Front Pediatr. 2025 Sep 22;13:1678818. doi: 10.3389/fped.2025.1678818. eCollection 2025. NO ABSTRACT PMID:41059475 | PMC:PMC12499354 | DOI:10.3389/fped.2025.1678818
Front Pediatr. 2025 Sep 22;13:1530177. doi: 10.3389/fped.2025.1530177. eCollection 2025. ABSTRACT OBJECTIVE: This report presents the inaugural case of Gaucher disease identified in Kashgar Prefecture, Xinjiang, …
Ther Adv Infect Dis. 2025 Oct 5;12:20499361251357521. doi: 10.1177/20499361251357521. eCollection 2025 Jan-Dec. ABSTRACT The resurgence of monkeypox (mpox), driven by Clade IIb of the monkeypox …
Appl Clin Genet. 2025 Oct 2;18:189-197. doi: 10.2147/TACG.S538739. eCollection 2025. ABSTRACT BACKGROUND: 3M syndrome is a rare autosomal recessive genetic disorder characterized by significant intrauterine …
Global Health. 2025 Oct 7;21(1):56. doi: 10.1186/s12992-025-01151-2. ABSTRACT BACKGROUND: Despite strong evidence supporting breastfeeding’s benefits for maternal and child health, breastfeeding rates (e.g. any breastfeeding, …
Orphanet J Rare Dis. 2025 Oct 7;20(1):504. doi: 10.1186/s13023-025-03995-8. ABSTRACT BACKGROUND: Cutaneous venous malformations (cVMs) are rare vascular anomalies characterized by progressive vessel ectasia, leading …
BMC Med Inform Decis Mak. 2025 Oct 7;25(1):364. doi: 10.1186/s12911-025-03203-4. NO ABSTRACT PMID:41057927 | DOI:10.1186/s12911-025-03203-4
Orphanet J Rare Dis. 2025 Oct 7;20(1):505. doi: 10.1186/s13023-025-03952-5. NO ABSTRACT PMID:41057893 | DOI:10.1186/s13023-025-03952-5
Trials. 2025 Oct 7;26(1):390. doi: 10.1186/s13063-025-09164-3. NO ABSTRACT PMID:41057906 | DOI:10.1186/s13063-025-09164-3
Hum Genomics. 2025 Oct 7;19(1):116. doi: 10.1186/s40246-025-00827-5. ABSTRACT BACKGROUND: Recurrent acute liver failure (RALF) is a rare and life-threatening disorder often triggered by infections or …
