Sara HABİF
Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Tıbbi Biyokimya Anabilim Dalı
Araştırma alanları: Tıp, Sağlık Bilimleri, Dahili Tıp Bilimleri, İç Hastalıkları, Endokrinoloji ve Metabolizma Hastalıkları, Tıbbi Ekoloji ve Hidroklimatoloji, Temel Tıp Bilimleri, Çocuk Sağlığı ve Hastalıkları, Tıbbi Genetik, Pediatrik Endokrinoloji ve Metabolizma
Yayınlar
- Author Correction to: “Assessment of hormone measurement methods in girls with premature adrenarche, polycystic ovary syndrome, and non-classical congenital adrenal hyperplasia.” [Turk J Pediatr 2025; 67: 692-699.] (2026)
- Response to “Perspectives on ‘Assessment of hormone measurement methods in girls with premature adrenarche, polycystic ovary syndrome, and non-classical congenital adrenal hyperplasia’” (2026)
- Treatment strategies, radiological recovery, and neurodevelopmental outcomes in paediatric Maple Syrup Urine Disease: a 20-year single-centre experience from Türkiye (2026)
- Assessment of hormone measurement methods in girls with premature adrenarche, polycystic ovary syndrome, and non-classical congenital adrenal hyperplasia (2025)
- Effect of large neutral amino acids treatment on blood phenylalanine, tyrosine, and tryptophan levels in adolescent and young adult PKU patients (2025)
- Assessment of hormone measurement methods in girls with premature adrenarche, polycystic ovary syndrome, and non-classical congenital adrenal hyperplasia (2025)
- Lens Superoxide Dismutase and Catalase Activities in Diabetic Cataract (2022)
- Methylmalonyl-CoA Epimerase Deficiency Case: Mimicking Ketolysis Defect (2021)
- Tetrahydrobiopterin deficiencies: Lesson from clinical experience (2021)
- Eight CPT II deficient patients: single center experience from Turkey (2021)
- Plasma steroid panel with liquid chromotographymass spectrometry (LC/MS-MS) method: utilization in differential diagnosis of hyperandrogenism (2021)
- Tetrahydrobiopterin deficiencies: Lesson from clinical experience. (2021)
- NADİR GÖRÜLEN BİR KOAGÜLOPATİ OLGUSU: EDİNSEL FAKTÖR IX İNHİBİTÖRÜ (2019)
- Tyrosinemia Type III: Outcome in Two Cases (2019)
- Acut metabolic decompensation of a maple syrup urine disease patient treated with hemodiafiltration (2018)
- Single center experience of biotinidase deficiency: 259 patients and six novel mutations (2018)
- Glutaric Aciduria Type I Diagnosis Case with Normal Glutaryl Carnitine and Urine Organic Acid Analysis (2018)
- Clinical and molecular features of 29 patients with hereditary tyrosinemia 1 in western Turkey. (2018)
- Clinical, Neuroimaging, and Genetic Features of the Patients with L-2-Hydroxyglutaric Aciduria (2018)
- Clinical Features of 29 Patients with Hereditary Tyrosinemia I in Western Turkey (2018)
- Insulin resistance in children with familia hyperlipidemia (2018)
- Recurrent ketoacidosis: Is it a ketone metabolism disorder? (2018)
- Glutaric aciduria type I diagnosis case with normal glutaryl carnitine and urine organic acid analysis. (2017)
- SİTRİN EKSİKLİĞİ TANISI İLE İZLENEN İKİ OLGU (2017)
- NORMAL GLUTARİL KARNİTİN VE İDRAR ORGANİK ASİT ANALİZİNE RAĞMEN GLUTARİK ASİDÜRİ TİP 1 (2017)
- Patients diagnosed with hepatocellular carcinoma with tyrosinemia tye I. (2017)
