Results 121 to 130 of about 66,605 (262)
Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach +23 more
wiley +1 more source
Fertility postponement and age norms in Poland: is there a deadline for parenthood? [PDF]
The postponement of childbearing is occurring across Europe, but the paths of this trend differ profoundly from country to country. Especially in Central and Eastern Europe, most women have their first child at a relatively young age.
Monika A. Mynarska
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Compound Heterozygote Friedreich Ataxia Patients With Covert Proximal FXN Gene Deletions
ABSTRACT We present Friedreich ataxia patients with frataxin gene deletions. Data and records were collected at the Children's Hospital of Philadelphia from patients enrolled in the FACOMS natural history study. Patients with proximal deletions initially diagnosed with only one GAA expanded allele had more severe disease than their homozygous expansion
Michael P. Lazaropoulos +5 more
wiley +1 more source
Diverging Paths: Heterogeneities in Single Parenthood and Consequences for Child Poverty
The authors propose an expanded conceptualization of single parenthood that acknowledges within-group heterogeneity and investigate differential short- and long-term poverty outcomes on the basis of pathways into single parenthood.
Roxana-Diana Burciu, Zachary Parolin
doaj +1 more source
Bearing children in unstable times: psychological traits and early parenthood in a lowest-low fertility context, Rostock 1990 - 1995 [PDF]
In this paper, we analyze a unique longitudinal data set from Rostock in Eastern Germany. Data collection began in the communist era and has been followed up until today.
Francesco C. Billari +2 more
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ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li +11 more
wiley +1 more source
Being a parent can be one of the most fulfilling experiences, but also the most challenging. Its complexity is reflected in the fact that the very thought of becoming a parent often fills people with mixed feelings and leads them to postpone the decision
Małgorzata Szcześniak +2 more
doaj +1 more source
Single Parenthood and Childhood Outcomes in the Mid-Nineteenth Century Urban South [PDF]
Families are the core social institution and a growing body of research documents the costs of single parenthood for children in the twentieth century.
Howard Bodenhorn
core

