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Werner syndrome

Werner's syndrome
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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Werner syndrome" returned 14 free, full-text review articles. First few results:
Studying Werner syndrome to elucidate mechanisms and therapeutics of human aging and age-related diseases.
Last Updated: Feb 17, 2020

Aging is a natural and unavoidable part of life. However, aging is also the primary driver of the dominant human diseases, such as cardiovascular disease, cancer, and neurodegenerative diseases, including Alzheimer's disease. Unraveling the sophisticated molecular mechanisms of the ...

Herlyn-Werner-Wunderlich Syndrome: Report of a Prenatally Recognised Case and Review of the Literature.
Last Updated: Jun 06, 2019

Herlyn-Werner-Wunderlich syndrome, defined by the triad of uterus didelphys, obstructed hemivagina and ipsilateral renal agenesis, is a rare Mullerian malformation, usually diagnosed after menarche, when symptoms related to hematocolpos arise. Rarely, this malformation is diagnosed ...

Werner Syndrome Protein and DNA Replication.
Last Updated: Feb 15, 2019

Werner Syndrome (WS) is an autosomal recessive disorder characterized by the premature development of aging features. Individuals with WS also have a greater predisposition to rare cancers that are mesenchymal in origin. Werner Syndrome Protein (WRN), the protein mutated in WS, is ...

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14 Free Review Articles 56 Review Articles

Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Werner syndrome" returned 1 free, full-text editorial articles. First 1 results:
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Werner syndrome" returned 202 free, full-text research articles. First few results:
Herlyn-Werner-Wunderlich syndrome presenting with dysmenorrhea: a case report.
Last Updated: Feb 04, 2020

Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly characterized by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. The most common presentation is abdominal pain, dysmenorrhea, and abdominal mass secondary to hematocolpos. We present the first ...

Diagnosis and gestational follow-up in a patient with Herlyn-Werner-Wünderlich syndrome, a case report.
Last Updated: Jan 24, 2020

Herlyn-Werner-Wünderlich syndrome (HWW) is a rare congenital malformation of the urogenital tract due to a fusion failure in the Müllerian ducts. This anomaly consists of a didelphus uterus with obstructed hemivagina and sometimes associated with ipsilateral renal agenesis. The ...

Oral squamous cell carcinoma arising in a patient with Werner syndrome.
Last Updated: Oct 29, 2019

Werner syndrome (WS) is an autosomal recessive disorder characterized by physical signs and symptoms, including premature aging and scleroderma-like skin changes. The gene responsible for WS is the WRN gene. A significant proportion of WS-related malignant tumours are non-epithelial ...

Full PubMed Research articles matches at NCBI:
202 Free Research Articles 414 Research Articles