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Similar articles for PubMed (Select 21506744)

1.

Case records of the Massachusetts General Hospital. Case 12-2011. A 9-month-old boy with acute liver failure.

Fearing MK, Israel EJ, Sahai I, Rapalino O, Lisovsky M.

N Engl J Med. 2011 Apr 21;364(16):1545-56. doi: 10.1056/NEJMcpc1013928. No abstract available.

PMID:
21506744
2.

A defect in the transport of long-chain fatty acids associated with acute liver failure.

Odaib AA, Shneider BL, Bennett MJ, Pober BR, Reyes-Mugica M, Friedman AL, Suchy FJ, Rinaldo P.

N Engl J Med. 1998 Dec 10;339(24):1752-7. No abstract available.

3.

Neutral lipid storage disease with fatty liver and cholestasis.

Igal RA, Rhoads JM, Coleman RA.

J Pediatr Gastroenterol Nutr. 1997 Nov;25(5):541-7. Review. No abstract available.

PMID:
9360211
4.

Acute liver failure in children: the role of defects in fatty acid oxidation.

Alonso EM.

Hepatology. 2005 Apr;41(4):696-9. Review. No abstract available.

PMID:
15789368
5.

Propionicacidemia, a new inborn error of metabolism.

Hommes FA, Kuipers JR, Elema JD, Jansen JF, Jonxis JH.

Pediatr Res. 1968 Nov;2(6):519-24. No abstract available.

PMID:
5727920
6.

Inborn errors of metabolism: the essentials of clinical diagnosis.

Roth KS.

Clin Pediatr (Phila). 1991 Mar;30(3):183-90. No abstract available.

PMID:
2009725
7.

Fatal familial steatosis of the liver and kidney in two siblings.

Räsänen O, Korhonen M, Similä S, Autere T, Hakosalo J.

Z Kinderheilkd. 1971;110(4):267-75. No abstract available.

PMID:
5567005
8.

A three-month-old infant with seizures, hypoglycemia, and apnea.

Chesney RW, Sveum RJ, Lacey M, Arya S, Shug A, Saari T, Berlow S, Ellefson R, Gilbert EF, Odell GB, et al.

Am J Med Genet. 1983 Nov;16(3):373-88. No abstract available.

PMID:
6650573
9.

Liver disease in pregnancy.

Williams MS.

N Engl J Med. 1997 Jan 30;336(5):378; author reply 379. No abstract available.

PMID:
9011803
10.

Dorfman-Chanarin syndrome.

Gandhi V, Aggarwal P, Dhawan J, Singh UR, Bhattacharya SN.

Indian J Dermatol Venereol Leprol. 2007 Jan-Feb;73(1):36-9.

11.

Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 41-1972.

[No authors listed]

N Engl J Med. 1972 Oct 12;287(15):763-8. No abstract available.

PMID:
4560356
12.

Novel heterozygous mutations in TALDO1 gene causing transaldolase deficiency and early infantile liver failure.

Balasubramaniam S, Wamelink MM, Ngu LH, Talib A, Salomons GS, Jakobs C, Keng WT.

J Pediatr Gastroenterol Nutr. 2011 Jan;52(1):113-6. doi: 10.1097/MPG.0b013e3181f50388. No abstract available.

PMID:
21119539
13.

Liver disease in pregnancy.

Rinaldo P, Treem WR, Riely CA.

N Engl J Med. 1997 Jan 30;336(5):377-8; author reply 379. No abstract available.

PMID:
9011801
14.

Hodgkin' s disease with fulminant non-alcoholic steatohepatitis.

Kosmidou IS, Aggarwal A, Ross JJ, Worthington MG.

Dig Liver Dis. 2004 Oct;36(10):691-3.

PMID:
15506670
15.

Fatty acid oxidation disorder as a cause of sudden infant death syndrome (SIDS)--a case report.

Thanka J, Padmasani, Krishnan L, Kuruvilla S.

Indian J Pathol Microbiol. 2005 Oct;48(4):485-7.

PMID:
16366103
16.

Recurrent acute fatty liver of pregnancy associated with a fatty-acid oxidation defect in the offspring.

Schoeman MN, Batey RG, Wilcken B.

Gastroenterology. 1991 Feb;100(2):544-8.

PMID:
1985050
17.

Neutral lipid storage disease. Case report and lipid studies.

Judge MR, Atherton DJ, Salvayre R, Hilaire N, Levade T, Johnston DI, Winchester B, Lake BD.

Br J Dermatol. 1994 Apr;130(4):507-10.

PMID:
8186119
18.

The critically ill child: acute metabolic disease in infancy and early childhood.

O'Brien D, Goodman SI.

Pediatrics. 1970 Oct;46(4):620-6. No abstract available.

PMID:
5503697
19.

[2 patients with Reye syndrome?].

Houwen RH, Nelck GF, Reijngoud DJ, Grond J, Smit GP, Bijleveld CM.

Ned Tijdschr Geneeskd. 1988 Oct 29;132(44):2025-8. Dutch. No abstract available.

PMID:
3185812
20.

[Involvement of the eye in hereditary metabolic diseases in children].

Bickel H, Jaeger W, Wollensak J, Teller W, Kraus E.

Ber Zusammenkunft Dtsch Ophthalmol Ges. 1969;69:13-68. German. No abstract available.

PMID:
4311270
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