Zobrazeno 1 - 10
of 153
pro vyhledávání: '"N Kalfakis"'
Publikováno v:
Acta Neurologica Scandinavica. 115:364-366
Objective – A family with a clinically heterogeneous progressive ataxia in two generations is presented. Methods – Having eliminated mutations within the known dominant spinocerebellar ataxia genes, the family was investigated for expansion at th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d13e33ca6e1521f1b2c8e0a089613f2e
https://doi.org/10.1111/j.1600-0404.2007.00734.x
https://doi.org/10.1111/j.1600-0404.2007.00734.x
Publikováno v:
The Journal of international medical research. 34(3)
The widespread use of antibiotics in recent years has caused a significant reduction in the incidence of neurosyphilis and changes in its clinical features. We present a case that initially presented as persistent headache and untreatable psychosis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f62c1a86c5cf5fb76542fc7499ede4a7
https://pubmed.ncbi.nlm.nih.gov/16866029
https://pubmed.ncbi.nlm.nih.gov/16866029
Publikováno v:
Acta Neurochirurgica. 131:226-228
The family trees of 142 patients, suffering from histologically proven brain tumour, were compared to those of an equal number of sex and age matched controls. The results showed no statistically significant differences in the occurrence of malignant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80f70a6aeaf9e13679978b4a04892a8e
https://doi.org/10.1007/bf01808618
https://doi.org/10.1007/bf01808618
Autor:
V. Kamtsadeli, Aspasia Nika, P. Sakka, Angeliki Tsapanou, N. Kalfakis, Ion Beratis, G. Tsilikopoulou, John Papatriantafyllou, Sokratis G. Papageorgiou, L. Margioti, Panagiotis D. Bamidis
Publikováno v:
Neuroscience Letters. 500:e5-e6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3cf9133029044faa3ac413d632d3ffe1
https://doi.org/10.1016/j.neulet.2011.05.078
https://doi.org/10.1016/j.neulet.2011.05.078
Publikováno v:
Headache. 36(9)
In order to study the prevalence of frequent headaches among the medical students of Athens University, an epidemiological survey was carried out among 588 medical students (318 men and 270 women), with mean age 23.5 years. Two questionnaires were de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfdfd7a80ddc57bdb00b30b481c4b913
https://pubmed.ncbi.nlm.nih.gov/8916565
https://pubmed.ncbi.nlm.nih.gov/8916565
Publikováno v:
Clinical neuropathology. 15(2)
Size and distribution of 2 histochemical types of muscle fibers within the human muscle fascicle were investigated. Cryostat sections (ATPase, pH 9.4) were studied from 15 quadriceps femoris, 15 biceps brachii and 15 deltoid muscles taken at autopsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d8afa504d7c9186bcad65eeae64612b2
https://pubmed.ncbi.nlm.nih.gov/8925596
https://pubmed.ncbi.nlm.nih.gov/8925596
Autor:
P, Manta, P, Kontoleon, A, Panousopoulou, N, Kalfakis, H, Christomanou, P, Papapetrou, C, Papageorgiou
Publikováno v:
Functional neurology. 11(2-3)
An eight-member family is presented with two female members suffering from the juvenile form of acid maltase deficiency (AMD), the diagnosis confirmed by biochemical study of muscle. Biochemical leucocyte investigation revealed reduced a-glucosidase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e3fd33c9aa27f27af109e3e1f2f2ed3a
https://pubmed.ncbi.nlm.nih.gov/8765758
https://pubmed.ncbi.nlm.nih.gov/8765758
Publikováno v:
Functional neurology. 10(4-5)
The cases of two elderly women with external ophthalmoplegia, generalized muscle weakness and serum anti-acetylcholine receptor antibodies, are presented. The electophysiological studies showed a myopathic pattern but no indications of myasthenia aft
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a9667e19705fb8773dd1c0522f5fd9a6
https://pubmed.ncbi.nlm.nih.gov/8749048
https://pubmed.ncbi.nlm.nih.gov/8749048
Publikováno v:
Functional neurology. 9(2)
The diagnosis of Stargardt's disease, in cases of macular degeneration associated with neurological symptomatology, has been questioned. A 23 year old man, suffering from well characterized Stargardt's disease since childhood, presented with progress
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4c19cf5b274098ea89355132376b7d29
https://pubmed.ncbi.nlm.nih.gov/7926893
https://pubmed.ncbi.nlm.nih.gov/7926893
