Results 141 to 150 of about 132,538 (304)

Outcomes and adverse effects of teduglutide treatment with periodic withdrawal in pediatric short bowel patients

open access: yesJournal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives We evaluated the efficacy and safety of teduglutide in a real‐world cohort in which national reimbursement policies required treatment interruptions. The primary outcomes were reduction in parenteral support (PS) and treatment‐related adverse effects, and the secondary outcome was the impact of the mandated withdrawal periods ...
Riikka Gunnar   +3 more
wiley   +1 more source

Treatment of Iron-deficiency Anemia in Patients with Subclinical Hypothyroidism [PDF]

open access: yes, 2013
Subclinical hypothyroidism is a health state that is associated with hypercholesterolemia, infertility, iron-deficiency anemia, and poor obstetric outcome. This article summarizes the results of a prospective clinical investigation of whether treatment
Asadipooya, Kamyar   +4 more
core  

Severe allergic reaction to ustekinumab reinitiation in a pediatric patient with Crohn's disease: A case report

open access: yesJPGN Reports, EarlyView.
Abstract Ustekinumab (UST) is a monoclonal antibody used in the management of moderate to severe inflammatory bowel disease. While generally well‐tolerated, serious adverse reactions, including hypersensitivity and anaphylaxis, have been documented, specifical following the initial intravenous (IV) dose.
Kennedy Sparling   +2 more
wiley   +1 more source

Evaluation of the Prevalence and Determinants of Iron Deficiency Anemia in a Sample of Preschool-Aged Children in Isfahan City, Iran

open access: yesمجله دانشکده پزشکی اصفهان, 2017
Background: Iron deficiency anemia (IDA) is a public health problem and the most common cause of anemia worldwide. The prevalence of iron deficiency anemia is 17-75 percent in preschool children in the Middle East. Early diagnosis and proper treatment of
Morteza Sadinejad   +4 more
doaj  

Menetrier's: A pediatric chronic state of disease with a possible heritable form

open access: yesJPGN Reports, EarlyView.
Abstract Menetrier's disease (MD) is a rare, typically transient, hypertrophic gastropathy with under 1000 adult cases and 50 pediatric cases known worldwide. Pediatric cases most often present with an infectious etiology. We present a case of a teenage male expressing a chronic state of disease without infectious origin.
MariaElena Terzis   +2 more
wiley   +1 more source

Anemia in North of Iran (South-east of Caspian Sea)

open access: yes, 2007
The main purpose of this study was set up to determine iron deficiency and anemia due to iron deficiency among the women in villages around of Gorgan.
Gholamreza, V.
core  

UNA PANORAMICA SULL\u2019ANEMIA SIDEROPENICA NEGLI ATLETI/AN OVERVIEW ON IRON DEFICIENCY ANEMIA IN ATHLETES [PDF]

open access: yes, 2012
Diversi studi in letteratura riportano come la capacit\ue0 prestativa degli atleti di endurance sia fortemente compromessa in seguito all\u2019insorgenza di anemia sideropenica.
Battaglia, G.   +6 more
core  

Juvenile polyposis in a SMAD4‐mutated child: A call for early surveillance

open access: yesJPGN Reports, EarlyView.
Abstract We report the case of a 10‐year‐old boy with hereditary hemorrhagic telangiectasia (HHT) and a family history of SMAD4‐related juvenile polyposis syndrome (JPS), presenting with hypoferritinaemia unresponsive to oral supplementation. Endoscopic evaluation revealed multiple gastrointestinal polyps, including duodenal, gastric, and colonic ...
Claudia Lorusso   +10 more
wiley   +1 more source

Prevalence of Iron Deficiency with and Without Anemia Among Immigrant’ People in Al-Azrakeen Area, Sana’a City, Yemen

open access: yesAnnals of Medicine and Medical Sciences
Background: The prevalence of iron deficiency with or without anemia is still remains the common clinical problem worldwide. Iron deficiency with and without anemia may be more prevalent among migrants due to disadvantaged life conditions.
Dekra El-Aghbary   +3 more
doaj  

Infantile exocrine pancreatic insufficiency due to a homozygous SPINK1 pathogenic variant in two siblings: A case report

open access: yesJPGN Reports, EarlyView.
Abstract Infantile exocrine pancreatic insufficiency is a rare condition, most often encountered in the context of cystic fibrosis or Shwachman–Diamond syndrome. The SPINK1 gene encodes a trypsin inhibitor protein that prevents the premature activation of digestive enzymes in pancreatic tissue.
France Chalon   +10 more
wiley   +1 more source

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