Case Report: Novel molecular characterization of rare primary mucinous adenocarcinoma of the renal pelvis. [PDF]
Front OncolTaylor MK +4 more
europepmc +1 more source
The Kidney Pelvis: Its Normal and Pathological Physiology [PDF]
, 1936 J. Leon Jona
openalex +1 more source
A role for epithelium‐derived 6‐nitrodopamine on human ureter contractility
British Journal of Pharmacology, EarlyView.Abstract Background and Purpose To investigate the basal release of 6‐nitrodopamine (6‐ND) from human isolated ureter and the role of this novel catecholamine in the ureter contractility. Experimental Approach Ureters from 67 brain‐dead organ donors (40 males and 27 females) were used during kidney transplantation procedures.
Wilmar Azal Neto +12 more
wiley +1 more source
Clinical analysis of percutaneous kidney-sparing surgery for upper tract urothelial carcinoma. [PDF]
BMC UrolTang S +7 more
europepmc +1 more source
307. Hitting the Kidney from All Angles: Using Direct Intrarenal Pelvis Injection Combined with Serotype and Promoter Targeting to Achieve Renal AAV Gene Delivery [PDF]
, 2016 Claire A. Schreiber +2 more
openalex +1 more source
Mitochondrial DNA Depletion Syndrome 1 (MTDPS1)—A Novel Cause of Premature Ovarian Insufficiency
Clinical Genetics, EarlyView.We describe a woman with MNGIE due to a novel homozygous TYMP nonsense variant and propose MNGIE as the cause of her premature ovarian insufficiency—a rarely reported association—highlighting the need to consider mitochondrial disease in unexplained POI, especially in atypical, consanguineous presentations. ABSTRACT Mitochondrial DNA depletion syndrome
Michael Matheou +3 more
wiley +1 more source
Reduced collagen degradation in pelvic urine precedes kidney fibrosis induced by unilateral ureteral obstruction. [PDF]
Sci RepFrattini T +14 more
europepmc +1 more source
Expanding the Genotype and Phenotype Diversity in a Chinese Cohort With TRPV4‐Related Dysplasia
Clinical Genetics, EarlyView.Exploring the genotype and phenotype diversity in a Chinese cohort with TRPV4‐related dysplasia. ABSTRACT Dominant mutations in the calcium permeable ion channel TRPV4 (transient receptor potential vanilloid 4) typically result in skeletal dysplasia or peripheral neuromuscular disease.
Lina Dong +8 more
wiley +1 more source
Gastroenterological disorders and hepatic disease in adults with cerebral palsy: A systematic review
Developmental Medicine &Child Neurology, EarlyView.Abstract Aim To describe the incidence, prevalence, and prognostic factors for gastroenterological disorders and hepatic disease in adults with cerebral palsy (CP), and to examine the effectiveness of any screening or interventions. Method Six databases were searched for articles published in any language since 1990 meeting eligibility criteria ...
Christina M. Marciniak +18 more
wiley +1 more source