Longitudinal Smartphone-Based Post-hospitalisation Symptom Monitoring in SARS-CoV-2 Associated Respiratory Failure: A Multi-Centre Observational Study von Kohlbrenner, Dario, Kuhn, Manuel, Stüssi-Helbling, Melina, Nordmann, Yves, Spielmanns, Marc, Clarenbach, Christian F.

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Variegate Porphyria in Western Europe: Identification of PPOX Gene Mutations in 104 Families, Extent of Allelic Heterogeneity, and Absence of Correlation between Phenotype and Type... von Whatley, Sharon D., Puy, Hervé, Morgan, Rhian R., Robreau, Anne-Marie, Roberts, Andrew G., Nordmann, Yves, Elder, George H., Deybach, Jean-Charles

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A Telemonitoring and Hybrid Virtual Coaching Solution “CAir” for Patients with Chronic Obstructive Pulmonary Disease: Protocol for a Randomized Controlled Trial von Gross, Christoph, Kohlbrenner, Dario, Clarenbach, Christian F, Ivankay, Adam, Brunschwiler, Thomas, Nordmann, Yves, v Wangenheim, Florian

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Homozygous hereditary coproporphyria caused by an arginine to tryptophane substitution in coproporphyrinogen oxidase and common intragenic polymorphisms von Martasek, Pavel, Nordmann, Yves, Grandchamp, Bernard

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A Telemonitoring and Hybrid Virtual Coaching Solution “CAir” for Patients with Chronic Obstructive Pulmonary Disease: Protocol for a Randomized Controlled Trial von Gross, Christoph, Kohlbrenner, Dario, Clarenbach, Christian F, Ivankay, Adam, Brunschwiler, Thomas, Nordmann, Yves, v Wangenheim, Florian

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Erythropoietic protoporphyria and hepatic complications von Nordmann, Yves

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Human hereditary hepatic porphyrias von Nordmann, Yves, Puy, Hervé

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Human Erythropoietic Protoporphyria: Two point mutations in the ferrochelatase gene von Lamoril, Jerôme, Boulechfar, Samia, de Verneuil, Hubert, Grandchamp, Bernard, Nordmann, Yves, Deybach, Jean-Charles

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Three novel mutations in the coproporphyrinogen oxidase gene von Lamoril, Jérôme, Deybach, Jean-Charles, Puy, Hervé, Grandchamp, Bernard, Nordmann, Yves

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Ferrochelatase Structural Mutant ( Fech m1Pas) in the House Mouse von Boulechfar, Samia, Lamoril, Jérôme, Montagutelli, Xavier, Guenet, Jean-Louis, Deybach, Jean-Charles, Nordmann, Yves, Dailey, Harry, Grandchamp, Bernard, de Verneuil, Hubert

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Improving body composition and physical activity in Prader-Willi Syndrome von Eiholzer, Urs, Nordmann, Yves, L'allemand, Dagmar, Schlumpf, Michael, Schmid, Silvia, Kromeyer-Hauschild, Katrin

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Hepatocellular carcinoma in patients with acute hepatic porphyria: frequency of occurrence and related factors von Andant, Christophe, Puy, Hervé, Bogard, Catherine, Faivre, Jean, Soulé, Jean-Claude, Nordmann, Yves, Deybach, Jean-Charles

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Inheritance in Erythropoietic Protoporphyria: A Common Wild-Type Ferrochelatase Allelic Variant With Low Expression Accounts for Clinical Manifestation von Gouya, Laurent, Puy, Herve, Lamoril, Jerôme, Da Silva, Vasco, Grandchamp, Bernard, Nordmann, Yves, Deybach, Jean-Charles

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Sudden Death of an Infant with Prader-Willi Syndrome – Not a Unique Case? von Nordmann, Yves, Eiholzer, Urs, l’Allemand, Dagmar, Mirjanic, Slavko, Markwalder, Christoph

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Fatal Outcome of Sleep Apnoea in PWS during the Initial Phase of Growth Hormone Treatment von Eiholzer, Urs, Nordmann, Yves, l’Allemand, Dagmar

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EFFECT OF GLUTEN‐CONTAINING DIET ON SERUM ZONULIN AND INTESTINAL PERMEABILITY IN TYPE 1 DIABETES CHILDREN AND THEIR RELATIVES von Sapone, Anna, Counts, Debra, Kryszak, Deborah, Palese, Teresa, Catassi, Carlo, Zampini, Lucia, Nordmann, Yves, Coppa, Giovanni Valentino, Fasano, Alessio

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Heme and acute inflammation von Lyoumi, Saïd, Puy, Hervé, Tamion, Fabienne, Bogard, Catherine, Leplingard, Antony, Scotté, Michel, Vranckx, Roger, Gauthier, Francis, Hiron, Martine, Daveau, Maryvonne, Nordmann, Yves, Deybach, Jean Charles, Lebreton, Jean Pierre

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Epidemiology of hepatitis C and G in sporadic and familial porphyria cutanea tarda von Lamoril, Jérôme, Andant, Christophe, Bogard, Catherine, Puy, Hervé, Gouya, Laurent, Pawlotsky, Jean‐Michel, Da Silva, Vasco, Soulé, Jean‐Claude, Deybach, Jean‐Charles, Nordmann, Yves

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Molecular characterization of homozygous variegate porphyria von ROBERTS, A. G, PUY, H, DAILEY, T. A, MORGAN, R. R, WHATLEY, S. D, DAILEY, H. A, MARTASEK, P, NORDMANN, Y, DEYBACH, J.-C, ELDER, G. H

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Correction of congenital erythropoietic porphyria by bone marrow transplantation von Thomas, Caroline, Ged, Cecile, Nordmann, Yves, de Verneuil, Hubert, Pellier, Isabelle, Fischer, Alain, Blanche, Stéphane

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