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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:1.1/Q3

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共收录本刊相关文章索引633
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
Svetlana Shalygina,Leticia Gracia Sáenz,Jerónimo Gonzálvez Piñera et al. Svetlana Shalygina et al.
Fetiform teratoma (FT) and fetus-in-fetu (FIF) represent a spectrum of rare retroperitoneal masses containing organoid structures. While FIF is classically defined by the presence of a vertebral axis, FT lacks this organized skeletal develo...
Erica Price,Sunitha Suresh,Linda M Ernst Erica Price
Background: Fetal hemorrhage (FH) is an important and difficult cause of death to recognize at perinatal autopsy. Existing literature is restricted to case reports and small case series, and none comprehensively describe ...
Kalyani R Patel,Juan Putra Kalyani R Patel
Drug-induced liver injury (DILI) in children remains a diagnostic challenge due to its broad clinical and histologic spectrum. Based on pathogenesis, DILI is classified as idiosyncratic, intrinsic (direct), or indirect. In the United States...
Chrystalle Katte Carreon,Stephen P Sanders,Elizabeth D Blume et al. Chrystalle Katte Carreon et al.
Background: Desmin-related cardiomyopathy is a rare disorder caused by pathogenic variants in desmin and associated protein genes. We aimed to describe the clinical, histopathological, immunohistochemical, ultrastructural...
Rachel Guest,John Van Arnam,Darryl Kinnear et al. Rachel Guest et al.
DICER1 syndrome is a rare autosomal dominant cancer predisposition syndrome caused by germline mutations in the DICER1 gene and several associated benign and malignant entities. This case describes a premature 8-day old neonate prenatally d...
Bilge S Akkelle,Emine Celik,Esra Dirimtekin et al. Bilge S Akkelle et al.
Persistent diarrhea that occurs in the first weeks of life and is caused by monogenic defects are defined as congenital diarrhea and enteropathies (CoDEs). The PERCC1 (proline and glutamate-rich protein with coiled-coil domain 1) gene which...
Chen Sun,Jiafen Zhang,Xiao Yang Chen Sun
Dermatofibrosarcoma protuberans (DFSP) is an uncommon soft tissue sarcoma with a high risk of local recurrence, of which the congenital atrophic variant is exceptionally rare and prone to misdiagnosis. We report a case of a 10-month-old mal...
Irena Manukyan,Christopher T Rossi,Priya Vaidyanathan et al. Irena Manukyan et al.
Most thyroid nodules encountered in clinical endocrinology are epithelial in origin. In contrast, primary thyroid mesenchymal tumors are exceedingly rare but increasingly recognized with advances in immunohistochemistry and molecular diagno...
Katelyn E Moss,Heather L Keir,Theonia K Boyd et al. Katelyn E Moss et al.
Background: Placental calcifications are common and often associated with post-term placentas and maternal vascular disorders. However, their significance in specific fetal disease contexts remains poorly understood. Anec...