1708-8569 - Search Results

Year	Number of Results
2008	55
2009	61
2010	86
2011	95
2012	79
2013	68
2014	96
2015	100
2016	113
2017	94
2018	112
2019	127
2020	104
2021	104
2022	182
2023	167
2024	53

1

Wang W, Liu CF. Wang W, et al. World J Pediatr. 2023 Oct;19(10):919-927. doi: 10.1007/s12519-023-00689-8. Epub 2023 Feb 3. World J Pediatr. 2023. PMID: 36735197 Review.

2

Prenatal risk factors and genetic causes of ADHD in children.

Kian N, Samieefar N, Rezaei N. Kian N, et al. World J Pediatr. 2022 May;18(5):308-319. doi: 10.1007/s12519-022-00524-6. Epub 2022 Mar 2. World J Pediatr. 2022. PMID: 35235183 Review.

3

Biomarkers of hypoxic-ischemic encephalopathy: a systematic review.

Caramelo I, Coelho M, Rosado M, Cardoso CMP, Dinis A, Duarte CB, Grãos M, Manadas B. Caramelo I, et al. World J Pediatr. 2023 Jun;19(6):505-548. doi: 10.1007/s12519-023-00698-7. Epub 2023 Apr 21. World J Pediatr. 2023. PMID: 37084165 Free PMC article. Review.

4

Analysis and validation of diagnostic biomarkers and immune cell infiltration characteristics in pediatric sepsis by integrating bioinformatics and machine learning.

Zhang WY, Chen ZH, An XX, Li H, Zhang HL, Wu SJ, Guo YQ, Zhang K, Zeng CL, Fang XM. Zhang WY, et al. World J Pediatr. 2023 Nov;19(11):1094-1103. doi: 10.1007/s12519-023-00717-7. Epub 2023 Apr 28. World J Pediatr. 2023. PMID: 37115484 Free PMC article.

5

Current status of human adenovirus infection in China.

Mao NY, Zhu Z, Zhang Y, Xu WB. Mao NY, et al. World J Pediatr. 2022 Aug;18(8):533-537. doi: 10.1007/s12519-022-00568-8. Epub 2022 Jun 18. World J Pediatr. 2022. PMID: 35716276 Free PMC article. Review.

6

Fever without a source in children: international comparison of guidelines.

Graaf S, Keuning MW, Pajkrt D, Plötz FB. Graaf S, et al. World J Pediatr. 2023 Feb;19(2):120-128. doi: 10.1007/s12519-022-00611-8. Epub 2022 Oct 26. World J Pediatr. 2023. PMID: 36287322 Free PMC article. Review.

7

Juvenile dermatomyositis: advances in clinical presentation, myositis-specific antibodies and treatment.

Wu JQ, Lu MP, Reed AM. Wu JQ, et al. World J Pediatr. 2020 Feb;16(1):31-43. doi: 10.1007/s12519-019-00313-8. Epub 2019 Sep 26. World J Pediatr. 2020. PMID: 31556011 Review.

8

Bartter's syndrome: clinical findings, genetic causes and therapeutic approach.

Mrad FCC, Soares SBM, de Menezes Silva LAW, Dos Anjos Menezes PV, Simões-E-Silva AC. Mrad FCC, et al. World J Pediatr. 2021 Feb;17(1):31-39. doi: 10.1007/s12519-020-00370-4. Epub 2020 Jun 1. World J Pediatr. 2021. PMID: 32488762 Review.

9

Haploinsufficiency of A20 (HA20): updates on the genetics, phenotype, pathogenesis and treatment.

Yu MP, Xu XS, Zhou Q, Deuitch N, Lu MP. Yu MP, et al. World J Pediatr. 2020 Dec;16(6):575-584. doi: 10.1007/s12519-019-00288-6. Epub 2019 Oct 5. World J Pediatr. 2020. PMID: 31587140 Review.

10

Inherited Fanconi syndrome.

Albuquerque ALB, Dos Santos Borges R, Conegundes AF, Dos Santos EE, Fu FMM, Araujo CT, Vaz de Castro PAS, Simões E Silva AC. Albuquerque ALB, et al. World J Pediatr. 2023 Jul;19(7):619-634. doi: 10.1007/s12519-023-00685-y. Epub 2023 Feb 2. World J Pediatr. 2023. PMID: 36729281 Review.

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