Results 241 to 250 of about 116,608 (309)

Two cases of neonatal hyperglycemia caused by a homozygous COQ9 stop‐gain variant

open access: yesJournal of Diabetes Investigation, EarlyView.
ABSTRACT Neonatal diabetes mellitus (NDM) is a monogenic condition diagnosed <6 months of age with >40 genetic causes. International guidelines recommend referral for genetic testing immediately after diagnosis since the genetic result guides clinical management. We used next‐generation sequencing to identify a homozygous pathogenic variant, p.(Arg244*)
Russell Donis   +5 more
wiley   +1 more source

Timolol-Induced Bradycardia

open access: bronze, 1980
Jin W. Kim, Porter H Smith
openalex   +1 more source

Efficacy and safety of etrasimod in alopecia areata: A multicentre, randomized, double‐blind, placebo‐controlled, Phase 2 study

open access: yesJournal of the European Academy of Dermatology and Venereology, EarlyView.
Patients with alopecia areata received etrasimod 2 mg, 3 mg or placebo oncedaily for 24 weeks, followed by a 28‐week open‐label extension period. Overall, etrasimod 2 mg and 3 mg were safe and well tolerated in patients; their efficacy was numerically higher than placebo and appeared to be dose dependent.
B. King   +5 more
wiley   +1 more source

Vagus Nerve Schwannoma: A Case Report and Literature Review. [PDF]

open access: yesClin Case Rep
Ronald K   +3 more
europepmc   +1 more source

Individualized Net Benefit of Intensive Blood Pressure Lowering Among Community‐Dwelling Older Adults in SPRINT

open access: yesJournal of the American Geriatrics Society, EarlyView.
ABSTRACT Background The optimal blood pressure (BP) target for older adults with hypertension remains controversial, particularly among those with advanced age, frailty, or polypharmacy. This study estimated the individualized net benefit of intensive BP lowering among community‐dwelling older adults in the Systolic Blood Pressure Intervention Trial ...
Mitra S. Jamshidian   +11 more
wiley   +1 more source

Potential Adverse Effects of Sugammadex Administration: A Scoping Review. [PDF]

open access: yesCureus
Liang WM   +6 more
europepmc   +1 more source

HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy.

open access: yesJournal of the American College of Cardiology, 2014
A. Milano   +16 more
semanticscholar   +1 more source

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