Results 181 to 190 of about 1,190,684 (378)

Specific Features of Proctectomy in a Pelvis Presenting Anatomical Variation Type: Bilateral Kidney Ectopia.

open access: bronze
N. Chadli   +12 more
openalex   +1 more source

Flexible and navigable suction access sheaths: balancing sheath and scope size for desired flows

open access: yesBJU International, EarlyView.
Objective To study the effects of ureteroscope diameter, ‘flexible and navigable suction’ access sheaths (FANS) diameter, and irrigation pressure on intrarenal pressure (IRP) and irrigation fluid flow rates in ex vivo porcine kidneys; these benchtop data were compared against mathematical modelling results.
Richard Menzies‐Wilson   +4 more
wiley   +1 more source

A role for epithelium‐derived 6‐nitrodopamine on human ureter contractility

open access: yesBritish 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

A case of incidental renal pelvic basaloid squamous cell carcinoma. [PDF]

open access: yesMedicine (Baltimore)
Li Z   +6 more
europepmc   +1 more source

Mitochondrial DNA Depletion Syndrome 1 (MTDPS1)—A Novel Cause of Premature Ovarian Insufficiency

open access: yesClinical 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

Expanding the Genotype and Phenotype Diversity in a Chinese Cohort With TRPV4‐Related Dysplasia

open access: yesClinical 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

Pancake kidney in infant: A case report with literature review. [PDF]

open access: yesRadiol Case Rep
Bapir R   +10 more
europepmc   +1 more source

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