Portuguese
Albanian
Arabic
Armenian
Azerbaijani
Belarusian
Bengali
Bosnian
Catalan
Czech
Danish
Deutsch
Dutch
English
Estonian
Finnish
Français
Greek
Haitian Creole
Hebrew
Hindi
Hungarian
Icelandic
Indonesian
Irish
Italian
Japanese
Korean
Latvian
Lithuanian
Macedonian
Mongolian
Norwegian
Persian
Polish
Portuguese
Romanian
Russian
Serbian
Slovak
Slovenian
Spanish
Swahili
Swedish
Turkish
Ukrainian
Vietnamese
Български
中文(简体)
中文(繁體)

hypoventilation/cefaleia

O link é salvo na área de transferência
Página 1 a partir de 50 resultados

Successful diaphragmatic pacing for idiopathic alveolar hypoventilation.

Apenas usuários registrados podem traduzir artigos
Entrar Inscrever-se
We describe the case of a 17-year-old woman noted to have idiopathic alveolar hypoventilation, with multiple Intensive Care Unit (ICU) admissions because of acute respiratory failure (ARF) due to respiratory infections. After two years of diaphragmatic pacing arterial blood gases have substantially
BACKGROUND Congenital central hypoventilation syndrome (CCHS) is a rare genetic disorder resulting from mutations in the PHOX2B gene located on chromosome 4p12.3, characterized by hypoventilation secondary to missing responses to both hypercapnia and hypoxia. METHODS Proband. A girl, hospitalised 5

Idiopathic hypoventilation syndrome: importance of preventing nocturnal hypoxemia and hypercapnia.

Apenas usuários registrados podem traduzir artigos
Entrar Inscrever-se
This report describes a young woman with unexplained chronic hypoventilation that was greatly exacerbated during sleep. Treatment with nocturnal O2 during a 2-yr period was associated with stable cardiovascular function but severe morning headaches and lethargy, presumably related to nightly bouts

The obesity hypoventilation syndrome can be treated with noninvasive mechanical ventilation.

Apenas usuários registrados podem traduzir artigos
Entrar Inscrever-se
OBJECTIVE To assess the effectiveness of nasal noninvasive mechanical ventilation (NIMV) in patients with obesity hypoventilation syndrome (OHS). METHODS Clinical assay that compares two groups of patients with hypercapnic respiratory failure, one group with OHS and the other group with
Lateral medullary infarction rarely leads to central hypoventilation syndrome (CHS). CHS is a life-threatening disorder characterized by hypoventilation during sleep. We report the first case of CHS as a complication of lateral medullary infarction after endovascular treatment. A 65-year-old man

Nocturnal hypoventilation in children with nonprogressive neuromuscular disease.

Apenas usuários registrados podem traduzir artigos
Entrar Inscrever-se
Eight patients between 4 and 24 years of age with nonprogressive neuromuscular disease sought medical attention because of severe nocturnal hypoventilation. There were two types of findings: subacute with progressive early morning headaches and daytime drowsiness and acute with ventilatory failure

HYPOVENTILATION, CYANOSIS AND POLYCYTHEMIA IN A THIN MAN.

Apenas usuários registrados podem traduzir artigos
Entrar Inscrever-se
A lack of respiratory centrogenic drive of undetermined origin is a rare cause of cyanosis. In this condition, voluntary hyperventilation restores arterial oxygen saturation to normal. Secondary changes consist of polycythemia, somnolence, headache and right heart failure. The present report of a

[Nocturnal hypoxia index: a new pulse oxymetry index of nocturnal hypoventilation in neuromuscular disorders].

Apenas usuários registrados podem traduzir artigos
Entrar Inscrever-se
Respiratory insufficiency due to progressive muscle wasting is a major cause of death in various neuromuscular disorders. Morning headache and anorexia leading to slowly progressive body weight loss are frequently observed as initial symptoms of insufficient ventilation. From our experience

[The congenital central hypoventilation syndrome (CCHS): a late presentation].

Apenas usuários registrados podem traduzir artigos
Entrar Inscrever-se
BACKGROUND The congenital central hypoventilation syndrome (CCHS) or Ondine's curse is a rare autosomal dominant disease, characterized by disorders of the autonomic nervous system, with abnormal ventilatory responses to hypercapnia and hypoxia. PHOX2B has been identified as the major gene causing

[Mechanical ventilation in neuromuscular diseases: do not start too early, but certainly not too late].

Apenas usuários registrados podem traduzir artigos
Entrar Inscrever-se
Three patients had chronic respiratory disorders: a 42-year-old man with glycogenosis type II was tired, had headaches, poor pulmonary function values and, according to the arterial blood gas values, hypercapnia; a man aged 24 with Duchenne's muscular dystrophy had variable moderate dyspnoea with

[Neuromuscular disease and sleep disturbance].

Apenas usuários registrados podem traduzir artigos
Entrar Inscrever-se
In neuromuscular diseases, respiratory disorder is related to sleep disorder. In Duchenne muscular dystrophy, respiratory muscle disorder progresses and induces alveolar hypoventilation. Hypoxemia and hypercapnia develop, requiring appropriate management. Hypoxemia first appears during sleep,

Arterial oxygen saturation for prediction of acute mountain sickness.

Apenas usuários registrados podem traduzir artigos
Entrar Inscrever-se
BACKGROUND Acute mountain sickness (AMS) is a usually self-limiting syndrome encompassing headache, nausea and dizziness. AMS is seen in those that go from low to high altitudes too quickly, without allowing sufficient time to acclimatize. At present, susceptibility to AMS cannot be predicted. One

[Late onset Ondine syndrome: literature review on a case report].

Apenas usuários registrados podem traduzir artigos
Entrar Inscrever-se
Ondine syndrome is the central congenital hypoventilation syndrome (CCHS) caused by the mutation of the PHOX2B gene. In late onset cases, the symptomatology often appears after an acute event (infection, general anesthesia, drug intake), increasing hypoventilation. We report a case of late onset

Sleep breathing disorders and nocturnal respiratory pattern in patients with glycogenosis type II.

Apenas usuários registrados podem traduzir artigos
Entrar Inscrever-se
Patients affected by glycogenosis type II frequently present sleep disordered breathing. The presence of symptoms suggestive of sleep breathing disorders was investigated, by a questionnaire, in 10 patients, affected by adult or juvenile forms of glycogenosis type II. Diurnal respiratory function,

Sleep studies and supportive ventilatory treatment in patients with congenital muscle disorders.

Apenas usuários registrados podem traduzir artigos
Entrar Inscrever-se
Eight ambulant children aged 6-13 years, four with congenital myopathy, two with congenital muscular dystrophy and two with the rigid spine syndrome, presented with recurrent chest infections, morning headaches, shallow breathing at night, or respiratory failure. Polysomnography confirmed the
Junte-se à nossa
página do facebook

O mais completo banco de dados de ervas medicinais apoiado pela ciência

  • Funciona em 55 idiomas
  • Curas herbais apoiadas pela ciência
  • Reconhecimento de ervas por imagem
  • Mapa GPS interativo - marcar ervas no local (em breve)
  • Leia publicações científicas relacionadas à sua pesquisa
  • Pesquise ervas medicinais por seus efeitos
  • Organize seus interesses e mantenha-se atualizado com as notícias de pesquisa, testes clínicos e patentes

Digite um sintoma ou doença e leia sobre ervas que podem ajudar, digite uma erva e veja as doenças e sintomas contra os quais ela é usada.
* Todas as informações são baseadas em pesquisas científicas publicadas

Google Play badgeApp Store badge