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期刊名:Pediatric and developmental pathology

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ISSN:1093-5266

e-ISSN:1615-5742

IF/分区:1.3/Q3

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Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Pauline Mae Dy,Rachel Santos,Erick Martin Yturralde Pauline Mae Dy
Introduction: There is a dearth of information regarding the epidemiology of biliary atresia and Kasai portoenterostomy (KPE) outcomes in the Philippines. Here we describe the histopathologic features of biliary atresia a...
Sze Jet Aw,Yingting Mok,Khurshid Merchant et al. Sze Jet Aw et al.
Background: Identifying the genetic signatures in bone and soft tissue tumors enhances our understanding of tumor biology and aids in the subclassification of tumors for personalized treatment. Histone H3.3 alterations pl...
Veronique Schiffer,Ina Thijs,Salwan Al-Nasiry et al. Veronique Schiffer et al.
We present a unique case of a 33-year-old gravida that was referred to our hospital with an umbilical vessel aneurysm presenting as a large placental cyst on ultrasound. Although the 20-week anomaly scan showed no structural abnormalities, ...
Ozlem Sumer Cosar,Hakan Öztürk,Deniz Gezgin Yıldırım et al. Ozlem Sumer Cosar et al.
Protein-losing enteropathy (PLE) is a rare condition characterized by clinical findings such as edema, ascites, pleural effusion, and diarrhea due to excessive protein loss from the gastrointestinal system. Although systemic lupus erythemat...
Conner Thompson,Katsiaryna Khatskevich,Cynthia T Welsh et al. Conner Thompson et al.
Lennox-Gastaut syndrome is a form of severe childhood epilepsy caused by a variety of etiologies including structural abnormalities, inflammatory conditions affecting the brain, malignancy, injury, or unknown causes. Sodium channelopathies ...
Apostolou Alexia,Joubert Madeleine,Poreau Brice et al. Apostolou Alexia et al.
Background: Pulmonary agenesis is characterized by the absence of bronchi and lung parenchyma and it differs from pulmonary aplasia by the presence of rudimentary bronchial buds. SOX2 expression is observed during the nor...