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Journal of Inherited Metabolic Disease

Ausgabe 6/2011

Inhalt (14 Artikel)

Editorial

Alkaptonuria: treasure your exceptions

Timothy M. Cox

Alkaptonuria

Collagen atomic scale molecular disorder in ochronotic cartilage from an alkaptonuria patient, observed by solid state NMR

Wing Ying Chow, Adam M. Taylor, David G. Reid, James A. Gallagher, Melinda J. Duer

Original Article

Natural history of alkaptonuria revisited: analyses based on scoring systems

Lakshminarayan R. Ranganath, Trevor F. Cox

Alkaptonuria

A quantitative assessment of alkaptonuria

Trevor F. Cox, Lakshminarayan Ranganath

Alkaptonuria

Redox-proteomics of the effects of homogentisic acid in an in vitro human serum model of alkaptonuric ochronosis

Daniela Braconi, Claretta Bianchini, Giulia Bernardini, Marcella Laschi, Lia Millucci, Adriano Spreafico, Annalisa Santucci

Alkaptonuria

Cardiovascular manifestations of Alkaptonuria

Stephen J. Pettit, Michael Fisher, James A. Gallagher, Lakshminarayan R. Ranganath

Open Access Review

Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and management

Elizabeth A. Braunlin, Paul R. Harmatz, Maurizio Scarpa, Beatriz Furlanetto, Christoph Kampmann, James P. Loehr, Katherine P. Ponder, William C. Roberts, Howard M. Rosenfeld, Roberto Giugliani

Original Article

Pitfalls in diagnosing mitochondrial neurogastrointestinal encephalomyopathy

Massimiliano Filosto, Mauro Scarpelli, Paola Tonin, Silvia Testi, Maria Sofia Cotelli, Mara Rossi, Andrea Salvi, Alberto Grottolo, Valentina Vielmi, Alice Todeschini, Gian Maria Fabrizi, Alessandro Padovani, Giuliano Tomelleri

Original Article

Mitochondrial diabetes is associated with insulin resistance in subcutaneous adipose tissue but not with increased liver fat content

Markus M. Lindroos, Ronald Borra, Nina Mononen, Terho Lehtimäki, Kirsi A. Virtanen, Virva Lepomäki, Letizia Guiducci, Patricia Iozzo, Kari Majamaa, Pirjo Nuutila

Original Article

Molecular insights into the pathogenicity of variants associated with the aromatic amino acid decarboxylase deficiency

Riccardo Montioli, Barbara Cellini, Carla Borri Voltattorni

Images in Metabolic Medicine

Cerebellar hypoplasia and brainstem thinning associated with severe white matter and basal ganglia abnormalities in a child with an mtDNA deletion

Roberta Biancheri, Claudio Bruno, Denise Cassandrini, Enrico Bertini, Filippo M. Santorelli, Andrea Rossi

Erratum

Erratum to: Isolated remethylation disorders: do our treatments benefit patients?

Manuel Schiff, Jean-François Benoist, Bogdana Tilea, Nicolas Royer, Stéphane Giraudier, Hélène Ogier de Baulny

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