Clin Pediatr Endocrinol. 2026 Apr;35(2):186-191. doi: 10.1297/cpe.2025-0105. Epub 2026 Feb 5. ABSTRACT Schaaf-Yang syndrome (SYS) is a rare neurodevelopmental disorder with overlapping features with Prader-Willi …
Clin Pediatr Endocrinol. 2026 Apr;35(2):152-160. doi: 10.1297/cpe.2025-0076. Epub 2025 Dec 28. ABSTRACT Head shape undergoes rapid changes during infancy, but the age-dependent changes in cranial …
Mol Genet Metab. 2026 Mar 27;148(2):109912. doi: 10.1016/j.ymgme.2026.109912. Online ahead of print. ABSTRACT BACKGROUND: Citrin deficiency is an autosomal recessive metabolic disorder caused by pathogenic …
Front Public Health. 2026 Mar 17;14:1758836. doi: 10.3389/fpubh.2026.1758836. eCollection 2026. ABSTRACT BACKGROUND: Using data from the Lanzhou Birth Cohort in China, this study examined the …
Br J Haematol. 2026 Apr 2. doi: 10.1111/bjh.70459. Online ahead of print. NO ABSTRACT PMID:41924946 | DOI:10.1111/bjh.70459
Pediatr Blood Cancer. 2026 Apr 2:e70306. doi: 10.1002/1545-5017.70306. Online ahead of print. ABSTRACT Palliative home care for pediatric cancer patients has become increasingly common in …
Br J Haematol. 2026 Apr 2. doi: 10.1111/bjh.70465. Online ahead of print. NO ABSTRACT PMID:41924942 | DOI:10.1111/bjh.70465
Haematologica. 2026 Apr 2. doi: 10.3324/haematol.2025.300154. Online ahead of print. ABSTRACT Not available. PMID:41924922 | DOI:10.3324/haematol.2025.300154
Haematologica. 2026 Apr 2. doi: 10.3324/haematol.2025.300403. Online ahead of print. ABSTRACT RUNX1 familial platelet disorder (RUNX1-FPD) is associated with a 35% to 50% lifetime risk …
Haematologica. 2026 Apr 2. doi: 10.3324/haematol.2025.300093. Online ahead of print. ABSTRACT Not available. PMID:41924914 | DOI:10.3324/haematol.2025.300093
