Results 41 to 50 of about 57,263 (279)

Fatherhood, intra-household employment dynamics, and men's earnings in a cross-national perspective [PDF]

open access: yes, 2013
Studies find fatherhood earnings premiums in several European countries and the United States. Yet little research investigates how intra-household dynamics shape the size of the fatherhood premium cross-nationally.
Boeckmann, Irene, Budig, Michelle
core  

Relative Exchangeable Copper Confirms Wilson Disease and Supports Reclassification of the ATP7B p.Met665Ile Variant With Conflicting Pathogenicity Evidence

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Wilson disease (WD) is an autosomal recessive disorder of copper metabolism caused by ATP7B mutations. Diagnosis is usually straightforward in symptomatic patients, but can be challenging in children and adolescents with mild liver disease, borderline urinary copper excretion, or inconclusive genetic findings.
Emanuele Nicastro   +10 more
wiley   +1 more source

STUDY OF IDEAS ABOUT RESPONSIBLE FATHERHOOD IN YOUNG PEOPLE WHO DO NOT HAVE THEIR OWN CHILDREN

open access: yesВестник университета, 2019
The problem of studying the ideas of responsible fatherhood in young people aged 18 to 25 years, who do not have their own children has been considered.
S. N. Savinkov, V. V. Kozyreva
doaj   +1 more source

Single fathers by choice using surrogacy. Why men decide to have a child as a single parent [PDF]

open access: yes, 2017
STUDY QUESTION: Why do men decide to have a child by surrogacy as a single parent? SUMMARY ANSWER: Reasons included feeling that it was the right time (i.e.
Baiocco, Roberto   +2 more
core   +2 more sources

Optimizing Diagnostic Accuracy of Clinical Red Flags in RASopathies

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT RASopathies are a group of genetic disorders caused by pathogenic variants in the RAS‐mitogen‐activated protein kinase (RAS–MAPK) signaling pathway, often presenting with congenital heart defects, craniofacial dysmorphisms, and developmental delays. To assess the diagnostic yield of genetic testing in patients with suspected RASopathies and to
Emanuele Bobbio   +16 more
wiley   +1 more source

Reading The Road with Paul Ricoeur and Julia Kristeva: The Human Body as a Sacred Connection [PDF]

open access: yes, 2014
Cormac McCarthy’s novel The Road confronts readers with a question: what is there to live towards after apocalypse? McCarthy locates his protagonists in the aftermath of the world’s fiery destruction, dramatizing a relationship between a father and a son,
Arel, Stephanie
core   +2 more sources

The 9th International RASopathies Symposium

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The RASopathies are a group of congenital disorders with overlapping clinical manifestations that are caused by pathogenic germline or early somatic variants that result in the hyperactivation of the RAS/mitogen‐activated protein kinase (MAPK) signaling pathway.
Pau Castel   +41 more
wiley   +1 more source

The prevalence of adolescent fatherhood and its associated factors in East African countries

open access: yesBMC Public Health
Background In developing nations, the phenomenon of adolescent fatherhood poses significant challenges, including increased risk of poverty, limited educational opportunities, and potential negative health outcomes for both the young fathers and their ...
Bewuketu Terefe   +5 more
doaj   +1 more source

Restoring Fathers to Families and Communities: Six Steps for Policymakers [PDF]

open access: yes, 2000
Presents a detailed strategy for legislative and administrative efforts that state and local officials can implement to promote father involvement, especially among low-income, unwed ...
Kathleen Sylvester, Kathy Reich
core  

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12‐Related Developmental Disorders

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken   +4 more
wiley   +1 more source

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