L Dolenc Grošelj

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Sirs, In our retrospective study [1], 60 out of 189 patients with amyotrophic lateral sclerosis (ALS) had presented the predominantly bulbar form at disease onset. The disease form was defined according to the patient’s history of first symptom and, if there was uncertain history, the patients were assigned in groups according to the predominant clinical(More)
OBJECTIVES In patients who exhibit myotonic dystrophy type 1 (DM1), sleep disorders and breathing impairments are common; however, in those with DM type 2 (DM2), limited studies on polysomnography (PSG) and none on phrenic compound motor action potential (CMAP) have been performed, which is the aim of this study. MATERIALS AND METHODS Sixteen patients(More)
BACKGROUND Various breathing abnormalities (Neurology 2009; 73: 1218) have been proposed as indicators for the introduction of non-invasive positive-pressure ventilation (NIV) in patients with amyotrophic lateral sclerosis (ALS). We were interested in the usefulness of symptoms of respiratory insufficiency and abnormal results of daytime arterial gas(More)
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