Results 181 to 190 of about 482,946 (280)

Short sleep duration in adults with congenital heart disease is associated with epicardial adipose tissue accumulation. [PDF]

open access: yesFront Psychiatry
Stapel B   +9 more
europepmc   +1 more source

Prevalence and Geographic Patterns of Self-Reported Short Sleep Duration Among US Adults, 2020. [PDF]

open access: yesPrev Chronic Dis, 2023
Pankowska MM   +6 more
europepmc   +1 more source

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young   +6 more
wiley   +1 more source

Sleep Irregularity and Short Sleep Duration Are Associated with Less Favorable Cardiometabolic Profiles in Healthy Adults: A Cross-Sectional Study. [PDF]

open access: yesNutrients
Lotti S   +9 more
europepmc   +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

Short Sleep Duration is Inversely Associated with the Prevalence of Underweight in a Young Japanese Population. [PDF]

open access: yesNat Sci Sleep
Ishikawa S   +18 more
europepmc   +1 more source

Brugada Syndrome: New Implications for Heterozygous Carriers of the Pathogenic SCN5A c.689T>C(p.Ile230Thr) Variant

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Pathogenic variants in the SCN5A gene and its subunits have been identified in individuals with Brugada Syndrome. One such SCN5A variant, c.689T>C(p.Ile230Thr), was previously reported as disease‐causing only in homozygous individuals, with heterozygous carriers being unaffected.
Shayla Shojaat   +2 more
wiley   +1 more source

Medical Students on Their Internal Medicine Clerkship Experience Short Sleep Duration. [PDF]

open access: yesATS Sch
Ge D   +8 more
europepmc   +1 more source

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