- GLUTARİC ACİDURİA TYPE I DİAGNOSİS CASE WİTH NORMAL GLUTARYL CARNİTİNE AND URİNE ORGANİC ACİD ANALYSİS (2017)
- patients diagnosed with hepatocelluler carsinoma with tyrosinemia type I (2017)
- determining the quality indicators and evaluating the laboratory performance in the preanalytical phase of testing (2017)
- Follow-up the two cases with the diagnosis of neonatal citrin deficiency (2017)
- patients diagnosed with hepatocellular carcinoma with tyrosinemia type 1 (2017)
- Glutaric aciduria type I diagnosis case with normal glutaryl carnitine and urine organic acid analysis. (2017)
- FOLLOW UP OF THE TWO CASES WİTH THE DİAGNOSİS OF NEONATAL CİTRİN DEFİCİENCY (2017)
- HEPATOSELÜLER KARSİNOM SAPTANAN TİROZİNEMİ TİP 1 TANILI OLGULARIMIZ (2017)
- Sitrin eksikliği tanısı ile izlenen iki olgu (2017)
- TANDEM MASS LC MS MS İLE VİTAMİN D ÖLÇÜMÜ (2016)
- Clinical Neuroimaging and genetic features of L 2hydroxyglutaric aciduria case series (2016)
- Presentation and management of classical urea cycle disorders: lessons from our experience (2016)
- Tandem Mass Spektrometri Çalışma Prensipleri (2016)
- Örnek Olgular (2016)
- Branched-Chain Aminoacidopathies: Our Experience in Ege University Faculty of Medicine (2016)
- İKİ KARDEŞİN METİLMALONİK ASİDÜRİ İLE SINAVI KARACİĞER TRANSPLANTASYONU VE SONRASI (2015)
- DALLLI ZİNCİRLİ AMİNOASİDOPATİLERDE NUTRİSYON VE BÜYÜME (2015)
- Nutrition and child development in branched chain aminoacidopathies (2015)
- Yeni Doğan Döneminde Bir uzamış sarılık Olgusu: Sitrullinemi Tip II? (2015)
- CENTER SPECIFIC MEDIANS FOR FREE beta HUMAN CHORIONIC GONADOTROPIN AND PREGNANCY ASSOCIATED PLASMA PROTEIN A IN FIRST TRIMESTER RISK CALCULATION FOR TRISOMY 21 (2015)
- SCOT EKSİKLİĞİ ATAK TEDAVİSİNDE PERİTON DİYALİZİNİN ROLÜ (2015)
- Challenge of two sublings with methylmslonic aciduria: Liver transplantataion and beyond (2015)
- Trizomi 21 İçin Birinci Trimester Risk Hesaplamasında Merkez özgü Medyan değerleri (2015)
- DALLI ZİNCİRLİ AMİNOASİDOPATİLER EGE TIP DENEYİMİ (2015)
- SCOT Deficiency: The Role of Peritoneal Dialysis in treatment of Attack (2015)
- MSUD Lİ BİR HASTA ATAK TEDAVİSİNDEBESLENME SODYUM FENİLBARBİTÜRİAT VE HEMODİYALİZ (2015)
- SSIEM 2015 Annual SymposiumSCOT DEFICIENCY THE ROLE OF PERITONEAL DIALYSIS IN TREARMENT OF ATTACK (2015)
- TRİZOMİ 21 İÇİN BİRİNCİ TRİMESTER RİSK HESAPLAMASINDA MERKEZE ÖZGÜ MEDYAN DEĞERLERİ (2015)
- METİLEN TETRA HİDROFOLAT EKSİKLİĞİ FARKLI KLİNİK BULGULARLA EGE TIP DENEYİMİ (2015)
- YENİ DOĞAN DÖEMİNDE BİR UZAMIŞ SARILIK OLGUSU SİTRULLİNEMİ TİP II (2015)
- LİZİNÜRİK PROTEİN İNTOLERANSI OLGULARI (2015)
- Metilen tetrahidrofolat redüktaz eksikliği farklı klinik bulgularla ege tıp deneyimi (2015)
- A MSUD Case: sodium phenybutyrate treatment during attack period (2015)
- 5 OKSOPROLİNAZ EKSİKLİĞİ İKİ FARKLI KLİNİK BULGU (2015)
- Two cases of oxoprolinuria: 5-oxoprolinase deficiency? (2014)
- The Comparison of the Effect of Tetrahydrobiopterin and Phenylalanine Deficient diet on Oxidative stress in Hyperphenyalaninenmia (2014)
- The comparison of the effect of tetrahydrobiopterin and phenylalanine deficient diet on oxidative stress in hyperphenylalaninemia (2014)
