BMC Pediatr. 2024 Apr 5;24(1):242. doi: 10.1186/s12887-024-04715-0. ABSTRACT EPIDERMOLYSIS: Bullosa is a rare hereditary skin condition that causes blisters. Genes encoding structural proteins at or …
BMC Pediatr. 2024 Apr 5;24(1):243. doi: 10.1186/s12887-024-04709-y. ABSTRACT Cholangiocarcinoma in patients with Choledochal cysts is rare in childhood; however, it seriously affects the prognosis of …
Orphanet J Rare Dis. 2024 Apr 5;19(1):146. doi: 10.1186/s13023-024-03154-5. ABSTRACT Angelman syndrome (AS) is a neurodevelopmental disorder caused by abnormal expression of the maternal ubiquitin …
BMC Pediatr. 2024 Apr 5;24(1):244. doi: 10.1186/s12887-024-04670-w. ABSTRACT BACKGROUND: β-Thalassemia major (BTM) is one of the most common hereditary anemias worldwide. Patients suffer from iron …
BMC Health Serv Res. 2024 Apr 5;24(1):435. doi: 10.1186/s12913-024-10860-0. ABSTRACT BACKGROUND: Despite being a global public health concern, there is a research gap in analyzing …
J Neurosurg Pediatr. 2024 Apr 5:1-9. doi: 10.3171/2024.1.PEDS23229. Online ahead of print. ABSTRACT OBJECTIVE: Congenital anomalies of the atlanto-occipital articulation may be present in patients …
J Neurosurg. 2024 Apr 5:1-2. doi: 10.3171/2024.1.JNS232800. Online ahead of print. NO ABSTRACT PMID:38579350 | DOI:10.3171/2024.1.JNS232800
J Neurosurg Pediatr. 2024 Apr 5:1-10. doi: 10.3171/2024.1.PEDS23128. Online ahead of print. ABSTRACT OBJECTIVE: A minority of pediatric patients who may benefit from epilepsy surgery …
Swiss Med Wkly. 2023 Nov 28;153:40129. doi: 10.57187/smw.2023.40129. ABSTRACT AIM OF THE STUDY: The global prevalence of scabies is estimated to be up to 200 …
J Neurosurg Pediatr. 2024 Apr 5:1-12. doi: 10.3171/2024.1.PEDS23444. Online ahead of print. ABSTRACT OBJECTIVE: More than one-third of pediatric patients who undergo resection of intradural …
