLU T., CANSEVER M. Ş., AKTUĞLU ZEYBEK A. Ç.
INTERNATIONAL INBORN ERRORS OF METABOLISM AND NUTRITION CONGRESS, Türkiye, 10 - 14 Nisan 2019, (Tam Metin Bildiri) Creative Commons License

6. The Evaluation of Patients with Diagnosis of infantile, juvenile and late onset Pompe Disease: A retrospective Study.

BELDE DOĞAN B., ÖGE ENVER E., KIYKIM E., CANSEVER M. Ş., ZÜBARİOĞLU T., AKTUĞLU ZEYBEK A. Ç.
INTERNATIONAL INBORN ERRORS OF METABOLISM AND NUTRITION CONGRESS, 10 - 14 Nisan 2019, (Tam Metin Bildiri) Creative Commons License

7. An Alternative Method for Diagnosing Inborn Metabolic Diseases Capillary Electrophoresis

CANSEVER M. Ş., ÖZTEKİN N., KIYKIM E., ZÜBARİOĞLU T., AKTUĞLU ZEYBEK A. Ç.
INTERNATIONAL INBORN ERRORS OF METABOLISM AND NUTRITION CONGRESS, İstanbul, Türkiye, 10 - 14 Nisan 2019, (Tam Metin Bildiri) Creative Commons License

8. Clinical Presentation and Follow Up of Patients with Lysinuric Protein Intolerance

AKTUĞLU ZEYBEK A. Ç., BAYRAMLI Z., SHAFİROVA S., ÖGE ENVER E., BELDE DOĞAN B., ZÜBARİOĞLU T., et al.
INTERNATIONAL INBORN ERRORS OF METABOLISM AND NUTRITION CONGRESS, 10 - 14 Nisan 2019, (Tam Metin Bildiri) Creative Commons License

9. Lysinuric Protein Intolerance in Differential Diagnosis of Hemophagocytic Lymphohistiocytosis

ZÜBARİOĞLU T., BEKTAŞ Ş., KIYKIM E., CANSEVER M. Ş., AKTUĞLU ZEYBEK A. Ç.
INTERNATIONAL INBORN ERRORS OF METABOLISM AND NUTRITION CONGRES, İstanbul, Türkiye, 10 - 14 Nisan 2019, (Özet Bildiri) Creative Commons License

10. Galactosemia Among Turkish Children: Presentation and Outcome from a Pediatric Metabolism Center

DOĞAN B. B., ÖGE ENVER E., KIYKIM E., CANSEVER M. Ş., ZÜBARİOĞLU T., UYGUR E., et al.
INTERNATIONAL INBORN ERRORS OF METABOLISM AND NUTRITION CONGRESS, İstanbul, Türkiye, 10 - 14 Nisan 2019, (Tam Metin Bildiri) Creative Commons License

11. DOĞUMSAL METABOLİZMA HASTALIKLARININ TEŞHİSİNDE KAPİLER ELEKTROFOREZ: L-OH-GLUTARİK ASİTİN İNDİREKT TAYİNİ

Cansever M. Ş., Kalaycıoğlu Z., Zübarioğlu T.
41.PEDİATRİ GÜNLERİ, İstanbul, Türkiye, 7 - 10 Nisan 2019, ss.238-395, (Özet Bildiri) Creative Commons License

12. METABOLİK HASTALIKLARDA TANI TESTLERİNİ YORUMLUYORUZ

Cansever M. Ş.
39.PEDİATRİ GÜNLERİ, İstanbul, Türkiye, 2 - 05 Nisan 2017, ss.1-13, (Tam Metin Bildiri) Creative Commons License

13. ÖZGÜN METABOLİK TETKİK SONUÇLARINI VAKA ÖRNEKLERİ İLE DEĞERLENDİRELİM

Aktuğlu Zeybek A. Ç., Cansever M. Ş.
38.PEDİATRİ GÜNLERİ, İstanbul, Türkiye, 3 - 06 Nisan 2016, ss.121-143, (Tam Metin Bildiri) Creative Commons License

14. NONKETOTİK HİPERGLİSİNEMİLERDE KETOJENİK DİYET ETKİNLİĞİ

Topuz H. Ş., Günaydın D., Aktuğlu Zeybek A. Ç., Kıykım E., Zübarioğlu T., Önal H., et al.
XIII. ULUSAL METABOLİK HASTALIKLAR VE BESLENME KONGRESİ, Adana, Türkiye, 14 - 18 Nisan 2015, ss.162, (Tam Metin Bildiri) Creative Commons License

