Results 51 to 60 of about 980 (143)
The authors report a case of primary hypothyroidism where the main symptoms were caused by muscular lesions and disappeared after treatment with L-thyroxine.
C Paiva +4 more
doaj +1 more source
Miopatía por interacción de ciclosporina, atorvastatina y verapamilo [PDF]
It has been described a higher muscle toxicity when cyclosporine is used mixed with other drugs that interact withenzymes from cytochrome P450 3A4 (CYP3A4), such as atorvastatin or verapamil. It is due to their shared metabolismby these enzymes.
Fernández-Canedo, María Inés +2 more
core +2 more sources
Miopatía secundaria a insuficiencia suprarrenal en paciente con síndrome de la silla turca vacía [PDF]
A 21 year-old female requests medical assistance for asthenia and proximal lower limbs weakness. Through a blood test and electromyogram, it is stated that she has high CPK levels with signs of myopathy.
Martínez-Pérez, María Almudena +4 more
core +2 more sources
La encefalopatía neurogastrointestinal mitocondrial (MNGIE) es una enfermedad genética que se manifiesta desde los primeros años de vida con episodios de íleo, obstrucción intestinal, trastorno de deglución, falla de medro, miopatía, neuropatía ...
Blair Ortiz Giraldo +4 more
doaj
Toxic myopathies: muscle biopsy features Miopatia tóxica: biópsia muscular
Several drugs and toxic substances can cause muscular abnormalities and are frequent causes of acquired myopathies. We present a series of 32 patients, predominance of young adult patients, diagnosed with toxic myopathy.
Rosana Herminia Scola +3 more
doaj +1 more source
A 21 year old male ingested podophyllin in a suicide attempt. The disorder was marked by seizures, coma, peripheral neuropathy, renal failure and acute necrotizing myopathy, an unusual finding.
Acary Souza Bulle Oliveira +5 more
doaj +1 more source
Miopatía y polineuropatía en el paciente crítico. Estudio PEC : parálisis del enfermo crítico [PDF]
Alguns pacients ingressats en la Unitat de Cures Intensives (UCI) desenvolupen una debilitat muscular en grau variable que pot arribar fins a la tetraparesia o tretraplejia. Aquesta condició és deguda a una disfunció neuromuscular perifèrica. No existeix
Oller Sales, Benjamín +5 more
core
Miopatia vacuolar do lupus eritematoso
Após considerações rápidas sôbre as miosites, particularmente sôbre a miopatia vacuolar do lúpus eritematoso, é relatado o caso de uma paciente no qual êsse diagnóstico pôde ser confirmado pelo exame histopatológico.
José Antonio Levy
doaj +1 more source
El splicing alternativo aberrante del mRNA-SMN2 induce en la SMA humana y murina (SMNΔ7) una miopatía de actina primaria: efecto corrector del tratamiento con el ASO Nusinersen [PDF]
RESUMEN: La atrofia muscular espinal (SMA) es una enfermedad hereditaria, con patología neuromuscular, considerada la principal causa de mortalidad infantil de base genética.
Berciano Blanco, María Teresa
core
Mecanismos de rabdomiólise com as estatinas Mechanisms of rhabdomyolysis with statins
A rabdomiólise é incomum, mas é o efeito adverso mais sério observado na terapia hipolipemiante com estatinas. A ocorrência de rabdomiólise fatal reportada nos Estados Unidos desde a introdução das estatinas no mercado, na década de 1980, foi muito rara (
Maria Eliane Campos Magalhães
doaj +1 more source

