Novel myophosphorylase mutation (p.Arg94Pro) with progressive exercise intolerance

por Nabavi Nouri, Maryam, Lamhonwah, Anne‐Marie, Tein, Ingrid
Publicado 2018

Attention deficit/hyperactivity disorder as an associated feature in OCTN2 deficiency with novel deletion (p.T440‐Y449)

por Lamhonwah, Anne‐Marie, Barić, Ivo, Lamhonwah, Jessica, Grubić, Marina, Tein, Ingrid
Publicado 2018

Vulnerability to Oxidative Stress In Vitro in Pathophysiology of Mitochondrial Short-Chain Acyl-CoA Dehydrogenase Deficiency: Response to Antioxidants

por Zolkipli, Zarazuela, Pedersen, Christina B., Lamhonwah, Anne-Marie, Gregersen, Niels, Tein, Ingrid
Publicado 2011