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1.
The Importance of Nontraditional and Sex-Specific Risk Factors in Young Women With Vasomotor Nonobstructive vs Obstructive Coronary Syndromes.
CJC Open
; 6(2Part B): 279-291, 2024 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-38487074
2.
Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy.
Nat Genet
; 32(2): 326-30, 2002 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-12172548
3.
Clinical characteristics and treatment experience of individuals with SCN8A developmental and epileptic encephalopathy (SCN8A-DEE): Findings from an online caregiver survey.
Seizure
; 97: 50-57, 2022 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-35325842
4.
NBI-921352, a first-in-class, NaV1.6 selective, sodium channel inhibitor that prevents seizures in Scn8a gain-of-function mice, and wild-type mice and rats.
Elife
; 112022 03 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-35234610
5.
Familial Hypercholesterolemia, Familial Combined Hyperlipidemia, and Elevated Lipoprotein(a) in Patients With Premature Coronary Artery Disease.
Can J Cardiol
; 37(11): 1733-1742, 2021 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34455025
6.
Capturing seizures in clinical trials of antiseizure medications for KCNQ2-DEE.
Epilepsia Open
; 6(1): 38-44, 2021 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-33681646
7.
Lipid-lowering therapy for primary prevention of premature atherosclerotic coronary artery disease: Eligibility, utilization, target achievement, and predictors of initiation.
Am J Prev Cardiol
; 2: 100036, 2020 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-34327459
8.
Premature Atherosclerotic Cardiovascular Disease: Trends in Incidence, Risk Factors, and Sex-Related Differences, 2000 to 2016.
J Am Heart Assoc
; 8(14): e012178, 2019 07 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-31280642
9.
Safety and Efficacy of a Topical Sodium Channel Inhibitor (TV-45070) in Patients With Postherpetic Neuralgia (PHN): A Randomized, Controlled, Proof-of-Concept, Crossover Study, With a Subgroup Analysis of the Nav1.7 R1150W Genotype.
Clin J Pain
; 33(4): 310-318, 2017 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-28266963
10.
Identification of Cadherin 2 (CDH2) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy.
Circ Cardiovasc Genet
; 10(2)2017 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-28280076
11.
Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates.
Am J Hum Genet
; 74(5): 1064-73, 2004 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-15060842
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