Medical care of patients with Wilson disease in Germany: a multidisciplinary survey among university centers
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U. Merle | K. Weiss | G. Denk | S. Hohenester | H. Bourhis | E. Kraft | F. Reiter | S. Weber | Sebastian Zimny | I. Mohr
[1] M. Washington,et al. A Multidisciplinary Approach to the Diagnosis and Management of Wilson Disease: 2022 Practice Guidance on Wilson Disease from the American Association for the Study of Liver Diseases. , 2022, Hepatology.
[2] Y. Izumi,et al. Copper and zinc concentrations in the breast milk of mothers undergoing treatment for Wilson’s disease: a prospective study , 2021, BMJ Paediatrics Open.
[3] T. Sandahl,et al. The Prevalence of Wilson’s Disease: An Update , 2020, Hepatology.
[4] Ren-min Yang,et al. The study of Wilson disease in pregnancy management , 2019, BMC Pregnancy and Childbirth.
[5] A. Poujois,et al. New tools for Wilson's disease diagnosis: exchangeable copper fraction. , 2019, Annals of translational medicine.
[6] J. Dooley,et al. ATP7B variant penetrance explains differences between genetic and clinical prevalence estimates for Wilson disease , 2020, Human Genetics.
[7] K. Zieniewicz,et al. 2018 Annual Report of the European Liver Transplant Registry (ELTR) – 50‐year evolution of liver transplantation , 2018, Transplant international : official journal of the European Society for Organ Transplantation.
[8] C. Lohse,et al. Long-term evaluation of urinary copper excretion and non-caeruloplasmin associated copper in Wilson disease patients under medical treatment , 2018, Journal of Inherited Metabolic Disease.
[9] L. D’Antiga,et al. Wilson's Disease in Children: A Position Paper by the Hepatology Committee of the European Society for Paediatric Gastroenterology, Hepatology and Nutrition. , 2017, Journal of pediatric gastroenterology and nutrition.
[10] A. Członkowska,et al. Measurement of urinary copper excretion after 48-h d-penicillamine cessation as a compliance assessment in Wilson's disease. , 2015, Functional neurology.
[11] J. Mayerle,et al. Erste Daten zur Versorgungssituation von Patienten mit nicht alkoholischer Fettlebererkrankung (NAFLD) in Deutschland – Eine Umfrage an universitären hepatologischen Zentren , 2014, Zeitschrift für Gastroenterologie.
[12] Raffaele Iorio,et al. Zinc monotherapy is effective in Wilson’s disease patients with mild liver disease diagnosed in childhood: a retrospective study , 2014, Orphanet Journal of Rare Diseases.
[13] Yan Lin,et al. Comprehensive analysis on clinical features of Wilson’s disease: an experience over 28 years with 133 cases , 2014, Neurological research.
[14] J. Walshe. The acute haemolytic syndrome in Wilson's disease--a review of 22 patients. , 2013, QJM : monthly journal of the Association of Physicians.
[15] W. Stremmel,et al. EASL Clinical Practice Guidelines: Wilson's disease. , 2012, Journal of hepatology.
[16] F. Woimant,et al. Relative exchangeable copper: a new highly sensitive and highly specific biomarker for Wilson's disease diagnosis. , 2011, Clinica chimica acta; international journal of clinical chemistry.
[17] M. Schaefer,et al. Zinc monotherapy is not as effective as chelating agents in treatment of Wilson disease. , 2011, Gastroenterology.
[18] Matthew T. Lorincz,et al. Neurologic Wilson's disease , 2010, Annals of the New York Academy of Sciences.
[19] F. Woimant,et al. Determination of ultrafiltrable and exchangeable copper in plasma: stability and reference values in healthy subjects , 2009, Analytical and bioanalytical chemistry.
[20] M. Schilsky,et al. Diagnosis and treatment of Wilson disease: An update , 2008, Hepatology.
[21] G. Arunodaya,et al. Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades , 2007, Medicine.
[22] M. Schaefer,et al. Clinical presentation, diagnosis and long-term outcome of Wilson’s disease: a cohort study , 2006, Gut.
[23] Ali Akbar Asadi Pooya,et al. Wilson disease in southern Iran. , 2005, The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology.
