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Association of M2 Haplotype of the Annexin A5 Gene with Recurrent Reproductive Losses

5. 5. 2023 Source: Genetics

Annexin A5 (ANXA5) is a placental anticoagulant protein that ensures adequate blood supply to the fetus during pregnancy, and its deficiency can increase the incidence of vascular thrombosis in the placenta. Current research shows that the M2 haplotype of the ANXA5 gene may be associated with recurrent reproductive losses and obstetric complications due to placental disorders.

ID 2124669452GENETIKA

Etiology of Recurrent Reproductive Losses – Focus on Genetics

Repeated pregnancy losses pose a significant threat to a woman's physical and mental health. The…
4. 5. 2023 Source: Genetics
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Li-Fraumeni Syndrome – Indication for Testing and Recommended Surveillance

A germline mutation of the TP53 gene, which causes Li-Fraumeni syndrome, results in a congenital predisposition...
3. 5. 2023 Source: Genetics
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Water Microjet as a Gentler Method of Debridement

Debridement is an integral part of chronic wound treatment. Currently, the most common method is…
3. 5. 2023 Source: Wound Healing
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INFOGRAPHIC: Eye Drops for Dry and Irritated Eyes – Mechanism of Action and Benefits

2. 5. 2023 Source: Ophthalmologic Diseases
Syndrom Dravetové

Dravet Syndrome – Get to Know It

Dravet syndrome is a severe myoclonic epilepsy occurring in early childhood. It is classified as a…
2. 5. 2023 Source: Rare Diseases in Neurology
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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
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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
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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
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