15. METABOLİK TETKİK SONUÇLARINI VAKA ÖRNEKLERİYLE DEĞERLENDİRELİM ( TANDEM MS İLE ASİLKARNİTİNLER VE AMİNOASİTLER, İDRARDA ORGANİK ASİTLER,VÜCUT SIVILARINDA AMİNOASİTLER, KARBONHİDRATTAN YOKSUN GLİKOPROTEİN ANALİSİ, ÇOK UZUNLU ZİNCİRLİ YAĞ ASİTLERİ)

Cansever M. Ş., Türkoğlu Ü. D., Aktuğlu Zeybek A. Ç.
37.PEDİATRİ GÜNLERİ, İstanbul, Türkiye, 8 - 11 Nisan 2015, ss.1-23, (Tam Metin Bildiri) Creative Commons License

16. LONG TERM FALLOW UP OF A PATIENT WITH GA TYPE I( 10 YEARS)

Altay İ. S., Aktuğlu Zeybek A. Ç., Cansever M. Ş., Aydın A.
VI.INTERNATIONAL NUTRITION AND DIETETICS CONGRESS, Antalya, Türkiye, 2 - 06 Nisan 2008, ss.234-235, (Tam Metin Bildiri) Creative Commons License

17. YÜKSEK BASINÇLI SIVI KROMATOGRAFİSİ (HPLC) İLE KANTİTATİF AMİNOASİT ANALİZİ

Cansever M. Ş.
IX. ULUSLARARASI KATILIMLI BESLENME VE METABOLİZMA KONGRESİ, İstanbul, Türkiye, 22 - 25 Ekim 2007, ss.36-40, (Tam Metin Bildiri) Creative Commons License
Kitaplar 6

1. Diagnostic Methods in Bile Acid Metabolism Disorders

Cansever M. Ş., İşat E.
Inborn Errors of Bile Acid Metabolism, Prof. Dr. Ertuğrul KIYKIM, Editör, Türkiye Klinikleri Yayınevi, Ankara, ss.68-76, 2024

2. Biopterin Metabolizması Bozukluklarında Tanısal Yöntemler

Cansever M. Ş.
Nörotransmitter Hastalıkları 2023, Doç. Dr. Tanyel Zübarioğlu, Editör, Türkiye Klinikleri, Ankara, ss.31-36, 2023 Creative Commons License

3. KALITSAL METABOLIZMA HASTALIKLARINDA LABORATUVAR İNCELEMELERI

Cansever M. Ş.
ÇOCUKLARDA NÖRODEJENERATİF VE NÖROMETABOLİK HASTALIKLAR Temel Bilgiler ve Olgularla Tanısal Yaklaşımlar, Cengiz HAVALI, Editör, Akademi Kitabevi Yayınları, Ankara, ss.5-16, 2022 Creative Commons License

4. Hereditary Tyrosinemia Type 1 in Turkey

Aktuğlu Zeybek A. Ç., Kıykım E., Cansever M. Ş.
Hereditary Tyrosinemia, Tanguay Robert M, Editör, Springer, London/Berlin , Quebec, ss.157-172, 2017

5. Hereditary Tyrosinemia Type 1 in Turkey.

AKTUĞLU ZEYBEK A. Ç., KIYKIM E., CANSEVER M. Ş.
Hereditary Tyrosinemia Pathogenesis, Screening and Management, Prof. Robert M. Tanguay, Editör, Springer, ss.157-172, 2017

6. Screening Mucopolysaccharidosis Type IX in Patients with Juvenile Idiopathic Arthritis

KIYKIM E., BARUT K., CANSEVER M. Ş., AKTUĞLU ZEYBEK A. Ç., ZÜBARİOĞLU T., AYDIN A., et al.
JIMD reports, Morava, E., Baumgartner, M., Patterson, M., Rahman, S., Zschocke, J., Peters, V, Editör, Springer, Berlin, ss.21-24, 2015
Metrikler

Yayın

97

Yayın (WoS)

70

Yayın (Scopus)

68

Atıf (WoS)

490

H-İndeks (WoS)

11

Atıf (Scopus)

569

H-İndeks (Scopus)

13

Atıf (Scholar)

9

H-İndeks (Scholar)

2

Proje

9

Fikri Mülkiyet

3

Tez Danışmanlığı

1

Açık Erişim

9
BM Sürdürülebilir Kalkınma Amaçları
SDG 3: AMAÇ 3: SAĞLIKLI BİREYLER
SDG 8: AMAÇ 8: İNSANA YAKIŞIR İŞ VE EKONOMİK BÜYÜME
SDG 10: AMAÇ 10: EŞİTSİZLİKLERİN AZALTILMASI