Results 161 to 170 of about 148,383 (342)
Propranolol in management of muscular subaortic stenosis. [PDF]
Graeme Sloman
openalex +1 more source
Beta‐Alanine Relieves Symptoms in Primary Orthostatic Tremor
Movement Disorders, EarlyView.
Karolina af Edholm
wiley +1 more source
ABSTRACT Aim The aim of this review is to systematically summarise the evidence on the effectiveness of riboflavin (vitamin B2) or supplements containing riboflavin in preventing paediatric migraines. Methods This systematic review followed the Joanna Briggs Institute methodology and is reported to adhere to the Preferred Reporting Items for Systematic
Elisa Martello+13 more
wiley +1 more source
ABSTRACT This article explores the relevance and future of social paediatrics, drawing on 50 years of experience in the Netherlands. Social paediatrics is a subspecialty focused on children's health in relation to their environment, including family, school and social networks.
E. M. van de Putte+2 more
wiley +1 more source
Propranolol in paroxysmal ventricular tachycardia. [PDF]
Robert J. Kernohan
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Therapy of angina pectoris with propranolol and long-acting nitrates. [PDF]
Alberto N. Goldbarg+4 more
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We report a 2‐year‐old male with clinical features of Takenouchi‐Kosaki syndrome, bilateral colobomas, and a de novo, likely pathogenic missense variant in CDC42. Supportive evidence includes a Cdc42 conditional knock‐out mouse model with colobomas.
Diana Brightman+11 more
wiley +1 more source
Abstract Epilepsy is a chronic neurological condition marked by recurrent, uncontrolled seizures. Identifying comorbidities in epilepsy is critical for preventing mortality. Among these, the autonomic nervous system's role in epilepsy often manifests as cardiac disorders. Patients with epilepsy (PWE), particularly those with poorly controlled seizures,
Enes Akyuz+2 more
wiley +1 more source
Sensitivity to propranolol after digoxin intoxication. [PDF]
D. A. L. Watt
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Familial adult myoclonus epilepsy: A comprehensive diagnostic strategy for clinical practice
Abstract Familial adult myoclonus epilepsy (FAME) is a genetic neurological disorder characterized by cortical myoclonus and epileptic seizures with clinical features that overlap with other movement disorders and epileptic syndromes, particularly essential tremor (ET), progressive myoclonic epilepsy (PME), and juvenile myoclonic epilepsy (JME).
Yitao Lu+14 more
wiley +1 more source