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Mitochondrial diseases
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#	Item
11	Myoclonus in Childhood Michael R . Pranzatelli The term "myoclonus" sounds esoteric, yet it is part of our normal physiology, occurring as a muscle jerk on drowsiness or falling asleep, during rapid eye movement (REM) sl Add to Reading List Source URL: www.omsusa.org Language: English - Date: 2005-04-04 15:14:38 Neurological disorders Seizure types Rare diseases Medical signs Myoclonus Mitochondrial diseases Progressive myoclonus epilepsies Opsoclonus myoclonus syndrome Health Brain Epilepsy
12	Genetic hearing loss March 2004 Add to Reading List Source URL: www.utmb.edu Language: English - Date: 2014-02-04 16:22:44 Channelopathy Mitochondrial diseases Rare diseases Nonsyndromic deafness Sensorineural hearing loss Pendred syndrome KCNQ4 Waardenburg syndrome Usher syndrome Health Syndromes Deafness
13	Study identifies molecular process behind form of non-syndromic deafness Add to Reading List Source URL: medicalxpress.com Language: English - Date: 2015-02-26 07:51:52 Nonsyndromic deafness Health Biology Sensorineural hearing loss Ectrodactyly–ectodermal dysplasia–cleft syndrome Deafness Mitochondrial diseases Channelopathy
14	Downloaded from http://mp.bmj.com/ on February 25, [removed]Published by group.bmj.com I Clin Pathol: Mol Pathol 1995;48:M285-M288 M285 Add to Reading List Source URL: mp.bmj.com Language: English MELAS syndrome Heteroplasmy Mitochondrion Mitochondrial DNA Mitochondrial myopathy Mitochondrial encephalomyopathy Lactic acidosis Thrombin Encephalopathy Genetics Biology Mitochondrial diseases
15	Microsoft Word - pocket facts.docx Add to Reading List Source URL: ndhealth.gov Language: English - Date: 2011-12-12 15:42:57 Rare diseases Pediatrics Inborn errors of carbohydrate metabolism Hepatology Epidemiology Newborn screening Very long-chain acyl-coenzyme A dehydrogenase deficiency Systemic primary carnitine deficiency Mitochondrial trifunctional protein deficiency Health Medicine Genetic genealogy
16	OBSERVATION A Family With X-linked Dystonia-Deafness Syndrome With a Novel Mutation of the DDP Gene Hiroshi Ujike, MD, PhD; Yasuyuki Tanabe, MD, PhD; Yasushi Takehisa, MD; Toshiyuki Hayabara, MD, PhD; Shigetoshi Kuroda, Add to Reading List Source URL: archneur.jamanetwork.com Language: English Health X-linked recessive inheritance Biology Medicine Mitochondrial diseases Rare diseases Pediatrics Neurological disorders Mohr–Tranebjærg syndrome Dystonia
17	Animal results may pave way to treating rare mitochondrial diseases in children Add to Reading List Source URL: medicalxpress.com Language: English - Date: 2015-02-10 03:17:37 Biochemistry Mitochondrial diseases Mitochondrion Rare diseases Coenzyme Q10 Antioxidant Amyotrophic lateral sclerosis Genetic disorder Human mitochondrial genetics Biology Chemistry Cellular respiration
18	Sleep Questionnaire Study Add to Reading List Source URL: www.ataxia.org Language: English - Date: 2014-09-03 12:26:28 Neurology Genetic genealogy Mitochondrial diseases Spinocerebellar ataxia Ataxia Neurodegenerative disorders Health
19	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:52:41 Fatty-acid metabolism disorder Mitochondrial trifunctional protein deficiency Newborn screening Fatty acid metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Malonyl-CoA decarboxylase deficiency Health Medicine Rare diseases
20	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:53 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty acids Fatty-acid metabolism disorder Acute fatty liver of pregnancy Hepatology Newborn screening Fatty acid metabolism Mitochondrial trifunctional protein Health Medicine Rare diseases