Bosnian
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)
glycolipid/seizures
Veza se sprema u međuspremnik
Page 1 od 39 rezultati
Effect of insulin-induced epileptic seizures on neutral glycolipids of rabbit cerebral cortex.
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
The neutral glycolipids of rabbit central cortex were analyzed during epileptic seizures produced by insulin or pentetrazol injection. The two agents gave similar results. A decrease of glycolipid content occurred in the cortex and in the neuronal fraction during seizures. The normal glycolipid
Adult-onset GM2 gangliosidosis. Seizures, dementia, and normal pressure hydrocephalus associated with glycolipid storage in the brain and arachnoid granulation.
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizures
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
Deficiency of the endoplasmic reticulum transmembrane protein ARV1 leads to epileptic encephalopathy in humans and in mice. ARV1 is highly conserved, but its function in human cells is unknown. Studies of yeast arv1 null mutants indicate that it is involved in a number of biochemical processes
Type 1 sialidosis presenting with ataxia, seizures and myoclonus with no visual involvement.
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
Sialidosis is an autosomal recessive lysosomal storage disease caused by pathogenic variants in NEU1 which encodes lysosomal sialidase (neuraminidase 1). Lysosomal neuraminidase catalyzes the removal of terminal sialic acid molecules from glycolipids, glycoproteins and oligosaccharides. Sialidosis
A likely pathogenic variant putatively affecting splicing of PIGA identified in a multiple congenital anomalies hypotonia-seizures syndrome 2 (MCAHS2) family pedigree via whole-exome sequencing.
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
Glycosylphosphatidylinositol (GPI) anchoring is a special type of protein posttranslational modification, by which proteins with diverse function are attached to cell membrane through a covalent linkage between the protein and the glycolipid. Phosphatidylinositol glycan anchor biosynthesis class A
Differential expression of mRNAs for sialyltransferase isoenzymes induced in the hippocampus of mouse following kindled seizures.
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
Sialic acids play important roles in various biological functions. In the brain, evidence suggests that sialylation of glycoproteins and glycolipids affects neural plasticity. While the 18 sialyltransferase isoenzymes (STs) identified to date synthesize individual sialyl-oligosaccharide structures,
[Vomiting associated with weight stagnation and convulsions: urea cycle disorder should be suspected].
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
In some inherited metabolic diseases, in particular in urea cycle disorders, which are usually diagnosed in neonatal period or in childhood, vomiting is often the first symptom. We report a case of late revelation of urea cycle disorder in a 13 years old female patient hospitalized for convulsions
Pathogenic Variants in PIGG Cause Intellectual Disability with Seizures and Hypotonia.
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
Glycosylphosphatidylinositol (GPI) is a glycolipid that anchors >150 various proteins to the cell surface. At least 27 genes are involved in biosynthesis and transport of GPI-anchored proteins (GPI-APs). To date, mutations in 13 of these genes are known to cause inherited GPI deficiencies (IGDs),
Platelets promote epileptic seizures by modulating brain serotonin level, enhancing neuronal electric activity, and contributing to neuroinflammation and oxidative stress.
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
The drugs currently available for treating epilepsy are only partially effective in managing this condition. Therefore, it is crucial to investigate new pathways that induce and promote epilepsy development. Previously, we found that platelets interact with neuronal glycolipids and actively secrete
Anesthetic considerations in the child with Gaucher disease.
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
We present the case of a 7-month-old girl with Gaucher disease who required anesthetic care during laryngoscopy, bronchoscopy, and central line placement. Gaucher disease is a familial disorder of lipid catabolism with autosomal recessive inheritance. Due to the defective function of the enzyme
Lysosomal Storage Disorders in Indian Children with Neuroregression Attending a Genetic Center.
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
OBJECTIVE
To study the etiology of neuroregression in children having deficiency of the lysosomal enzymes.
METHODS
Review of medical records.
METHODS
Specialized Genetic Center.
METHODS
432 children aged 3 mo-18 y having regression in a learned skill, selected from 1453 patients referred for
Resin glycosides evoke the Gaba release by sodium- and/or calcium-dependent mechanism.
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
Ipomoea tyrianthina Lindley (syn. I. orizabensis Pelletan, Lebed. ex Steud., Convolvulaceae) is known as a purgative, but it has been also used in Mexican traditional medicine in the treatment of seizures and pain for their anticonvulsive, hypnotic and sedative properties. Some glycolipids isolated
Resin glycosides from the roots of Ipomoea tyrianthina and their biological activity.
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
Seven new tetrasaccharide glycosides, tyrianthins 1-7 (1-7), along with six known glycolipids were isolated from the roots of Ipomoea tyrianthina, and their structures were elucidated by spectroscopic and chemical methods. The content of resin glycosides in samples collected in three different
Phenotypic spectrum of fucosidosis in Tunisia.
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
Fucosidosis (OMIM 230000) is a rare autosomal recessive lysosomal disorder due to deficient α-L-fucosidase activity(EC 3.2.1.51), leading to the accumulation of fucose-containing glycolipids and glycoproteins in various tissues. This study contained the largest ever Tunisian survey of fucosidosis
Disease state awareness in Gaucher disease: a Q&A expert roundtable discussion.
Samo registrirani korisnici mogu prevoditi članke
Prijavite se / prijavite se
Gaucher disease is an inherited lysosomal storage disorder caused by mutations in the gene that encodes the lysosomal enzyme glucocerebrosidase. Inadequate enzymatic activity causes cells to become engorged due to an accumulation of glycolipids. Engorged cells then accumulate in various organs,
Najkompletnija baza ljekovitog bilja potpomognuta naukom
- Radi na 55 jezika
- Biljni lijekovi potpomognuti naukom
- Prepoznavanje biljaka po slici
- Interaktivna GPS karta - označite bilje na lokaciji (uskoro)
- Pročitajte naučne publikacije povezane sa vašom pretragom
- Pretražite ljekovito bilje po učincima
- Organizirajte svoja interesovanja i budite u toku sa istraživanjem vijesti, kliničkim ispitivanjima i patentima
Upišite simptom ili bolest i pročitajte o biljkama koje bi mogle pomoći, unesite travu i pogledajte bolesti i simptome protiv kojih se koristi.
* Sve informacije temelje se na objavljenim naučnim istraživanjima
