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Microwave ablation of symptomatic benign thyroid nodules: Short‐ and long‐term effects on thyroid function tests, thyroglobulin and thyroid autoantibodies

Clinical endocrinology (Oxford), 2021-04, Vol.94 (4), p.677-683

2021

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Periferik Kanında 100 HbF Bulunan Talasemi İntermedia Olgusu

Genel tip dergisi, 2021-06, Vol.31 (2), p.180-181

2021

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Determining the genital hygiene behaviours of visually impaired women

The British journal of visual impairment, 2023-09, Vol.41 (3), p.542-558

2023

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Glycosaminoglycan-induced proinflammatory cytokine levels as disease marker in mucopolysaccharidosis

Cytokine (Philadelphia, Pa.), 2024-01, Vol.173, p.156410-156410, Article 156410

2024

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Long-term clinical outcomes and management of hypertriglyceridemia in children with Apo-CII deficiency

Nutrition, metabolism, and cardiovascular diseases, 2024-07, Vol.34 (7), p.1798-1806

2024

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Case stories and Post-violence behavior of women seeking medical attention at the emergency department due to physical violence

Journal of forensic and legal medicine, 2021-05, Vol.80, p.102174-102174, Article 102174

2021

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Crystallized phenol application and modified Limberg flap procedure in treatment of pilonidal sinus disease: A comparative retrospective study

Asian journal of surgery, 2016-07, Vol.39 (3), p.172-177

2016

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Two siblings with galactose mutarotase deficiency: Clinical differences

JIMD reports, 2022-01, Vol.63 (1), p.25-28

2022

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Unique clinical presentations and follow-up outcomes from experience with congenital disorders of glycosylation: PMM2-PGM1-DPAGT1-MPI-POMT2-B3GALNT2-DPM1-SRD5A3-CDG

Journal of Pediatric Endocrinology and Metabolism, 2023-06

2023

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Severe perinatal hypophosphatasia case with a novel mutation

Archivos argentinos de pediatría, 2022-02, Vol.120 (1), p.e21

2022

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Experience with carnitine palmitoyltransferase II deficiency: diagnostic challenges in the myopathic form

Journal of Pediatric Endocrinology and Metabolism, 2024-01, Vol.37 (1), p.33-41

2024

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Un caso de hipofosfatasia perinatal grave con una mutación novedosa

Archivos argentinos de pediatría, 2022-02, Vol.120 (1), p.121-130

2022

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Clinical Characteristics and Outcomes of Cancer Cases Among Syrian Refugees From Southern Turkey

JAMA network open, 2023-05, Vol.6 (5), p.e2312903-e2312903

2023

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Percutaneous left atrial appendage closure in a patient with haemophilia and atrial fibrillation: a case report

European heart journal : case reports, 2019-09, Vol.3 (3)

2019

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Mild Aromatic L-Amino Acid Decarboxylase Deficiency Causing Hypoketotic Hypoglycemia in a 4-year-old Girl

Journal of clinical research in pediatric endocrinology, 2024-09, Vol.16 (3), p.361-366

2024

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Long-term personalized high-protein, high-fat diet in pediatric patients with glycogen storage disease type IIIa: Evaluation of myopathy, metabolic control, physical activity, growth, and dietary compliance

Journal of inherited metabolic disease, 2024-04, Vol.47 (5), p.1001-1017

2024

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Assessment of Antioxidant Effect of Beta-Glucan on the Whole Blood Oxidative DNA Damage with the Comet Assay in Colorectal Cancer

Current molecular pharmacology, 2022-01, Vol.15 (2), p.446-453

2022

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Mild Aromatic L-Amino Acid Decarboxylase Deficiency: As A Reason For Hypoketotic Hypoglycemia In A 4-Year-Old Girl

Journal of clinical research in pediatric endocrinology, 2024-07

2024

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Single center experience of biotinidase deficiency: 259 patients and six novel mutations

