Results 51 to 60 of about 35,299,302 (406)
Therapeutic approach for Amyand’s hernia; a case report [PDF]
In very few cases stated in the literature, the vermiform appendix might be contained in a hernial sac. This distinctive pathology is described as Amyand\u27s hernia and has the very small occurrence of about 1%.
Ardeleanu, Valeriu +4 more
core +2 more sources
Adrenal insufficiency in coronavirus disease 2019: a case report
Background Novel coronavirus disease 2019 presents with fever, dry cough, fatigue, and shortness of breath in most cases; however, some rare manifestations in other organs have also been reported so far.
M. Heidarpour +4 more
semanticscholar +1 more source
ABSTRACT Background While Wilms tumor (WT) typically has a favorable prognosis, relapsed cases—especially those with high‐risk histology—remain therapeutically challenging after intensive frontline therapy. The combination of vincristine and irinotecan has demonstrated activity in pediatric solid tumors, and pazopanib, a multi‐targeted tyrosine kinase ...
Maria Debora De Pasquale +6 more
wiley +1 more source
Gastrointestinal Ulceration as a Manifestation of Severe Dermatomyositis -
Please view the PDF to see the formatted meeting abstract.
Daniel O’Shea
doaj +1 more source
Scleroderma is an autoimmune connective tissue disorder which is characterized by fibrosis of visceral organs, skin and blood vessels. This condition can be localized or systemic. Its estimated prevalence is 250 cases in a million and it is more common in women than in men.
ALTAN, Gülay +3 more
openaire +5 more sources
Resistance to autosomal dominant Alzheimer’s in an APOE3-Christchurch homozygote: a case report
We identified a PSEN1 (presenilin 1) mutation carrier from the world’s largest autosomal dominant Alzheimer’s disease kindred, who did not develop mild cognitive impairment until her seventies, three decades after the expected age of clinical onset.
Joseph F. Arboleda-Velasquez +43 more
semanticscholar +1 more source
Bone Marrow Failure as an Underrecognized Feature of KAT6A Syndrome
ABSTRACT KAT6A syndrome (Arboleda–Tham syndrome) is a rare disorder caused by heterozygous pathogenic variants in KAT6A, a histone acetyltransferase essential for chromatin remodeling and hematopoietic stem cell function. While neurodevelopmental features are well established, hematologic manifestations are underrecognized.
Ye Jee Shim +8 more
wiley +1 more source
ERCP in Patient with Situs Inversus Totalis
Please view the PDF to see the formatted meeting abstract.
David Farrow
doaj +1 more source
Peculiar and Unusual Drowning in Waste Oil from Motor Vehicles: Case Report [PDF]
Drowning is one of the most frequent causes of accidental or suicidal death, and more rarely it is associated with a homicide. Cases of drowning in water or in the sea are common.
Cardia, Giulio +3 more
core +1 more source
ABSTRACT The pediatric hematology‐oncology fellowship training curriculum has not substantially changed since its inception. The first year of training is clinically focused, and the second and third years are devoted to scholarship. However, this current structure leaves many fellows less competitive in the current job market, resulting in ...
Scott C. Borinstein +3 more
wiley +1 more source

