Results 121 to 130 of about 114,162 (186)

Computing Individual Risks based on Family History in Genetic Disease in the Presence of Competing Risks [PDF]

arXiv, 2017
When considering a genetic disease with variable age at onset (ex: diabetes , familial amyloid neuropathy, cancers, etc.), computing the individual risk of the disease based on family history (FH) is of critical interest both for clinicians and patients. Such a risk is very challenging to compute because: 1) the genotype X of the individual of interest
arxiv  

Echocardiographic characteristics of autosomal dominant polycystic kidney disease

Scientific Reports
Cardiovascular complications in patients with autosomal dominant polycystic kidney disease (ADPKD) are frequently investigated extrarenal manifestations with contradictory outcomes.
Agata Koska-Ścigała, Hanna Jankowska, Magdalena Jankowska, Maria Dudziak, Marcin Hellmann, Alicja Dębska-Ślizień   +5 more
doaj   +1 more source

Unusual familial cystic kidney disease: combining fine radiologic and genetic evaluation to solve the case

BMC Nephrology
Background Autosomal dominant polycystic kidney disease (ADPKD) is the most prevalent hereditary kidney disease, characterized by enlarged kidneys with numerous cysts, high blood pressure, and a variety of extrarenal complications.
Sylvain Bodard, Rim Nabbout, Olivier Hélénon, Bertrand Knebelmann   +3 more
doaj   +1 more source

AI-Driven Predictive Analytics Approach for Early Prognosis of Chronic Kidney Disease Using Ensemble Learning and Explainable AI [PDF]

arXiv
Chronic Kidney Disease (CKD) is one of the widespread Chronic diseases with no known ultimo cure and high morbidity. Research demonstrates that progressive Chronic Kidney Disease (CKD) is a heterogeneous disorder that significantly impacts kidney structure and functions, eventually leading to kidney failure. With the progression of time, chronic kidney
arxiv  

Polycystic kidney disease in a Persian cat [PDF]

, 2015
A 6-year-old intact Persian cat was presented for the primary complaint of inappetence and weight loss. Irregular surface of kidneys was palpated during physical examination. Abdominal radiograph findings were indicative of renomegaly.
Khor, Kuan Hua, Lau, Seng Fong, Phoon, Melissa Hoi Ee, Saw, Ming Hooi   +3 more
core  

New Therapies Targeting Cystogenesis in Autosomal Polycystic Kidney Disease

European Medical Journal Nephrology, 2017
Autosomal dominant polycystic kidney disease is the most common inherited kidney disease and results from mutations in the polycystin 1 gene (PKD1) or the polycystin 2 gene (PKD2).
Maurizio Salvadori, Aris Tsalouchos
doaj  

Cerebral Microbleeds in Autosomal Dominant Polycystic Kidney Disease [PDF]

Journal of Stroke, 2020
Li-Kai Tsai, Pei-Lung Chen, Hsin-Hsi Tsai, Ya-Fang Chen, Ping-Chun Wu, Jiann-Shing Jeng, Jenq-Wen Huang, Tzong-Shinn Chu, Juliana Tze-Wah Kao   +8 more
doaj   +1 more source

No relationship between total kindey volume class or genotype and 24h blood pressure control in adult ADPKD patients [PDF]

, 2018
Allamani, Mandelina, Devos, Hannes, Schots, Lisa, Tonnelier, Annelies, Van der Niepen, Patricia   +4 more
core   +2 more sources

Endovascular Management of Renal Artery Pseudoaneurysm in Autosomal Dominant Polycystic Kidney Disease: A Case Report

Vascular Specialist International
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common hereditary kidney diseases. In addition to renal involvement, vascular complications including intracranial arterial, aortic aneurysms and dissections are common in these ...
Garima Sharma, Hira Lal, Narayan Prasad
doaj   +1 more source

Insights into autosomal dominant polycystic kidney disease by quantitative mass spectrometry-based proteomics [PDF]

, 2018
Autosomal dominant polycystic kidney disease (ADPKD) is a common monogenetic disorder that is caused by mutations in the genes PKD1 and PKD2 encoding polycystin-1 and polycystin-2, respectively.
Dengjel, Jörn, Diedrich, Britta
core