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Mitochondrial diseases
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51	T he Official News Letter of the Mitochondria Research Society Vol 1, Issue 2, Summer 2002 The Official Newsletter of the Mitochondria Research Society, Volume 1, Issue 3, 2002 Add to Reading List Source URL: mitoresearch.org Language: English - Date: 2002-10-09 20:07:52 Cellular respiration Health Mitochondrion Kearns–Sayre syndrome Human mitochondrial genetics Mitochondrial DNA MELAS syndrome Chronic progressive external ophthalmoplegia Coenzyme Q10 Biology Genetics Mitochondrial diseases
52	T he Official News Letter of the Mitochondria Research Society Vol 1, Issue 2, Summer 2002 The Official Newsletter of the Mitochondria Research Society, Volume 1, Issue 2, 2002 Add to Reading List Source URL: mitoresearch.org Language: English - Date: 2002-08-30 11:52:43 Cellular respiration Mitochondrion Organelles Human mitochondrial genetics Mitochondrial DNA Chronic progressive external ophthalmoplegia Fatty acid metabolism Insulin resistance Adipose tissue Biology Anatomy Mitochondrial diseases
53	Welcome to MitoMatters, the official newsletter for the Mitochondria Research Society-MRS Add to Reading List Source URL: mitoresearch.org Language: English - Date: 2002-02-06 20:38:09 Mitochondrial diseases Rare diseases Cellular respiration Mitochondrion Kearns–Sayre syndrome Mitochondrial DNA Succinate dehydrogenase National Institutes of Health Mitochondrial Eve Genetics Biology Health
54	23068 Mitomatters Newsletter 5.indd Add to Reading List Source URL: www.mitoresearch.org Language: English - Date: 2005-04-08 07:46:45 Chemistry Integral membrane proteins Mitochondrial diseases Mitochondrion Rare diseases Mitochondrial DNA NADH dehydrogenase Reactive oxygen species Electron transport chain Biology Cellular respiration Genetics
55	Long-chain L-3-hydroxy acyl-CoA Dehydrogenase Deficiency (LCHAD) Trifunctional Protein Deficiency (TFP) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 10:42:23 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Newborn screening Mitochondrial trifunctional protein deficiency Fatty-acid metabolism disorder Mitochondrial trifunctional protein Health Medicine Rare diseases
56	Medical frontier: Debating mitochondria replacement Annex VI: Patient focus group Report to HFEA February 2013 Add to Reading List Source URL: www.hfea.gov.uk Language: English - Date: 2014-08-05 11:03:51 Medical genetics Mitochondrial diseases Mitochondrial genetics DNA Mitochondrion Spindle transfer Mitochondrial DNA MELAS syndrome Preimplantation genetic diagnosis Biology Genetics Fertility medicine
57	2013 MeSH Tree Structures. C11 - DISEASES-OCULAR Add to Reading List Source URL: www.nlm.nih.gov Language: English - Date: 2012-08-22 14:06:13 Blindness Syndromes Rare diseases Mitochondrial diseases Eye disease Uveitis Optic neuropathy ICD-10 Chapter VII: Diseases of the eye adnexa Optic disc drusen Health Ophthalmology Medicine
58	Physician ethics and genetic testing Add to Reading List Source URL: www.peds.ufl.edu Language: English - Date: 2008-03-12 11:18:28 Channelopathy Sensorineural hearing loss Mitochondrial diseases Congenital hearing loss Rare diseases Nonsyndromic deafness Hearing impairment Pendred syndrome Treacher Collins syndrome Health Deafness Syndromes
59	Minnesota Department of Health[removed]Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency Action required Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:21 Rare diseases Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Newborn screening Carnitine 3-hydroxyacyl-CoA dehydrogenase Hypoglycemia 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Mitochondrial trifunctional protein Health Medicine Chemistry
60	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: www.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