Results 61 to 70 of about 119,125 (302)
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency (LCHADD) is an autosomal recessive mitochondrial defect of long‐chain fatty acid β‐oxidation, caused by biallelic pathogenic variants in HADHA or HADHB. We report a 22‐year‐old male with an atypically mild presentation of LCHADD who was referred to the Undiagnosed Diseases Network (UDN ...
Yutaka Furuta +9 more
wiley +1 more source
Maternal mortality ratio in Colombian municipalities, 2011. [PDF]
, 2015 Maternal mortality ratio in Colombian municipalities, 2011.
Fernando De la Hoz-Restrepo (704964) +6 more
core +1 more source
Maternal mortality in a tertiary care hospital: A 10-year review
International Journal of Preventive Medicine, 2013 Background: Epidemiological data pertaining to maternal mortality is valuable in each set up to design interventional programs to favourably reduce the ratio.
Bhaskar K Murthy +2 more
doaj
Asian Pacific Journal of Reproduction, 2016 Objective: To determine the trend, causes and characteristics of maternal deaths in a tertiary hospital in Northern Tanzania. Methods: A descriptive retrospective review of hospital based maternal death data that occurred at Kilimanjaro Christian Medical
Eusebious W. Maro +4 more
doaj +1 more source
Trends and Determinants of The Maternal Mortality Ratio Based on Healthcare Resources
Unnes Journal of Public Health, 2023 ABSTRACT Health resources play an essential role in realizing the unattainable Sustainable Development Goals targets in lowering maternal mortality ratio (MMR) globally. The study aimed to analyze trends and determinants of MMR based on the number of healthcare resources in Indonesia.
Bayu Anggileo Pramesona +2 more
openaire +1 more source
A Case of Multiple Mitochondrial Dysfunctions Syndrome 1 and Review of the Literature
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Multiple mitochondrial dysfunctions syndrome 1 (MMDS1, MIM #605711) due to NFU1 gene defects is an ultra‐rare autosomal recessive inborn error of metabolism associated with reduced function of NFU1 iron–sulfur cluster (ISC) scaffold protein.
Charles R. DiFalco +6 more
wiley +1 more source
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.ABSTRACT The present longitudinal study focuses on FMR1 premutation carrier women during midlife and early old age (n = 115). Bringing together the genetic risk factor of a family history of FXTAS and the environmental protective factor of higher education, the goal of the study was to determine how these factors potentially interact to predict self ...
Jinkuk Hong +4 more
wiley +1 more source
Maternal mortality in jos nigeria: a facility based prospective review [PDF]
International Journal of Biological and Medical Research, 2011 Objectives The study was designed to determine the maternal mortality ratio at the Jos University teaching Hospital and ascertain the causes of maternal death.
Stephen D. Ngwan, Terrumun Z. Swende
doaj
Public health approach to address maternal mortality
Indian Journal of Public Health, 2012 Reducing maternal mortality is one of the major challenges to health systems worldwide, more so in developing countries that account for nearly 99% of these maternal deaths.
Sanjay K Rai +4 more
doaj +1 more source
Over the edge: Empirical evidence for the cliff‐edge model of obstetric selection
The Anatomical Record, EarlyView.Abstract The cliff‐edge model of obstetric selection maintains that larger neonates and smaller birth canals confer a positive selective advantage until labor becomes obstructed and vaginal delivery is no longer possible, eliciting an abrupt reduction in fitness.
Laura M. Watson +6 more
wiley +1 more source