Search Results - "Fetal and pediatric pathology"

Vertical Transmission of Coronavirus Disease 19 (COVID-19) from Infected Pregnant Mothers to Neonates: A Review by Karimi-Zarchi, Mojgan, Neamatzadeh, Hossein, Dastgheib, Seyed Alireza, Abbasi, Hajar, Mirjalili, Seyed Reza, Behforouz, Athena, Ferdosian, Farzad, Bahrami, Reza

“…Background: Since early December 2019, the Coronavirus Disease 19 (COVID-19) infection has been prevalent in China and eventually spread to other countries…”
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Fatal Eosinophilic Myocarditis in a Healthy 17-Year-Old Male with Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2c) by Craver, Randall, Huber, Samantha, Sandomirsky, Marrianna, McKenna, Dwight, Schieffelin, John, Finger, Leron

“…Background: Cardiac damage is frequently referred to in patients with SARS-CoV-2, is usually diagnosed by enzyme elevations, and is generally thought to be due…”
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Histopathology of Third Trimester Placenta from SARS-CoV-2-Positive Women by He, Mai, Skaria, Priya, Kreutz, Kasey, Chen, Ling, Hagemann, Ian S., Carter, Ebony B., Mysorekar, Indira U., Nelson, D. Michael, Pfeifer, John, Dehner, Louis P.

“…Background: This study aims to investigate whether maternal SARS-CoV-2 status affects placental pathology. Methods: A retrospective case-control study was…”
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Early Pregnancy Losses: Review of Nomenclature, Histopathology, and Possible Etiologies by Pinar, M. Halit, Gibbins, Karen, He, Mai, Kostadinov, Stefan, Silver, Robert

“…Miscarriage is a frequent complication of human pregnancy: ∼50% to 70% of spontaneous conceptions are lost prior to the second trimester. Etiology of…”
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Exploring Causal Correlations Between Inflammatory Cytokines and Kawasaki Disease: A Mendelian Randomization by Pan, Yan, Jiao, Fuyong

“…The role of inflammatory cytokines in Kawasaki disease (KD) pathogenesis is known, but causal relationships are unclear. This study investigates these…”
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A Rare Case of Meckel-Gruber Syndrome with Congenital Intestinal Atresia and Abdominal Pseudocyst Clinic by Ulusoy Tangul, Sevgi, Gencan, Gizem

“…Meckel-Gruber syndrome (MGS) is a rare disease with a fatal, autosomal recessive inheritance pattern. This article mentions the neonatal MGS case followed by…”
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New Marker in the Umbilical Cord Blood of Fetuses with Fetal Growth Restriction: Serum Sortilin-1 Level by Karabay, Gulsan, Bayraktar, Burak, Seyhanli, Zeynep, Tokguz Cakir, Betul, Aktemur, Gizem, Topkara Sucu, Serap, Tonyali, Nazan Vanlı, Ipek, Selma, Kolomuc Gayretli, Tugba, Celen, Sevki

“…To determine the role of sortilin in the pathogenesis of fetal growth restriction (FGR) by examining serum sortilin levels in fetal cord blood. This…”
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Cornelia de Lange Syndrome: Expanding the Neuropathological Spectrum and Clinical Correlations by Della Giustina, Elvio, Salviato, Tiziana, Caramaschi, Stefania, Fabbiani, Luca, Reggiani Bonetti, Luca

“…Reporting new neuropathological findings and clinicopathological correlations in Cornelia de Lange syndrome. Cornelia de Lange syndrome has received much…”
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Secondary TFE3 -Rearranged Renal Cell Carcinoma in a Chinese Girl Treated for Wilms Tumor: Case Report and Literature Review by Chu, Jing, Chen, Lian

“…With the development of modern medicine and the application of multimodal treatment strategies, the survival rate after childhood malignant tumors as well as…”
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Pediatric Angiosarcoma with Novel Phenotypic and Genotypic Profile in Chinese Children by Shao, Bo, Fang, Yuan, Wang, Yizhen, Chen, Lian

“…Angiosarcoma is an exceedingly rare entity in pediatric population. Herein, we report two pediatric angiosarcoma with novel phenotypic and genotypic profile…”
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Prompt Cytopathological Diagnosis of Multiple Xanthomatous Skin Nodules in an Adolescent Girl Opening the Doors to Detection of Familial Hypercholesterolemia by Malik, Shaivy, Kandwal, Preeti, Madan, Neha Kawatra, Agrawal, Meetu, Ranga, Sunil

