Results 151 to 160 of about 120,079,059 (280)

Causes and consequences of uncertainty about illness risk perceptions. [PDF]

open access: yesJ Health Psychol, 2020
Orom H   +5 more
europepmc   +1 more source

Psychosocial Adjustment to Illness : Uncertainty and Coping in the Implantable Cardioverter Defibrillator Population

open access: yes, 2000
The implantable defibrillator is the treatment of choice in patients with life threatening ventricular arrhythmias. While defibrillators reduce the incidence of death, the psychosocial impact on the patient and family can be profound.
Provell, Evelyn M.
core   +1 more source

COX14 Variants Are Associated With Mitochondrial Complex IV Deficiency Nuclear Type 10 (MC4DN10)

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT COX14 encodes a transmembrane protein essential for cytochrome c oxidase (COX) complex assembly. A homozygous missense variant in COX14 was reported in three siblings from a single consanguineous family with severe, fatal infantile mitochondrial complex IV deficiency nuclear type 10 (MC4DN10; MIM# 619053).
Elias K. Awad   +7 more
wiley   +1 more source

Swallowing function, body image and uncertainty in illness after reconstruction in oral cancer survivors

open access: yes
Background: Swallowing and body image are the main concerns after reconstruction for oral cancer. Perceiving uncertainty or an unpredictable future is a significant psychosocial stressor in cancer survivors.
Chun-Ta Liao   +2 more
core   +1 more source

Care strategies for people with cancer in light of Uncertainty in Illness Theory. [PDF]

open access: yesRev Bras Enferm
Silveira JM   +7 more
europepmc   +1 more source

Spinal Involvement in Charge Syndrome: Implications for Management

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT CHARGE syndrome (OMIM #214800) is an autosomal dominant disorder caused by mutations in the CHD7 gene in most cases. Although originally defined by the CHARGE acronym (coloboma, heart defects, choanal atresia, growth restriction, genital hypoplasia, and ear anomalies), the recognized phenotype has expanded considerably to include highly ...
Adriana Gomes   +5 more
wiley   +1 more source

A Rare Form of Microcephalic Primordial Dwarfism due to NSMCE2 Deficiency (Seckel Syndrome Type 10): A Report of Macular Involvement

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto   +5 more
wiley   +1 more source

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