Results 151 to 160 of about 3,401 (187)

Clinical characteristics of patients with SALL1-related disorder. [PDF]

open access: yesPediatr Nephrol
Asagai Y   +9 more
europepmc   +1 more source

Multiple Stones in a Single-System Ureterocele in a Child.

open access: green, 2015
Sevgi Büyükbeşe Sarsu   +2 more
openalex   +1 more source

Emphysematous pyelonephritis in a diabetic child: a case report and review of the literature. [PDF]

open access: yesJ Med Case Rep
Bazargani B   +4 more
europepmc   +1 more source

Primary renal neuroendocrine tumor: A rare case and review of diagnostic and therapeutic challenges. [PDF]

open access: yesUrol Case Rep
Kokoneshi K   +9 more
europepmc   +1 more source

New Anhydramnios after 22 Weeks and Pulmonary Hypoplasia.

open access: yesFetal Diagn Ther
Roberts AW   +7 more
europepmc   +1 more source
Some of the next articles are maybe not open access.

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Stenotic Ureterocele

Australian and New Zealand Journal of Surgery, 1972
The incidence, clinical and radiological features and histopathology of the structure of stenotic ureteroceles are described, together with the correlation of muscle content with function and its significance in the choice of treatment.
N, Subbiah, D, Stephens
openaire   +3 more sources

Ureterocele Calculi

British Journal of Urology, 1973
Summary The clinical and radiographic findings in 3 cases of calculi in ureteroceles are described.
A G, Nash, M, Knight
openaire   +2 more sources

Prolapsed Ureterocele

European Urology, 1985
Although rare, the prolapsed ureterocele constitutes a urologic emergency that can rapidly evolve to severe conditions due to congestion and necrosis, and to obstruction of the urinary tract. A simple external resection resolves the emergency, allowing a postoperative investigation of the whole urinary tract to be performed, in order to adequately ...
F T, Dénes   +4 more
openaire   +2 more sources

Blind Ureterocele

European Urology, 1986
Ureterocele without corresponding renal tissue (blind ureterocele) represents a very rare malformation which is of special interest for the understanding of the embryogenesis of this anomaly. Two cases, the first without corresponding kidney seen in an adult and the second in connection with a small multicystic kidney observed in a boy, are considered.
G, Passerini Glazel   +4 more
openaire   +2 more sources

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