“…Xanthomas are papulo-nodular, yellow, soft, painless, dermal-based non-neoplastic cutaneous lesions that comprise of localized aggregates of lipid-laden…”
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A Comprehensive Consolidation of Data on the Relationship Between Surfactant Protein-B (SFTPB) Polymorphisms and Susceptibility to Bronchopulmonary Dysplasia by Bahrami, Reza, Golshan-Tafti, Mohammad, Dastgheib, Seyed Alireza, Alijanpour, Kamran, Yeganegi, Maryam, Lookzadeh, Mohamad Hosein, Mirjalili, Seyed Reza, Azizi, Sepideh, Aghasipour, Maryam, Shiri, Amirmasoud, Noorishadkam, Mahmood, Neamatzadeh, Hossein

“…This meta-analysis aims to evaluate the potential link between common variations in the Surfactant Protein-B (SFTPB) gene and the risk of bronchopulmonary…”
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Orbital Sarcoma with BCOR Genetic Alterations in the Pediatric Age Group by Salman, Syed Saad, Kakkar, Aanchal, Kashyap, Seema, Rastogi, Sameer, Meel, Rachna

“…Pediatric orbital tumors encompass a wide spectrum of neoplasms, many of which are malignant small round cell tumors with overlapping histology. Sarcomas with…”
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A Comprehensive Compilation of Data on the Relationship Between Surfactant Protein-B (SFTPB) Polymorphisms and Susceptibility to Neonatal Respiratory Distress Syndrome by Golshan-Tafti, Mohammad, Bahrami, Reza, Dastgheib, Seyed Alireza, Lookzadeh, Mohamad Hosein, Mirjalili, Seyed Reza, Yeganegi, Maryam, Marzbanrad, Zahra, Aghasipour, Maryam, Shahbazi, Amirhossein, Masoudi, Ali, Noorishadkam, Mahmood, Neamatzadeh, Hossein

“…This study aims to explore the association between variations in the Surfactant Protein-B (SFTPB) gene and the risk of neonatal respiratory distress syndrome…”
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Correlation Between the Expression of DNA Damage Repair Protein OGG1 and Ubiquitination Pathway Protein STUB1 in Pediatric Neuroblastoma by Shao, Bo, Wang, Yi-Zhen, Fang, Yuan

“…Neuroblastoma, a pediatric malignancy, is significantly influenced by genetic factors. Prior research indicates that the rs1052133 G > C polymorphism…”
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Assessment of Matrix Metalloprotease - 7 (MMP7) Immunohistochemistry in Biliary Atresia and Other Pediatric Cholestatic Liver Diseases by Biswal, Sandhya, Biswas, Dipanwita, Mahalik, Santosh Kumar, Purkait, Suvendu, Mitra, Suvradeep

“…Biliary atresia (BA) is a progressive fibro-obliterative cholangiopathy. The histopathological diagnosis is often challenging and an immunohistochemical marker…”
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Early Onset Inflammatory Bowel Disease Due to Immunodeficiency as a Result of ICOS Gene Homozygous Mutation by Arsoy, Hanife Ayşegül, Hafızoğlu, Demet, Terzi, Hatice Zeynep, Turhan, Ezgi Işıl

“…Inflammatory bowel disease (IBD) is classified as very early-onset IBD (VEO-IBD) if it occurs before age six. VEO-IBD may progress with more severe and…”
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Performance Validation of the NeoBase 2 Non-Derivatized MSMS Assay Kit and Cutoff Values Establishment of Term and Preterm Neonates by Wan, Zhihui, Liu, Wei, Zhai, Yanhong, Ma, Zhijun, Cao, Zheng

“…NeoBase 2 Non-derivatized MSMS assay kit (NeoBase 2 kit) was used for newborn screening, the performance of the NeoBase 2 kit should be validated before its…”
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Construction of a Cancer Stem Cell Marker Genes-Related 22-Gene Signature for Overall Survival Prediction in High-Risk Wilms' Tumor by Duan, Lihong, Xia, Wudie

“…This study aimed to investigate the comprehensive expression profile of cancer stem cell (CSC)-related genes and construct a prognostic signature for overall…”
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Association of Endothelial Nitric Oxide Synthase 894G > T Polymorphism with Preeclampsia Risk: A Systematic Review and Meta-Analysis based on 35 Studies by Abbasi, Hajar, Dastgheib, Seyed Alireza, Hadadan, Amaneh, Karimi-Zarchi, Mojgan, Javaheri, Atiyeh, Meibodi, Bahare, Zanbagh, Leila, Tabatabaei, Razieh Sadat, Neamatzadeh, Hossein

“…Several case-control studies have been performed to investigate the association between 894 G > T polymorphism in endothelial nitric oxide synthase (eNOS) gene…”
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