Jsou Rána Tíživá

Masaryka a jeho spoluzakladatele M. Pro: Petr P. Velice jsem se divil. Z ceske strany Nova Ves v mosteckem okrese? Je mozne toto "tvrzeni" nejak dolozit? Myslim oficialne od nejakeho vysokeho ekonoma z tehdejsi doby? Nulovy dluh CSSR se jevi jako blbost i kdyz samozrejme nebyl tak katastroficky jako polsky a rumunskem ani nemluve.

Podepsal Chartu Zatim mi nikdo neodpovedel, kde je mozne dohledat, ze CSSR Jsou Rána Tíživá nulovy dluh. Pouze seriozni zdroje prosim, ne neco podobneho jako John Bok. Tech skoro 28 let venku je znat. Nechci rict, ze jsem uplne blbej jenom trochu ztracim prehled o dnesni tvrde realite v Cechach.

Neco jineho na to koukat pres Internet a neco jineho byt v tom kazdy den. No, ale co dal? Kam myslite, ze to az povede nebo kde to skonci? Nemyslim, ze by doslo k nejakemu povstani a kdyby prece jenom zaclo jit do tuheho Jsou Rána Tíživá by vladnouci moci zase prisla "bratrska pomoc" tentokrat z jine svetove strany.

Nechci malovat certa na zed, ale karty jsou rozdany a ted par lidi co skutecne ridi tento svet nemyslim politiky si to bude delat tak jak uzna za vhodne.

Bajky Bidpajovy. Jsou Rána Tíživá Svrchovanost. Jsou Rána Tíživá Planeta opic. Boye: Kallocain. Camus: Cizinec. Cervantes: Don Quijote. France: Epikurova zahrada. Gaia Liberation Front. Goethe: Egmont. Goethe: Faust. Gogol: Vij. Grimmelshausen: Simplicius Simplicissimus. Hitler: Mein Kampf. Hitler: Monology. Huxley: Kontrapunkt. Huysmans: Naruby. Chesterton: Eseje.

Ibsen: Hry. Iuvenalis: Satiry. Lec: Aforismy. Maupassant: Horla. The markers of muscle metabolism creatine kinase and transaminases were normal, myoglobin was slightly increased. With the therapeutically achieved normalization of potassium, the above-mentioned clinical symptoms resolved within three hours. Upon exclusion of the secondary causes of hypokalaemia especially thyrotoxicosis and renal tubular disorders the diagnosis of hypokalaemic periodic paralysis was suspected.

Molecular genetic testing detected a heterozygous point mutation in SCN4A gene located on chromosome 17 17q23encoding the alpha-subunit of the sodium channel, thus confirming the diagnosis of familial hypokalemic periodic paralysis of type 2.

The identical pathogenic variant was found in the asymptomatic father of the patient. Conclusion: The diagnosis of primary PP is based on the characteristic clinical presentation and confirmed by genetic testing. The absence of previous spontaneously receding episodes of muscle weakness in the family or personal history does not exclude the primary familial form of PP.

Bloomfield 3,4 ; Jsou Rána Tíživá. Magner 3,6 ; K. Review of the diagnosis and treatment of periodic paralysis. Muscle Nerve ; 57 4 : — Jabor A, et al. Praha: Grada Publishing, a.

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