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Quoted phrase not found in phrase index: "Abnormal peroxisomal morphology"
Page 1
Diabetes and Cognitive Impairment.
Zilliox LA, Chadrasekaran K, Kwan JY, Russell JW. Zilliox LA, et al. Curr Diab Rep. 2016 Sep;16(9):87. doi: 10.1007/s11892-016-0775-x. Curr Diab Rep. 2016. PMID: 27491830 Free PMC article. Review.
Both type 1 (T1DM) and type 2 diabetes mellitus (T2DM) have been associated with reduced performance on multiple domains of cognitive function and with evidence of abnormal structural and functional brain magnetic resonance imaging (MRI). ...The duration of diabetes and gl …
Both type 1 (T1DM) and type 2 diabetes mellitus (T2DM) have been associated with reduced performance on multiple domains of cognitive functi …
What are the epileptic encephalopathies?
Trivisano M, Specchio N. Trivisano M, et al. Curr Opin Neurol. 2020 Apr;33(2):179-184. doi: 10.1097/WCO.0000000000000793. Curr Opin Neurol. 2020. PMID: 32049741 Review.
PURPOSE OF REVIEW: To review the evolution of the concept of epileptic encephalopathy during the course of past years and analyze how the current definition might impact on both clinical practice and research. ...DNA repair, transcriptional regulation, axon myelination, me …
PURPOSE OF REVIEW: To review the evolution of the concept of epileptic encephalopathy during the course of past years and analyze how …
Human peroxisomal disorders.
Depreter M, Espeel M, Roels F. Depreter M, et al. Microsc Res Tech. 2003 Jun 1;61(2):203-23. doi: 10.1002/jemt.10330. Microsc Res Tech. 2003. PMID: 12740827 Review.
Peroxisomes are single membrane-bound cell organelles performing numerous metabolic functions. ...Together with other laboratory investigations and clinical data, this approach continues to contribute to the diagnosis and further characterization of peroxisomal diso …
Peroxisomes are single membrane-bound cell organelles performing numerous metabolic functions. ...Together with other laboratory inve …
Neonatal adrenoleukodystrophy.
Aubourg P, Scotto J, Rocchiccioli F, Feldmann-Pautrat D, Robain O. Aubourg P, et al. J Neurol Neurosurg Psychiatry. 1986 Jan;49(1):77-86. doi: 10.1136/jnnp.49.1.77. J Neurol Neurosurg Psychiatry. 1986. PMID: 2420940 Free PMC article.
Nine cases of neonatal adrenoleukodystrophy are described. All patients had abnormal facial features, moderate to severe hypotonia, hepatomegaly, and retinitis pigmentosa. The clinical course was rapidly progressive in six cases and more protracted in three others. …
Nine cases of neonatal adrenoleukodystrophy are described. All patients had abnormal facial features, moderate to severe hypotonia, h …
Molecular Pathogenesis in Huntington's Disease.
Illarioshkin SN, Klyushnikov SA, Vigont VA, Seliverstov YA, Kaznacheyeva EV. Illarioshkin SN, et al. Biochemistry (Mosc). 2018 Sep;83(9):1030-1039. doi: 10.1134/S0006297918090043. Biochemistry (Mosc). 2018. PMID: 30472941 Free article. Review.
Huntington's disease (HD) is a severe autosomal dominant neurodegenerative disorder characterized by a combination of motor, cognitive, and psychiatric symptoms, atrophy of the basal ganglia and the cerebral cortex, and inevitably progressive course resulting in death 5-20 …
Huntington's disease (HD) is a severe autosomal dominant neurodegenerative disorder characterized by a combination of motor, cognitive, and …
Clinical diagnosis, biochemical findings and MRI spectrum of peroxisomal disorders.
Poll-The BT, Gärtner J. Poll-The BT, et al. Biochim Biophys Acta. 2012 Sep;1822(9):1421-9. doi: 10.1016/j.bbadis.2012.03.011. Epub 2012 Mar 28. Biochim Biophys Acta. 2012. PMID: 22483868 Free article. Review.
Peroxisomal disorders are an important group of neurometabolic diseases. The clinical presentation is varied in terms of age of onset, severity, and different neurological symptoms. The clinical course spans from death in infancy, rapid functional decline, slow decl …
Peroxisomal disorders are an important group of neurometabolic diseases. The clinical presentation is varied in terms of age of onset …
Nuclear receptors and pathogenesis of pancreatic cancer.
Polvani S, Tarocchi M, Tempesti S, Galli A. Polvani S, et al. World J Gastroenterol. 2014 Sep 14;20(34):12062-81. doi: 10.3748/wjg.v20.i34.12062. World J Gastroenterol. 2014. PMID: 25232244 Free PMC article. Review.
Pancreatic ductal adenocarcinoma (PDAC) is a devastating disease with a median overall survival time of 5 mo and the five years survival less than 5%, a rate essentially unchanged over the course of the years. A well defined progression model of accumulation of genetic alt …
Pancreatic ductal adenocarcinoma (PDAC) is a devastating disease with a median overall survival time of 5 mo and the five years survival les …
The value of autopsy in determining the cause of failure to respond to resuscitation at birth.
Squier W, Cowan FM. Squier W, et al. Semin Neonatol. 2004 Aug;9(4):331-45. doi: 10.1016/j.siny.2004.01.003. Semin Neonatol. 2004. PMID: 15251149 Review.
Disorders of the spinal cord, peripheral nerve and muscle as well as some metabolic diseases may cause a baby to be both floppy and weak. Metabolic disease, including peroxisomal disorders, non-ketotic hyperglycinaemia, lipid and glycogen storage disorders and mitochondria …
Disorders of the spinal cord, peripheral nerve and muscle as well as some metabolic diseases may cause a baby to be both floppy and weak. Me …
Nuclear Receptors in Hepatic Glucose and Lipid Metabolism During Neonatal and Adult Life.
Cai D, Liu H, Zhao R. Cai D, et al. Curr Protein Pept Sci. 2017;18(6):548-561. doi: 10.2174/1389203717666160627081751. Curr Protein Pept Sci. 2017. PMID: 27356935 Review.
Research efforts focusing on metabolic diseases have established a close conjunction between glucolipid abnormalities and nuclear receptors, a large superfamily of receptors including classic peroxisome proliferation-activated receptors (PPARs), liver X receptors (L …
Research efforts focusing on metabolic diseases have established a close conjunction between glucolipid abnormalities and nuclear rec …
Bile acid synthetic defects and liver disease: a comprehensive review.
Bove KE, Heubi JE, Balistreri WF, Setchell KD. Bove KE, et al. Pediatr Dev Pathol. 2004 Jul-Aug;7(4):315-34. doi: 10.1007/s10024-002-1201-8. Epub 2004 Jul 15. Pediatr Dev Pathol. 2004. PMID: 15383928 Review.
Bile acid synthetic defects (BASD), uncommon genetic disorders that are responsible for approximately 2% of persistent cholestasis in infants, are reviewed with emphasis on morphology of associated liver disease. The associated liver diseases may be life threatening, and a …
Bile acid synthetic defects (BASD), uncommon genetic disorders that are responsible for approximately 2% of persistent cholestasis in infant …
85 results