Results 141 to 150 of about 9,152,470 (385)

Polycystic Kidney Disease without an Apparent Family History.

open access: yesJournal of the American Society of Nephrology, 2017
The absence of a positive family history (PFH) in 10%-25% of patients poses a diagnostic challenge for autosomal dominant polycystic kidney disease (ADPKD).
Ioan-Andrei Iliuta   +17 more
semanticscholar   +1 more source

Genetic linkage study of family members of a patient with adult polycystic kidney disease [PDF]

open access: yes, 1999
OBJECTIVE. To study the feasibility of making an early diagnosis of adult polycystic kidney disease by using genetic linkage analysis in Hong Kong. DESIGN. Genetic linkage study. SETTING. University teaching hospital, Hong Kong. PARTICIPANTS.
Chan, DTM   +4 more
core  

Androgens and Hypertension in Men and Women: a Unifying View. [PDF]

open access: yes, 2017
This review was designed to revaluate the androgen role on the mechanisms of hypertension and cardiovascular risks in both men and women. Sex steroids are involved in the regulation of blood pressure, but pathophysiological mechanism is not well ...
Carmina, E. 4.   +4 more
core   +1 more source

Plant extracellular vesicles: A promising bionic medicine platform for disease treatment and drug delivery

open access: yesInterdisciplinary Medicine, EarlyView.
We introduced the basic characterization and isolation methods of PEVs, reviewed the PEVs‐related articles pertaining to disease therapy and drug delivery system, and summarized the drug loading methods, storage techniques, and engineering modification strategies of the carrier, to establish a safer, more efficient and more affordable approach for ...
Jichun Yang   +14 more
wiley   +1 more source

Mitotic CDK1 and 4E-BP1 I: Loss of 4E-BP1 serine 82 phosphorylation promotes proliferative polycystic disease and lymphoma in aged or sublethally irradiated mice. [PDF]

open access: yesPLoS One, 2023
Sun R   +13 more
europepmc   +1 more source

Ciliary Mechanisms of Cyst Formation in Polycystic Kidney Disease.

open access: yesCold Spring Harbor Perspectives in Biology, 2017
Autosomal-dominant polycystic kidney disease (ADPKD) is a disease of defective tissue homeostasis resulting in active remodeling of nephrons and bile ducts to form fluid-filled sacs called cysts.
Ming Ma, A. Gallagher, S. Somlo
semanticscholar   +1 more source

Fuelling Recovery: Is There a Role for Radiation Therapists in Optimising Nutrition for Women With Breast Cancer?

open access: yesJournal of Medical Radiation Sciences, EarlyView.
A study of 90 Australian women receiving breast cancer radiation therapy found none met dietary guidelines, with only 33% consuming enough fruit and 12% enough vegetables daily, indicating a crucial need for improvement in nutritional support during treatment.
Laura Feighan   +3 more
wiley   +1 more source

Isolated Polycystic Liver Disease: An Unusual Cause of Recurrent Variceal Bleed

open access: yesCase Reports in Gastrointestinal Medicine, 2018
Isolated polycystic liver disease is a rare disorder. Majority of the patients with isolated polycystic liver disease are asymptomatic with incidental detection of liver cysts on imaging studies done for other purposes.
Mohammad Saud Khan   +7 more
doaj   +1 more source

Should a paediatrician perform abdominal ultrasonography inchildren of parents with polycystic kidney disease?

open access: yesPediatria i Medycyna Rodzinna, 2016
Autosomal dominant polycystic kidney disease produces symptoms mainly in adulthood. Renal cysts and/or elevated blood pressure can be the first signs of the disease in children.
Krzysztof Wróblewski   +4 more
doaj   +1 more source

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