Danish
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)
pseudotumor cerebri/epileptisk anfald
Linket gemmes på udklipsholderen
Side 1 fra 46 resultater
Hypophosphatasia presenting with pyridoxine-responsive seizures, hypercalcemia, and pseudotumor cerebri: case report.
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
Hypophosphatasia (HPP) is an inborn error of metabolism characterized by defective bone mineralization caused by a deficiency in alkaline phosphatase (ALP) activity due to mutations in the tissue-nonspecific ALP (TNALP) gene. The clinical expression of the disease is variable. Six forms of HPP are
The Use of Endoscopic Third Ventriculostomy as Treatment for Idiopathic Intracranial Hypertension: Case Report and a Review of Previously Reported Cases
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
Background: Idiopathic intracranial hypertension (IIH), or pseudotumor cerebri (PTC), is a rare disorder marked by the increase of CSF pressure that may cause severe headaches, papilledema, vision loss, and more. IIH is typically treated
[Systemic lupus erythematosus associated with benign intracranial hypertension: a case report].
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
A case of systemic lupus erythematosus (SLE) with benign intracranial hypertension (BIH) is reported. A 41-year-old male with a history of SLE starting in 1982 was admitted to our hospital in December 1989 because of headache and vertigo. Laboratory examinations on admission showed proteinuria, mild
Drug-induced pseudotumor cerebri.
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
Pseudotumor Cerebri (PTC) is an uncommon disorder whose etiology is largely unknown, although its association with steroid withdrawal, hypervitaminosis A, and the use of the tetracycline group of drugs has been well documented. We report here a case in which a patient on chronic divalproex therapy
Lennox-Gastaut syndrome and idiopathic intracranial hypertension.
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
Lennox-Gastaut Syndrome is a severe childhood epilepsy syndrome characterised by the diagnostic triad of a slow spike and wave pattern on electroencephalogram, multiple seizure types and developmental delay. Idiopathic intracranial hypertension is a syndrome characterised by raised cerebrospinal
Benign intracranial hypertension with particular reference to its occurrence in fat young women.
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
Benign intracranial hypertension (pseudotumor cerebri), a syndrome common to a number of disorders, is characterized by headaches and blurred vision. The patient is alert and has papilledema without localizing signs. Air studies show normal ventricles under increased pressure. The authors describe
Internal cranial expansion surgery for the treatment of refractory idiopathic intracranial hypertension.
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
OBJECTIVE
Idiopathic intracranial hypertension (IIH) may be refractory to available medical and surgical therapies. Patients with this condition may suffer from intractable headaches, experience visual deterioration, or have other symptoms related to elevated intracranial pressure. Internal cranial
Headaches, idiopathic intracranial hypertension, and pseudopapilledema.
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
A young woman with frontal headaches of several months' evolution and monocular transient "tunnel" obscurations that developed after a generalized seizure is described. She had elevation of the optic discs (pseudopapilledema), greater on the side of her visual symptoms. No intracranial lesions were
Posterior Reversible Encephalopathy Syndrome and Subarachnoid Hemorrhage After Lumboperitoneal Shunt for Fulminant Idiopathic Intracranial Hypertension.
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
A 33-year-old woman presented with severe visual loss from fulminant idiopathic intracranial hypertension. Her lumbar puncture opening pressure was 97 cm H2O. Soon after lumboperitoneal shunt surgery, she had a generalized tonic-clonic seizure. Magnetic resonance imaging demonstrated frontal
Temporal lobe epilepsy due to meningoencephaloceles into the greater sphenoid wing: a consequence of idiopathic intracranial hypertension?
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
OBJECTIVE
Antero-inferior temporal lobe meningoencephaloceles are a rare, but increasingly recognized cause of drug-resistant temporal lobe epilepsy (TLE). In order to evaluate whether these lesions are related to idiopathic intracranial hypertension (IIH), we analyzed clinical and MRI findings of a
Postoperative management of patients with spontaneous cerebrospinal fluid leak.
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
Serious Diagnoses for Headaches After ED Discharge
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
Background: Headache is a common complaint among children presenting to the emergency department (ED) and can be due to serious neurologic and nonneurologic diagnoses (SNNDs). We sought to characterize the children discharged from the ED
[A case of intracranial arteriovenous malformation presenting with intracranial hypertension].
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
A case of unruptured arteriovenous malformations (AVMs) presenting benign intracranial hypertension is reported. A 14-year-old male suffered from headache and papilledema. Intracranial pressure was 260 mmH2O. Unenhanced CT demonstrated no evidence of hemorrhage or hydrocephalus. Angiogram
Cerebral venous sinus thrombosis: a clinical study of 23 cases.
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
OBJECTIVE
To describe the etiologies, clinical features and diagnosis of cerebral venous sinus thrombosis.
METHODS
We reviewed the records of 23 patients admitted with a documented diagnosis of cerebral venous sinus thrombosis from 1991 through 1999 in the Beijing Tiantan Hospital.
RESULTS
Infection
Multiple small cavernous angiomas of the brain with increased intracranial pressure.
Kun registrerede brugere kan oversætte artikler
Log ind / Tilmeld
Small vascular malformations of the central nervous system are generally considered cryptic, or silent, because they are an incidental but frequent finding at autopsy. When they are symptomatic, these malformations have been associated with intracranial hemorrhage or seizures. The patient reported
Den mest komplette database med medicinske urter understøttet af videnskab
- Arbejder på 55 sprog
- Urtekurer, der understøttes af videnskab
- Urtegenkendelse ved billede
- Interaktivt GPS-kort - tag urter på stedet (kommer snart)
- Læs videnskabelige publikationer relateret til din søgning
- Søg medicinske urter efter deres virkninger
- Organiser dine interesser og hold dig opdateret med nyhedsundersøgelser, kliniske forsøg og patenter
Skriv et symptom eller en sygdom, og læs om urter, der kan hjælpe, skriv en urt og se sygdomme og symptomer, den bruges mod.
* Al information er baseret på offentliggjort videnskabelig forskning
