Sait Karaman,Semiha Bahçeci Erdem,Hikmet Tekin Nacaroğlu et al.
Sait Karaman et al.
Aim: Allergic sensitization in infancy generally develops against food allergens. We aimed to investigate the frequency of aero-allergens sensitization at older ages in infants with food allergy. ...
Dinçer Yıldızdaş,Nagehan Aslan
Dinçer Yıldızdaş
In recent years, the use of point-of-care ultrasound by non-radiologist physicians has become widespread. Especially for clinicians working in pediatric emergency departments and pediatric intensive care units, point-of-care ultrasound has ...
COVID-19 and re-opening of schools: Opinions with scientific evidence [0.03%]
新冠肺炎疫情下的复课：基于科学证据的观点分析
Mustafa Hacımustafaoğlu
Mustafa Hacımustafaoğlu
Due to the COVID-19 pandemic, more than 90% of students worldwide were affected by education loss. Moreover, for school-age children and adolescents, there may be worsening of nutrition, increasing mental health disorders, lack of physical ...
Özgür Kasapçopur
Özgür Kasapçopur
Authors' Response [0.03%]
作者回应
Rui Ping Zhang,Jing Chen,Xiao-Li Hu et al.
Rui Ping Zhang et al.
Mahmood D Al-Mendalawi
Mahmood D Al-Mendalawi
Some considerations about the association between autism spectrum disorder and epilepsy [0.03%]
有关自闭症谱系障碍和癫痫之间关联的一些思考
Annio Posar,Paola Visconti
Annio Posar
Alpha-lipoic acid intoxication in an adolescent girl: Case report and review of the literature [0.03%]
青少年女孩的α-硫辛酸中毒：病例报告及文献回顾
Sinem Polat,Önder Kılıçaslan,Feruza Turan Sönmez
Sinem Polat
Alpha-lipoic acid is a widely used medication that does not need a prescription. Although it is safely used in adults, hitherto no safe dose for children has been reported, and there is no known antidote. The medical literature provides fou...
Recurrent infections, neurologic signs, low serum uric acid levels, and lymphopenia in childhood: Purine nucleoside phosphorylase deficiency, an emergency for infants [0.03%]
儿童反复感染，神经症状，血清尿酸水平低和淋巴细胞减少：核糖核苷磷酸化缺乏症，婴儿期的一种紧急情况
Necil Kütükçüler,Ezgi Bölük,Nazan Tökmeci et al.
Necil Kütükçüler et al.
Purine nucleoside phosphorylase deficiency is one of the severe combined immunodeficiencies, which often clinically manifests with recurrent infections, neurologic symptoms and autoimmune diseases, and leads to thymocyte development and per...
A case of classic galactosemia manifesting as neonatal early and profound indirect hyperbilirubinemia [0.03%]
经典半乳糖血症表现为新生儿早期和严重的间接高胆红素血症一例报告
Zohreh Kavehmanesh,Mohammad Torkaman,Fatemeh Beiraghdar
Zohreh Kavehmanesh
Galactosemia is a rare autosomal recessive metabolic disorder that has three major types. The most common type is classic galactosemia. These patients have deficient galactose-1-phosphate-urydiltransferase. The enzyme deficiency often resul...