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R J Wanders Selected Research

Alpha-Methylacyl-CoA Racemase Deficiency

1/2001Plasma analysis of di- and trihydroxycholestanoic acid diastereoisomers in peroxisomal alpha-methylacyl-CoA racemase deficiency.
11/2000Subcellular localization and physiological role of alpha-methylacyl-CoA racemase.

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R J Wanders Research Topics

Disease

6Fever (Fevers)
05/2001 - 04/2000
5Refsum Disease (Refsum's Disease)
01/2009 - 01/2000
5Mevalonate Kinase Deficiency
04/2001 - 04/2000
5Zellweger Syndrome (Zellweger's Syndrome)
02/2001 - 03/2000
3Disease Progression
01/2005 - 09/2000
3Adrenoleukodystrophy (Adrenoleukodystrophy, X-Linked)
12/2001 - 11/2001
3Sjogren-Larsson Syndrome
07/2001 - 02/2000
3Smith-Lemli-Opitz Syndrome
05/2001 - 05/2000
3Trifunctional Protein Deficiency With Myopathy And Neuropathy
08/2000 - 01/2000
2Infantile Refsum Disease (Infantile Phytanic Acid Storage Disease)
01/2005 - 10/2000
2Reye Syndrome (Reye's Syndrome)
11/2001 - 08/2000
2Hyperammonemia
11/2001 - 08/2000
2Hypoglycemia (Reactive Hypoglycemia)
11/2001 - 08/2000
2Neurocutaneous Syndromes (Phakomatoses)
07/2001 - 01/2001
2Liver Diseases (Liver Disease)
01/2001 - 01/2000
2Alpha-Methylacyl-CoA Racemase Deficiency
01/2001 - 11/2000
2Peroxisomal Disorders (Peroxisomal Disorder)
01/2001 - 10/2000
2Peroxisome biogenesis disorders
10/2000 - 02/2000
2Seizures (Absence Seizure)
08/2000 - 01/2000
2Coma (Comas)
08/2000 - 01/2000
1Inflammation (Inflammations)
09/2011
1Type I 3-Methylglutaconic Aciduria
09/2010
1Protein Deficiency
01/2005
1Galactosemias (Galactosemia)
11/2001
1Hepatomegaly
11/2001
1Ornithine Carbamoyltransferase Deficiency Disease
11/2001
1Desmosterolosis
10/2001
1Medium chain acyl CoA dehydrogenase deficiency
05/2001
1Schizophrenia (Dementia Praecox)
03/2001
1Hypertrophic Pyloric Stenosis
03/2001
1Chondrodysplasia Punctata (Stippled Epiphyses)
02/2001
1Barth Syndrome
12/2000
1Skin Abnormalities
12/2000
1Acute-Phase Reaction
12/2000
1Syndromic 10 X-Linked Mental Retardation
12/2000
1Neurologic Manifestations (Neurological Manifestations)
12/2000
12-Methylbutyryl-CoA Dehydrogenase Deficiency
11/2000
1Cardiomyopathies (Cardiomyopathy)
08/2000
1Hemolysis
08/2000
1Heart Failure
08/2000
1HELLP Syndrome
08/2000
1type 2 Rhizomelic chondrodysplasia punctata
07/2000
1Multiple Abnormalities
03/2000

Drug/Important Bio-Agent (IBA)

18EnzymesIBA
12/2001 - 01/2000
9Fatty Acids (Saturated Fatty Acids)IBA
01/2005 - 01/2000
6Proteins (Proteins, Gene)FDA Link
12/2001 - 09/2000
5mevalonate kinaseIBA
05/2001 - 04/2000
4Phytanic AcidIBA
11/2001 - 05/2000
4CholesterolIBA
10/2001 - 12/2000
2pristanic acidIBA
01/2009 - 11/2000
2sterol carrier proteinsIBA
12/2001 - 03/2000
2Carnitine (L-Carnitine)FDA LinkGeneric
11/2001 - 08/2000
2SterolsIBA
10/2001 - 12/2000
2long-chain-aldehyde dehydrogenaseIBA
07/2001 - 01/2001
2Immunoglobulin D (IgD)IBA
05/2001 - 07/2000
27-dehydrocholesterol reductaseIBA
05/2001 - 12/2000
2Leukotriene B4IBA
01/2001 - 02/2000
2AcidsIBA
01/2001 - 08/2000
2Isoleucine (L-Isoleucine)FDA Link
12/2000 - 11/2000
2phytanoyl-coenzyme A (phytanoyl CoA)IBA
07/2000 - 05/2000
2Mixed Function Oxygenases (Monooxygenases)IBA
07/2000 - 05/2000
2CatalaseIBA
02/2000 - 01/2000
1Insulin (Novolin)FDA Link
09/2011
1Leucine (L-Leucine)FDA Link
09/2010
1type 1 Rhizomelic chondrodysplasia punctataIBA
12/2001
1Acyl-CoA OxidaseIBA
12/2001
1TransferasesIBA
11/2001
1Systemic carnitine deficiencyIBA
11/2001
1DesmosterolIBA
10/2001
13beta-hydroxysterol delta24-reductaseIBA
10/2001
17-dehydrocholesterolIBA
05/2001
1Immunoglobulins (Immunoglobulin)IBA
05/2001
1acylcarnitineIBA
05/2001
1Phospholipids (Phosphatides)FDA LinkGeneric
03/2001
1Carnitine Acyltransferases (Carnitine-Acylcarnitine Translocase)IBA
02/2001
1TaurineFDA Link
01/2001
1Bile Acids and Salts (Bile Acids)IBA
01/2001
1Coenzyme A (CoA)IBA
01/2001
1alpha-methylacyl-CoA racemaseIBA
01/2001
1Racemases and Epimerases (Epimerases and Racemases)IBA
01/2001
1Cardiolipins (Cardiolipin)IBA
12/2000
1PhosphatidylglycerolsIBA
12/2000
1Terpenes (Terpenoids)IBA
12/2000
1Valine (L-Valine)FDA Link
11/2000
1Acyl-CoA DehydrogenasesIBA
11/2000
1PeroxinsIBA
10/2000
13-Hydroxyacyl-CoA DehydrogenaseIBA
08/2000
1Carnitine-Acylcarnitine Translocase DeficiencyIBA
08/2000
1Peroxisomal Targeting SignalsIBA
07/2000
1Acyl Coenzyme A (Acyl CoA)IBA
07/2000
1Complementary DNA (cDNA)IBA
07/2000
1glycerone-phosphate O-acyltransferaseIBA
07/2000
1Acute-Phase Proteins (Acute-Phase Protein)IBA
07/2000
12-hydroxyphytanoyl-coenzyme A lyaseIBA
06/2000
1RNA Splice SitesIBA
05/2000
1Long-Chain-3-Hydroxyacyl-CoA DehydrogenaseIBA
04/2000
1Adenosine Triphosphate (ATP)IBA
04/2000
1Congenital disorder of glycosylation type 1AIBA
03/2000

Therapy/Procedure

1Liver Transplantation
01/2005
1Transplantation
01/2005