Publications by authors named "Alev Hasanoglu"

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High incidence of co-existing factors significantly modifying the phenotype in patients with Fabry disease.
Serhat Koca, Leyla Tümer, İlyas Okur, Yasemin Erten, Sevcan Bakkaloğlu

Gene· March 2019

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Hematologic Findings of Inherited Metabolic Disease: They are More Than Expected.
Ertan Sal, Idil Yenicesu, Ilyas Okur, Zuhre Kaya, Fatih S Ezgu, Alev Hasanoglu

J Pediatr Hematol Oncol· July 2018

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Zinc deficiency in the pediatric age group is common but underevaluated.
Dogus Vuralli, Leyla Tumer, Alev Hasanoglu

World J Pediatr· August 2017

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Secondary Hemophagocytosis in Propionic Acidemia.
Cigdem Seher Kasapkara, Murat Kangin, Banu Oflaz Ozmen, Mehmet Nuri Ozbek, Remezan Demir, Alev Hasanoglu

Iran J Pediatr· June 2015

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Diagnostic dilemma: osteopetrosis with superimposed rickets causing neonatal hypocalcemia.
Asburçe Olgaç, Leyla Tümer, Öznur Boyunağa, Metehan Kızılkaya, Alev Hasanoğlu

J Trop Pediatr· April 2015

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Could GSD type I expand the spectrum of disorders with elevated plasma chitotriosidase activity?
Leyla Tümer, Çiğdem Seher Kasapkara, Gürsel Biberoğlu, Fatih Ezgü, Alev Hasanoğlu

J Pediatr Endocrinol Metab· July 2014

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BCS1L gene mutation causing GRACILE syndrome: case report.
Çiğdem Seher Kasapkara, Leyla Tümer, Fatih Suheyl Ezgü, Aynur Küçükçongar, Alev Hasanoğlu

Ren Fail· July 2014

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Vitamin A status and factors associated in healthy school-age children.
Dogus Vuralli, Leyla Tumer, Alev Hasanoglu, Gürsel Biberoglu, Hatice Pasaoglu

Clin Nutr· June 2014

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Serum dipeptidyl peptidase-IV: a better screening test for early detection of mucopolysaccharidosis?
Ismail Kurt, Erdim Sertoglu, Ilyas Okur, Serkan Tapan, Metin Uyanık, Alev Hasanoglu

Clin Chim Acta· April 2014

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Home sleep study characteristics in patients with mucopolysaccharidosis.
Çiğdem Seher Kasapkara, Leyla Tümer, Ayşe Tana Aslan, Alev Hasanoğlu, Fatih Süheyl Ezgü

Sleep Breath· March 2014

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Diagnosis of glycine encephalopathy in a pediatric patient by detection of a GLDC mutation during initial next generation DNA sequencing.
Fatih Ezgu, Bahattin Çiftci, Burcu Topçu, Gülcan Adıyaman, Hatice Gökmenoğlu

Metab Brain Dis· March 2014

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Rapid molecular diagnosis of genetic diseases by high resolution melting analysis: fabry and glycogen storage 1A diseases.
Fatih Ezgu, Yoruk Divanoglu, Murat Polat, Sitkiye Bahceci, Alev Hasanoglu

Genet Test Mol Biomarkers· January 2014

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Oxidized low-density lipoprotein levels and carotid intima-media thickness as markers of early atherosclerosis in prepubertal obese children.
Ilyas Okur, Leyla Tumer, Fatih Suheyl Ezgu, Ediz Yesilkaya, Arzu Aral, Alev Hasanoglu

J Pediatr Endocrinol Metab· December 2013

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DGUOK-related mitochondrial DNA depletion syndrome in a child with an early diagnosis of glycogen storage disease.
Ciğdem S Kasapkara, Leyla Tümer, Aynur Küçükçongar, Alev Hasanoğlu, Sara Seneca

J Pediatr Gastroenterol Nutr· November 2013

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Severe renal tubulopathy in a newborn due to BCS1L gene mutation: effects of different treatment modalities on the clinical course.
Fatih Ezgu, Sara Senaca, Mehmet Gunduz, Leyla Tumer, Alev Hasanoglu

Gene· October 2013

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Screening for Fabry disease in patients undergoing dialysis for chronic renal failure in Turkey: identification of new case with novel mutation.
Ilyas Okur, Fatih Ezgu, Gursel Biberoglu, Leyla Tumer, Yasemin Erten, Alev Hasanoglu

Gene· September 2013

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Asymmetric dimethylarginine (ADMA) and L-arginine levels in children with glycogen storage disease type I.
Çiğdem Seher Kasapkara, Leyla Tümer, Gursel Biberoglu, Ahmet Kasapkara, Alev Hasanoğlu

J Pediatr Endocrinol Metab· August 2013

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Quality of life in children treated with restrictive diet for inherited metabolic disease.
Tuba F Eminoglu, Sebnem A Soysal, Leyla Tumer, Ilyas Okur, Alev Hasanoglu

Pediatr Int· August 2013

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Rhabdomyolysis and acute kidney injury in two children: questions.
Kibriya Fidan, Yasar Kandur, Leyla Tumer, Alev Hasanoglu, Oguz Soylemezoglu

Pediatr Nephrol· June 2013

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Apheresis-inducible cytokine pattern change in children with homozygous familial hypercholesterolemia.
Aynur Küçükçongar, Idil Yenicesu, Leyla Tümer, Ciğdem Seher Kasapkara, Fatih Süheyl Ezgü

Transfus Apher Sci· June 2013

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Rapid screening of 12 common mutations in Turkish GSD 1a patients using electronic DNA microarray.
Tuba Fatma Eminoglu, Fatih Süheyl Ezgu, Alev Hasanoglu, Leyla Tumer

Gene· April 2013

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Assessment of atherosclerosis risk due to the homocysteine-asymmetric dimethylarginine-nitric oxide cascade in children taking antiepileptic drugs.
Hamdi Cihan Emeksiz, Ayse Serdaroglu, Gürsel Biberoglu, Ozlem Gulbahar, Ebru Arhan, Alev Hasanoglu

Seizure· March 2013

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Hypercalcemia in glycogen storage disease type I patients of Turkish origin.
Ciğdem Seher Kasapkara, Leyla Tümer, Ilyas Okur, Tuba Eminoğlu, Fatih Süheyl Ezgü

Turk J Pediatr· April 2012

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The levels of asymmetric dimethylarginine, homocysteine and carotid intima-media thickness in hypercholesterolemic children.
Alev Hasanoğlu, Ilyas Okur, Ayşe Ceyda Oren, Gürsel Biberoğlu, Suna Oktar

Turk J Pediatr· February 2012

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Analysis of acylcarnitine levels by tandem mass spectrometry in epileptic children receiving valproate and oxcarbazepine.
Ali Cansu, Ayse Serdaroglu, Gursel Biberoglu, Leyla Tumer, Tugba Luleci Hirfanoglu, Alev Hasanoglu

Epileptic Disord· December 2011

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