Results 161 to 170 of about 217,621 (296)

Assessing the costs of antenatal care in Eastern Ethiopia: implications for improving the free maternity services policy. [PDF]

Health Policy Plan
Tolossa T, Gold L, Lau EHY, Dheresa M, Abimanyi-Ochom J.   +4 more
europepmc   +1 more source

Accurate identification and documentation of First Nations women and babies attending maternity services: How can we 'close the gap' if we can't get this right? [PDF]

Aust N Z J Obstet Gynaecol, 2023
McLardie-Hore FE, McLachlan HL, Newton MS, Bundle G, Druce T, Jackomos M, Forster DA.   +6 more
europepmc   +1 more source

Genome Sequencing in 19 Families With Bladder Exstrophy and Epispadias Complex Indicates Involvement of the ADGR‐Gene Family

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Bladder exstrophy and epispadias complex (BEEC) is one of the most severe congenital malformations of the urogenital tract, significantly impacting continence, sexual function, and renal function. To date, the only recurrent genetic aberration identified is the 22q.11.2 microduplication, but several candidate regions and genes including ...
Agneta Nordenskjöld, Samara Alm, Jesper Eisfeldt, Jia Cao, Magnus Anderberg, Gillian Barker, Hans Matsson, Gundela Holmdahl, Anna Lindstrand, Kristina Lagerstedt‐Robinson   +9 more
wiley   +1 more source

Improving the quality of induction of labour in maternity services. [PDF]

BMJ Open Qual
Elnasharty M, Al-Dabbagh R, Makramallah I, Ismail A.   +3 more
europepmc   +1 more source

Black, Asian and minority ethnic women's experiences of maternity services in the UK: A qualitative evidence synthesis. [PDF]

J Adv Nurs, 2022
MacLellan J, Collins S, Myatt M, Pope C, Knighton W, Rai T.   +5 more
europepmc   +1 more source

Facilitating Genetic Testing for Perinatal Demise: Development of a Multidisciplinary Workflow

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Genetic contributors to perinatal demise are common but frequently undiagnosed due to clinical and logistical barriers. We aimed to improve access to genetic for intrauterine fetal demise (IUFD), stillbirth, and early neonatal death by developing a multidisciplinary workflow.
Mackenzie Mosera, Samantha Stover, Elise Boos, Molly Casey, Joseph Fanning, Chelsea Fechter, Matthew Grace, L. Dupree Hatch, Michaela Ibach, Carla Jackson, Jiancong Liang, Caitlin Mann, Emily A. Morris, Jessica Turnbull, Marie Williams, Bryce A. Schuler   +15 more
wiley   +1 more source

The role of social risk factors and engagement with maternity services in ethnic disparities in maternal mortality: A retrospective case note review. [PDF]

EClinicalMedicine, 2022
Cosstick E, Nirmal R, Cross-Sudworth F, Knight M, Kenyon S.   +4 more
europepmc   +1 more source

Longitudinal Behavior Phenotype Hallmarks in RNU4‐2 Syndrome: Implications for Clinical Management

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Pathogenic variants in the non‐coding spliceosomal gene RNU4‐2 underlie ReNU syndrome, one of the most prevalent monogenic causes of neurodevelopmental disorders, accounting for ~0.4% of cases. Despite increasing recognition, little is known about the longitudinal behavioral and neuropsychiatric phenotype of affected individuals. We report two
Paola Francesca Ajmone, Claudia Rigamonti, Francesca Brasca, Donatella Milani, Chiara Ranci Ortigosa, Maria Iascone, Lucrezia Goisis, Annalaura Torella, Maria Antonella Costantino   +8 more
wiley   +1 more source

How Woman-Centred Care Is Experienced and Understood in Maternity Services by Women and Professionals: A Rapid Review. [PDF]

Scand J Caring Sci
Gregory S, Caffrey L, Daly D, Sheaf G.
europepmc   +1 more source

Transformational Change in maternity services in England: a longitudinal qualitative study of a national transformation programme 'Early Adopter'. [PDF]

BMC Health Serv Res, 2022
Taylor B, Hewison A, Cross-Sudworth F, Morrell K.   +3 more
europepmc   +1 more source