EDITORIAL
Published on 24 Jan 2022
Editorial: New Therapeutic Options for Rare Diseases
doi 10.3389/fped.2021.832395
- 1,870 views
- 1 citation
- Frontiers in Pediatrics
- Genetics of Common and Rare Diseases
- Research Topics
- New Therapeutic Options for Rare Diseases
New Therapeutic Options for Rare Diseases
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Articles
ORIGINAL RESEARCH
Published on 15 Oct 2021
Effect of Sirolimus on the Level of Peripheral Blood Lymphocyte Autophagy in Children With Systemic Lupus Erythematosus
doi 10.3389/fped.2021.685497
- 2,273 views
- 2 citations
CASE REPORT
Published on 18 Aug 2021
Case Report: ISPD Gene Mutation Leads to Dystroglycanopathies: Genotypic Phenotype Analysis and Treatment Exploration
doi 10.3389/fped.2021.710553
- 2,096 views
- 3 citations
CASE REPORT
Published on 10 Jun 2021
Case Report: Cerebral Revascularization in a Child With Mucopolysaccharidosis Type I
doi 10.3389/fped.2021.606905
- 1,901 views
- 1 citation
ORIGINAL RESEARCH
Published on 29 Apr 2021
Identification of Hub Genes and MicroRNAs Associated With Idiopathic Pulmonary Arterial Hypertension by Integrated Bioinformatics Analyses
doi 10.3389/fgene.2021.636934
- 3,887 views
- 11 citations
CORRECTION
Published on 05 Mar 2021
Corrigendum: Characteristics of Genetic Variations Associated With Lennox-Gastaut Syndrome in Korean Families
doi 10.3389/fgene.2021.669107
- 1,114 views
- 2 citations
BRIEF RESEARCH REPORT
Published on 04 Mar 2021
Novel Gross Deletion Mutations in NTRK1 Gene Associated With Congenital Insensitivity to Pain With Anhidrosis
doi 10.3389/fped.2021.638190
- 3,676 views
- 8 citations
CASE REPORT
Published on 04 Mar 2021
Case Report: A Novel PAX3 Mutation Associated With Waardenburg Syndrome Type 1
doi 10.3389/fgene.2021.609040
- 3,825 views
- 2 citations
MINI REVIEW
Published on 19 Feb 2021
Liver Transplantation for Glycogen Storage Disease Type IV
doi 10.3389/fped.2021.633822
- 3,941 views
- 14 citations
CORRECTION
Published on 15 Feb 2021
Corrigendum: Pediatric NMOSD: A Review and Position Statement on Approach to Work-Up and Diagnosis
doi 10.3389/fped.2020.642203
- 1,235 views
- 2 citations
ORIGINAL RESEARCH
Published on 20 Jan 2021
Characteristics of Genetic Variations Associated With Lennox-Gastaut Syndrome in Korean Families
doi 10.3389/fgene.2020.590924
- 7,511 views
- 3 citations
REVIEW
Published on 23 Nov 2020
New Therapeutics Options for Pediatric Neuromuscular Disorders
doi 10.3389/fped.2020.583877
- 5,824 views
- 12 citations
Published in
Frontiers in Pediatrics
- Genetics of Common and Rare Diseases
- Pediatric Immunology
- Pediatric Neurology
Participating Journals
Frontiers in Genetics
- 2.8 impact factor
- 5.5 citescore
Frontiers in Neurology
- 2.7 impact factor
- 4.9 citescore
Impact
- 149kTopic views
- 120kArticle views
- 27kArticle downloads