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The results of the test and any samples taken are sent directly to your GP. This can take up to 5 weeks.

Instead of cots, babies often sleep in a warm box called an incubator.

Feelings of anger, frustration, anxiety and depression are common after a stroke.

She described how, despite there being none of the usual signs of blood clots, the ED staff rapidly identified what treatment was needed.

Adenovirus may cause a variety of clinical manifestations including (but not exclusively) conjunctivitis, pharyngitis, pneumonitis, haemorrhagic cystitis

which will have a positive impact on the future of patient care in Gloucestershire.

FCAL >150 µg/g: please refer to Gastroenterology for further investigation of the cause of this raised result.

Paraneoplastic disorders are characterised by the presence of neuronal autoantibodies.

Our aim is to offer emotional support to patients and staff while not getting in the way of the vital work of hospital staff.”

Date of move

Area of expertise Vascular Neurology and Stroke Inpatient services: All patients requiring an overnight stay in the hospital under the care of Dr.

Chemical Pathology Notes Liver function tests are a requestable test profile which locally consists of: Total protein Albumin Alkaline phosphatase ALT

Blood test services The majority of blood test services are carried out at GP surgeries and other community settings, in order to: improve services reduce

It is important for you to know the signs of labour and to be prepared.

Department of Immunology Notes Antibodies to cardiac muscle antigens are found in a proportion of patients with Dressler's syndrome (following myocardial

Patients with pleural infection should be managed with antibiotics and drainage of the pleural cavity.

Department of Immunology Notes Useful for prognosis and monitoring of lymphoproliferative disease such as multiple myeloma.

Send at ambient temperature to the laboratory on day of sample collection.

This section profiles some of the work that we do

Chemical Pathology Notes Biotinidase deficiency (late-onset multiple carboxylase deficiency) is an autosomal recessively inherited disorder of biotin recycling