Serveur d'exploration sur le lymphœdème - Exploration (Accueil)

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List of bibliographic references indexed by disorders

Number of relevant bibliographic references: 195.
[0-20] [0 - 20][0 - 50][20-40]
Ident.Authors (with country if any)Title
000082 (2017) Pui Wong [République populaire de Chine] ; Victoria Laxton ; Saurabh Srivastava ; Yin Wah Fiona Chan [Royaume-Uni] ; Gary Tse [République populaire de Chine]The role of gap junctions in inflammatory and neoplastic disorders (Review)
000243 (2017) Readability of Wikipedia Pages on Autoimmune Disorders: Systematic Quantitative Assessment
000482 (2017) Eberhard Rabe [Allemagne] ; Hugo Partsch [Autriche] ; Juerg Hafner [Suisse] ; Christopher Lattimer [Royaume-Uni] ; Giovanni Mosti [Italie] ; Martino Neumann [Pays-Bas] ; Tomasz Urbanek [Pologne] ; Monika Huebner [Suisse] ; Sylvain Gaillard [Suisse] ; Patrick Carpentier [France]Indications for medical compression stockings in venous and lymphatic disorders: An evidence-based consensus statement.
000539 (2017) Tohru FujiwaraGATA Transcription Factors: Basic Principles and Related Human Disorders.
000578 (2017) Suresh Parmar ; Iryna Khodasevych ; Olga TroynikovEvaluation of Flexible Force Sensors for Pressure Monitoring in Treatment of Chronic Venous Disorders
000825 (2017) Kohji Ohki ; Hiromichi Wakui ; Kengo Azushima [Singapour] ; Kazushi Uneda ; Sona Haku ; Ryu Kobayashi ; Kotaro Haruhara ; Sho Kinguchi ; Miyuki Matsuda ; Masato Ohsawa ; Akinobu Maeda ; Shintaro Minegishi ; Tomoaki Ishigami ; Yoshiyuki Toya ; Akio Yamashita ; Satoshi Umemura [Japon] ; Kouichi TamuraATRAP Expression in Brown Adipose Tissue Does Not Influence the Development of Diet-Induced Metabolic Disorders in Mice
000919 (2016) Aisha Al-Shamsi ; Jozef L. Hertecant ; Abdul-Kader Souid ; Fatma A. Al-JasmiWhole exome sequencing diagnosis of inborn errors of metabolism and other disorders in United Arab Emirates
000A35 (2016) Giuseppe Maccagnano [Italie] ; Angela Notarnicola [Italie] ; Vito Pesce [Italie] ; Simona Mudoni [Italie] ; Silvio Tafuri [Italie] ; Biagio Moretti [Italie]The Prevalence of Fragility Fractures in a Population of a Region of Southern Italy Affected by Thyroid Disorders
000E36 (2016) Rie Yagi Yoshida [Japon] ; Shuji Kariya [Japon] ; Sangkil Ha-Kawa [Japon] ; Noboru Tanigawa [Japon]Lymphoscintigraphy for Imaging of the Lymphatic Flow Disorders.
000E60 (2016) Antoine Louveau ; Sandro Da Mesquita ; Jonathan KipnisLymphatics in Neurological Disorders: A neuro-lympho-vascular Component of Multiple Sclerosis and Alzheimer’s Disease
001107 (2016) Alessandro Guidotti [États-Unis] ; Dennis R. Grayson [États-Unis] ; Hector J. Caruncho [Canada]Epigenetic RELN Dysfunction in Schizophrenia and Related Neuropsychiatric Disorders
001594 (2015) Debora Karetová[Chronic venous disorders - necessity of specific differentiation to determination of the best medical treatment].
001943 (2015) Jana Trebatická [Slovaquie] ; Zde Ka Ura Ková [Slovaquie]Psychiatric Disorders and Polyphenols: Can They Be Helpful in Therapy?
001B72 (2015) Andrea Ranghino [Italie] ; Giuseppe Paolo Segoloni [Italie] ; Fedele Lasaponara [Italie] ; Luigi Biancone [Italie]Lymphatic disorders after renal transplantation: new insights for an old complication
001D55 (2015) Matthias Griese [Allemagne] ; Ralf Zarbock [Allemagne] ; Ulrich Costabel [Allemagne] ; Jenna Hildebrandt [Allemagne] ; Dirk Theegarten [Allemagne] ; Michael Albert [Allemagne] ; Antonia Thiel [Allemagne] ; Andrea Schams [Allemagne] ; Joanna Lange [Pologne] ; Katazyrna Krenke [Pologne] ; Traudl Wesselak [Allemagne] ; Carola Schön [Allemagne] ; Matthias Kappler [Allemagne] ; Helmut Blum [Allemagne] ; Stefan Krebs [Allemagne] ; Andreas Jung [Allemagne] ; Carolin Kröner [Allemagne] ; Christoph Klein [Allemagne] ; Ilaria Campo [Italie] ; Maurizio Luisetti [Italie] ; Francesco Bonella [Allemagne]GATA2 deficiency in children and adults with severe pulmonary alveolar proteinosis and hematologic disorders
001D57 (2015) Juehua Gao [États-Unis] ; Yi-Hua Chen [États-Unis] ; Loann C. Peterson [États-Unis]GATA family transcriptional factors: emerging suspects in hematologic disorders
001F24 (2015) Norihito Shibata ; Nobumichi Ohoka ; Yusuke Sugaki ; Chiaki Onodera ; Mizuho Inoue ; Yoshiyuki Sakuraba ; Daisuke Takakura ; Noritaka Hashii ; Nana Kawasaki ; Yoichi Gondo ; Mikihiko NaitoDegradation of Stop Codon Read-through Mutant Proteins via the Ubiquitin-Proteasome System Causes Hereditary Disorders*
001F25 (2015) Jonathan Baets [Belgique] ; Xiaohui Duan [États-Unis] ; Yanhong Wu [États-Unis] ; Gordon Smith [États-Unis] ; William W. Seeley [États-Unis] ; Inès Mademan [Belgique] ; Nicole M. Mcgrath [Nouvelle-Zélande] ; Noah C. Beadell [États-Unis] ; Julie Khoury [États-Unis] ; Maria-Victoria Botuyan [États-Unis] ; Georges Mer [États-Unis] ; Gregory A. Worrell [États-Unis] ; Kaori Hojo [Japon] ; Jessica Deleon [États-Unis] ; Matilde Laura [Royaume-Uni] ; Yo-Tsen Liu [Royaume-Uni, Taïwan] ; Jan Senderek [Allemagne] ; Joachim Weis [Allemagne] ; Peter Van Den Bergh [Belgique] ; Shana L. Merrill [États-Unis] ; Mary M. Reilly [Royaume-Uni] ; Henry Houlden [Royaume-Uni] ; Murray Grossman [États-Unis] ; Steven S. Scherer [États-Unis] ; Peter De Jonghe [Belgique] ; Peter J. Dyck [États-Unis] ; Christopher J. Klein [États-Unis]Defects of mutant DNMT1 are linked to a spectrum of neurological disorders
002105 (2015) Bo Hoon Lee [États-Unis] ; Tristram Smith [États-Unis] ; Alex R. Paciorkowski [États-Unis]Autism Spectrum Disorder and Epilepsy: disorders with a shared biology
002346 (2014) Michael D. Stubblefield [États-Unis] ; Nandita KeoleUpper body pain and functional disorders in patients with breast cancer.
002458 (2014) Amy E. Dezern ; Mikkael A. SekeresThe Challenging World of Cytopenias: Distinguishing Myelodysplastic Syndromes From Other Disorders of Marrow Failure

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