Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Krisztina, Boór"'
Autor:
Anikó, Rózsa, Krisztina, Kovács, Krisztina, Boór, Agnes, Vagyóczky, Ildikó, Szilvássy, Gyula, Gács
Publikováno v:
Ideggyogyaszati szemle. 66(11-12)
We present three cases, where young patients had unilateral disc edema with normal optic nerve function. We diagnosed their disease as big blind spot syndrome (BBSS). What is remarkable, however, is that in two of the three cases the extent of the vi
Publikováno v:
Ideggyogyaszati szemle. 64(7-8)
In this study, we present two cases of different eye movement disorders with variable case histories but with the same end stage; abduction paresis of one of the eyes, which ceased when the other eye was covered. Our differential diagnosis is that ei
Publikováno v:
Ideggyogyaszati szemle. 63(1-2)
We present the characteristics of posterior cortical atrophy--a very rare cortical dementia--in a 69 year old woman's case. Our patient's symptoms began with a visual problem which was initially explained by ophthalmological disorder. After neurologi
Autor:
Krisztina, Boór, Krisztina, Kovács, Anikó, Rózsa, Gyula, Pánczél, Iidikó, Szilvássy, Gyula, Gács
Publikováno v:
Ideggyogyaszati szemle. 62(5-6)
Here one case report of the posterior ischaemic optic neuropathy, a rare and underdiagnosed form of the non arteritic ischaemic optic neuropathy is presented, to underline the value of the MRI in the diagnosis. The ischaemic optic neuropathy is the i
Autor:
Agnes, Szilágyi, Csaba, Barta, Krisztina, Boór, Anna, Székely, Zsolt, Demetrovics, József, Csorba, Huba, Kalász, Mária, Sasvári-Székely
Publikováno v:
Neuropsychopharmacologia Hungarica : a Magyar Pszichofarmakologiai Egyesulet lapja = official journal of the Hungarian Association of Psychopharmacology. 9(2)
Several studies suggested a possible link between substance use disorder and attention deficit hyperactivity syndrome (ADHD). The ADHD Rating Scale (ADHD-RS) completed by parents is a tool for diagnosing ADHD in childhood. We adapted this questionnai
Autor:
Iren Orosz, Ágnes Szilágyi, Eszter Szantai, Huba Kalász, Krisztina Boór, Viktor Farkas, Anna Szekely, Maria Sasvari-Szekely
Publikováno v:
Headache. 46(3)
Background.—The serotonin transporter gene is a promising candidate locus for the genetic susceptibility of migraine. Objective.—Two functional polymorphisms of the serotonin transporter gene (5-HTTLPR and STin2) were analyzed to assess whether t
Autor:
Agnes, Szilagyi, Krisztina, Boór, Anna, Székely, Péter, Gaszner, Huba, Kalász, Mária, Sasvári-Székely, Csaba, Barta
Publikováno v:
Neuropsychopharmacologia Hungarica : a Magyar Pszichofarmakologiai Egyesulet lapja = official journal of the Hungarian Association of Psychopharmacology. 7(1)
Dopamine D4 receptor (DRD4) and serotonin transporter (SERT) gene polymorphisms were studied, as possible genetic risk factors for substance dependence. The case-control study involved a large cohort (n = 362) of healthy Caucasian population, and an
Autor:
Péter Gaszner, Maria Sasvari-Szekely, Zsolt Ronai, András Guttman, Krisztina Boór, Zsofia Nemoda, Huba Kalász
Publikováno v:
Current medicinal chemistry. 9(8)
A noninvasive DNA sampling method has been implemented collecting buccal mucosa cells by cotton wool swabs. An amount of 0.2 2 microg DNA per patient was obtained after the phenol-extraction procedure and 0.2 2 ng DNA template was sufficient for PCR
Publikováno v:
Scopus-Elsevier
The polymorphic human DNA sequence in the promoter region of the dopamine D4 receptor gene has been investigated by means of non-invasive DNA sampling, amplification by means of the polymerase chain reaction, and subsequent separation of the reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60444060790d36aefeae661429d7edf7
http://www.scopus.com/inward/record.url?eid=2-s2.0-0036084159&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0036084159&partnerID=MN8TOARS