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The Turkish Journal of Pediatrics|February 28, 2020
Congenital long-QT syndrome in type 1 diabetes: a unique associationErdal Kurnaz, Şenay Savaş Erdeve, Senem Özgür, et al.
The Turkish Journal of Pediatrics|February 28, 2020
Acute ophthalmoparesis and persistent mydriasis: expanding the clinical spectrum of anti-GQ1b positive cranial neuropathy in a 5.5-year-old girlAyfer Sakarya Güneş, Hülya Maraş Genç, Emek Uyur Yalçın, et al.
The Turkish Journal of Pediatrics|February 28, 2020
Assessment of pediatric cricopharyngeal achalasia with high resolution manometryÖzlem Boybeyi Türer, Numan Demir, Thomas Ciecieraga, et al.
The Turkish Journal of Pediatrics|February 28, 2020
Syncope due to acute rheumatic fever with pacemaker-like syndromeDenizhan Bağrul
The Turkish Journal of Pediatrics|January 18, 2020
Renal features of Bardet Biedl syndrome: A single center experienceBahriye Atmış, Aysun Karabay-Bayazıt, Engin Melek, et al.
The Turkish Journal of Pediatrics|January 18, 2020
Clinical signs and symptoms of toxic serum digoxin levels in neonatesMehmet Mutlu, Yakup Aslan, Şebnem Kader, et al.
The Turkish Journal of Pediatrics|January 18, 2020
A novel mutation in the SLC19A2 gene in a Turkish male with thiamine-responsive megaloblastic anemia syndromeIşık Odaman-Al, Alper Gezdirici, Melek Yıldız, et al.
The Turkish Journal of Pediatrics|January 18, 2020
A rare chromosomal disorder in a newborn: Trisomy 3qDilek Kahvecioğlu, Hatice Tatar-Aksoy, Eren Yıldız, et al.
The Turkish Journal of Pediatrics|January 18, 2020
An infant with an extremely rare cobalamin disorder: Methionine synthase deficiency and importance of early diagnosis and treatmentÇiğdem Seher Kasapkara, Ebru Yılmaz-Keskin, Ferda Özbay-Hoşnut, et al.
The Turkish Journal of Pediatrics|January 18, 2020
Alpha methyl acyl CoA racemase deficiency: Diagnosis with isolated elevated liver enzymesMehmet Gündüz, Özlem Ünal, Aynur Küçükçongar-Yavaş, et al.
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