Number of the records: 1
Obezita a metabolický syndróm
Title Obezita a metabolický syndróm Par.title Obesity and metabolic syndrome Author info Ivan Majerčák Author Majerčák Ivan
Note Bibliogr. odkazy. - Res. angl., slov. Sign. C 3046 Source Kardiológia pre prax : recenzovaný, postgraduálne zameraný odborný lekársky časopis. - ISSN 1336-3433. - Bratislava : SAMEDI , 2011 . - Roč. 9, č. 1 (2011), s. 6-11 : ilustr. (fareb.), obr., tab. MeSH Subject syndróm metabolický
obezita : diagnostika : dietoterapia : terapia
obezita : farmakoterapia : chirurgia : prevencia a kontrola
index telesnej hmotnosti
obvod pása
index centrálnej obezity WHR
štýl životný
Subj. Headings parametre antropometrické * hmotnosť tela * tuk a svalstvo Language Slovak Country Slovak Republic Document kind Rozpis článkov z periodík Database ARTICLES 
article
MeSH Tree Structures - xeroderma pigmentosum
[c04.834.867]- nádory [c04] +
- prekancerózy [c04.834] +
- ohniská aberantných krýpt [c04.834.020]
- Barrettov pažerák [c04.834.154]
- erytroplázia [c04.834.288]
- keratóza aktinická [c04.834.450]
- leukoplakia [c04.834.512] +
- granulomatóza lymfomatoidná [c04.834.567]
- preleukémia [c04.834.770]
- myelóm tlejúci mnohopočetný [c04.834.794]
- dysplázia krčka maternice [c04.834.818] +
- xeroderma pigmentosum
[c04.834.867]
- prekancerózy [c04.834] +
[c16.131.831.936]- choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
- abnormality vrodené [c16.131] +
- abnormality kožné [c16.131.831] +
- akrodermatitída [c16.131.831.066]
- Carneyho komplex [c16.131.831.108]
- dyskeratóza kongenitálna [c16.131.831.150]
- dysplázia ektodermálna [c16.131.831.350] +
- Ehlersov-Danlosov syndróm [c16.131.831.428] +
- epidermolysis bullosa [c16.131.831.493] +
- ichtyóza [c16.131.831.512] +
- incontinentia pigmenti [c16.131.831.580]
- naevus flammeus [c16.131.831.675]
- deficit prolidázy [c16.131.831.720]
- pseudoxanthoma elasticum [c16.131.831.766]
- Rothmundov-Thomsonov syndróm [c16.131.831.775]
- scleredema neonatorum [c16.131.831.812]
- syndrómy trichotiodystrofie [c16.131.831.874]
- xeroderma pigmentosum
[c16.131.831.936]
- abnormality kožné [c16.131.831] +
- abnormality vrodené [c16.131] +
[c16.320.850.970]- choroby a abnormality novorodenecké, vrodené a dedičné [c16] +
- choroby genetické, vrodené [c16.320] +
- choroby kožné genetické [c16.320.850] +
- albinizmus [c16.320.850.080] +
- cutis laxa [c16.320.850.180]
- Darierova choroba [c16.320.850.190]
- dermatitída atopická [c16.320.850.210]
- dyskeratóza kongenitálna [c16.320.850.235]
- dysplázia ektodermálna [c16.320.850.250] +
- Ehlersov-Danlosov syndróm [c16.320.850.260] +
- epidermolysis bullosa [c16.320.850.275] +
- erythrokeratodermia variabilis [c16.320.850.337]
- syndróm hyalínovej fibromatózy [c16.320.850.368]
- erytroderma ichtyoziformná vrodená [c16.320.850.400] +
- Siemensova bulózna ichtyóza [c16.320.850.402]
- ichthyosis vulgaris [c16.320.850.405]
- ichtyóza viazaná na chromozóm X [c16.320.850.408]
- incontinentia pigmenti [c16.320.850.420]
- keratodermia palmoplantárna [c16.320.850.475] +
