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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1970 1
1974 1
1977 1
1978 1
1982 1
1989 1
1993 1
1998 2
2001 2
2002 1
2005 1
2016 1
2017 1
2019 1
2024 0

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15 results

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Page 1
Can LDL cholesterol be too low? Possible risks of extremely low levels.
Olsson AG, Angelin B, Assmann G, Binder CJ, Björkhem I, Cedazo-Minguez A, Cohen J, von Eckardstein A, Farinaro E, Müller-Wieland D, Parhofer KG, Parini P, Rosenson RS, Starup-Linde J, Tikkanen MJ, Yvan-Charvet L. Olsson AG, et al. J Intern Med. 2017 Jun;281(6):534-553. doi: 10.1111/joim.12614. J Intern Med. 2017. PMID: 28295777 Free article. Review.
Acanthocytosis and neurological disorders.
Stevenson VL, Hardie RJ. Stevenson VL, et al. J Neurol. 2001 Feb;248(2):87-94. doi: 10.1007/s004150170241. J Neurol. 2001. PMID: 11284140 Review.
At least three hereditary neurological conditions are associated with it, although as yet the pathogenesis of the neurological features is unknown. In abetalipoproteinaemia, an autosomal recessive condition, vitamin E deficiency results in a progressive spinocerebellar syn …
At least three hereditary neurological conditions are associated with it, although as yet the pathogenesis of the neurological features is u …
Medium chain triglycerides in paediatric practice.
Gracey M, Burke V, Anderson CM. Gracey M, et al. Arch Dis Child. 1970 Aug;45(242):445-52. doi: 10.1136/adc.45.242.445. Arch Dis Child. 1970. PMID: 4918706 Free PMC article. Review.
Keys to overcoming the challenge of diagnosing autosomal recessive spinocerebellar ataxia.
Arias M. Arias M. Neurologia (Engl Ed). 2019 May;34(4):248-258. doi: 10.1016/j.nrl.2016.06.006. Epub 2016 Jul 25. Neurologia (Engl Ed). 2019. PMID: 27460185 Free article. Review. English, Spanish.
A positive genetic test result is necessary to determine prognosis and provide adequate genetic counselling, and will also permit appropriate treatment of some entities (abetalipoproteinaemia, ataxia with vitamin E deficiency, Refsum disease, cerebrotendinous xanthomatosis …
A positive genetic test result is necessary to determine prognosis and provide adequate genetic counselling, and will also permit appropriat …
Clinical features and molecular bases of neuroacanthocytosis.
Rampoldi L, Danek A, Monaco AP. Rampoldi L, et al. J Mol Med (Berl). 2002 Aug;80(8):475-91. doi: 10.1007/s00109-002-0349-z. Epub 2002 Jun 18. J Mol Med (Berl). 2002. PMID: 12185448 Review.
Acanthocytosis is found to be associated with at least three hereditary neurological disorders that are generally referred to as neuroacanthocytosis. Abetalipoproteinaemia is an autosomal recessive condition, characterised by absence of serum apolipoprotein B containing li …
Acanthocytosis is found to be associated with at least three hereditary neurological disorders that are generally referred to as neuroacanth …
Platelet and neutrophil function and eicosanoid release in a subject with abetalipoproteinaemia.
Croft KD, Beilin LJ. Croft KD, et al. Thromb Res. 1993 Feb 15;69(4):333-42. doi: 10.1016/0049-3848(93)90032-j. Thromb Res. 1993. PMID: 8385810
To evaluate the possible biological effects of LDL further we have studied platelet aggregation, leukocyte function and eicosanoid release in a young woman with abetalipoproteinaemia (ABL) who totally lacks LDL. The subject showed decreased platelet response to threshold d …
To evaluate the possible biological effects of LDL further we have studied platelet aggregation, leukocyte function and eicosanoid release i …
Monogenic hypocholesterolaemic lipid disorders and apolipoprotein B metabolism.
Hooper AJ, van Bockxmeer FM, Burnett JR. Hooper AJ, et al. Crit Rev Clin Lab Sci. 2005;42(5-6):515-45. doi: 10.1080/10408360500295113. Crit Rev Clin Lab Sci. 2005. PMID: 16390683 Review.
Truncation-causing mutations in the APOB gene cause familial hypobetalipoproteinaemia, whereas mutations in MTP result in abetalipoproteinaemia; both rare conditions are characterised by marked hypocholesterolaemia. ...
Truncation-causing mutations in the APOB gene cause familial hypobetalipoproteinaemia, whereas mutations in MTP result in abetalipoprotei …
Acanthocytosis and neurological impairment--a review.
Hardie RJ. Hardie RJ. Q J Med. 1989 Apr;71(264):291-306. Q J Med. 1989. PMID: 2687930 Review.
They occur in association with at least three neurological syndromes. In abetalipoproteinaemia, a progressive spinocerebellar ataxia and retinopathy occurs secondary to malabsorption of vitamin E. ...
They occur in association with at least three neurological syndromes. In abetalipoproteinaemia, a progressive spinocerebellar ataxia …
The assembly of triacylglycerol-rich lipoproteins: an essential role for the microsomal triacylglycerol transfer protein.
White DA, Bennett AJ, Billett MA, Salter AM. White DA, et al. Br J Nutr. 1998 Sep;80(3):219-29. Br J Nutr. 1998. PMID: 9875061 Review.
After absorption in the intestine, dietary fat and fat-soluble vitamins are incorporated into chylomicrons in the intestinal epithelial cells, and these lipoproteins reach the bloodstream via the lymphatic system. Patients with the rare genetic disorder, abetalipoproteinaemia …
After absorption in the intestine, dietary fat and fat-soluble vitamins are incorporated into chylomicrons in the intestinal epithelial cell …
Long-term assessment of combined vitamin A and E treatment for the prevention of retinal degeneration in abetalipoproteinaemia and hypobetalipoproteinaemia patients.
Chowers I, Banin E, Merin S, Cooper M, Granot E. Chowers I, et al. Eye (Lond). 2001 Aug;15(Pt 4):525-30. doi: 10.1038/eye.2001.167. Eye (Lond). 2001. PMID: 11767031 Clinical Trial.
PURPOSE: To assess the long-term efficacy of combined vitamin A and E treatment in preventing retinal degeneration in patients with abetalipoproteinaemia (ABL) or homozygous hypobetalipoproteinaemia (HBL). ...
PURPOSE: To assess the long-term efficacy of combined vitamin A and E treatment in preventing retinal degeneration in patients with abeta …
15 results