Italian
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)
tuberous sclerosis/potassio
Il collegamento viene salvato negli appunti
15 risultati
Impaired astrocytic gap junction coupling and potassium buffering in a mouse model of tuberous sclerosis complex.
Solo gli utenti registrati possono tradurre articoli
Entra registrati
Abnormalities in astrocytes occur in the brains of patients with Tuberous Sclerosis Complex (TSC) and may contribute to the pathogenesis of neurological dysfunction in this disease. Here, we report that knock-out mice with Tsc1 gene inactivation in glia (Tsc1(GFAP)CKO mice) exhibit decreased
Epileptogenesis and reduced inward rectifier potassium current in tuberous sclerosis complex-1-deficient astrocytes.
Solo gli utenti registrati possono tradurre articoli
Entra registrati
OBJECTIVE
Individuals with tuberous sclerosis complex (TSC) frequently have intractable epilepsy. To gain insights into mechanisms of epileptogenesis in TSC, we previously developed a mouse model of TSC with conditional inactivation of the Tsc1 gene in glia (Tsc1(GFAP)CKO mice). These mice develop
Successful treatment of adenoma sebaceum with the potassium titanyl phosphate laser.
Solo gli utenti registrati possono tradurre articoli
Entra registrati
Abnormal intracellular granules of the renal papilla in a child with potassium depletion (Bartter's syndrome) and renal tuberous sclerosis.
Solo gli utenti registrati possono tradurre articoli
Entra registrati
Tuberous sclerosis and epilepsy: role of astrocytes.
Solo gli utenti registrati possono tradurre articoli
Entra registrati
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder that is among the most common genetic causes of epilepsy. Focal brain lesions in TSC, known as cortical tubers, have been implicated in promoting epileptogenesis in TSC. Histological, cellular, and molecular abnormalities in
[Tuberous sclerosis and organic bipolar disorder in a 15-year-old adolescent].
Solo gli utenti registrati possono tradurre articoli
Entra registrati
We present the case of a 15-year-old girl with tuberous sclerosis who developed rapid cycling bipolar disorder under treatment with the anticonsulvant oxcarbazepine. Because of first occurrence of grand mal-seizures combined treatment with Valproate became necessary, but failed to prevent relapses
Diadenosine-Polyphosphate Analogue AppCH2ppA Suppresses Seizures by Enhancing Adenosine Signaling in the Cortex.
Solo gli utenti registrati possono tradurre articoli
Entra registrati
Epilepsy is a multifactorial disorder associated with neuronal hyperexcitability that affects more than 1% of the human population. It has long been known that adenosine can reduce seizure generation in animal models of epilepsies. However, in addition to various side effects, the instability of
Incidental cardiac rhabdomyomas: a significant finding necessitating additional investigation at the time of autopsy.
Solo gli utenti registrati possono tradurre articoli
Entra registrati
Cardiac rhabdomyomas are rare lesions forming part of the tuberous sclerosis complex that may be responsible for sudden death. As well as remaining clinically occult for variable periods of time, they may, along with other manifestations of tuberous sclerosis, be quite difficult to detect clinically
Effects of rapamycin on gene expression, morphology, and electrophysiological properties of rat hippocampal neurons.
Solo gli utenti registrati possono tradurre articoli
Entra registrati
OBJECTIVE
We assayed the effects of rapamycin, an immunomodulatory agent known to inhibit the activity of the mammalian target of rapamycin (mTOR) cascade, on candidate gene expression and single unit firing properties in cultured rat hippocampal neurons as a strategy to define the effects of
Disorders of hypopigmentation in children.
Solo gli utenti registrati possono tradurre articoli
Entra registrati
The most common disorders of hypopigmentation in children are pityriasis alba, vitiligo, nevus depigmentosus, and tinea versicolor. Pityriasis alba usually presents as ill defined, scaly patches of hypomelanosis on the cheeks of children with an atopic diathesis. The face is also a favored site for
Polycystic kidney disease: etiology, pathogenesis, and treatment.
Solo gli utenti registrati possono tradurre articoli
Entra registrati
Once viewed as hopelessly incurable disorders and the dustbin for careers in academic medicine, the polycystic kidney diseases have emerged as prime targets of pathophysiologic study and palliative and definitive treatment in the era of molecular medicine. Polycystic kidney disease (PKD) may be
Activation of mTORC1 in collecting ducts causes hyperkalemia.
Solo gli utenti registrati possono tradurre articoli
Entra registrati
Mutation of TSC (encoding tuberous sclerosis complex protein) and activation of mammalian target of rapamycin (mTOR) have been implicated in the pathogenesis of several renal diseases, such as diabetic nephropathy and polycystic kidney disease. However, the role of mTOR in renal potassium excretion
Expression of astrocyte-related receptors in cortical dysplasia with intractable epilepsy.
Solo gli utenti registrati possono tradurre articoli
Entra registrati
Epilepsy is one of the major neurologic diseases, and astrocytes play important roles in epileptogenesis. To investigate possible roles of astrocyte-related receptors in patients with intractable epilepsy associated with focal cortical dysplasia (FCD) and other conditions, we examined resected
The two-pore domain K+ channel TASK-1 is closely associated with brain barriers and meninges.
Solo gli utenti registrati possono tradurre articoli
Entra registrati
Impairment of the blood-brain barrier (BBB), the blood-cerebrospinal fluid (CSF) barrier and brain-CSF barrier has been implicated in neuropathology of several brain disorders, such as amyotrophic lateral sclerosis, cerebral edema, multiple sclerosis, neural inflammation, ischemia and stroke.
GSK-3β at the crossroads in the signalling of heart preconditioning: implication of mTOR and Wnt pathways.
Solo gli utenti registrati possono tradurre articoli
Entra registrati
OBJECTIVE
Ischaemic preconditioning (IPC) protects the heart against prolonged lethal ischaemia through a signalling cascade involving Akt, glycogen synthase kinase-3β (GSK-3β), and mitochondrial ATP-sensitive potassium channels (mitoK(ATP)). We previously demonstrated the involvement of the Wnt
Il database di erbe medicinali più completo supportato dalla scienza
- Funziona in 55 lingue
- Cure a base di erbe sostenute dalla scienza
- Riconoscimento delle erbe per immagine
- Mappa GPS interattiva - tagga le erbe sul luogo (disponibile a breve)
- Leggi le pubblicazioni scientifiche relative alla tua ricerca
- Cerca le erbe medicinali in base ai loro effetti
- Organizza i tuoi interessi e tieniti aggiornato sulle notizie di ricerca, sperimentazioni cliniche e brevetti
Digita un sintomo o una malattia e leggi le erbe che potrebbero aiutare, digita un'erba e osserva le malattie ei sintomi contro cui è usata.
* Tutte le informazioni si basano su ricerche scientifiche pubblicate
