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Items: 1 to 20 of 74

1.

Familial metabolic disorder with fatty metamorphosis of the viscera.

Peremans J, De Graef PJ, Strubbe G, De Block G.

J Pediatr. 1966 Dec;69(6):1108-12. No abstract available.

PMID:
5953838
2.

Familial disease characterized by neonatal jaundice, and probable hepatosteatosis and kernicterus: a new syndrome?

Wadlington WB, Riley HD Jr.

Pediatrics. 1973 Feb;51(2):192-8. No abstract available.

PMID:
4695852
3.

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
4.

An inborn error of short-chain fatty acid metabolism. The odor-of-sweaty-feet syndrome.

Sidbury JB Jr, Smith EK, Harlan W.

J Pediatr. 1967 Jan;70(1):8-15. No abstract available.

PMID:
6016812
5.

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

Treem WR, Rinaldo P, Hale DE, Stanley CA, Millington DS, Hyams JS, Jackson S, Turnbull DM.

Hepatology. 1994 Feb;19(2):339-45.

PMID:
8294091
6.

Mitochondrial fatty acid oxidation and acute fatty liver of pregnancy.

Treem WR.

Semin Gastrointest Dis. 2002 Jan;13(1):55-66. Review.

PMID:
11944635
7.

Metabolic disease in the fetus predisposes to maternal hepatic complications of pregnancy.

Tein I.

Pediatr Res. 2000 Jan;47(1):6-8. No abstract available.

PMID:
10625076
8.

Familial infantile apnea and immature beta oxidation.

Iafolla AK, Browning IB 3rd, Roe CR.

Pediatr Pulmonol. 1995 Sep;20(3):167-71.

PMID:
8545168
9.

Sudden neonatal death in carnitine transporter deficiency.

Rinaldo P, Stanley CA, Hsu BY, Sanchez LA, Stern HJ.

J Pediatr. 1997 Aug;131(2):304-5.

PMID:
9290621
10.

Liver disease in pregnancy.

Williams MS.

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

PMID:
9011803
11.

Mitochondrial carnitine-acylcarnitine translocase deficiency presenting as sudden neonatal death.

Chalmers RA, Stanley CA, English N, Wigglesworth JS.

J Pediatr. 1997 Aug;131(2):220-5.

PMID:
9290607
12.

Inborn errors of lipid metabolism. Familial hyperlipoproteinaemia type 3. Detection of heterozygotes.

Sobra J, Heyrovský A.

Rev Czech Med. 1972;18(1):34-9. No abstract available.

PMID:
5022312
13.

Hereditary metabolic cardiomyopathies.

Servidei S, Bertini E, DiMauro S.

Adv Pediatr. 1994;41:1-32. Review. No abstract available.

PMID:
7992680
15.

A cause of fatty liver: neutral lipid storage disease with ichthyosis--electron microscopic findings.

Gürakan F, Kaymaz F, Koçak N, Ors U, Yüce A, Atakan N.

Dig Dis Sci. 1999 Nov;44(11):2214-7. No abstract available.

PMID:
10573364
16.

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
17.

Fatal neonatal heptic steatosis: a new familial disorder.

Satran L, Sharp HL, Schenken JR, Krivit W.

J Pediatr. 1969 Jul;75(1):39-46. No abstract available.

PMID:
5790404
18.

[A new disease caused by accumulation of glycolipids. (Ceramide tetrahexosides)].

Durand P, Philippart M, Borrone C, Della Cella G, Bugiani O.

Minerva Pediatr. 1967 Dec 8;19(49):2187-96. Italian. No abstract available.

PMID:
5607240
19.

Neonatal pancreatitis associated with familial lipoprotein lipase deficiency.

Siafakas CG, Brown MR, Miller TL.

J Pediatr Gastroenterol Nutr. 1999 Jul;29(1):95-8. No abstract available.

PMID:
10400113
20.

Steatohepatitis and unsuspected micronodular cirrhosis in Dorfman-Chanarin syndrome with documented ABHD5 mutation.

Srinivasan R, Hadzić N, Fischer J, Knisely AS.

J Pediatr. 2004 May;144(5):662-5.

PMID:
15127008

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