Halise Neslihan Onenli Mungan (Neslihan Önenli-Mungan, Halise Neslihan Mungan, Halise Neslihan Önenli Mungan, Neslihan Onenli Mungan, Halise Neslihan Önenli Mungan, Neslihan Önenli Mungan)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 10

Top Topics

Replacement Therapy

Top Venues

American journal of medical genetics. Part A

Metabolic brain disease

Turkish archives of pediatrics

International journal of paediatric dentistry

This page only lists publications with an associated author ORCID identifier.

Publications

Ezgi Burgac, İrem Kaplan, Burcu Köseci, Esra Kara, Deniz Kor, Fatma Derya Bulut, Anıl Atmıs, Ferhat Can Piskin, Sevcan Tuğ Bozdoğan, Gizem Ürel-Demir, Faruk Incecik, Halise Neslihan Onenli Mungan
Early diagnostic clues of mucolipidosis type II: Significance of radiological findings. American journal of medical genetics. Part A 194 (6) (2024)
Ezgi Burgac, İrem Kaplan, Burcu Köseci, Esra Kara, Deniz Kor, Fatma Derya Bulut, Anıl Atmıs, Ferhat Can Piskin, Sevcan Tuğ Bozdoğan, Gizem Ürel-Demir, Faruk Incecik, Halise Neslihan Onenli Mungan
Early diagnostic clues of mucolipidosis type II: Significance of radiological findings. American journal of medical genetics. Part A 194 (6) (2024)
Ezgi Burgac, İrem Kaplan, Burcu Köseci, Esra Kara, Deniz Kor, Fatma Derya Bulut, Anıl Atmıs, Ferhat Can Piskin, Sevcan Tuğ Bozdoğan, Gizem Ürel-Demir, Faruk Incecik, Halise Neslihan Onenli Mungan
Early diagnostic clues of mucolipidosis type II: Significance of radiological findings. American journal of medical genetics. Part A (2024)
Fatma Derya Bulut, Deniz Kor, Sebile Kılavuz, Ebru Cicek, Burcu Köseci, Esra Kara, Ezgi Burgac, İrem Kaplan, Halise Neslihan Onenli Mungan
Actions speak louder than words: Home visits and its effect on dietary adherence in patients with phenylketonuria. Journal of paediatrics and child health (2023)
Sebile Kılavuz, Murat Basaranoglu, Serdar Epcacan, Derya Bako, Arife Ozer, Yasemin Nuran Donmez, Emine Ipek Ceylan, Ajlan Tukun, Serdar Ceylaner, Hadi Geylani, Halise Neslihan Onenli Mungan
A rare cause of hydrops fetalis in two Gaucher disease type 2 patients with a novel mutation. Metabolic brain disease 37 (4) (2022)
Sebile Kılavuz, Sibel Basaran, Deniz Kor, Fatma Derya Bulut, Sevcan Erdem, Hüseyin Tuğsan Ballı, Muhammed Dağkıran, Serdar Ceylaner, Halise Neslihan Onenli Mungan
Morquio A syndrome and effect of enzyme replacement therapy in different age groups of Turkish patients: a case series. Orphanet journal of rare diseases 16 (1) (2021)
Mehmet Satar, Ahmet İbrahim Kurtoğlu, Hacer Yapıcıoğlu Yıldızdaş, Halise Neslihan Onenli Mungan, Ferda Ozlü, Serdar Ceylaner
Coexistence of molybdenum cofactor deficiency type A and hypertrophic pyloric stenosis, a new case. Turkish archives of pediatrics 56 (1) (2021)
Sebile Kılavuz, Fatma Derya Bulut, Deniz Kor, Berna Seker Yilmaz, Neslihan Özcan, Faruk Incecik, Hasan Bilen Onan, Gülay Ceylaner, Halise Neslihan Onenli Mungan
The outcome of 41 Late-Diagnosed Turkish GA-1 Patients: A Candidate for the Turkish NBS. Neuropediatrics 52 (5) (2021)
Berna Seker Yilmaz, Deniz Kor, Fatma Derya Bulut, Sebile Kılavuz, Serdar Ceylaner, Halise Neslihan Onenli Mungan
Clinical and molecular findings in 37 Turkish patients with isolated methylmalonic acidemia Turkish journal of medical sciences 51 (3) (2021)
Volkan Çiftçi, Sebile Kılavuz, Fatma Derya Bulut, Halise Neslihan Onenli Mungan, Serdar Ceylaner, Muharrem Cem Dogan
Congenital erythropoietic porphyria with erythrodontia: A case report. International journal of paediatric dentistry 29 (4) (2019)