These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

266 related articles for article (PubMed ID: 18059381)

  • 1. Screening for familial hypercholesterolemia: what is the most effective strategy?
    Daniels SR
    Nat Clin Pract Cardiovasc Med; 2008 Mar; 5(3):130-1. PubMed ID: 18059381
    [No Abstract]   [Full Text] [Related]  

  • 2. Femoral atherosclerosis in heterozygous familial hypercholesterolemia: influence of the genetic defect.
    Junyent M; Gilabert R; Zambón D; Pocoví M; Mallén M; Cofán M; Núñez I; Civeira F; Tejedor D; Ros E
    Arterioscler Thromb Vasc Biol; 2008 Mar; 28(3):580-6. PubMed ID: 18096825
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A review of genetic mutation in familial Hirschsprung's disease in South Africa: towards genetic counseling.
    Moore SW; Zaahl MG
    J Pediatr Surg; 2008 Feb; 43(2):325-9. PubMed ID: 18280283
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial hypercholesterolemia in Spain: case-finding program, clinical and genetic aspects.
    Pocovi M; Civeira F; Alonso R; Mata P
    Semin Vasc Med; 2004 Feb; 4(1):67-74. PubMed ID: 15199435
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cost-effectiveness analysis of the genetic screening program for familial hypercholesterolemia in The Netherlands.
    Wonderling D; Umans-Eckenhausen MA; Marks D; Defesche JC; Kastelein JJ; Thorogood M
    Semin Vasc Med; 2004 Feb; 4(1):97-104. PubMed ID: 15199439
    [TBL] [Abstract][Full Text] [Related]  

  • 6. No certain predictors for mutation status in a Danish cohort with familial hypercholesterolemia: a descriptive study.
    Nybo M; Brusgaard K; Hansen AB
    Clin Biochem; 2007 Dec; 40(18):1347-52. PubMed ID: 17961529
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Genetic screening for familial hypercholesterolemia in 1992-1997: primarily younger patients in the care of family physicians].
    ten Asbroek AH; van Lunsen S; Marang-van de Mheen PJ; Gunning-Schepers LJ
    Ned Tijdschr Geneeskd; 2000 Jan; 144(3):125-9. PubMed ID: 10674119
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Heterozygous Familial Hypercholesterolemia.
    Onorato A; Sturm AC
    Circulation; 2016 Apr; 133(14):e587-9. PubMed ID: 27045133
    [No Abstract]   [Full Text] [Related]  

  • 9. The type of LDLR gene mutation predicts cardiovascular risk in children with familial hypercholesterolemia.
    Guardamagna O; Restagno G; Rolfo E; Pederiva C; Martini S; Abello F; Baracco V; Pisciotta L; Pino E; Calandra S; Bertolini S
    J Pediatr; 2009 Aug; 155(2):199-204.e2. PubMed ID: 19446849
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Comparison of genetic versus clinical diagnosis in familial hypercholesterolemia.
    Civeira F; Ros E; Jarauta E; Plana N; Zambon D; Puzo J; Martinez de Esteban JP; Ferrando J; Zabala S; Almagro F; Gimeno JA; Masana L; Pocovi M
    Am J Cardiol; 2008 Nov; 102(9):1187-93, 1193.e1. PubMed ID: 18940289
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cascade genetic screening for familial hypercholesterolemia.
    Leren TP
    Clin Genet; 2004 Dec; 66(6):483-7. PubMed ID: 15521974
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical features, diagnosis and frequency of familial hypercholesterolemia.
    Khachadurian AK
    Beitr Infusionsther; 1988; 23():26-32. PubMed ID: 2484779
    [No Abstract]   [Full Text] [Related]  

  • 13. Low-density lipoprotein apheresis in children with familial hypercholesterolemia: follow-up to 21 years.
    Palcoux JB; Atassi-Dumont M; Lefevre P; Hequet O; Schlienger JL; Brignon P; Roussel B
    Ther Apher Dial; 2008 Jun; 12(3):195-201. PubMed ID: 18503695
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Application of molecular genetics for diagnosing familial hypercholesterolemia in Norway: results from a family-based screening program.
    Leren TP; Manshaus T; Skovholt U; Skodje T; Nossen IE; Teie C; Sørensen S; Bakken KS
    Semin Vasc Med; 2004 Feb; 4(1):75-85. PubMed ID: 15199436
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diagnosis of familial hypercholesterolemia in general practice using clinical diagnostic criteria or genetic testing as part of cascade genetic screening.
    Leren TP; Finborud TH; Manshaus TE; Ose L; Berge KE
    Community Genet; 2008; 11(1):26-35. PubMed ID: 18196915
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial hypercholesterolemias: prevalence, genetics, diagnosis and screening recommendations from the National Lipid Association Expert Panel on Familial Hypercholesterolemia.
    Hopkins PN; Toth PP; Ballantyne CM; Rader DJ;
    J Clin Lipidol; 2011 Jun; 5(3 Suppl):S9-17. PubMed ID: 21600530
    [No Abstract]   [Full Text] [Related]  

  • 17. Patient profile: familial hypercholesterolaemia.
    Schuster H
    Int J Clin Pract Suppl; 2002 Jul; (130):20-1. PubMed ID: 12296604
    [No Abstract]   [Full Text] [Related]  

  • 18. [The lipid patient. Case 3. Polygene hypercholesterolemia].
    Richter WO
    Fortschr Med; 1997 Dec; 115(34):38-40. PubMed ID: 9465474
    [No Abstract]   [Full Text] [Related]  

  • 19. Reverse Cascade Screening for Familial Hypercholesterolemia.
    Vinson A; Guerra L; Hamilton L; Wilson DP; Fnla
    J Pediatr Nurs; 2019; 44():50-55. PubMed ID: 30683281
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [A case with homozygote familial hypercholesterolemia treated with LDL apheresis and coronary bypass in adolescence period].
    Altinel E; Cetinkaya S; Kara C; Orün UA; Aydin H; Kutsal A
    Anadolu Kardiyol Derg; 2008 Jun; 8(3):231-2. PubMed ID: 18524734
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 14.