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Mitochondrial diseases
Results: 104

#	Item
31	Facts About Mitochondrial Myopathies Updated December 2009 Add to Reading List Source URL: mdausa.org Language: English - Date: 2011-09-19 18:47:32 Biology Rare diseases MELAS syndrome Chronic progressive external ophthalmoplegia Kearns–Sayre syndrome Mitochondrion Mitochondrial myopathy Myopathy Mitochondrial DNA Health Mitochondrial diseases Genetics
32	ABSTRACT: Mitochondrial trifunctional protein (TFP) deﬁciency is a rare disorder of the fatty acid ␤-oxidation cycle with heterogeneous phenotypes and occurs secondary to either ␣- or ␤-subunit mutations. We char Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:17 Rare diseases Hepatology Mitochondrial trifunctional protein Proteins Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty acids HADHB Hydroxyacyl-Coenzyme A dehydrogenase Mitochondrial trifunctional protein deficiency Health Medicine Genetic genealogy
33	Cyclic Vomiting Syndrome Association USA/Canada 3585 Cedar Hill Rd. NW, Canal Winchester, OH[removed]Telephone[removed]Fax[removed]Email [removed] Website http://www.cvsaonline.org As Reprinted from Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:40:42 Medicine Vomiting Cyclic vomiting syndrome Mitochondrial diseases Gastroparesis MELAS syndrome Migraine Mitochondrion Ondansetron Health Biology Rare diseases
34	A Modern Approach to the Treatment of Mitochondrial Disease Sumit Parikh, MD Russell Saneto, DO, PhD Marni J. Falk, MD Irina Anselm, MD Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-09-02 09:34:52 Mitochondrial diseases Coenzyme Q10 Carnitine MELAS syndrome Mitochondrion Ubiquinol Fatty-acid metabolism disorder Mitochondrial myopathy Creatine Chemistry Biology Health
35	Facts About Genetics and Neuromuscular Diseases Add to Reading List Source URL: mdausa.org Language: English - Date: 2011-10-03 18:31:08 Mitochondrial disease Mitochondrion Non-Mendelian inheritance Mutation Mitochondrial DNA Human genome Chromosome Duchenne muscular dystrophy Genetic testing Biology Genetics Genetic disorder
36	Final Progress Report: RSDSA and RSDhope Grant Researcher’s Name: E-mail Address: Institution: Project Title: Date: Add to Reading List Source URL: www.rsds.org Language: English - Date: 2013-01-11 01:34:01 DNA Neurological disorders Syndromes Pain Rare diseases Complex regional pain syndrome Mitochondrial DNA Mitochondrion Cyclic vomiting syndrome Health Biology Medicine
37	J Inherit Metab Dis[removed]:488–497 DOI[removed]s10545[removed]ORIGINAL ARTICLE Management and outcome in 75 individuals with long-chain fatty Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:02 Fatty acids Hepatology Metabolism Rare diseases Fatty-acid metabolism disorder Mitochondrial trifunctional protein deficiency Newborn screening Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Mitochondrial trifunctional protein Biology Health Medicine
38	Coenzyme Q10 in the Treatment of Mitochondrial Disorders Barbara Marriage, PhD RD Ross Metabolics Ross Products Division, Abbott Laboratories Metabolic Hotline[removed]removed] Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:14 Health Cellular respiration Antioxidants Benzoquinones Coenzyme Q10 Coenzymes MELAS syndrome Kearns–Sayre syndrome Mitochondrion Mitochondrial diseases Biology Chemistry
39	The n e w e ng l a n d j o u r na l of Add to Reading List Source URL: www.infanthearing.org Language: English - Date: 2010-04-22 17:51:15 Otolaryngology Otology Sensorineural hearing loss Mitochondrial diseases Hearing impairment Syndromes GJB2 KCNQ4 Congenital hearing loss Deafness Health Medicine
40	Microsoft Word - LCHADD_update_2013 Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-12-01 03:02:07 Rare diseases Fatty acids Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Mitochondrial trifunctional protein deficiency 3-hydroxyacyl-coenzyme A dehydrogenase deficiency 3-hydroxyacyl-CoA dehydrogenase Newborn screening Fatty acid metabolism Health Medicine Biology