Français
Albanian
Arabic
Armenian
Azerbaijani
Belarusian
Bengali
Bosnian
Catalan
Czech
Danish
Deutsch
Dutch
English
Estonian
Finnish
Français
Greek
Haitian Creole
Hebrew
Hindi
Hungarian
Icelandic
Indonesian
Irish
Italian
Japanese
Korean
Latvian
Lithuanian
Macedonian
Mongolian
Norwegian
Persian
Polish
Portuguese
Romanian
Russian
Serbian
Slovak
Slovenian
Spanish
Swahili
Swedish
Turkish
Ukrainian
Vietnamese
Български
中文(简体)
中文(繁體)
hepatolenticular degeneration/crise épileptique
Le lien est enregistré dans le presse-papiers
Page 1 de 16 résultats
Was Cavum Septum Pellucidum the Cause of Intractable Seizure in a 17-Year-Old Boy with Wilson Disease?
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
BACKGROUND
Cavum septum pellucidum (CSP), which is often found incidentally in a few populations, occasionally becomes symptomatic if enlarged significantly. Wilson disease (WD) is an uncommon autosomal recessive inborn defect in copper metabolism characterized by abnormal accumulation of copper in
Predictors of seizure in Wilson disease: A clinico-radiological and biomarkers study.
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
Acute extrapyramidal syndrome and seizures as heralding manifestation of Wilson disease.
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
Neurological Wilson disease in children: a three years experience from Multan.
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
OBJECTIVE
To describe the neurological manifestations, results of investigations and response to treatment in Wilson disease in children from Multan.
METHODS
This cross sectional study was conducted at Neurology Department of Children Hospital and Institute of Child Health Multan from June 2005 to
Anesthetic management of a pediatric patient with wilsons disease.
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
Wilsons disease, characterized by cirrhosis, extrapyramidal symptoms and Kayser-Fleischer corneal rings, is a rare hereditary disease of human copper metabolism. Clinical findings in Wilsons disease are complex and neurological symptoms such as tremor, dysarthria, rigid dystonia, seizures,
[Clinical study on manifestation of hepatolenticular degeneration complicated with epilepsy and therapeutic effect of integrative Chinese and Western medicine treatment].
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
OBJECTIVE
To observe the clinical manifestation of 155 patients with hepatolenticular degeneration (HLD) complicated with epilepsy and the therapeutic effect of integrative Chinese and Western medicine treatment on them.
METHODS
Clinical manifestation of patients and its relationship with
Psychological presentations without hepatic involvement in Wilson disease.
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
Wilson disease is an autosomal recessive inborn error of copper metabolism that leads to neurologic symptoms and variable degrees of hepatic damage. The most common characteristic signs clinically are liver disease, psychiatric disease, neurologic disease, or a combination of these. Early
Early childhood hepatocerebral degeneration misdiagnosed as valproate hepatotoxicity.
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
Four unrelated children were thought to have valproate-associated hepatotoxicity. They presented with recurrent partial secondarily generalized status epilepticus and epilepsia partialis continua followed by mental and motor regression. Despite treatment with multiple antiepileptic medications, they
Misidentification of Wilson Disease as Schizophrenia (1998-2013): Case Report and Review.
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
Wilson's disease (WD) is a neurodegenerative disorder due to copper metabolism. Schizophrenia-like psychosis and delusional disorder are rare forms of psychiatric manifestations of WD. The lack of recognition of these signs and symptoms as being attributable to WD often leads to delays in diagnosis
Clinical features and outcome of Wilson's disease with generalized epilepsy in Chinese patients.
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
Neuromuscular complication after liver transplant in children: a single-center experience.
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
OBJECTIVE
Neurologic complications are a significant cause of morbidity in children after liver transplant. In this study, we sought to evaluate the neurologic complications in children after liver transplant.
METHODS
All children aged younger than 18 years old who had undergone liver transplant
Infantile diffuse cerebral degeneration with hepatic cirrhosis.
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
Four children had progressive degeneration of the cerebral cortex, with hepatic cirrhosis. They and four previously described ones, are representative of a distinct form of hepatocerebral degeneration. Onset of the neurological disorder is between ages 1 and 3 years, at times with mild developmental
Primary and secondary defects of the mitochondrial respiratory chain.
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
Over 100 mutations of mitochondrial DNA (mtDNA) have been associated with human disease. The phenotypic manifestation of mtDNA mutations is extremely broad, from oligosymptomatic patients with isolated deafness, diabetes, ophthalmoplegia, etc., to complex encephalomyopathic disorders that may
[Basal ganglia calcification: clinical manifestations and diagnostic evaluation].
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
Physiological intracranial calcification occurs in about 0,3-1,5% of cases. It is asymptomatic and is detected incidentally by neuroimaging. Pathological basal ganglia calcification is due to various causes, such as: metabolic disorders, infectious and genetic diseases and other. Hypoparathyroidism
Leukoencephalopathy syndrome after living-donor liver transplantation.
Seuls les utilisateurs enregistrés peuvent traduire des articles
Se connecter S'inscrire
OBJECTIVE
Leukoencephalopathy syndrome is a neurologic complication after organ transplantation caused predominantly by the neurotoxic effects of immunosuppressive agents on cerebral white matter. We determined the incidence and features of leukoencephalopathy syndrome in recipients after
La base de données d'herbes médicinales la plus complète soutenue par la science
- Fonctionne en 55 langues
- Cures à base de plantes soutenues par la science
- Reconnaissance des herbes par image
- Carte GPS interactive - étiquetez les herbes sur place (à venir)
- Lisez les publications scientifiques liées à votre recherche
- Rechercher les herbes médicinales par leurs effets
- Organisez vos intérêts et restez à jour avec les nouvelles recherches, essais cliniques et brevets
Tapez un symptôme ou une maladie et lisez des informations sur les herbes qui pourraient aider, tapez une herbe et voyez les maladies et symptômes contre lesquels elle est utilisée.
* Toutes les informations sont basées sur des recherches scientifiques publiées
