Author

Alev Hasanoğlu

Observed names: A Hasanoglu, A Hasanoğlu, A. HASANOGLU, A. Hasanoglu, A. Hasano lu, A. Hasanoğlu, A. Hasanoǧlu, ALEV HASANOGLU, Alev HASANOGLU, Alev HASANOĞLU, Alev Hasanoglu, Alev Hasanoğlu, Alev Hasanoĝlu, Alev HasanoǦLu, Dr.Alev Hasanoğlu, HASANOĞLU, ALEV

Institution: Gazi University

Observed institutions: Karadeniz Technical University, Akdeniz University, Gazi Hastanesi, Hacettepe University, Erciyes University, Gazi University

ORCID: 0000-0001-7490-2064

Observed ORCID: 0000-0001-7490-2064

OpenAlex ID: A5088569343

An overview of L-2-hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype-phenotype study

2010 · Marjan E. Steenweg, Cornelis Jakobs, et al. · Human Mutation · 126

PDF

Evaluation of Bone Mineral Metabolism in Children Receiving Carbamazepine and Valproic Acid

2000 · E. Erbayat Altay, A. Serdaroğlu, et al. · Journal of Pediatric Endocrinology and Metabolism · 89

Serum leptin, oxidized low density lipoprotein and plasma asymmetric dimethylarginine levels and their relationship with dyslipidaemia in adolescent girls with polycystic ovary syndrome

2007 · Fatma Demirel, Aysun Bideci, et al. · Clinical Endocrinology · 78

Arm Anthropometry in Evaluation of Malnutrition in Children With Cancer

1999 · Aynur Oguz, Ceyda Karadeniz, et al. · Pediatric Hematology and Oncology · 67

Frequency of vitamin D insufficiency in healthy children between 1 and 16 years of age in Turkey

2011 · Alkim Oden Akman, Leyla Tumer, et al. · Pediatrics International · 66

Bone Mineral Density in Childhood Obesity

2000 · A. Hasanoǧlu, A. Bideci, et al. · Journal of Pediatric Endocrinology and Metabolism · 52

N-carbamylglutamate treatment for acute neonatal hyperammonemia in isovaleric acidemia

2011 · Cigdem Seher Kasapkara, Fatih Suheyl Ezgu, et al. · European Journal of Pediatrics · 45

Screening for Fabry disease in patients undergoing dialysis for chronic renal failure in Turkey: Identification of new case with novel mutation

2013 · Ilyas Okur, Fatih Ezgu, et al. · Gene · 44

Endothelial activation and inflammation in prepubertal obese Turkish children

2005 · Fatih Süheyl Ezgü, Alev Hasanoğlu, et al. · Metabolism · 43

Continuous glucose monitoring in children with glycogen storage disease type I

2013 · Ç S Kasapkara, G Cinasal Demir, et al. · European Journal of Clinical Nutrition · 41

Endomysium antibodies in the diagnosis of celiac disease in short‐statured children with no gastrointestinal symptoms

2001 · Leyla Tümer, Alev Hasanoglu, et al. · Pediatrics International · 40

Asymmetrical dimethylarginine level in atrial fibrillation

2008 · A. Cengel, A. Sahinarslan, et al. · Acta Cardiologica · 37

Quality of life in children treated with restrictive diet for inherited metabolic disease

2013 · Tuba F. Eminoglu, Sebnem A. Soysal, et al. · Pediatrics International · 35

Adjuvant effect of vitamin A on recurrent lower urinary tract infections

2007 · AYGEN YILMAZ, ELIF BAHAT, et al. · Pediatrics International · 35

SRD5A3-CDG: A patient with a novel mutation

2012 · C.S. Kasapkara, L. Tümer, et al. · European Journal of Paediatric Neurology · 33

Excitatory amino acids and taurine levels in cerebrospinal fluid of hypoxic ischemic encephalopathy in newborn

1999 · Kıvılcım Gücüyener, Yıldız Atalay, et al. · Clinical Neurology and Neurosurgery · 33

Serum Levels of Insulin-like Growth Factor-I and Insulin-like Growth Factor Binding Protein-3 in Obese Children

1997 · Aysun Bideci, Peyami Cinaz, et al. · Journal of Pediatric Endocrinology and Metabolism · 31

Zinc deficiency in the pediatric age group is common but underevaluated

2017 · Dogus Vuralli, Leyla Tumer, et al. · World Journal of Pediatrics · 29

Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R

2010 · Alev Hasanoglu, Manisha Balwani, et al. · Journal of Inherited Metabolic Disease · 28

Cholesteryl ester storage disease in a young child presenting as isolated hepatomegaly treated with simvastatin

2006 · Buket Dalgıç, Sinan Sarı, et al. · The Turkish Journal of Pediatrics · 28

PDF

Vitamin D intoxication and hypercalcaemia in an infant treated with pamidronate infusions

2004 · Fatih Suheyl Ezgu, Necla Buyan, et al. · European Journal of Pediatrics · 28

Severe renal tubulopathy in a newborn due to BCS1L gene mutation: Effects of different treatment modalities on the clinical course

2013 · Fatih Ezgu, Sara Senaca, et al. · Gene · 27

BCS1L gene mutation causing GRACILE syndrome: case report

2014 · Çiğdem Seher Kasapkara, Leyla Tümer, et al. · Renal Failure · 26

PDF

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): case report with a new mutation

2010 · Zeren Barış, Tuba Eminoğlu, et al. · European Journal of Pediatrics · 26

Plasma homocysteine and lipoprotein (a) levels as risk factors for atherosclerotic vascular disease in epileptic children taking anticonvulsants

2002 · L Tümer, A Serdaroğlu, et al. · Acta Paediatrica · 25

Works count: 217

Citation count: 1,715

H-index: 25

I10-index: 52