- leukokeratóza sliznice, dedičná [c16.320.850.542]
- Urbachova-Wiethova lipoidproteinóza [c16.320.850.595]
- monilethrix [c16.320.850.647]
- Nethertonov syndróm [c16.320.850.673]
- pemfigus benígny familiárny [c16.320.850.700]
- porokeratóza [c16.320.850.730]
- porfýria erytropoetická [c16.320.850.738]
- porfýrie hepatálne [c16.320.850.742] +
- deficit prolidázy [c16.320.850.746]
- pseudoxanthoma elasticum [c16.320.850.750]
- Rothmundov-Thomsonov syndróm [c16.320.850.765]
- Sjögrenov-Larssonov syndróm [c16.320.850.820]
- syndrómy trichotiodystrofie [c16.320.850.895]
- xeroderma pigmentosum
[c16.320.850.970]
- choroby kožné genetické [c16.320.850] +
- choroby genetické, vrodené [c16.320] +
[c17.800.600.925][c17.800.621.936][c17.800.804.936]- choroby kože a spojivového tkaniva [c17] +
- choroby kožné [c17.800] +
- abnormality kožné [c17.800.804] +
- akrodermatitída [c17.800.804.066]
- Anetoderma [c17.800.804.108]
- dyskeratóza kongenitálna [c17.800.804.150]
- dysplázia ektodermálna [c17.800.804.350] +
- Ehlersov-Danlosov syndróm [c17.800.804.428] +
- epidermolysis bullosa [c17.800.804.493] +
- ichtyóza [c17.800.804.512] +
- incontinentia pigmenti [c17.800.804.580]
- naevus flammeus [c17.800.804.675]
- pseudoxanthoma elasticum [c17.800.804.766]
- Rothmundov-Thomsonov syndróm [c17.800.804.775]
- scleredema neonatorum [c17.800.804.812]
- syndrómy trichotiodystrofie [c17.800.804.874]
- xeroderma pigmentosum
[c17.800.804.936]
- abnormality kožné [c17.800.804] +
- choroby kožné [c17.800] +
[c17.800.827.970]- choroby kože a spojivového tkaniva [c17] +
- choroby kožné [c17.800] +
- choroby kožné genetické [c17.800.827] +
- albinizmus [c17.800.827.080] +
- cutis laxa [c17.800.827.180]
- Darierova choroba [c17.800.827.190]
- dermatitída atopická [c17.800.827.210]
- dyskeratóza kongenitálna [c17.800.827.235]
- dysplázia ektodermálna [c17.800.827.250] +
- Ehlersov-Danlosov syndróm [c17.800.827.260] +
- epidermolysis bullosa [c17.800.827.275] +
- erythrokeratodermia variabilis [c17.800.827.337]
- choroby dedičné autozápalové [c17.800.827.368] +
- syndróm hyalínovej fibromatózy [c17.800.827.384]
- erytroderma ichtyoziformná vrodená [c17.800.827.400] +
- Siemensova bulózna ichtyóza [c17.800.827.403]
- ichthyosis vulgaris [c17.800.827.405]
- ichtyóza viazaná na chromozóm X [c17.800.827.408]
- incontinentia pigmenti [c17.800.827.420]
- keratodermia palmoplantárna [c17.800.827.475] +
- leukokeratóza sliznice, dedičná [c17.800.827.595]
- monilethrix [c17.800.827.602]
- Muirov-Torreho syndróm [c17.800.827.610]
- Nethertonov syndróm [c17.800.827.655]
- pemfigus benígny familiárny [c17.800.827.700]
- porokeratóza [c17.800.827.730]
- porfýria erytropoetická [c17.800.827.738]
- porfýrie hepatálne [c17.800.827.742] +
- pseudoxanthoma elasticum [c17.800.827.750]
- Rothmundov-Thomsonov syndróm [c17.800.827.775]
- Sjögrenov-Larssonov syndróm [c17.800.827.820]
- syndrómy trichotiodystrofie [c17.800.827.895]
- xeroderma pigmentosum
[c17.800.827.970]
- choroby kožné genetické [c17.800.827] +
- choroby kožné [c17.800] +
- nádory [c04] +
Number of the records: 1