- Lysinuric protein intolerance: keep hyperammonemia in mind (2014)
- BH4 Responsiveness: Ege University Experience (2014)
- Two cases with cıtrullinemia type 1 diagnosed during neonatal period. (2013)
- The Case of Lysinuric Protein Intolerance With a Novel Mutation (2013)
- A Patient with HMGCOA Lyase Deficiency (2013)
- The Case of Lysinuric Protein Intolerance With a Novel Mutation. (2013)
- Two Cases With Citrullinemia Type 1 Diagnosed During Neonatal Period (2013)
- Paciente diabético de 54 años de edad con bajos niveles de colesterol sérico (2012)
- PATIENTS WITH BIOTINIDASE DEFICIENCY DETECTED THROUGH NEWBORN SCREENING IN EGE REGION OF TURKEY (2012)
- A NEW CASE WITH BIOTINIDASE DEFICIENCY AND ALKAPTONURIA (2012)
- A 54-Year-Old Diabetic Man with Low Serum Cholesterol (2012)
- A 54-year-old diabetic man with low serum cholesterol (2012)
- L-CARNITINE DEFICIENCY IN BETA-THALASSEMIA MAJOR (2012)
- Sağlıklı yenidoğanlarda ve biyotinidaz eksikliği sağtanan olgularda biyotinidaz aktiviteleri (2011)
- Chitotriosidase enzyme activity in patients with metabolic syndrome (2011)
- 54-year-old diabetic man with unexpectedly low serum cholesterol levels (2011)
- CHITOTRIOSIDASE ENZYME ACTIVITY IN PATIENTS WITH METABOLIC SYNDROME (2011)
- Fatty liver and dyslipidemia as important clues for diagnosis of cholesterol ester storage (2010)
- Establishment of reference intervals for free carnitine and acylcarnitines from birth to adulthood: a posteriori sampling approach (2010)
- REFERENCE INTERVAL DETERMINATION OF BIOTINIDASE ACTIVITY IN HEALTHY CHILDREN AND ADULTS (2010)
- Çekirdekli eritrositlerin hastane ölümlerinde risk belirleyici rolü (2010)
- Reference interval determination of biotinidase activity in healthy children and adults (2010)
- A case of neonatal type carbamoyl phosphate synthetase 1 deficiency with R233C mutation (2010)
- Effect of telmisartan on vascular endothelium in hypertensive and type 2 diabetic hypertensive patients (2010)
- False Negative High Density Lipoprotein- Cholesterol in an Autoimmune Hepatitis Patient: Case Report (2010)
- ESTABLISHMENT OF REFERENCE INTERVALS FOR FREE CARNITINE AND ACYLCARNITINES FROM BIRTH TO ADULTHOOD: A POSTERIORI SAMPLING APPROACH (2010)
- The first use of N-carbamylglutamate in a patient with decompensated maple syrup urine disease (2009)
- Önemi bilinmeyen monoklonal gammopatinin eşlik ettiği bir ailesel hipobetalipoproteinemi olgusu (2009)
- Late onset very long chain acyl CoA dehydrogenase deficiency presentedwith rhabdomyolysis (2008)
- Insulin resistance in pediatric patents with familial hyperlipidemia (2008)
- Late-onset very-long-chain acyl-CoA dehydrogenase deficiency presented with rhabdomyolysis (2008)
- Unusual presentation of carnitine membrane transporter deficiency: Bicytopenia (2008)
- Pleural fluid neopterin levels in tuberculous pleurisy (2007)
- Unexpected death of a case with argininosuccinate lyase deficiency (2007)
- Unexpected death of a case with argininosuccinate lyase deficiency (2007)
- Prostat Kanseri Değerlendirmesinde İnflamasyon Göstergeleri ve Fibrin Yıkım Ürünlerinin Rolü (2006)
- C-Reactive protein and neopterin levels in healthy non-obese adults (2006)