Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    ISSN: 1468-2982
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Cluster headache is a disorder of unknown origin. Some studies have focused their attention on neuroendocrine derangement, others on immunity. To probe central alterations in cluster headache (CH), immune parameters were investigated in cluster headache patients in comparison to low back pain patients and healthy controls. Increases in peripheral blood monocytes found in remission cluster headache patients may be attributable to chronic central nervous system (hypothalamic?) noradrenergic dysfunction or altered b-endorphin. Alterations in NK+, CD3+ and CD4+ levels found in cluster period cluster headache and low back pain patients are probably pain or stress-related.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 0010-4655
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Computer Science , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 0168-9002
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 1590-3478
    Keywords: Cluster headache ; hypothalamic involvement ; plasma cortisol levels ; night-time melatonin peak ; THS response to TRH
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Sommario L'origine della cefalea a grappolo è a tutt'oggi sconosciuta. Il tipico periodismo e la presenza di sintomi autonomici relativi sia all'attività simpatica che parasimpatica suggeriscono l'interessamento di strutture del Sistema Nervoso Centrale, in particolare dell'ipotalamo. Allo scopo di esplorare il coinvolgimento dell'ipotalamo nella cefalea a grappolo, abbiamo condotto uno studio di tipo neuroendocrino. I nostri risultati indicano che il test di soppressione al desametazone (DST) è normale nella CH, mentre i livelli ematici di cortisolo alle ore 8 di mattino, prima e dopo DST, sono più elevati nei pazienti in remissione sia nei confronti dei controlli che dei cluster in fase di grappolo. La risposta del TSH al TRH è ridotta e il picco notturno della melatonina è più basso nei pazienti solo durante il periodo di grappolo. Le alterazioni neuroendocrine rilevate sia in fase di remissione che di grappolo confortano l'ipotesi di un coinvolgimento dell'ipotalamo nella cefalea a grappolo.
    Notes: Abstract The origin of Cluster Headache (CH) is still unknown. The periodicty and presence of symptoms due to both sympathetic and parasympathetic activity suggest the involvement of central nervous system structures, particularly the hypothalamus. To investigate hypothalamic involvement in CH, we employed a neuroendocrinological approach. We observed a normal dexamethasone suppression test (DST) in all patients, increased cortisol plasma levels in remission patients at 8.00am before and at the end of the DST, while only in CH patients during cluster period did we find a reduced TSH response to TRH and a reduced night-time melatonin peak. The neuroendocrinological derangements found in CH may be consistent with hypothalamic involvement.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    ISSN: 1432-5233
    Keywords: Key words Protein oxidation ; Glycation ; Carbonyl groups ; Antioxidants ; Vitamins ; Type 2 diabetes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Carbonyl groups result from protein oxidation and their level in tissues and plasma is a relatively stable marker of oxidative damage. Carbonyl content of plasma proteins in 43 type 2 diabetic subjects, 30–87 years of age (25 males and 18 females) and in 20 age-matched healthy controls (31–89 years of age, 12 males and 8 females) was evaluated with 2,4-dinitro-phenyl-hydrazine method. In both groups, lipids, tocopherols (HPLC) and glycated hemoglobin (HPLC) were studied. Fasting blood glucose, glycated hemoglobin and lipids were significantly higher in the diabetic group; carbonyl content and α-tocopherol were slightly, but not significantly higher in the diabetic group (1.06 ± 0.03 vs. 0.97 ± 0.04 nmol/mg protein, 27.07 ± 2.82 vs. 31.55 ± 2.11 μmol/l, respectively). Significant relationships between age and lipids, α-tocopherol and proteins were found in controls, but not in diabetics. Alpha-tocopherol correlated with lipids in both groups; glycated hemoglobin, a marker of glycemic control, was related to lipids, α-tocopherol and protein carbonyl groups in diabetics, while only the correlation with carbonyls was found in controls. These results suggest that impaired glycemic control is connected to protein oxidation. Glycation cascade also releases free radicals, becoming responsible for further oxidative attacks. In conclusion, increased oxidative stress, if any, in the diabetic group, is doubtlessly induced by hyperglycemia, and the tocopherols are not seriously affected by a worsening of the metabolic control.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Studia logica 39 (1980), S. 245-256 
    ISSN: 1572-8730
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics , Philosophy
    Notes: Abstract Global properties of canonical derivability predicates (the standard example is Pr() in Peano Arithmetic) are studied here by means of a suitable propositional modal logic GL. A whole book [1] has appeared on GL and we refer to it for more information and a bibliography on GL. Here we propose a sequent calculus for GL and, by exhibiting a good proof procedure, prove that such calculus admits the elimination of cuts. Most of standard results on GL are then easy consequences: completeness, decidability, finite model property, interpolation and the fixed point theorem.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Neurological sciences 12 (1991), S. 581-584 
    ISSN: 1590-3478
    Keywords: Migraine without aura ; genetic hypothesis ; family history ; “sex-limited” transmission
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Sommario Allo scopo di comprovare la teoria genetica dell'emicrania, abbiamo studiato 68 pazienti consecutivi affetti da emicrania senz'aura insieme ai loro parenti attraverso quattro generazioni (N=394). Significativamente la maggior parte dei probandi erano donne e l'emicrania era più frequente tra i parenti di sesso femminile. Un'età di esordio più bassa era più comune tra i probandi di sesso maschile. L'esistenza di una componente genetica dell'emicrania senz'aura è indicata dall' alta incidenza di storia familiare positiva (almeno un parente affetto) uguale all'85.3% e da una costante prevalenza di malattia nei parenti di primo e secondo grado. Dall'analisi dei dati riguardanti le percentuali di probandi con genitori affetti da emicrania, sembra improbabile l'esistenza di una trasmissione di tipo autosomico. Viene proposta una trasmissione “sex-limited”.
    Notes: Abstract 68 randomly selected patients with migraine without aura (M) and 4 generations of their relatives (N=394) were studied in order to probe the genetic hypothesis of migraine. Significantly more of the probands were women and M was significantly more frequent among female relatives. Earlier onset was commoner among male probands. A genetic component of M is indicated by the very high frequency of at least one affected relative (85.3%) and by a disease prevalence that is similar among both first and second degree relatives. A simple autosomal mode of transmission seems unlikely from analysis of the data on the affected relatives, while a “sex-limited” transmission mode is suggested.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...