Results 81 to 90 of about 742,158 (388)

A study of diabetes mellitus within a large sample of Australian twins. [PDF]

open access: yes, 2008
Udgivelsesdato: 2008-FebTwin studies of diabetes mellitus can help elucidate genetic and environmental factors in etiology and can provide valuable biological samples for testing functional hypotheses, for example using expression and methylation studies
David L. Duffy   +9 more
core   +1 more source

Mortality Patterns and Phenotypic Clusters in Trisomy 13: A Population‐Based Study From Japan

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Trisomy 13, the third most common autosomal trisomy after trisomy 21 and trisomy 18, is associated with a significantly high infant mortality rate. However, large‐scale studies examining causes of death in trisomy 13 remain scarce. Therefore, we aimed to better understand the mortality patterns.
Narumi Kato   +2 more
wiley   +1 more source

Hyperglycemia and Adverse Pregnancy Outcome Follow-up Study (HAPO FUS): Maternal Gestational Diabetes Mellitus and Childhood Glucose Metabolism

open access: yesDiabetes Care, 2019
OBJECTIVE Whether hyperglycemia in utero less than overt diabetes is associated with altered childhood glucose metabolism is unknown. We examined associations of gestational diabetes mellitus (GDM) not confounded by treatment with childhood glycemia in ...
W. Lowe   +17 more
semanticscholar   +1 more source

Association of Maternal Prepregnancy Diabetes and Gestational Diabetes Mellitus With Congenital Anomalies of the Newborn

open access: yesDiabetes Care, 2020
OBJECTIVE To examine the association of maternal prepregnancy diabetes, gestational diabetes mellitus (GDM), and 12 subtypes of congenital anomalies of the newborn.
Yuxiao Wu   +7 more
semanticscholar   +1 more source

A Confirmatory Case of Severe Spondylocostal Dysostosis Caused by Biallelic Loss‐of‐Function of DMRT2

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Spondylocostal dysostosis (SCDO) is a rare genetic disorder characterized by abnormal development of the axial skeleton, resulting in malformations of the vertebrae and ribs that often impair lung development and lead to significant respiratory morbidity.
Jonathan Rips   +8 more
wiley   +1 more source

Is There An Association Between Kisspeptin Levels And Gestational Diabetes Mellitus?

open access: yesGynecology Obstetrics & Reproductive Medicine, 2020
Objective: To find out the relationship of maternal serum levels of kisspeptin with gestational diabetes mellitus status. Study Design: A total of 158 pregnant women between 24 and 28 weeks of gestation were divided into two groups according to ...
Emine Arslan, Umit Gorkem, Cihan Togrul
doaj   +1 more source

Diagnosis of gestational diabetes in Uganda: The reactions of women, family members and health workers

open access: yesWomen's Health, 2021
Objectives: In Uganda, as in many other low- and middle-income countries, screening for gestational diabetes mellitus is suboptimal and is rarely embedded in routine antenatal care.
Flavia Zalwango   +5 more
doaj   +1 more source

Impact of gestational weight gain on obstetric and neonatal outcomes in obese diabetic women [PDF]

open access: yes, 2015
Both obesity and gestational diabetes mellitus are increasing in prevalence, being a major health problem in pregnancy with independent and additive impact on obstetrics outcomes. It is recognized that inadequate gestational weight gain is an independent
AM Egan   +29 more
core   +1 more source

Perinatal Outcomes of Two Screening Strategies for Gestational Diabetes Mellitus

open access: yesObstetrics and Gynecology, 2021
Compared with Carpenter-Coustan criteria, the International Association of Diabetes and Pregnancy Study Groups criteria resulted in more women being diagnosed and treated for gestational diabetes without reducing the incidence of large-for-gestational ...
E. Davis   +11 more
semanticscholar   +1 more source

The HRAS Variant c.175G>A (p.Ala59Thr) Causes a Predominantly Ectodermal Phenotype Lacking Classic Costello Syndrome Features

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Costello syndrome (CS) is a rare dominant HRAS RASopathy characterized by curly hair, cardiac abnormalities, craniofacial anomalies, and developmental delay. HRAS codon 58, 59, and 60 variants are associated with milder phenotypes. We describe a three‐generation family with a previously unreported heterozygous HRAS variant c.175G>A (p.Ala59Thr)
Nikole Rautiainen   +10 more
wiley   +1 more source

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