Results 111 to 120 of about 22,210 (303)
Journal of Advanced Nursing, EarlyView.ABSTRACT Aim To test the feasibility and acceptability of a newly developed model of neonatal nurse‐controlled analgesia to manage pain in the post‐operative infant. Design The study utilised a single‐centre two‐arm parallel, unblinded randomised controlled external pilot trial design.
Renee Muirhead +5 more
wiley +1 more source
Intestinal synthesis and secretion of bile salts as an adaptation to developmental biliary atresia in the sea lamprey [PDF]
, 2012 Chu‐Yin Yeh +4 more
openalex +1 more source
Pathology Seen in Myenteric Plexus in Two Subjects With Waardenburg Syndrome
Neurogastroenterology &Motility, EarlyView.Ganglion cells immunohistochemically labeled with pan‐neuronal marker HuC/D in sections from ileum. Note the different number of stained cells in the myenteric plexus. A, control subject, B, patient with SOX10 mutation (hypoganglionosis) C, patient with EDN3 mutation (aganlionosis). Both patients diagnosed with Waardenburg syndrome type 4 including gut
Björn Ersson +3 more
wiley +1 more source
014. Localized Meconium Peritonitis Due to Perforation of Ileum Atresia: Case Report
JBN (Jurnal Bedah Nasional)Background: Ileal atresia is a congenital disorder that can cause serious complications such as intestinal obstruction, intestinal ischemia, and intestinal rupture.
Gina Amalia, Avriana Pety Wardhani
doaj +1 more source
ATRESIA Y ESTENOSIS INTESTINALES COMO CAUSA DE OCLUSIÓN EN EL RECIÉN NACIDO [PDF]
, 2022 José Miguel Maldonado Macías +4 more
openalex +1 more source
A Population‐Based Study of Limb Body Wall Complex With Proposed Features for Prenatal Diagnosis
American Journal of Medical Genetics Part A, Volume 197, Issue 11, November 2025.ABSTRACT Limb body wall complex (LBWC) is a lethal condition comprising major congenital anomalies. Although currently diagnosed in the early prenatal period, historical diagnostic criteria are based on detailed pathological assessments. Prenatal and postnatal findings of LBWC and their phenotypic overlap with body stalk anomaly (BSA) and recurrent ...
Mary Ann Thomas +2 more
wiley +1 more source
Exome sequencing identifies mutations in the geneTTC7Ain French-Canadian cases with hereditary multiple intestinal atresia [PDF]
, 2013 Mark E. Samuels +19 more
openalex +1 more source
American Journal of Medical Genetics Part A, Volume 197, Issue 11, November 2025.ABSTRACT Gastrointestinal (GI) symptoms are common in CHARGE syndrome, but their frequency and characteristics remain poorly documented due to the complex nature of CHARGE syndrome. This study aimed to determine the prevalence of GI issues in CHARGE syndrome and their impact on quality of life (QoL).
Annie Kakamousias, Kim Blake
wiley +1 more source
Medisur, 2005 Esophageal atresia is the congenital lack of continuity of the esophagus with or without communication to the airway. Incidence is estimateed in 1 by 3000 to 4500 alive newborns. Cases in brothers are found and children of parents with atresia esophagus,
Crisanto Abad Celuria +2 more
doaj +2 more sources
Tubular intestinal duplication extending from the stomach to the ileum associated with multiple intestinal atresia and situs inversus: a case report [PDF]
, 2023 Naruki Higashidate +9 more
openalex +1 more source