|2.||Retinitis Pigmentosa (Pigmentary Retinopathy)
|1.||Houlden, H: 2 articles (10/2006 - 11/2003)|
|2.||Husby, Steffen: 1 article (05/2010)|
|3.||Kjaersgaard, Lars: 1 article (05/2010)|
|4.||Hansen, Anne-Birthe Bo: 1 article (05/2010)|
|5.||Brusgaard, Klaus: 1 article (05/2010)|
|6.||Higuera Domínguez, F: 1 article (03/2009)|
|7.||Bacardí-Gascón, M: 1 article (03/2009)|
|8.||Velasco-Martínez, R M: 1 article (03/2009)|
|9.||Jiménez-Cruz, A: 1 article (03/2009)|
|10.||Domínguez de la Piedra, E: 1 article (03/2009)|
|2.||Adrenal Cortex Hormones (Corticosteroids)IBA
01/01/2005 - "PV patients (n=55, including 27 patients with CHD) had predominant hypolipoproteinemia with normal proportion of various lipoprotein classes. "
03/01/1983 - "These data demonstrate the relative deficiency of lipoprotein lipolysis in the type of hypolipoproteinemia studied."
01/01/1989 - "Whereas the lipid accumulation of hyperlipoproteinemia may be representative of excessive insudation of lipoprotein from plasma into the cornea that of hypolipoproteinemia is more likely to be a consequence of defective lipid clearance. "
12/29/1983 - "The very rare inherited hypolipoproteinemias are of great help to understand the relations between lipoproteins and atherosclerosis; moreover, in this field, they raise questions, which are discussed in this paper."
09/01/1983 - "The very rare inherited hypolipoproteinemias are of great help to understand the relations between lipoproteins and atherosclerosis; moreover, they raise questions in this field, which are discussed in this paper."
06/01/2008 - "Recently, the hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa and pallidal degeneration syndrome (HARP syndrome) has been genetically shown to be an allelic form of PKAN. "
11/25/2003 - "The authors describe a patient with hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration (HARP) who has two compound heterozygote mutations of the PANK2 gene. "
03/01/1995 - "Acanthocytosis, retinitis pigmentosa, and pallidal degeneration: a report of three patients, including the second reported case with hypoprebetalipoproteinemia (HARP syndrome)."
01/01/1992 - "Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration (HARP syndrome)."
06/11/2002 - "HARP (hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration) is a rare syndrome with many clinical similarities to pantothenate kinase-associated neurodegeneration (PKAN, formerly Hallervorden-Spatz syndrome). "
|5.||LDL Lipoproteins (beta Lipoproteins)IBA
01/01/1992 - "Investigations revealed hypoprebetalipoproteinemia, acanthocytosis, atypical retinitis pigmentosa, and evidence of iron deposition in the pallidal nuclei. "
10/23/2006 - "This included cases with neurodegeneration and brain iron accumulation, corticobasal degeneartion, progressive supranuclear palsy (PSP), Parkinson's disease (PD), multiple system atropy, giant axonal neuropathy (GAN), neuroaxonal dystrophy (NAD), Guam dementia and HARP syndrome (pallido-pyramidal syndrome and hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa and pallidal degeneration). "
01/01/1985 - "40 micrograms/kg of glucagon which is known as an inhibitory factor of apoprotein production in the liver, was injected for 2 weeks into the rat tail vein and resulted in apparent fatty liver and hypolipoproteinemia. "
02/01/1986 - " Regarding genetic predisposition, single-gene mutations in apoproteins, lipoproteins, and some of the enzymes involved in lipoprotein may underlie disorders of hyperlipoproteinemia or hypolipoproteinemia."
|10.||Vitamin EFDA LinkGeneric