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 *

136 related articles for article (PubMed ID: 12747894)

  • 1. Homozygous familial hypercholesterolaemia in identical twins.
    Zschocke J; Schaefer JR
    Lancet; 2003 May; 361(9369):1641. PubMed ID: 12747894
    [No Abstract]   [Full Text] [Related]  

  • 2. Homozygous familial hypercholesterolaemia and treatment by LDL apheresis.
    King RI; Scott RS; Florkowski CM; Laurie AD; Reid N; George PM
    N Z Med J; 2010 Jul; 123(1319):79-82. PubMed ID: 20717180
    [No Abstract]   [Full Text] [Related]  

  • 3. Yellowish intertriginous plaques in a young girl: a clue to homozygous familial hypercholesterolaemia.
    Bhatia R; Chakraborty A; Durgapal P; Walia R; Kaur D
    Postgrad Med J; 2020 Nov; 96(1141):718. PubMed ID: 31911449
    [No Abstract]   [Full Text] [Related]  

  • 4. Managing familial hypercholesterolaemia.
    Jones JL; Lakasing E; Archontakis S
    Practitioner; 2009 Jun; 253(1719):28-31. PubMed ID: 19606612
    [No Abstract]   [Full Text] [Related]  

  • 5. Homozygous familial hypercholesterolaemia.
    Macchiaiolo M; Gagliardi MG; Toscano A; Guccione P; Bartuli A
    Lancet; 2012 Apr; 379(9823):1330. PubMed ID: 22285056
    [No Abstract]   [Full Text] [Related]  

  • 6. Hypercholesterolaemia: management and nursing implications.
    Babb Y; Eyre C
    Paediatr Nurs; 2005 Mar; 17(2):35-8. PubMed ID: 15793988
    [No Abstract]   [Full Text] [Related]  

  • 7. Managing homozygous familial hypercholesterolaemia from cradle to grave.
    Thompson GR
    Atheroscler Suppl; 2015 May; 18():16-20. PubMed ID: 25936299
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Acute effect of a single session of lipoprotein apheresis on central haemodynamics in patients with familial hypercholesterolaemia.
    Ellins EA; Watkins S; Rees DA; Datta DBN; Halcox JP
    Atherosclerosis; 2021 May; 325():121-123. PubMed ID: 33883085
    [No Abstract]   [Full Text] [Related]  

  • 9. [Homozygous familial hypercholesterolaemia: Spanish adaptation of the position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society. Consensus document of the Spanish Society of Arteriosclerosis (SEA) and Familial Hypercholesterolaemia Foundation (FHF)].
    Ascaso JF; Mata P; Arbona C; Civeira F; Valdivielso P; Masana L
    Clin Investig Arterioscler; 2015; 27(2):80-96. PubMed ID: 25757840
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Long-term efficacy of lipoprotein apheresis in homozygous familial hypercholesterolaemia.
    Meier P; Blanc E
    Nephrol Dial Transplant; 2000 May; 15(5):738-40. PubMed ID: 10809830
    [No Abstract]   [Full Text] [Related]  

  • 11. [Niemann-Pick disease type C in monozygotic twins].
    Orecchia L; Signorile G; Pezzano A; Bianco R; Iavarone A; Stradoni P; De Sario PN
    Minerva Pediatr; 1992 Oct; 44(10):491-5. PubMed ID: 1287434
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Management of homozygous familial hypercholesterolaemia--unmet needs, updated recommendations, and clinical experience with the MTP inhibitor, lomitapide. Concluding comments.
    Catapano AL
    Atheroscler Suppl; 2014 Sep; 15(2):52. PubMed ID: 25257077
    [No Abstract]   [Full Text] [Related]  

  • 13. Null receptor homozygous familial hypercholesterolaemia:
    Sampietro T; Sbrana F; Bigazzi F; Ripoli A; Dal Pino B
    Eur J Prev Cardiol; 2020 Dec; 27(19):2105-2108. PubMed ID: 31299859
    [No Abstract]   [Full Text] [Related]  

  • 14. Retroperitoneal catecholamine-producing ganglioneuroma with a birth history of monozygotic twins who both suffered from neuroblastoma during their childhoods: a case report with genome analysis.
    Ishihara H; Kikuno N; Hayakawa N; Ryoji O; Tanabe K
    J Neurol Sci; 2015 Oct; 357(1-2):329-31. PubMed ID: 26248704
    [No Abstract]   [Full Text] [Related]  

  • 15. Monozygotic twins with LRRK2 mutations: genetically identical but phenotypically discordant.
    Schneider SA; Johnson MR
    Mov Disord; 2012 Sep; 27(10):1203-4. PubMed ID: 22976776
    [No Abstract]   [Full Text] [Related]  

  • 16. Essential palatal myoclonus in monozygotic male twins.
    Kutukcu Y; Imirzalioglu N; Odabasi Z; Gokcil Z; Vural O
    J Neurol; 2003 Jul; 250(7):885-6. PubMed ID: 12883939
    [No Abstract]   [Full Text] [Related]  

  • 17. Monozygotic twins discordant for the oculo-oto-radial syndrome (IVIC syndrome).
    Elçioğlu N; Berry AC
    Genet Couns; 1997; 8(3):201-6. PubMed ID: 9327262
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Homozygous familial hypercholesterolaemia: update on management.
    France M
    Paediatr Int Child Health; 2016 Nov; 36(4):243-247. PubMed ID: 27967828
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial hypercholesterolaemia.
    Phillips T; Leigh IM
    J R Soc Med; 1987 Oct; 80(10):649-51. PubMed ID: 3320364
    [No Abstract]   [Full Text] [Related]  

  • 20. Anatomic brain abnormalities in monozygotic twins discordant for attention deficit hyperactivity disorder.
    Castellanos FX; Sharp WS; Gottesman RF; Greenstein DK; Giedd JN; Rapoport JL
    Am J Psychiatry; 2003 Sep; 160(9):1693-6. PubMed ID: 12944348
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.