Publications by authors named "Safak Gucer"

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AP-1-dependent fibrosis: Exploring its potential role in the pathogenesis of placental transmogrification of the lung (PTL) via tissue-level transcriptome analysis.
Beren Karaosmanoglu, Gozde Imren, Meral Uner, Diclehan Orhan, Safak Gucer

Pathol Res Pract· June 2024

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Homozygous Missense Epithelial Cell Adhesion Molecule Variant in a Patient with Congenital Tufting Enteropathy and Literature Review.
Merve Güvenoğlu, Pelin Özlem Şimşek-Kiper, Can Koşukcu, Ekim Z Taskiran, İnci Nur Saltık-Temizel, Safak Gucer

Pediatr Gastroenterol Hepatol Nutr· November 2022

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Fetal Mediastinal Fibrosarcoma. Report of Two Cases.
Murat Cagan, Selma Yildirim, Gulenay Gencosmanoglu Turkmen, Ozgur Ozyuncu, Zuhal Akcoren, Safak Gucer

Fetal Pediatr Pathol· October 2022

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Glomerulonephritis with crescents in childhood; etiologies and significance of M2 macrophages.
Gözdem Kaykı, Diclehan Orhan, Bora Gülhan, Rezan Topaloğlu, Zuhal Akçören

Turk J Pediatr· May 2022

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Giant Right Atrial Myxoma with Fulminant Progression in an Infant.
Ebru Azapagasi, Mutlu Uysal Yazici, Mehmet Emre Ari, Rabia Sedef Karakaya, Hasibe Gökçe Cınar, Safak Gucer

J Pediatr Intensive Care· March 2022

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Acute kidney injury in a patient with COVID-19: Questions.
Tugba Tastemel Ozturk, Demet Baltu, Eda Didem Kurt Sukur, Yasemin Ozsurekci, Safak Gucer

Pediatr Nephrol· December 2021

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Acute kidney injury in a patient with COVID-19: Answers.
Tugba Tastemel Ozturk, Demet Baltu, Eda Didem Kurt Sukur, Yasemin Ozsurekci, Safak Gucer

Pediatr Nephrol· December 2021

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A very rare cause of protein losing enteropathy: Gaucher disease.
Mehmet Akif Göktaş, Ersin Gümüş, Hülya Demir, Hayriye Hızarcıoğlu Gülşen, İnci Nur Saltık-Temizel

Turk J Pediatr· September 2021

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Inflammatory milieu of muscle biopsies in juvenile dermatomyositis.
Erdal Sag, Gulsev Kale, Goknur Haliloglu, Yelda Bilginer, Zuhal Akcoren, Safak Gucer

Rheumatol Int· January 2021

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Atypical Presentation of Sengers Syndrome: A Novel Mutation Revealed with Postmortem Genetic Testing.
Naz Guleray, Can Kosukcu, Zihni Ekim Taskiran, Pelin Ozlem Simsek Kiper, Gulen Eda Utine, Safak Gucer

Fetal Pediatr Pathol· April 2020

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BK virus associated nephropathy and severe pneumonia in a kidney transplanted adolescent with Schimke immuneosseous- dysplasia.
Ali Düzova, Bora Gülhan, Rezan Topaloğlu, Fatih Özaltın, Ali Bülent Cengiz

Turk J Pediatr· January 2020

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Non-immune hydrops fetalis: A retrospective analysis of 151 autopsies performed at a single center.
Gözdem Kaykı, Şafak Güçer, Zuhal Akçören, Diclehan Orhan, Beril Talim

Turk J Pediatr· June 2019

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Erratum to 'Response to early coenzyme Q10 supplementation is not sustained in CoQ10 deficiency caused by CoQ2 mutation' [Pediatric Neurology 88 (2018) 71-74].
Fehime K Eroglu, Fatih Ozaltin, Nazli Gönç, Hülya Nalçacıoğlu, Z Birsin Özçakar

Pediatr Neurol· May 2019

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Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation.
Fehime K Eroglu, Fatih Ozaltin, Nazlı Gönç, Hülya Nalçacıoğlu, Z Birsin Özçakar

Pediatr Neurol· November 2018

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Are Congenital Urinary Tract Abnormalities Linked to Maternal Methylenetetrahydrofolate Reductase Polymorphisms in Fetuses of Intentionally Terminated Pregnancies with Oligo- or Anhydramnios ?
M Sinan Beksac, Alp Tuna Beksac, Melek Buyukeren, Atakan Tanacan, Hatice Bektas, Safak Gucer

Fetal Pediatr Pathol· June 2018

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Coexistence of Trisomy 13 and SRY (-) XX Ovotesticular Disorder of Sex Development.
Gizem Ürel Demir, Özlem Akgün Doğan, Pelin Özlem Şimşek Kiper, Gülen Eda Utine, Koray Boduroğlu, Safak Gucer

Fetal Pediatr Pathol· December 2017

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Epidermal cyst in the patent processus vaginalis: An unusual inguinal mass in a girl.
İbrahim Karnak, Mithat Haliloğlu, Şafak Güçer

Turk J Pediatr· September 2017

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Congenital Microvillus Inclusion Disease in the Differential Diagnosis of Intractable Metabolic Acidosis.
Nilufer Guzoglu, Didem Aliefendioglu, Fulya Gulerman, Safak Gucer, Figen Kaymaz

Pediatr Neonatol· June 2017

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A probable new syndrome with the storage disease phenotype caused by the VPS33A gene mutation.
Ali Dursun, Dilek Yalnizoglu, Omer F Gerdan, Didem Yucel-Yilmaz, Mahmut S Sagiroglu, Safak Gucer

Clin Dysmorphol· January 2017

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Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency.
Rikke K J Olsen, Eliška Koňaříková, Teresa A Giancaspero, Signe Mosegaard, Veronika Boczonadi, Safak Gucer

Am J Hum Genet· June 2016

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ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS.
Emine Korkmaz, Beata S Lipska-Ziętkiewicz, Olivia Boyer, Olivier Gribouval, Cecile Fourrage, Safak Gucer

J Am Soc Nephrol· January 2016

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Diagnosis: Melanoderma after Hematopoietic Stem Cell Transplantation.
Şule Ünal, İlhan Tezcan, Şafak Güçer, Meryem Seda Boyraz, Deniz Çağdaş

Turk J Haematol· December 2015

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Index of suspicion.
Hayriye Hızarcioglu-Gulsen, Yusuf Aydemir, Safak Gucer, Burcu Berberoglu-Ates, Gulin Hizal

Pediatr Rev· December 2014

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Mucopolysaccharidosis: Otolaryngologic findings, obstructive sleep apnea and accumulation of glucosaminoglycans in lymphatic tissue of the upper airway.
Burhanettin Gönüldaş, Taner Yılmaz, H Serap Sivri, K Şafak Güçer, Kamer Kılınç

Int J Pediatr Otorhinolaryngol· June 2014

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Recurrent hemoptysis and a mass in the thorax in an infant: the split notochord syndrome.
Mutlu Uysal Yazici, Saniye Ekinci, Ozlem Keskin Turkmen, Ebru Gunes Yalcin, Arbay O Ciftci, Safak Gucer

European J Pediatr Surg Rep· June 2014

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