The role of argyrophilic nucleolar organizing region-associated proteins in clinical exacerbation of chronic obstructive pulmonary disease von Turan Sönmez, Feruza, Eröz, Recep

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A novel pathogenic variant in the 3ʹ end of the AGTPBP1 gene gives rise to neurodegeneration without cerebellar atrophy: an expansion of the disease phenotype? von Türay, Sevim, Eröz, Recep, Başak, A. Nazlı

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A rare cause of delayed puberty and primary amenorrhea: 17α-hydroxylase enzyme deficiency von Beştaş, Aslı, Bolu, Semih, Unal, Edip, Aktar Karakaya, Amine, Eröz, Recep, Tekin, Mehmet, Haspolat, Yusuf Kenan

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A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del) von Yavaş, Cüneyd, Doğan, Mustafa, Eröz, Recep, Türegün, Kübra

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Short- and long-term effects of rapamycin on ischemic damage and apoptotic changes in torsion of rat testes von Kabaklıoğlu, Murat, Kaya, Murat, Şahin, Ibrahim Ethem, Gamsızkan, Mehmet, Bahçıvan, Atike, Eröz, Recep

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Clinical, radiological and computational studies on two novel GNPTG variants causing mucolipidosis III gamma phenotypes with varying severity von Doğan, Mustafa, Eröz, Recep, Terali, Kerem, Gezdirici, Alper, Bolu, Semih

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An integrated clinical and molecular study of a cohort of Turkish patients with Marfan syndrome harboring known and novel FBN1 variants von Gezdirici, Alper, Terali, Kerem, Gulec, Elif Yilmaz, Bornaun, Helen, Dogan, Mustafa, Eroz, Recep

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Evaluation of HLA-B51 frequency and its relationship with clinical findings in patients with Behçet’s disease: 4-year analysis in a single center von Erdem Sultanoğlu, Tuba, Eröz, Recep, Ataoğlu, Safinaz

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The diagnosis to be kept in mind in resistant epilepsy; tuberous sclerosis von Kurt, Fatih, Eröz, Recep, Doğan, Mustafa

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The Relationship Between Clinical Phenotypes and Chromosomal Microdeletions/Duplications in Pediatric Neurology von TÜRAY, Sevim, ERÖZ, Recep, HABİLOĞLU, Esra, SAV, Nadide Melike

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Does capsaicin have therapeutic benefits in human colon adenocarcinoma? Selection of the most reliable dose via AgNOR von Nisari, Mustafa, Eroz, Recep

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White–Sutton syndrome with hot water epilepsy and coexistence of SHOX gene variations von Turay, Sevim, Eroz, Recep

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Evaluation of both expression and serum protein levels of caspase-8 and mitogen-activated protein kinase 1 genes in patients with different severities of COVID-19 infection von Acat, Murat, Yıldız Gülhan, Pınar, Eröz, Recep, Ertınmaz Özkan, Ayşegül, Koca, Oğuzhan, Çınar, Caner

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Study of ten causal genes in Turkish patients with clinically suspected maturity-onset diabetes of the young (MODY) using a targeted next-generation sequencing panel von Doğan, Mustafa, Eröz, Recep, Bolu, Semih, Yüce, Hüseyin, Gezdirici, Alper, Arslanoğlu, İlknur, Teralı, Kerem

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Association of Endothelial Nitric Oxide Synthase Gene Polymorphisms (894G/T, −786T/C, G10T) and Clinical Findings in Patients with Migraine von Eröz, Recep, Bahadir, Anzel, Dikici, Suber, Tasdemir, Sener

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Atypical presentation in patients with 17 alpha-hydroxylase deficiency caused by a deletion in the CYP17A1 gene: short stature von Bolu, Semih, Eroz, Recep, Tekin, Mehmet, Dogan, Mustafa

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Investigation of the AgNOR (Argyrophilic Nucleolar Organizing Region) Protein Levels in Patients with Coronary Artery Diseases: The Prognostic Role of AgNOR Proteins in Acute Myoca... von Turan Sönmez, Feruza, Eröz, Recep, Yurdakul, Bilge

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Argyrophilic Nucleolar Organizer Regions as New Biomarkers in ST-Elevation Myocardial Infarction von Damar, İbrahim Halil, Eroz, Recep

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Evaluation of Cases with Myotonia Congenita for Cardiovascular Risk von Damar, Ibrahim Halil, Eroz, Recep

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May Argyrophilic Nucleolar Organizer Regions Be Used as a Biomarker for the Detection of the Degree of Ischemic Damage Instead of Tunel in Testicular Torsion? von Kabaklioglu, Murat, Eroz, Recep, Kaya, Murat

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