Extracellular collagen matrix in the treatment of chronic wounds in patients with diabetic foot syndrome

Autor: Artem D. Zakharov, Valeriy I. Nikol'skiy, Konstantin I. Sergatskiy, Aleksandr N. Mitroshin, Mikhail M. Mironov

Publikováno v: Известия высших учебных заведений. Поволжский регион: Медицинские науки, Iss 1 (2024)

Background. Treatment of chronic wounds in patients suffering from diabetic foot syndrome is one of the serious problems of practical surgery. Despite the constant improvement of methods aimed at improving the results of treatment of purulent-necroti

Externí odkaz: https://doaj.org/article/9b8dd65ed47448acbcacff0cb9c90054

Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy.

Autor: Mignot C; Département de Génétique, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France Centre de Référence 'Déficiences Intellectuelles de Causes Rares, Paris, France Groupe de Recherche Clinique (GRC) 'Déficience Intellectuelle et Autisme', UPMC, Paris, France., von Stülpnagel C; Hospital for Neuropediatrics and Neurological Rehabilitation, Epilepsy Center for Children and Adolescents, Vogtareuth, Germany Paracelsus Medical University Salzburg, Austria., Nava C; Département de Génétique, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France Sorbonne Universités, UPMC Univ Paris 06, INSERM UMR S 1127, CNRS UMR 7225, ICM, Paris, France., Ville D; Service de Neurologie Pédiatrique, Hôpital Femme Mère Enfant, CHU de Lyon, Bron, France., Sanlaville D; Service de Génétique, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France Université Claude-Bernard Lyon 1, Villeurbanne, France CRNL, CNRS UMR 5292, INSERM U1028, bâtiment IMBL, Villeurbanne, France., Lesca G; Service de Génétique, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France Université Claude-Bernard Lyon 1, Villeurbanne, France CRNL, CNRS UMR 5292, INSERM U1028, bâtiment IMBL, Villeurbanne, France., Rastetter A; Sorbonne Universités, UPMC Univ Paris 06, INSERM UMR S 1127, CNRS UMR 7225, ICM, Paris, France., Gachet B; Sorbonne Universités, UPMC Univ Paris 06, INSERM UMR S 1127, CNRS UMR 7225, ICM, Paris, France., Marie Y; Sorbonne Universités, UPMC Univ Paris 06, INSERM UMR S 1127, CNRS UMR 7225, ICM, Paris, France., Korenke GC; Klinikum Oldenburg, Zentrum für Kinder- und Jugendmedizin (Elisabeth Kinderkrankenhaus), Klinik für Neuropädiatrie u. angeborene Stoffwechselerkrankungen, Oldenburg, Germany., Borggraefe I; Department of Pediatric Neurology and Developmental Medicine and Epilepsy Center, University of Munich, Munich, Germany., Hoffmann-Zacharska D; Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland., Szczepanik E; Clinic of Neurology of Children and Adolescents, Institute of Mother and Child, Warsaw, Poland., Rudzka-Dybała M; Clinic of Neurology of Children and Adolescents, Institute of Mother and Child, Warsaw, Poland., Yiş U; Division of Child Neurology, Department of Pediatrics, School of Medicine, Dokuz Eylül University, İzmir, Turkey., Çağlayan H; Department of Molecular Biology and Genetics Istanbul, Boğaziçi University, Istanbul, Turkey., Isapof A; AP-HP, Hôpital Trousseau, Service de Neuropédiatrie, Paris, France., Marey I; Département de Génétique, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France., Panagiotakaki E; Epilepsy, Sleep and Pediatric Neurophysiology Department (ESEFNP), University Hospitals of Lyon (HCL), France., Korff C; Département de l'Enfant et de l'Adolescent, Neuropédiatrie-Hôpitaux Universitaires de Genève, Genève, Switzerland., Rossier E; Institute of Human Genetics, University of Tuebingen, Tuebingen, Germany., Riess A; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany., Beck-Woedl S; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany., Rauch A; Institute of Medical Genetics, University of Zurich, Schwerzenbach, Switzerland., Zweier C; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany., Hoyer J; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany., Reis A; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany., Mironov M; Svt. Luka's Institute of Child Neurology and Epilepsy, Moscow, Russia., Bobylova M; Svt. Luka's Institute of Child Neurology and Epilepsy, Moscow, Russia., Mukhin K; Svt. Luka's Institute of Child Neurology and Epilepsy, Moscow, Russia., Hernandez-Hernandez L; Department of Clinical and Experimental Epilepsy, Institute of Neurology, University College London, London, UK., Maher B; Department of Clinical and Experimental Epilepsy, Institute of Neurology, University College London, London, UK., Sisodiya S; Department of Clinical and Experimental Epilepsy, Institute of Neurology, University College London, London, UK., Kuhn M; Genetikum, Neu-Ulm, Germany., Glaeser D; Genetikum, Neu-Ulm, Germany., Weckhuysen S; Sorbonne Universités, UPMC Univ Paris 06, INSERM UMR S 1127, CNRS UMR 7225, ICM, Paris, France Neurogenetics Group, Department of Molecular Genetics, VIB, Antwerp, Belgium., Myers CT; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, USA., Mefford HC; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, USA., Hörtnagel K; CeGaT GmbH, Tübingen, Germany., Biskup S; CeGaT GmbH, Tübingen, Germany., Lemke JR; CeGaT GmbH, Tübingen, Germany., Héron D; Département de Génétique, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France Centre de Référence 'Déficiences Intellectuelles de Causes Rares, Paris, France Groupe de Recherche Clinique (GRC) 'Déficience Intellectuelle et Autisme', UPMC, Paris, France Hospital for Neuropediatrics and Neurological Rehabilitation, Epilepsy Center for Children and Adolescents, Vogtareuth, Germany., Kluger G; Hospital for Neuropediatrics and Neurological Rehabilitation, Epilepsy Center for Children and Adolescents, Vogtareuth, Germany Paracelsus Medical University Salzburg, Austria., Depienne C; Département de Génétique, AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France Sorbonne Universités, UPMC Univ Paris 06, INSERM UMR S 1127, CNRS UMR 7225, ICM, Paris, France.

Publikováno v: Journal of medical genetics [J Med Genet] 2016 Aug; Vol. 53 (8), pp. 511-22. Date of Electronic Publication: 2016 Mar 17.