Recent advances in neurometabolic diseases: The genetic role in the modern era von Tein, Ingrid

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L-arginine effects on cerebrovascular reactivity, perfusion and neurovascular coupling in MELAS (mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes) synd... von Rodan, Lance H, Poublanc, Julien, Fisher, Joseph A, Sobczyk, Olivia, Mikulis, David J, Tein, Ingrid

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New treatments in mitochondrial disorders von Tein, Ingrid

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Novel localization of OCTN1, an organic cation/carnitine transporter, to mammalian mitochondria von Lamhonwah, Anne-Marie, Tein, Ingrid

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L-Arginine Affects Aerobic Capacity and Muscle Metabolism in MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes) Syndrome von Rodan, Lance H, Wells, Greg D, Banks, Laura, Thompson, Sara, Schneiderman, Jane E, Tein, Ingrid

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Cystic fibrosis transmembrane conductance regulator in human muscle: Dysfunction causes abnormal metabolic recovery in exercise von Lamhonwah, Anne-Marie, Bear, Christine E., Huan, Ling Jun, Chiaw, Patrick Kim, Ackerley, Cameron A., Tein, Ingrid

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NDST1 Preferred Promoter Confirmation and Identification of Corresponding Transcriptional Inhibitors as Substrate Reduction Agents for Multiple Mucopolysaccharidosis Disorders von Tkachyova, Ilona, Fan, Xiaolian, LamHonWah, Anne-Marie, Fedyshyn, Bohdana, Tein, Ingrid, Mahuran, Don J, Schulze, Andreas

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Obituary for Dr. Brian H. Robinson, PhD von Cameron, Jessie, Tein, Ingrid

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Expression patterns of the organic cation/carnitine transporter family in adult murine brain von Lamhonwah, Anne Marie, Hawkins, Cynthia E, Tam, Carolyn, Wong, Jeannie, Mai, Lydia, Tein, Ingrid

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Tribute to Linda Joanna DE MEIRLEIR von Tein, Ingrid

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Impact of fatty acid oxidation disorders in child neurology: from Reye syndrome to Pandora's box von Tein, Ingrid

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Vulnerability to oxidative stress in vitro in pathophysiology of mitochondrial short-chain acyl-CoA dehydrogenase deficiency: response to antioxidants von Zolkipli, Zarazuela, Pedersen, Christina B, Lamhonwah, Anne-Marie, Gregersen, Niels, Tein, Ingrid

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Mitochondrial diseases: need for international collaborations? von Tein, Ingrid

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CPT2 gene mutations resulting in lethal neonatal or severe infantile carnitine palmitoyltransferase II deficiency von Isackson, Paul J., Bennett, Michael J., Lichter-Konecki, Uta, Willis, Mary, Nyhan, William L., Sutton, V. Reid, Tein, Ingrid, Vladutiu, Georgirene D.

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Obituary for Dr. Brian H. Robinson, PhD von Cameron, Jessie, Tein, Ingrid

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A third human carnitine/organic cation transporter ( OCTN3) as a candidate for the 5q31 Crohn’s disease locus ( IBD5) von Lamhonwah, Anne-Marie, Skaug, Jennifer, Scherer, Stephen W., Tein, Ingrid

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l‐Carnitine Supplementation in Childhood Epilepsy: Current Perspectives von Vivo, Darryl C., Bohan, Timothy P., Coulter, David L., Dreifuss, Fritz E., Greenwood, Robert S., Nordli, Douglas R., Shields, W. Donald, Stafstrom, Carl E., Tein, Ingrid

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Expression of the organic cation/carnitine transporter family (Octn1,-2 and-3) in mdx muscle and heart: Implications for early carnitine therapy in Duchenne muscular dystrophy to i... von Lamhonwah, Anne-Marie, Tein, Ingrid

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Peripheral neuropathy, episodic myoglobinuria, and respiratory failure in deficiency of the mitochondrial trifunctional protein von Spiekerkoetter, Ute, Bennett, Michael J., Ben-Zeev, Bruria, Strauss, Arnold W., Tein, Ingrid

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Clinical and radiologic reversal of stroke-like episodes in MELAS with high-dose L-arginine von Siddiq, Ishita, Widjaja, Elysa, Tein, Ingrid

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