Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Low serum ceruloplasmin"'
Publikováno v:
Zeitschrift für Gastroenterologie.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6191cb6d731201e37d0ae11e118f3e41
https://doi.org/10.1055/s-0039-1691921
https://doi.org/10.1055/s-0039-1691921
Publikováno v:
Indian Journal of Gastroenterology. 34:174-177
Wilson disease and cholestatic liver diseases may present as a diagnostic dilemma if standard guidelines incorporating markers of copper overload are followed. We hereby present a series of four cases of sclerosing cholangitis masquerading as Wilson
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6838e8dc4475b451914ad9acc40965cf
https://doi.org/10.1007/s12664-015-0552-9
https://doi.org/10.1007/s12664-015-0552-9
Publikováno v:
Mustafa Kemal Üniversitesi Tıp Dergisi, Vol 6, Iss 21, Pp 43-45 (2015)
Wilson’s disease is an autosomal recessive disorder of copper metabolism characterized by excessive amount of copper in liver, brain, eye and other body tissues. Diagnosis is based on the presence of Kayser-Fleischer rings, typical neurological sym
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29f6e246d46c1829617d5e08558a3690
https://doi.org/10.17944/mkutfd.47284
https://doi.org/10.17944/mkutfd.47284
Autor:
Paulo Virgolino da Nóbrega, José Correia de Farias Brito, Mário de Almeida Pereira Coutinho, Hermano José Falcone de Almeida
Publikováno v:
Arquivos de Neuro-Psiquiatria v.63 n.1 2005
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 63, Issue: 1, Pages: 176-179, Published: MAR 2005
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 63, Issue: 1, Pages: 176-179, Published: MAR 2005
Homem de 25 anos de idade foi internado com sintomatologia polimorfa típica das afecções dos gânglios da base, associada a manifestações psiquiátricas. Fez uso de periciazina; no entanto, a suspensão do medicamento não melhorou a sintomatolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ec5ceb43452114b6e317f8746558183
https://doi.org/10.1590/s0004-282x2005000100034
https://doi.org/10.1590/s0004-282x2005000100034
Autor:
E. D’Acunto, H. Freeze, A. Di Nuzzi, Pietro Vajro, B.G. Ng, M. Maccarana, K. Zielinska, Claudia Mandato, Marco Poeta, E. Ecklund, Luca Pierri
Publikováno v:
Digestive and Liver Disease. 49:e249
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b3e71dc9573dd5a3ff34e52f655f0e2
https://doi.org/10.1016/j.dld.2017.09.021
https://doi.org/10.1016/j.dld.2017.09.021
Publikováno v:
Neurological research. 36(2)
Here, we reported our experience over 28 years with 133 cases of patients with Wilson's disease (WD) in order to illustrate the diverse clinical presentation and to improve understanding and early diagnosis of WD.We reviewed the medical records of pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cb34b68f601f20223be074db9b0cefd
https://pubmed.ncbi.nlm.nih.gov/24107488
https://pubmed.ncbi.nlm.nih.gov/24107488
Publikováno v:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 19(4)
We present a 28-year-old woman with a diagnosis of Niemann–Pick type C disease which was initially diagnosed as Wilson disease due to low serum ceruloplasmin and elevated free copper. This report supports the hypothesis that NPC1 could play a role
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5c59864a151a03b0aa7ffde917e8dd8
https://pubmed.ncbi.nlm.nih.gov/22269206
https://pubmed.ncbi.nlm.nih.gov/22269206
Publikováno v:
Canadian Journal of Gastroenterology, Vol 9, Iss 2, Pp 78-80 (1995)
A 65-year-old man with Fanconi’s syndrome was investigated for the cause of chronic liver disease. Wilson’s disease was diagnosed based on the detection of bilateral Kayser-Fleischer rings, a low serum ceruloplasmin level, increased urine copper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9330a3080554359a156c42e8f15c704b
https://doi.org/10.1155/1995/352692
https://doi.org/10.1155/1995/352692
Autor:
D. Alagille
Publikováno v:
Inborn Metabolic Diseases ISBN: 9783662026151
Wilson’s disease is characterized by copper accumulation in various organs and low serum ceruloplasmin levels. In children copper toxicity in the liver predominates, whereas later on neurological symptoms predominate in adults. D-Penicillamine is t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99c263fe592c213de490c6ac0aa0424d
https://doi.org/10.1007/978-3-662-02613-7_38
https://doi.org/10.1007/978-3-662-02613-7_38
Autor:
Henning J. Konig, Christoph J. G. Lang, Andreas Engelhardt, Gabriele Kobras, Peter Rabas-Kolominsky
Publikováno v:
Archives of Neurology. 50:1007-1008
To the Editor. —In their letter to the editor, Hoogenraad and van Hattum claimed that "worsening of neurologic signs after the start of zinc therapy has never been described." 1 Herein, we report such a case. Report of a Case. —A 30-year-old righ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4827371bf4bde04827015f7e6fef6c2f
https://doi.org/10.1001/archneur.1993.00540100008005
https://doi.org/10.1001/archneur.1993.00540100008005