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Syndrom Dravetové

Dravet Syndrome – Get to Know It

2. 5. 2023 Source: Rare Diseases in Neurology

Dravet syndrome is a severe myoclonic epilepsy occurring in early childhood. It is classified as a rare progressive epileptic encephalopathy, characterized by generalized or lateralized clonic seizures often prolonged and linked to febrile infections. Other forms of seizures later appear, leading to deterioration in psychomotor development and the onset of mental retardation. Early diagnosis and treatment are desirable.

Bolest svalů_muž

When and why to consider the diagnosis of myasthenia gravis in neurological practice, and what treatment options do we currently have?

Myasthenia gravis (MG) is a clinically heterogeneous disease characterized by fluctuating muscle…
2. 5. 2023 Source: Rare Diseases in Neurology
Syndrom suchého oka_žena

Sjögren's Syndrome as a Cause of Dry Eye Syndrome

Primary Sjögren's syndrome represents a complex autoimmune disease primarily affecting glands with…
2. 5. 2023 Source: Ophthalmologic Diseases
plíce 3D model

Infographic and Commentary from Practice: Reasons and Pathways for Patients to Biological Treatment of Asthma

For asthma patients with the most severe forms of the disease to access targeted biological…
28. 4. 2023 Source: Systemic treatment of atopic dermatitis, asthma, and chronic rhinosinusitis with nasal polyposis – Type 2 inflammation
studie.

Subcutaneous pdC1-INH in Patients with Hereditary Angioedema in Real-World Practice

Italian authors published a series of cases of patients with hereditary angioedema caused by C1 inhibitor...
27. 4. 2023 Source: Hereditary Angioedema
screening

Efficacy and Safety of an Activated FXII Inhibitor in Preventing HAE Attacks

Hereditary angioedema (HAE) is a rare, potentially life-threatening inherited disorder characterized...
27. 4. 2023 Source: Hereditary Angioedema
pacient

To what extent does the delay between symptom onset and diagnosis of AATD affect patient survival?

The risk of chronic obstructive pulmonary disease (COPD) is increased, among other things, by a deficiency...
26. 4. 2023 Source: Deficiency of Alpha-1-Antitrypsin
pacientka

Augmentation Therapy of Bronchiectasis Due to AATD – Case Report

Alpha-1-antitrypsin deficiency (AATD) is a rare cause of bronchiectasis unrelated to cystic fibrosis....
26. 4. 2023 Source: Deficiency of Alpha-1-Antitrypsin
tehotenstvi

Pregnancy and Childbirth in a Woman with VWD − A Case Study

Pregnancy and childbirth are relatively demanding periods and situations for women with von Willebrand...
26. 4. 2023 Source: Von Willebrand Disease
leg ulcers

Benefits and Cost-Effectiveness of Superabsorbent Dressings in the Treatment of Venous Leg Ulcers

A recent cost-effectiveness analysis based on German data showed that using superabsorbent…
26. 4. 2023 Source: Wound Healing
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XIII. Celostátní kongres České společnosti pro léčbu rány s mezinárodní účastí

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