muscular atrophy/opkast

Linket gemmes på udklipsholderen

Vælg sorteringstype

13 resultater

Severe ketoacidosis in a patient with spinal muscular atrophy.

Kun registrerede brugere kan oversætte artikler

Log ind / Tilmeld

Spinal muscular atrophy (SMA) is a genetic neuromuscular disease characterized by progressive muscle weakness and atrophy. We report a case of a 36-year-old man with SMA type 3 who presented to our emergency department with epigastric pain and vomiting. He was found to have severe ketoacidosis on

[Severe ketoacidosis induced by short-term starvation in a patient with spinal muscular atrophy].

Kun registrerede brugere kan oversætte artikler

Log ind / Tilmeld

We report a case of a 29-year-old woman with spinal muscular atrophy (SMA) type II who developed severe ketoacidosis after short-term starvation. She was hospitalized with lower respiratory tract infection. Although her symptoms improved after administration of intravenous antibiotic agents, her

Evaluating Benefit-risk Decision-making in Spinal Muscular Atrophy: A First-ever Study to Assess Risk Tolerance in the SMA Patient Community.

Kun registrerede brugere kan oversætte artikler

Log ind / Tilmeld

Patients' perceptions of benefit-risk are essential to informing the regulatory process and the context in which potential therapies are evaluated. To bring this critical information to regulators, Cure SMA launched a first-ever Benefit-Risk Survey for spinal muscular atrophy (SMA) to

Safety and efficacy of olesoxime in patients with type 2 or non-ambulatory type 3 spinal muscular atrophy: a randomised, double-blind, placebo-controlled phase 2 trial.

Kun registrerede brugere kan oversætte artikler

Log ind / Tilmeld

Spinal muscular atrophy (SMA) is a progressive motor neuron disease causing loss of motor function and reduced life expectancy, for which limited treatment is available. We investigated the safety and efficacy of olesoxime in patients with type 2 or non-ambulatory type 3 SMA. This randomised,

An Integrated Safety Analysis of Infants and Children with Symptomatic Spinal Muscular Atrophy (SMA) Treated with Nusinersen in Seven Clinical Trials.

Kun registrerede brugere kan oversætte artikler

Log ind / Tilmeld

Treatment with nusinersen has demonstrated significant and clinically meaningful benefits in clinical trials in infants and children with spinal muscular atrophy (SMA).The objective of this analysis was to characterize the safety of nusinersen across the

Surgical complications in neuromuscular scoliosis operated with posterior- only approach using pedicle screw fixation.

Kun registrerede brugere kan oversætte artikler

Log ind / Tilmeld

BACKGROUND There are no reports describing complications with posterior spinal fusion (PSF) with segmental spinal instrumentation (SSI) using pedicle screw fixation in patients with neuromuscular scoliosis. METHODS Fifty neuromuscular patients (18 cerebral palsy, 18 Duchenne muscular dystrophy, 8

[Mechanism of development of space motion sickness].

Kun registrerede brugere kan oversætte artikler

Log ind / Tilmeld

Astronauts and scientists are scheduled to stay aboard the International Space Station (ISS) for three-month periods, and various problems relating to the human ability to live in space for such long periods of time, as well as medical problems, are being studied. For the crews that have operated

[Diagnosis and treatment of methylmalonic acidemia in 14 cases].

Kun registrerede brugere kan oversætte artikler

Log ind / Tilmeld

OBJECTIVE Methylmalonic acidemia (MMA) is one of the most common disorders of congenital organic acid metabolism. This study aimed at exploring the clinical characteristics and treatment of the disease to help improve our understanding of it. METHODS The clinical data of 14 patients with MMA

Percutaneous endoscopic gastrostomy in children: 15 cases experience.

Kun registrerede brugere kan oversætte artikler

Log ind / Tilmeld

For long-term tube feeding in children, percutaneous endoscopic gastrostomy (PEG) has the advantages of a short surgical time, early feeding following surgery, and lower rate of complications. From July 2000 to September 2002, we enrolled fifteen children (mean age: 8.2 years old) who underwent PEG

[Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) associated with hypothalamo-pituitary hypofunction--a case report].

Kun registrerede brugere kan oversætte artikler

Log ind / Tilmeld

A case of 25-year-old woman with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) was reported. She had short stature, episodic vomiting with headache, several episodes with homonymous hemianopsia, progressive intellectual decline, generalized convulsion, muscular

[Gastric emphysema, a critical condition accompanied by eating disorders: a case report].

Kun registrerede brugere kan oversætte artikler

Log ind / Tilmeld

Gastric emphysema encompasses a broad spectrum of diseases. A 31-year-old woman presented with severe vomiting and epigastric pain. She had lost body weight for several months, and was later diagnosed as having anorexia nervosa. A radiological study demonstrated intramural gas with huge gastric

Subjective global assessment of nutrition a useful diagnostic tool for nurses?

Kun registrerede brugere kan oversætte artikler

Log ind / Tilmeld

Malnutrition in maintenance haemodialysis (HD) patients is closely related with morbidity and mortality in this population. OBJECTIVE To evaluate feasibility, performance and information given by SGA (subjective global assessment), a semi-quantitative method of nutritional evaluation (based on a

CPEO and carnitine deficiency overlapping in MELAS syndrome.

Kun registrerede brugere kan oversætte artikler

Log ind / Tilmeld

Mitochondrial myopathy, encephalopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome is one of the mitochondrial encephalomyopathies that has distinct clinical features including stroke-like episodes with migraine-like headache, nausea, vomiting, encephalopathy and lactic acidosis.

Deltag i vores
facebook-side

Herbal & Natural Medicine

Den mest komplette database med medicinske urter understøttet af videnskab

Arbejder på 55 sprog
Urtekurer, der understøttes af videnskab
Urtegenkendelse ved billede
Interaktivt GPS-kort - tag urter på stedet (kommer snart)
Læs videnskabelige publikationer relateret til din søgning
Søg medicinske urter efter deres virkninger
Organiser dine interesser og hold dig opdateret med nyhedsundersøgelser, kliniske forsøg og patenter

Skriv et symptom eller en sygdom, og læs om urter, der kan hjælpe, skriv en urt og se sygdomme og symptomer, den bruges mod.
* Al information er baseret på offentliggjort videnskabelig forskning