Results 181 to 190 of about 360,718 (298)
The Pathology of the Pituitary and Adrenal Glands in Systemic Disease in Man [PDF]
A Currie, T. Symington
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This analysis included quantification of intrafraction motion in pancreas stereotactic ablative radiotherapy treated on the MR‐Linac, leading to the development of adjusted (PTV) margins. Intrafraction motion indicated an average target displacement of 1–3 mm, resulting in an adjusted PTV margin of 2 mm in the right–left and superior–inferior ...
Ashleigh Fasala +6 more
wiley +1 more source
A patient with an adrenal metastasis and periadrenal lymph node metastases of a laryngeal squamous cell carcinoma: a case report. [PDF]
Gimm O, Nilsson CM, Stefanis A.
europepmc +1 more source
Circulatory collapse requiring mechanical circulatory support in a child with autoimmune adrenal insufficiency: a case report [PDF]
Yahia Hejazi +3 more
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Abstract Objectives Pediatric patients with chronic gastrointestinal (GI) conditions including inflammatory bowel diseases (IBD) and irritable bowel syndrome (IBS) on average endorse lower health related quality of life (HRQOL) than their healthy counterparts.
S. Taylor Younginer +6 more
wiley +1 more source
Clinical and Biochemical Progression in a Patient With Cortisol-Producing Adenoma. [PDF]
Nanba K +5 more
europepmc +1 more source
Abstract Objectives Pediatric intestinal pseudo‐obstruction (PIPO) is a severe bowel motility disorder characterized by impaired propulsion of gastrointestinal contents without mechanical obstruction. PIPO encompasses congenital and acquired disorders, including neuropathies, myopathies, and mesenchymopathies.
Sharon Wolfson +8 more
wiley +1 more source
An Adrenal Crisis After Denosumab Use in a Patient With Addison's Disease: A Case Report. [PDF]
Caglar H, Hira S, Caglar SO.
europepmc +1 more source
Adrenal Crisis: From Perioperative Clinic to Diagnosis [PDF]
Ahmet Gültekin +4 more
openalex +1 more source
Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea
Abstract Among congenital diarrhea and enteropathies (CODEs), proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency is a rare monogenic disorder, associated with severe neonatal diarrhea and polyendocrinopathies. We report an 18‐day‐old male neonate, born to consanguineous parents, presenting with persistent watery diarrhea, metabolic ...
Eleonora Saraceno +7 more
wiley +1 more source