Journal of Pediatric Endocrinology and Metabolism, 2018-08, Vol.31 (8), p.917-926

2018

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Nephrotic syndrome in a patient with Glycogen Storage Disease Type IXb

Journal of pediatric academy, 2022-12, Vol.3 (3), p.132-134

2022

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Long-term follow-up of alkaptonuria patients: single center experience

Journal of Pediatric Endocrinology and Metabolism, 2022-07, Vol.35 (7), p.913-923

2022

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Persistent moderate methylmalonic aciduria in a patient with methylmalonyl CoA epimerase deficiency

Turkish journal of pediatrics, 2022-09, Vol.64 (5), p.946-950

2022

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Development of a New Amperometric Biosensor for Measurement of Plasma Galactose Levels

ACS omega, 2024-02, Vol.9 (7), p.7621-7633

2024

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Özel Eğitim Öğretmenlerinin Yardımcı Teknoloji Kullanmaya İlişkin Deneyimleri

Yaşadıkça eğitim (Online), 2024-05, Vol.38 (2), p.354-371

2024

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Four cases of Chanarin-Dorfman syndrome presenting with different types of erythrokeratoderma

Pediatric dermatology, 2024-06

2024

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Microwave ablation of symptomatic benign thyroid nodules: Short‐ and long‐term effects on thyroid function tests, thyroglobulin and thyroid autoantibodies

Periferik Kanında 100 HbF Bulunan Talasemi İntermedia Olgusu

Determining the genital hygiene behaviours of visually impaired women

Glycosaminoglycan-induced proinflammatory cytokine levels as disease marker in mucopolysaccharidosis

Long-term clinical outcomes and management of hypertriglyceridemia in children with Apo-CII deficiency

Case stories and Post-violence behavior of women seeking medical attention at the emergency department due to physical violence

Crystallized phenol application and modified Limberg flap procedure in treatment of pilonidal sinus disease: A comparative retrospective study

Two siblings with galactose mutarotase deficiency: Clinical differences

Unique clinical presentations and follow-up outcomes from experience with congenital disorders of glycosylation: PMM2-PGM1-DPAGT1-MPI-POMT2-B3GALNT2-DPM1-SRD5A3-CDG

Severe perinatal hypophosphatasia case with a novel mutation

Experience with carnitine palmitoyltransferase II deficiency: diagnostic challenges in the myopathic form

Un caso de hipofosfatasia perinatal grave con una mutación novedosa

Clinical Characteristics and Outcomes of Cancer Cases Among Syrian Refugees From Southern Turkey

Percutaneous left atrial appendage closure in a patient with haemophilia and atrial fibrillation: a case report

Mild Aromatic L-Amino Acid Decarboxylase Deficiency Causing Hypoketotic Hypoglycemia in a 4-year-old Girl

Long-term personalized high-protein, high-fat diet in pediatric patients with glycogen storage disease type IIIa: Evaluation of myopathy, metabolic control, physical activity, growth, and dietary compliance

Assessment of Antioxidant Effect of Beta-Glucan on the Whole Blood Oxidative DNA Damage with the Comet Assay in Colorectal Cancer

Mild Aromatic L-Amino Acid Decarboxylase Deficiency: As A Reason For Hypoketotic Hypoglycemia In A 4-Year-Old Girl

Single center experience of biotinidase deficiency: 259 patients and six novel mutations

Nephrotic syndrome in a patient with Glycogen Storage Disease Type IXb

Long-term follow-up of alkaptonuria patients: single center experience

Persistent moderate methylmalonic aciduria in a patient with methylmalonyl CoA epimerase deficiency

Development of a New Amperometric Biosensor for Measurement of Plasma Galactose Levels

Özel Eğitim Öğretmenlerinin Yardımcı Teknoloji Kullanmaya İlişkin Deneyimleri

Four cases of Chanarin-Dorfman syndrome presenting with different types of erythrokeratoderma

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