[24] D. Cox,et al. Diagnosis and phenotypic classification of Wilson disease 1 , 2003, Liver international : official journal of the International Association for the Study of the Liver.
[25] A. Herneth,et al. Wilson's disease in patients presenting with liver disease: a diagnostic challenge. , 1997, Gastroenterology.
[26] G. Brewer,et al. Wilson Disease , 1992, Medicine.
[27] H. Hefter,et al. Wilson disease: clinical presentation, treatment, and survival. , 1991, Annals of internal medicine.
[28] H. Ikematsu,et al. Fulminant hepatic failure during perinatal period in a pregnant woman with Wilson’s disease , 1991, Gastroenterologia Japonica.
[29] M. Aladjem,et al. Hypercalciuria and nephrolithiasis as a presenting sign in Wilson disease , 1989, European Journal of Pediatrics.
[30] E. Picard,et al. Wilson's disease associated with pancreatitis. , 1988, Journal of pediatric gastroenterology and nutrition.
[31] A. Aisen,et al. Worsening of neurologic syndrome in patients with Wilson's disease with initial penicillamine therapy. , 1987, Archives of neurology.
[32] T. Hoogenraad,et al. Management of Wilson's disease with zinc sulphate Experience in a series of 27 patients , 1987, Journal of the Neurological Sciences.
[33] A. Dixon,et al. DANGERS OF NON-COMPLIANCE IN WILSON'S DISEASE , 1986, The Lancet.
[34] D. Wiebers,et al. Renal stones in Wilson's disease. , 1979, The American journal of medicine.
[35] T. Hoogenraad,et al. ORAL ZINC IN WILSON'S DISEASE , 1979, The Lancet.
[36] S. Sherlock,et al. Fulminant Wilson's disease with haemolysis and renal failure: copper studies and assessment of dialysis regimens. , 1977, British medical journal.
[37] J. Benhamou,et al. Acute intravascular hemolysis and acute liver failure associated as a first manifestation of Wilson's disease. , 1977, Annals of internal medicine.
[38] A. Członkowska. A study of haemolysis in Wilson's disease. , 1972, Journal of the neurological sciences.
[39] B. Fleischer. Über eine der „Pseudosklerose“ nahestehende bisher unbekannte Krankheit (gekennzeichnet durch Tremor, psychische Störungen, bräunliche Pigmentierung bestimmter Gewebe, insbesondere auch der Hornhautperipherie, Lebercirrhose) , 1912, Deutsche Zeitschrift für Nervenheilkunde.
[40] S. A. Wilson. PROGRESSIVE LENTICULAR DEGENERATION : A FAMILIAL NERVOUS DISEASE ASSOCIATED WITH CIRRHOSIS OF THE LIVER. , 1912 .
[41] S. A. Wilson,et al. PROGRESSIVE LENTICULAR DEGENERATION: A FAMILIAL NERVOUS DISEASE ASSOCIATED WITH CIRRHOSIS OF THE LIVER , 1912 .
[42] F. Tacke,et al. [First data concerning the medical supply of patients with non-alcoholic fatty liver disease in Germany - a survey in university hospital centers of hepatology]. , 2015, Zeitschrift fur Gastroenterologie.
[43] Red.. Leitlinien für Diagnostik und Therapie in der Neurologie , 2012, NeuroTransmitter.
[44] C. Klötzsch,et al. Leitlinien für Diagnostik und Therapie in der Neurologie , 2012 .
[45] Meier,et al. Leitlinien für Diagnostik und Therapie in der Neurologie: Herausgegeben von der Kommission „Leitlinien“ der Deutschen Gesellschaft für Neurologie (DGN) , 2008 .
[46] Peter Bross,et al. The Metabolic and Molecular Basis of Inherited Disease: Protein Folding and Misfolding: the Role of Cellular Protein Quality Control Systems in Inherited Disorders , 2005 .
[47] S. Factor,et al. The cardiomyopathy of Wilson's disease , 2004, Virchows Archiv A.
[48] Hilde van der Togt,et al. Publisher's Note , 2003, J. Netw. Comput. Appl..
[49] H. Cheong,et al. Recurrent Hypokalemic Muscle Weakness as an Initial Manifestation of Wilson’s Disease , 1996 .