Results 61 to 70 of about 14,675 (263)

A case of congenital myopathy masquerading as paroxysmal dyskinesia

open access: yesAnnals of Indian Academy of Neurology, 2014
Gastroesophageal reflux (GER) disease is a significant comorbidity of neuromuscular disorders. It may present as paroxysmal dyskinesia, an entity known as Sandifer syndrome.
Harsh Patel   +4 more
doaj   +1 more source

Structural insights and therapeutic targets in Acinetobacter baumannii capsule biosynthesis

open access: yesFEBS Letters, EarlyView.
Hypervirulent KL49 A. baumannii's capsular polysaccharide contains the nonulosonic acid 8‐epi‐Leg5,7Ac2, synthesized by epimerization via ElaA, ElaB, and ElaC. Crystal structures of ElaA, ElaB, and ElaC reveal their role in CMP‐Leg5,7Ac2 synthesis and regioselective C8 epimerization.
Woo Cheol Lee   +7 more
wiley   +1 more source

Effect of cardiac resynchronization therapy on ventricular tachycardias in patients with dilated cardiomyopathy and severe heart failure

open access: yesПатология кровообращения и кардиохирургия, 2015
The aim of the study was to elucidate the effects of cardiac resynchronization therapy (CRT) on ventricular tachycardias in patients with dilated cardiomyopathy and to analyze the prospects of radionuclide diagnostic methods for prediction of life ...
Д. И. Лебедев   +6 more
doaj   +1 more source

Modelling stem cell differentiation related processes—A practical overview for biologists

open access: yesFEBS Letters, EarlyView.
Stem cell differentiation is complex and difficult to control experimentally. This review introduces suitable computational modelling approaches that can support stem cell research, from mechanistic ODE and abstract models to multiscale and deep learning methods.
Ricco Zeegelaar   +4 more
wiley   +1 more source

EEG after Febrile Seizure is Predictive of Epilepsy

open access: yesPediatric Neurology Briefs, 2012
Researchers in pediatric neurology and electroencephalography at the University of Yamanashi, Japan, studied the EEG in children referred within 7-20 days after a febrile seizure (FS), and determined the utility of localization of paroxysmal discharges ...
J Gordon Millichap
doaj   +1 more source

A pharmacotherapy of atrial fibrillation in subclinical thyrotoxicosis

open access: yesИзвестия высших учебных заведений. Поволжский регион: Медицинские науки, 2021
Background. Pharmacological therapy of atrial fibrillation (AF) in subclinical dysfunction of the thyroid – is the most important problem of modern clinical medicine.
R.F. Rakhmatullov   +3 more
doaj   +1 more source

Identification of a Shiga toxin A‐derived peptide internalized into Gb3 receptor‐bearing cells via interaction with the Shiga toxin B subunit

open access: yesFEBS Letters, EarlyView.
The process of internalization of the Shiga toxin A subunit via formation of a complex with the Shiga toxin B subunit, which specifically binds to the Gb3 receptor. The peptide is designed to act as a carrier of drugs into cancer cells. Here, we explored the potential of peptides derived from the catalytic A subunit of Shiga toxin (STxA) to be drug ...
Giulia Opassi   +6 more
wiley   +1 more source

Propafenone in complex anti-recurrent therapy of persistent atrial fibrillation

open access: yesРоссийский кардиологический журнал, 2007
Effectiveness and safety of Class IС antiarrhythmic agent, propafenone (Propanorm, PRO. MED. CS Praha a.s., Czech Republic), was studied inpatients with persistent atrial fibrillation (PAF) after sinus rhythm conversion, during long-term ant-recurrent ...
V. V. Skibitsky   +3 more
doaj  

Episodic Mydriasis as Migraine Equivalent

open access: yesPediatric Neurology Briefs, 1991
A 14-year-old girl who presented with yearly attacks of bilateral internal ophthalmoplegia, nausea and headache since the age of 9 is the subject of a case report from the Department of Child Neurology, University Hospital Nijmegen, The Netherlands.
J Gordon Millichap
doaj   +1 more source

Paroxysmal Nocturnal Hemoglobinuria [PDF]

open access: yesBlood, 2014
AbstractParoxysmal nocturnal hemoglobinuria (PNH) is a rare bone marrow failure disorder that manifests with hemolytic anemia, thrombosis, and peripheral blood cytopenias. The absence of two glycosylphosphatidylinositol (GPI)-anchored proteins, CD55 and CD59, leads to uncontrolled complement activation that accounts for hemolysis and other PNH ...
openaire   +2 more sources

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