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Items: 1 to 20 of 24

1.

Oncology Drug Dosing in Gilbert Syndrome Associated with UGT1A1: A Summary of the Literature.

Ha VH, Jupp J, Tsang RY.

Pharmacotherapy. 2017 Aug;37(8):956-972. doi: 10.1002/phar.1946. Epub 2017 Jun 28. Review.

PMID:
28494109
2.

Developmental, Genetic, Dietary, and Xenobiotic Influences on Neonatal Hyperbilirubinemia.

Yueh MF, Chen S, Nguyen N, Tukey RH.

Mol Pharmacol. 2017 May;91(5):545-553. doi: 10.1124/mol.116.107524. Epub 2017 Mar 10. Review.

PMID:
28283555
3.

<i>EPB42</i>-Related Hereditary Spherocytosis.

Kalfa TA, Connor JA, Begtrup AH.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mefford HC, Stephens K, Amemiya A, Ledbetter N, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2014 Mar 13 [updated 2016 Nov 10].

4.

Acquired von Willebrand syndrome associated with left ventricular assist device.

Nascimbene A, Neelamegham S, Frazier OH, Moake JL, Dong JF.

Blood. 2016 Jun 23;127(25):3133-41. doi: 10.1182/blood-2015-10-636480. Epub 2016 May 3. Review.

5.

[Role of bilirubin in the prevention of cardiovascular diseases and cancer].

Vítek L.

Cas Lek Cesk. 2016;155(2):10-4. Review. Czech.

PMID:
27088786
6.

GILBERT'S SYNDROME - A CONCEALED ADVERSITY FOR PHYSICIANS AND SURGEONS.

Rasool A, Sabir S, Ashlaq M, Farooq U, Khan MZ, Khan FY.

J Ayub Med Coll Abbottabad. 2015 Jul-Sep;27(3):707-10. Review.

PMID:
26721045
7.

Inherited disorders of bilirubin clearance.

Memon N, Weinberger BI, Hegyi T, Aleksunes LM.

Pediatr Res. 2016 Mar;79(3):378-86. doi: 10.1038/pr.2015.247. Epub 2015 Nov 23. Review.

8.

A pediatrician's practical guide to diagnosing and treating hereditary spherocytosis in neonates.

Christensen RD, Yaish HM, Gallagher PG.

Pediatrics. 2015 Jun;135(6):1107-14. doi: 10.1542/peds.2014-3516. Review.

9.

[Hereditary spherocytosis. Review. Part II. Symptomatology, outcome, complications, and treatment].

Comité Nacional de Hematología, Donato H, Crisp RL, Rapetti MC, García E, Attie M.

Arch Argent Pediatr. 2015 Apr;113(2):168-76. doi: 10.5546/aap.2015.168. Review. Spanish.

10.

Bilirubin, platelet activation and heart disease: a missing link to cardiovascular protection in Gilbert's syndrome?

Kundur AR, Singh I, Bulmer AC.

Atherosclerosis. 2015 Mar;239(1):73-84. doi: 10.1016/j.atherosclerosis.2014.12.042. Epub 2014 Dec 24. Review.

PMID:
25576848
11.

Mechanisms of atrial fibrillation: rotors, ionic determinants, and excitation frequency.

Berenfeld O, Jalife J.

Cardiol Clin. 2014 Nov;32(4):495-506. doi: 10.1016/j.ccl.2014.07.001. Epub 2014 Oct 23. Review.

12.

Gene replacement therapy for genetic hepatocellular jaundice.

van Dijk R, Beuers U, Bosma PJ.

Clin Rev Allergy Immunol. 2015 Jun;48(2-3):243-53. doi: 10.1007/s12016-014-8454-7. Review.

PMID:
25315738
13.

[Interest of UGT1A1 genotyping within digestive cancers treatment by irinotecan].

Boyer JC, Etienne-Grimaldi MC, Thomas F, Quaranta S, Picard N, Loriot MA, Poncet D, Gagnieu MC, Ged C, Broly F, Le Morvan V, Bouquié R, Gaub MP, Philibert L, Ghiringhelli F, Le Guellec C.

Bull Cancer. 2014 Jun;101(6):533-53. doi: 10.1684/bdc.2014.1933. Review. French.

PMID:
24977443
14.

Hereditary hyperbilirubinemias.

Radlović N.

Srp Arh Celok Lek. 2014 Mar-Apr;142(3-4):257-60. Review.

15.

Inherited disorders of bilirubin transport and conjugation: new insights into molecular mechanisms and consequences.

Erlinger S, Arias IM, Dhumeaux D.

Gastroenterology. 2014 Jun;146(7):1625-38. doi: 10.1053/j.gastro.2014.03.047. Epub 2014 Apr 1. Review.

PMID:
24704527
16.

[Crigler-Najjar type 1 in children].

Bach Knudsen K, Ebbesen F.

Ugeskr Laeger. 2013 Oct 14;175(42):2489-91. Review. Danish.

PMID:
24629116
17.

The roles of MRP2, MRP3, OATP1B1, and OATP1B3 in conjugated hyperbilirubinemia.

Keppler D.

Drug Metab Dispos. 2014 Apr;42(4):561-5. doi: 10.1124/dmd.113.055772. Epub 2014 Jan 23. Review.

18.

Oxidative stress and endothelial dysfunction: clinical evidence and therapeutic implications.

Higashi Y, Maruhashi T, Noma K, Kihara Y.

Trends Cardiovasc Med. 2014 May;24(4):165-9. doi: 10.1016/j.tcm.2013.12.001. Epub 2013 Dec 4. Review.

PMID:
24373981
19.

Neurophysiological follow-up of two siblings with Crigler-Najjar syndrome type I and review of literature.

Bayram E, Öztürk Y, Hız S, Topçu Y, Kılıç M, Zeytunlu M.

Turk J Pediatr. 2013 May-Jun;55(3):349-53. Review.

PMID:
24217087
20.

New insights in bilirubin metabolism and their clinical implications.

Sticova E, Jirsa M.

World J Gastroenterol. 2013 Oct 14;19(38):6398-407. doi: 10.3748/wjg.v19.i38.6398. Review.

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