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Mina Hızal

Showing results (1-10 of 25) with videos related to

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The Turkish Journal of Pediatrics|October 27, 2020
Takayasu arteritis presenting with spontaneous pneumothoraxMina Hızal, Selcan Demir, Sanem Eryılmaz Polat, et al.
The Turkish Journal of Pediatrics|June 20, 2020
Two cases of Vici syndrome presenting with corpus callosum agenesis, albinism, and severe developmental delayMina Hızal, Batuhan Yeke, Yılmaz Yıldız, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|November 22, 2022
The role of flexible bronchoscopy in the diagnostic pathway of children with unexplained peripheral eosinophiliaMina Hızal, Sanem Eryilmaz Polat, Nagehan Emiralioğlu, et al.
Pediatric Pulmonology|December 28, 2020
Differentially expressed genes associated with disease severity in siblings with cystic fibrosisİlksen Berfin Ekinci, Mina Hızal, Nagehan Emiralioğlu, et al.
The Turkish Journal of Pediatrics|April 8, 2020
A rare cause of acute abdominal pain in a patient with Primary ciliary dyskinesia with situs inversus totalisKısmet Çıkı, Özlem Boybeyi Türer, Mina Hızal, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 21, 2020
Mutations of the CFTR gene and novel variants in Turkish patients with cystic fibrosis: 24-years experienceDidem Dayangaç-Erden, Merve Atalay, Nagehan Emiralioğlu, et al.
Pediatric Pulmonology|March 3, 2020
Impact of mannose-binding lectin 2 gene polymorphisms on disease severity in noncystic fibrosis bronchiectasis in childrenDeniz Dogru, Sanem E Polat, Çağman Tan, et al.
The Turkish Journal of Pediatrics|July 18, 2024
The relationship between lung function, exercise capacity, oxidant and antioxidant response in primary ciliary dyskinesia and cystic fibrosisYasemin Kartal, Cemile Bozdemir Özel, Aslıhan Çakmak, et al.
Respiratory Medicine|August 19, 2021
Sleep disordered breathing in patients with Prader willi syndrome: Impact of underlying genetic mechanismBeste Ozsezen, Nagehan Emiralioglu, Alev Özön, et al.
Pediatric Pulmonology|April 3, 2026
Childhood Interstitial Lung Disease in Metabolic Disorders: Prevalence, Genotypic and Clinical Characteristics, and Management Approaches: An Analysis of the Child-Turkey RegistryMerve Selçuk Balcı, Fazılcan Zirek, Handan Kekeç, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
The Turkish Journal of Pediatrics|October 27, 2020
Takayasu arteritis presenting with spontaneous pneumothoraxMina Hızal, Selcan Demir, Sanem Eryılmaz Polat, et al.
The Turkish Journal of Pediatrics|June 20, 2020
Two cases of Vici syndrome presenting with corpus callosum agenesis, albinism, and severe developmental delayMina Hızal, Batuhan Yeke, Yılmaz Yıldız, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|November 22, 2022
The role of flexible bronchoscopy in the diagnostic pathway of children with unexplained peripheral eosinophiliaMina Hızal, Sanem Eryilmaz Polat, Nagehan Emiralioğlu, et al.
Pediatric Pulmonology|December 28, 2020
Differentially expressed genes associated with disease severity in siblings with cystic fibrosisİlksen Berfin Ekinci, Mina Hızal, Nagehan Emiralioğlu, et al.
The Turkish Journal of Pediatrics|April 8, 2020
A rare cause of acute abdominal pain in a patient with Primary ciliary dyskinesia with situs inversus totalisKısmet Çıkı, Özlem Boybeyi Türer, Mina Hızal, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 21, 2020
Mutations of the CFTR gene and novel variants in Turkish patients with cystic fibrosis: 24-years experienceDidem Dayangaç-Erden, Merve Atalay, Nagehan Emiralioğlu, et al.
Pediatric Pulmonology|March 3, 2020
Impact of mannose-binding lectin 2 gene polymorphisms on disease severity in noncystic fibrosis bronchiectasis in childrenDeniz Dogru, Sanem E Polat, Çağman Tan, et al.
The Turkish Journal of Pediatrics|July 18, 2024
The relationship between lung function, exercise capacity, oxidant and antioxidant response in primary ciliary dyskinesia and cystic fibrosisYasemin Kartal, Cemile Bozdemir Özel, Aslıhan Çakmak, et al.
Respiratory Medicine|August 19, 2021
Sleep disordered breathing in patients with Prader willi syndrome: Impact of underlying genetic mechanismBeste Ozsezen, Nagehan Emiralioglu, Alev Özön, et al.
Pediatric Pulmonology|April 3, 2026
Childhood Interstitial Lung Disease in Metabolic Disorders: Prevalence, Genotypic and Clinical Characteristics, and Management Approaches: An Analysis of the Child-Turkey RegistryMerve Selçuk Balcı, Fazılcan Zirek, Handan Kekeç, et al.
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