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期刊名:Molecular and cellular pediatrics

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e-ISSN:2194-7791

IF/分区:3.4/Q1

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共收录本刊相关文章索引241
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
Zhijuan Kang,Liang Zhang Zhijuan Kang
Here, we report a female (aged 1 year and 8 months) who presented with recurrent skin lesions, hepatosplenomegaly, lymphadenopathy, and fever. She was diagnosed initially with systemic lupus erythematosus and lupus nephritis with mild anemi...
Katja Linz,Felix Wachter,Merle Claßen et al. Katja Linz et al.
Background and aims: Altered bile acids (BA) are key drivers of hepatic disorders and beyond. The breakdown of BA profiles could serve as advanced biomarkers, but data in pediatric patients is scarce. In this work we retr...
Nesma M Elaraby,Ammal M Metwally,Sara M Sayed et al. Nesma M Elaraby et al.
Background: Inherited kidney diseases (IKDs) are a significant cause of chronic kidney disease (CKD) and end-stage kidney disease (ESKD), especially in children. While next-generation sequencing (NGS) has enhanced IKD dia...
Nadine Freitag,Dirk Schramm,Anja Stefanski et al. Nadine Freitag et al.
Background: Bronchoalveolar lavage fluid (BALF) is a valuable diagnostic and research tool in paediatric respiratory medicine. Mass spectrometry-based proteomic analysis of BALF can contribute to uncover disease mechanism...
Devesh Srivastava,Anurag Gupta,Nishant Verma et al. Devesh Srivastava et al.
Background: B-cell acute lymphoblastic leukemia (B-ALL) is characterized by the malignant burgeoning of abnormal B-cell lymphoblasts. In recent years, the use of chimeric antigen receptor T-cell (CAR-T) therapy which targ...
Mohamed El-Mezayen,Abdelrahman M Tawfik,Abdalla M Hadhoud et al. Mohamed El-Mezayen et al.
Background: Acid sphingomyelinase deficiency (ASMD), also known as Niemann-Pick disease types A and B, is a rare autosomal recessive lysosomal storage disorder caused by SMPD1 mutations. It is characterized by sphingomyel...
Unai Illarregi,Nerea Bilbao-Aldaiturriaga,Angela Gutierrez-Camino et al. Unai Illarregi et al.
Background: B-cell Acute Lymphoblastic Leukemia (B-ALL) remains an important cause of cancer-related death in children. Therefore, accurate identification at diagnosis of patients at high risk of relapse is crucial. In th...
Emmanuelle Zakheim,Sonal Sachdeva,Daniel Moon et al. Emmanuelle Zakheim et al.
Achondroplasia, the most prevalent skeletal dysplasia, is a genetic disorder caused by activating mutations in the FGFR3 gene impairing endochondral ossification of long bones. Clinical manifestations include disproportionate short stature ...
Calvin Kurz,Marcia Roeper,Alena Welters et al. Calvin Kurz et al.
Neonatal hypothermia and hypoglycemia are among the most common clinical disturbances in the immediate postnatal period and contribute to short- and long-term morbidity. While both conditions have been well described individually, particula...