Results 51 to 60 of about 2,201 (201)

Essential embryology for the Canadian pathologists’ assistant

open access: yesAnatomical Sciences Education, EarlyView.
Abstract Pathologists' assistants (PAs) are pivotal in healthcare, conducting autopsies and examining tissues under a pathologist's guidance. Embryology knowledge is crucial for PAs to accurately assess anomalies and identify pathologies. Yet, it is often overlooked in academic PA training programs.
Samantha H. Nacci   +4 more
wiley   +1 more source

SİTRÜLİNEMİ HASTASINDA MECKEL DİVERTİKÜL PERFORASYONU / SWALLOWİNG MECKEL DİVERTICULUM PERFORATİON IN A CİTRULİNNEMİA PATİENT [PDF]

open access: yes, 2016
Sitrülinemi, argininosüksinik asit sentetaz eksikliğinin neden olduğu üre siklus bozukluklarından birisidir. Nadir görülür ve otozomal resesif geçişlidir.
İhtiyar, Enver   +2 more
core   +1 more source

Paediatric development of radiopharmaceutical imaging agents and radioligand therapeutics

open access: yesBritish Journal of Clinical Pharmacology, EarlyView.
Abstract This review focuses on the development of radiopharmaceutical imaging agents and radioligand therapeutics for paediatric use. Nuclear medicine plays an important role in the diagnosis and treatment of various childhood conditions, including cancers, infections and brain disorders.
Justin L. Hay   +5 more
wiley   +1 more source

Large Enterolith Complicating a Meckel Diverticulum Causing Obstructive Ileus in an Adolescent Male Patient. [PDF]

open access: yesCase Rep Surg, 2017
We present a unique case of a 16-year-old male patient who was eventually diagnosed with a large enterolith arising from a Meckel's diverticulum. The enterolith had caused intermittent intestinal symptoms for three years before resulting in small ...
Nastos C   +7 more
europepmc   +2 more sources

Gastrointestinal Bleeding Caused by Meckel’s Diverticulum Diagnosed by Double Balloon Enteroscopy: Three Cases and a Brief Literature Review

open access: yesMedicine Science, 2015
Meckel's diverticulum is a small bulge in the small intestine present at birth and is the most frequent malformation of the gastrointestinal tract. Although Meckel diverticulum is usually of no medical significance, tendency to gastrointestinal bleeding ...
Mehmet Ibis   +4 more
doaj   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken   +4 more
wiley   +1 more source

Jejunal Diverticulosis as a Rare Cause of Severe Obscure Gastrointestinal Bleeding in an Elderly Patient: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Jejunal diverticulosis is a rare cause of obscure gastrointestinal bleeding (OGIB) that can present with life‐threatening hemorrhage. We report a 69‐year‐old male with recurrent melena, severe anemia, and hemodynamic instability requiring multiple transfusions. Upper and lower endoscopy were nondiagnostic, and CT angiography failed to localize
Mahmoud Draidi   +5 more
wiley   +1 more source

COMPLICAȚIILE DIVERTICULULUI MECKEL. REVISTA LITERATURII

open access: yesArta Medica, 2022
Obiective. Scopul articolului a fost de a analiza datele din sursele existente de literatură, referitor la complicațiile diverticulului Meckel. Material  și  metode.  Au  fost  studiate  un  număr  de  publicații  științifice  ce  prezintă  informații 
Iurii Bazeliuc, Alin Bour
doaj  

Intussusception secondary to Meckel's diverticulum in a 3-month-old girl. Case report

open access: yesRevista Médica del Hospital General de México, 2018
A 3-month-old female patient is presented, with ileo-ileal intussusception secondary to Meckel's diverticulum. The patient underwent emergency surgery due to a diagnosis of intestinal obstruction secondary to intussusception.
I. Camacho-Guerrero, L. Ramírez-Patiño
doaj   +1 more source

Bilateral Gonadoblastoma in a 12‐Year‐Old Girl 4 Years After Wilms' Tumor: A Rare Pediatric Case

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT This case of a 12‐year‐old patient who developed bilateral gonadoblastoma 4 years after treatment for Wilms tumor highlights the importance of rigorous, risk‐adapted long‐term surveillance and careful evaluation of incidental gonadal findings, even in asymptomatic patients.
Ahmed Quraish   +4 more
wiley   +1 more source

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