To address the question of whether altered function of the... Y Fueta,LA Vasilets,K Takeda,... - 《Neuroscience》 被引量: 31发表: 2003年 Intranasal midazolam for febrile seizures. A step forward in treating a common and distressing condition Papers p 83 Despite their benign nature and ...
The kidneys remove the body's wastes from the blood. If hypertension thickens the arteries to the kidneys, less waste can be filtered from the blood. As the condition worsens, the kidneys fail and wastes build up in the blood. Dialysis or a kidney transplant is needed when the kidneys fail...
Kallmann's syndrome is a type of hypogonadotropic hypogonadism which affects males and females and is characterized by eunuchoidal habitus, lack of sexual development, and anosmia, caused by a defective development of the olfactory bulbs. Cleft palate, deafness, seizures, short fourth metacarpal bon...
The business, results of operation or financial condition of EADS could be materially adversely affected by the risks described below. These are not the only risks EADS faces. Additional risks and uncertainties not presently known to EADS or that it currently considers immaterial may also impair ...
There have been many lessons learned since the initial description of the condition in humans in 2003. In this article, we will focus on pathophysiology, clinical manifestations, with particular focus on seizures because of its relevance to the medical practitioners and rese...
VSGP is a hallmark of NP-C and becomes highly specific of the disease when it occurs in combination with other manifestations (e.g. splenomegaly, ataxia). In young infants (<2 years), abnormal saccades may first manifest as slowing and shortening of upward saccades, long before gaze palsy...
This condition, which has been traditionally related to Alzheimer’s disease, is, on the contrary, quite frequent in the normal aging process, and it is dramatically evident in the SVD process. It is related to a consistent deposition of amyloid b-peptide (Ab) in the walls of the small ...
Following the initial paper in 2019 by O’Donnell-Luria and collaborators [1], other patients with the condition have been reported, and the evidence shows that individuals with missense mutations usually have a more severe phenotype than those with non-sense mutations or gene deletions, which ...
Hanukkah, the Festival of Lights Why Do Jeans Have That Tiny Pocket? 13 Iconic Buildings to Visit in New York City The Time a Law Clerk Successfully Forged a New Shakespeare Play to Impress His Dad traumatic brain injury medical condition ...
and K+ channels.18 The 19q13.11 deleted region includes the SCN1B gene encoding a sodium channel b-1 subunit whose heterozygous mutations may result in generalized epilepsy with febrile seizures plus, Brugada syndrome 5, and defects in cardiac conduction.19,20 Thus, SCN1B haploinsufficiency might...