Quality of Life and Related Factors in Patients Diagnosed with Mucopolysaccharidosis and Their Caregivers [0.03%]
黏多糖贮积症患者及其照料者的生活质量及影响因素研究
Merve Koç Yekedüz,Kubra Cilesiz,İlknur Sürücü Kara et al.
Merve Koç Yekedüz et al.
Objectives: Quality of life (QoL) is directly associated with physical-psychological well-being, family and environmental factors in patients with Mucopolysaccharidosis (MPS). The present study aims to investigate the fac...
Evaluation of Postnatal Echocardiographic Screening for Congenital Heart Defects - a Prospective Cohort Study at a German University Hospital [0.03%]
先天性心脏病的产后超声心动图筛查评估——德国大学医院前瞻性队列研究
Victoria Delphine Haberkern,Laura Luisa Kilarski,Thomas Schaible
Victoria Delphine Haberkern
Background: Congenital heart defects (CHD) being the most common congenital malformation, significantly impact mortality and morbidity in children and adults. Early detection greatly improves treatment and prognosis. Rout...
Do Systemic Inflammatory Indices, Urinalysis, and Radiological Findings Vary by Causative Pathogen in Neonatal Urinary Tract Infections? [0.03%]
病原体不同会改变新生儿泌尿道感染的炎症指标、尿液分析和影像学特征吗？
Sarkhan Elbayiyev,Gülsüm Kadıoğlu Şimşek,Tevfik Çevirici et al.
Sarkhan Elbayiyev et al.
Objectives: Urinary tract infections (UTI) are the most common occult infections in infants under three months of age with high fever, caused by various pathogens, and can progress with different symptoms from mild to sev...
Three Birds With One Stone: Successful Management Of Peritonitis Induced Pediatric Septic Shock With Peritoneal Washing [0.03%]
一石三鸟：腹腔灌洗成功治疗儿童腹膜炎性感染性休克
Osman Oğuz Demir,Gül Nihal Erdemir,Selman Kesici et al.
Osman Oğuz Demir et al.
[Pediatric pneumological aspects in the care of children with neuromuscular diseases with focus on Duchenne muscular dystrophy] [0.03%]
[神经肌肉疾病儿童护理中的儿科肺部问题以及杜氏肌营养不良症的治疗焦点]
Hans Fuchs,Lennart Gunst,Anke Wendt et al.
Hans Fuchs et al.
Duchenne muscular dystrophy is the most common inherited neuromuscular disease in children. In addition to the progressive loss of motor skills and cardiac involvement, respiratory muscle weakness leads to a restrictive lung disease and cou...
Severe Neonatal Episodic Laryngospasm (SNEL) due to Mutation in the SCN4A Gene as a Rare Differential Diagnosis in Paroxysmal Inspiratory Stridor with Cyanosis in Infancy [0.03%]
由于SCN4A基因突变导致的重症新生儿间质性喉痉挛(SNEL)作为婴儿阵发性吸气性喘鸣伴紫绀的罕见鉴别诊断
Julia Westhoff,Rahel Schuler,Lutz Nährlich et al.
Julia Westhoff et al.
SGLT2 Inhibition: A New Glimmer of Hope to Slow Chronic Kidney Disease Progression in Children? [0.03%]
钠-葡萄糖协同转运蛋白2抑制剂能阻止儿童期慢性肾脏病的发展吗？
Emre Leventoğlu,Sevcan A Bakkaloğlu
Emre Leventoğlu
Finding of a Homozygous SLC26A3 Mutation in a German Newborn with Congenital Chloride Diarrhea Presenting with Polyhydramnios and Dilated Bowel Loops [0.03%]
在一位出现羊水过多和肠管扩张的先天性氯化物腹泻德国新生儿中发现SLC26A3同合子突变
Philipp Fecher,Eric Frieauff,Rebecca Paul et al.
Philipp Fecher et al.
Urethral Catheterization as a cause of Kidney Failure after Successfully Treated Hemolytic Uremic Syndrome [0.03%]
成功治疗溶血性尿毒症综合症后的患者发生肾衰的元凶-导尿管所致尿道损伤
Emre Leventoglu,Ali Sezer,Bilge Türedi et al.
Emre Leventoglu et al.
David Topitz,Maria Rothensteiner,Sebastian Baier-Grabner et al.
David Topitz et al.