The hipopotasemic tiroxic periodic paralysis is an entity of low frequency, with incidence of 2 % in the western countries; in our means the incidence is smaller, and predominates between masculine young adults with hyperthyroidism antecedent; clinically one appears like episodes of acute muscular weakness; that they can put in risk the life of the patient; raising a diagnostic challenge occasions about which it does not exist previous antecedent of disease, taking the great majority of the times to think about diagnoses differential slike syndrome of Guillain- Barre-Landry, transverse myelitis, hysteria and acute medullary compression. The following is a patient with picture of acute muscular weakness exposes itself, that raised initially ...
The term ‘porphyria’ comes from the Greek ‘porphyra’. It refers to a heterogeneous group of metaboli...
Introduction: Guillain-Barre syndrome is an acute motor polyneuropathy of the immune mechanism, char...
La esclerosis lateral amiotrófica (ELA) es un trastorno neurodegenerativo que afecta principal...
La hipokalemia aguda es una causa poco frecuente de debilidadmuscular. La parálisis periódica tirotó...
Thyrotoxic periodic paralysis is a rare condition, frequently underdiagnosed and potentially deadly ...
A paralisia periódica hipocaliémica é uma complicação neurológica do hipertiroidismo, especialmente ...
La parálisis periódica hipocalemia es un trastorno autosómico dominante neuromuscular, que forma par...
Periodic paralysis is a rare disease, characterized by transient weakness associated with abnormal l...
In humans, skeletal muscle channelopathies are genetic disease with very low incidence. Regarding th...
Congenital myopathies are a heterogeneous group of muscle diseases of genetic origin, which present ...
La parálisis neuromuscular aguda (PNMA, por sus siglas en inglés) es um síndrome clínico caracteriza...
De Morsier syndrome dysplasia septo-optic (DSO), was described by De Morsier in 1956, who recognized...
Acute neuromuscular paralysis (PNMA) is a clinical syndrome characterized by rapid onset muscle weak...
Normal 0 21 false false false ES X-NONE X-NONE MicrosoftInternetExplorer4 ...
140 p.Antecedentes: El accidente cerebrovascular supone la tercera causa de muerte en hombres, así c...
The term ‘porphyria’ comes from the Greek ‘porphyra’. It refers to a heterogeneous group of metaboli...
Introduction: Guillain-Barre syndrome is an acute motor polyneuropathy of the immune mechanism, char...
La esclerosis lateral amiotrófica (ELA) es un trastorno neurodegenerativo que afecta principal...
La hipokalemia aguda es una causa poco frecuente de debilidadmuscular. La parálisis periódica tirotó...
Thyrotoxic periodic paralysis is a rare condition, frequently underdiagnosed and potentially deadly ...
A paralisia periódica hipocaliémica é uma complicação neurológica do hipertiroidismo, especialmente ...
La parálisis periódica hipocalemia es un trastorno autosómico dominante neuromuscular, que forma par...
Periodic paralysis is a rare disease, characterized by transient weakness associated with abnormal l...
In humans, skeletal muscle channelopathies are genetic disease with very low incidence. Regarding th...
Congenital myopathies are a heterogeneous group of muscle diseases of genetic origin, which present ...
La parálisis neuromuscular aguda (PNMA, por sus siglas en inglés) es um síndrome clínico caracteriza...
De Morsier syndrome dysplasia septo-optic (DSO), was described by De Morsier in 1956, who recognized...
Acute neuromuscular paralysis (PNMA) is a clinical syndrome characterized by rapid onset muscle weak...
Normal 0 21 false false false ES X-NONE X-NONE MicrosoftInternetExplorer4 ...
140 p.Antecedentes: El accidente cerebrovascular supone la tercera causa de muerte en hombres, así c...
The term ‘porphyria’ comes from the Greek ‘porphyra’. It refers to a heterogeneous group of metaboli...
Introduction: Guillain-Barre syndrome is an acute motor polyneuropathy of the immune mechanism, char...
La esclerosis lateral amiotrófica (ELA) es un trastorno neurodegenerativo que afecta principal...