Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 254

1.

The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy.

Sims HF, Brackett JC, Powell CK, Treem WR, Hale DE, Bennett MJ, Gibson B, Shapiro S, Strauss AW.

Proc Natl Acad Sci U S A. 1995 Jan 31;92(3):841-5.

2.

Prospective screening for pediatric mitochondrial trifunctional protein defects in pregnancies complicated by liver disease.

Yang Z, Yamada J, Zhao Y, Strauss AW, Ibdah JA.

JAMA. 2002 Nov 6;288(17):2163-6.

PMID:
12413376
3.

A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women.

Ibdah JA, Bennett MJ, Rinaldo P, Zhao Y, Gibson B, Sims HF, Strauss AW.

N Engl J Med. 1999 Jun 3;340(22):1723-31.

5.

Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant allele.

Isaacs JD Jr, Sims HF, Powell CK, Bennett MJ, Hale DE, Treem WR, Strauss AW.

Pediatr Res. 1996 Sep;40(3):393-8.

PMID:
8865274
7.

Elevated hydroxyacylcarnitines in a carrier of LCHAD deficiency during acute liver disease of pregnancy - a common feature of the pregnancy complication?

Eskelin PM, Laitinen KA, Tyni TA.

Mol Genet Metab. 2010 Jun;100(2):204-6. doi: 10.1016/j.ymgme.2010.03.006.

PMID:
20363656
8.

Long-chain fatty acid oxidation during early human development.

Oey NA, den Boer ME, Wijburg FA, Vekemans M, Augé J, Steiner C, Wanders RJ, Waterham HR, Ruiter JP, Attié-Bitach T.

Pediatr Res. 2005 Jun;57(6):755-9.

PMID:
15845636
9.
10.

Absence of the G1528C (E474Q) mutation in the alpha-subunit of the mitochondrial trifunctional protein in women with acute fatty liver of pregnancy.

Maitra A, Domiati-Saad R, Yost N, Cunningham G, Rogers BB, Bennett MJ.

Pediatr Res. 2002 May;51(5):658-61. Review.

PMID:
11978893
11.

No mutation was found in the alpha-subunit of the mitochondrial tri-functional protein in one patient with severe acute fatty liver of pregnancy and her relatives.

Kong XF, Zhang XX, Yu YY, Shi Q, La DD, Zhu-Ge CD, Deng L, Gong QM, Shen BY, Peng CH, Li HW.

J Gastroenterol Hepatol. 2007 Dec;22(12):2107-11.

PMID:
18031367
12.

Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications.

Strauss AW, Bennett MJ, Rinaldo P, Sims HF, O'Brien LK, Zhao Y, Gibson B, Ibdah J.

Semin Perinatol. 1999 Apr;23(2):100-12. Review.

PMID:
10331463
13.

[Variation of long-chain 3-hydroxyacyl-CoA dehydrogenase DNA methylation in placenta of different preeclampsia-like mouse models].

Han Y, Yang Z, Ding X, Yu H, Yi Y.

Zhonghua Fu Chan Ke Za Zhi. 2015 Oct;50(10):740-6. Chinese.

PMID:
26675572
14.

Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.

Treem WR, Shoup ME, Hale DE, Bennett MJ, Rinaldo P, Millington DS, Stanley CA, Riely CA, Hyams JS.

Am J Gastroenterol. 1996 Nov;91(11):2293-300.

PMID:
8931405
15.

Acute fatty liver of pregnancy and neonatal long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency.

Gutiérrez Junquera C, Balmaseda E, Gil E, Martínez A, Sorli M, Cuartero I, Merinero B, Ugarte M.

Eur J Pediatr. 2009 Jan;168(1):103-6. doi: 10.1007/s00431-008-0696-z.

PMID:
18408953
16.

Trifunctional protein deficiency: three families with significant maternal hepatic dysfunction in pregnancy not associated with E474Q mutation.

Chakrapani A, Olpin S, Cleary M, Walter JH, Wraith JE, Besley GT.

J Inherit Metab Dis. 2000 Dec;23(8):826-34.

PMID:
11196108
17.

[Long chain 3-hydroxyacyl-coA dehydrogenase deficiency, association with HELLP and magnetic resonance spectroscopy findings].

Deltetto N, Maxit C, Marchione D, Szlago M, Schenone A, Besada CH, Vaccarezza M, Agosta G.

Arch Argent Pediatr. 2012 Aug;110(4):e63-6. doi: 10.1590/S0325-00752012000400014. Spanish.

18.
19.

Mutations in long-chain 3-hydroxyacyl coenzyme a dehydrogenase are associated with placental maternal floor infarction/massive perivillous fibrin deposition.

Griffin AC, Strauss AW, Bennett MJ, Ernst LM.

Pediatr Dev Pathol. 2012 Sep-Oct;15(5):368-74. doi: 10.2350/12-05-1198-OA.1.

PMID:
22746996
Items per page

Supplemental Content

Support Center