Conclusion: Over half of the patients with chronic hepatitis C attending the DGH have a neurological manifestation, mainly presenting as sensoryperipheralneuropathy.
1
Peripheralsensoryneuropathies occurring in patients receiving both drugs are attributed to the chemotherapy.
Uso de sensory neuropathy en inglés
1
One patient experienced a postoperative complication, transient left lower extremity sensoryneuropathy.
2
Background: Painful sensoryneuropathy is a common complication of HIV infection.
3
Electrodiagnostic tests diagnosed a lower limb sensoryneuropathy in four patients.
4
Clinical and electrophysiological features supported the diagnosis of hereditary motor and sensoryneuropathy.
5
We recruited a large French-Canadian family with a dominantly inherited late-onset painful sensoryneuropathy.
6
Febrile neutropenia and sensoryneuropathy incidences were similar across groups.
7
Purpose: Diabetic cystopathy resulting from sensoryneuropathy may potentially be treated by direct gene therapy.
8
In addition, there was no significant association between active HCV replication and distal sensoryneuropathy.
9
The severity of the resultant sensoryneuropathy was compared with behavioral, physiological, and pathological measures.
10
Conclusion: CD is commonly associated with sensoryneuropathy and should be considered even in the absence of gastrointestinal symptoms.
11
Nearly all patients developed grade 1-2 toxicity consisting of fatigue, sensoryneuropathy, constipation and dizziness.
12
For both HTLV-I and -II participants, higher odds of sensoryneuropathy by monofilament examination were no longer significant after adjustment for confounding.
13
Mice expressing mutant, but not wild type, SIMPLE develop a late-onset motor and sensoryneuropathy that recapitulates key clinical features of CMT1C disease.
14
Hereditary motor and sensoryneuropathy-Lom is an autosomal recessive disorder of the peripheral nervous system, which occurs only in the european Roma population.
15
The electrophysiological findings in our patient with primary SS confirmed trigeminal sensoryneuropathy with abnormal blink reflexes and abnormal cutaneous masseter inhibitory reflexes.
16
A wide variety of neuropathies can be associated with WM, but most commonly it is a mild length-dependent sensoryneuropathy of unclear etiology.