Pelin Teke Kisa - Division of Pediatric Metabolism and Nutrition, Dokuz Eylül University School of Medicine

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论文共 29 篇作者统计合作学者相似作者

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A Novel PNPLA2 Variant in a Female Patient with Neutral Lipid Storage Disease with Myopathy and Hypogonadotropic Hypogonadism

Hüseyin Bahadır Şenol,Pelin Teke Kısa, Bahar Kulu, Hale Ören,Nur Arslan,Uluç Yiş

Molecular Syndromology（2024）

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SCOT Deficiency Mimicking Sepsis: an Unusual Cause of Increased Anion Gap Metabolic Acidosis

Pelin Teke Kisa,Semra Gursoy,Pinar Seven, Neslihan Pirinc,Ozlem Sarac Sandal,Gulhan Atakul,Filiz Hazan,Tijen Tanyalcin

JOURNAL OF BASIC AND CLINICAL HEALTH SCIENCESno. 2 (2024): 507-510

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Experience with Cascade Screening: A Comprehensive Family Pedigree Analysis of Two Index Patients with Fabry Disease

Pelin Teke Kisa,Burcu Ozturk Hismi,Mehmet Kocabey,Zumrut Arslan Gulten,Bulent Huddam,Selim Ekinci, Evrim Bozkaya,Harun Akar, Ozge K. Karalar Pekuz,Ayca Aydogan,Nur Arslan

AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 7 (2024)

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Clinical, Biochemical, and Molecular Insights into Cerebrotendinous Xanthomatosis: A Nationwide Study of 100 Turkish Individuals

Tanyel Zubarioglu,Ertugrul Kiykim,Engin Kose,Fatma Tuba Eminoglu,Pelin Teke Kisa,Mehmet Cihan Balci,Isil Ozer,Asli Inci, Kubra Cilesiz,Ebru Canda,Havva Yazici, Burcu Ozturk-Hismi,Fatma Derya Bulut,Sevil Dorum,Abdurrahman Akgun, Guel Yalcin-Cakmakli,Gonca Kilic-Yildirim,Erdogan Soyucen,Aylin Akcali, Dilek Gunes,Asli Durmus,Aysegul Gunduz,cigdem Seher Kasapkara,Emine Goksoy,Halil Tuna Akar,Melike Ersoy,Sahin Erdol,Yilmaz Yildiz, Hasmet Ayhan Hanagasi,Nur Arslan,Cigdem Aktuglu-Zeybek

MOLECULAR GENETICS AND METABOLISMno. 2 (2024)

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Expression of Autophagy-Related Proteins in Microlissencephaly Associated with a Novel Variant in the WDR81 Gene

Hatice Yelda Yalcin,Ufkay Karabay,Tayfun Cinleti,Pelin Teke Kisa, Mehtap Yueksel Egrilmez, Akif Ayaz, Nihal Aydin

MOLECULAR SYNDROMOLOGY (2024)

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A Challenging Etiology of Myopathy: the Late-Onset Pompe Disease

Tuba Yüce İnel,Aydan Köken Avşar,Pelin Teke Kısa,Erdener Özer,İ̇smail Sarı

openalex（2023）

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Evaluation of the Genetically Diagnosed Mitochondrial Disease Cases with Neuromuscular Involvement

Cagatay Gunay,Cem Paketci,Pinar Edem,Gamze Sarikaya Uzan,Ayse Semra Hiz Kurul,Zumrut Arslan Gulten,Pelin Teke Kisa,Nur Arslan,Uluc Yis

Journal of Dr Behcet Uz Children s Hospitalno. 1 (2022): 27-36

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A Novel Homozygous GALK1 Variant Combined with Cataract and Prolonged Jaundice

Oguz Ozler,Bugra Han Egeli,Selcan Zeybek,Erdem Eris,Pelin Teke Kisa

Clinical pediatricsno. 6 (2022): 537-540

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Positive Effects of Ketogenic Diet on Weight Control in Children with Obesity Due to Prader–Willi Syndrome

Pelin Teke Kisa,Orkide Guzel,Nur Arslan,Korcan Demir

Clinical endocrinology（2022）

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