Zobrazeno 1 - 10
of 1 574
pro vyhledávání: '"11"'
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 33:923-930
Objectives To investigate the clinical and genetic characteristics of children with glycogen storage disease type IIIa (GSD IIIa) and to explore the muscle involvement and manifestations of GSD IIIa patients. Methods The clinical data of 11 patients
Autor:
Wei-Hua Sun, Hong-Jiang Wu, Bin Yang, Xinran Dong, Wenhao Zhou, Meng-Yuan Wu, Yaqiong Wang, Ping Zhang, Min Zhang, Wei Lu, Bingbing Wu, Yue-ping Zhang
Publikováno v:
World Journal of Pediatrics. 16:401-410
Maple syrup urine disease (MSUD) is an autosomal recessive inherited disorder that affects the degradation of branched-chain amino acids and is associated with acute and chronic brain dysfunction. This study presents 11 new patients with MSUD and des
Publikováno v:
American Journal of Perinatology. 38:683-689
Objective An observed disparity in population-scale data are a larger number of males among preterm births (PTBs). We investigated spontaneous PTB risk among women of various race/ethnic groups in combination with infants' sex. Study Design This obse
Autor:
Minhaj S. Khaja, Jeffrey Forris Beecham Chick, Wael A. Saad, Kyle J. Cooper, Ravi N. Srinivasa, Bill S. Majdalany
Publikováno v:
Pediatric Radiology. 48:235-240
Interventional radiology treatment of chylothorax is well described in adults, with high technical and clinical success that decreases patient morbidity and mortality. However there is limited experience in children. To report the technical and clini
Autor:
Murat Karaoglan, Mehmet Keskin
Publikováno v:
Journal of paediatrics and child healthReferences. 56(5)
Aim Although newly diagnosed type 1 diabetes mellitus (T1DM) occurs sporadically in childhood, there is an increased risk of T1DM for first-degree relatives of patients that endure into the advanced years. Determination of T1DM incidence in siblings
Treatment of complex idiopathic clubfoot using the modified Ponseti method: up to 11 years follow-up
Publikováno v:
Journal of Pediatric Orthopaedics B. 26:137-142
Complex idiopathic clubfeet are distinguished by significant shortening, rigid equinus with a deep crease above the heel, severe plantar flexion of all metatarsals, a deep plantar crease seven across the full width of the sole of the foot and high ca
Autor:
Martin Ward-Platt, Jonathan Wyllie, Sundeep Harigopal, Nishant Banait, Nicola Miller, Majd Abu-Harb
Publikováno v:
The journal of maternal-fetalneonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 33(12)
Background: Pulse oximetry (POS) has been proposed as a screening tool for CCHD in newborn. The aim was to identify the effect of POS on the rate of diagnosis after discharge and survival to one year in cases with CCHD.Material and Methods: All cases
Autor:
Ashwin Pimpalwar, Annie Hsiao
Publikováno v:
European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie. 29(3)
Introduction External angular dermoid cysts, or epidermoid inclusion cysts, are a common subcutaneous tumor of the head and neck. For the majority of these lesions, excision is relatively simple and performed through an incision immediately overlying
Publikováno v:
Journal of pediatric urology. 14(3)
Summary Introduction One of the goals of hypospadias repair is to create a neourethra with normal urinary stream and normal growth. Several studies have reported that dorsal inlay graft urethroplasty (DIG) has wide indications for various clinical ph
Publikováno v:
Pediatric Surgery International. 32:239-243
Inflammatory myofibroblastic tumor (IMT) is a rare benign neoplasm. The purpose of this study was to review the clinical characteristics, imaging and pathological features, and outcomes of children with IMTs from a single center in China. A retrospec