Results 51 to 60 of about 79,262 (343)

Alternative versus conventional institutional settings for birth [PDF]

open access: yes, 2010
Background: Alternative institutional settings have been established for the care of pregnant women who prefer and require little or no medical intervention.
Downe, Soo   +2 more
core   +1 more source

Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat   +4 more
wiley   +1 more source

Comparison of the Combined versus Conventional Apgar Scores in Predicting Adverse Neonatal Outcomes. [PDF]

open access: yesPLoS ONE, 2016
OBJECTIVES:Assessing the value of the Combined-Apgar score in predicting neonatal mortality and morbidity compared to the Conventional-Apgar. METHODS:This prospective cohort study evaluated 942 neonates (166 very preterm, 233 near term, and 543 term ...
Hosein Dalili   +5 more
doaj   +1 more source

Thrombocytopenia in Preterm Infants with Intrauterine Growth Restriction [PDF]

open access: yes, 2008
Sick preterm infants often have thrombocytopenia at birth, and this is often associated with intrauterine growth restriction (IUGR), or birth weights less than the 10th percentile.
Akahori, Yo-ichiro   +7 more
core   +1 more source

Expanding the Genotype–Phenotype Correlation of Marden–Walker Syndrome due to PIEZO2 Gene Variants: A Case Report From Brazil

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Marden–Walker syndrome (MWS; OMIM 248700) is an extremely rare congenital disorder characterized by multiple joint contractures, craniofacial dysmorphism, neurological abnormalities, and multisystem involvement. Although historically diagnosed on clinical grounds, only a few cases have been molecularly confirmed.
Guilherme Sotto Battiston   +35 more
wiley   +1 more source

Surgical Apgar Score Predicts Postoperative Complications in Traumatic Brain Injury ​

open access: yesThe Annals of African Surgery, 2016
Background: Predicting complications in neurotrauma patients by using an effective scoring system can reduce morbidity and mortality while facilitating objective clinical decision making during recovery.
Yusufali TS   +3 more
doaj  

Prevalence of Electrolyte Imbalance in Hypoxic-ischemic Encephalopathy: A Hospital-based Prospective Observational Study [PDF]

open access: yesIranian Journal of Neonatology, 2019
Background: The present study aimed to investigate the prevalence of electrolyte imbalance in hypoxic-ischemic encephalopathy (HIE). Moreover, the correlation of this condition with Apgar score is evaluated.
Jehangir Allam Bhat   +2 more
doaj   +1 more source

Prevalence and Immediate Outcomes of Hypoxic Ischaemic Encephalopathy (HIE) Among Infants with Birth Asphyxia Admitted at the Neonatal ward of Muhimbili National Hospital in Dar es Salaam, Tanzania [PDF]

open access: yes, 2007
\ud To determine the prevalence and immediate outcome of infant with hypoxic ischemic encephalopathy (HIE) admitted at the Neonatal ward [ward 36] of Muhimbili National Hospital.
Juma, Athuman
core  

The psychosocial impact of vaginal delivery and cesarean section in primiparous women [PDF]

open access: yes, 2018
The aim of this study was to identify how the method of delivery and birth experience interfere with maternal psychological status early after puerperium.
Alexandroaia, Camelia   +6 more
core   +3 more sources

Homozygous Achondroplasia With Long‐Term Survival: Growth Patterns, Medical Interventions, and Practice Implications

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Homozygous achondroplasia is widely considered perinatal lethal by the medical community. In this case series, we report two children from a single family with longer‐term survival. One child lived for 17 months and the other was 60 months at the time of publication.
Hannah Singerline   +3 more
wiley   +1 more source

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