Results 41 to 50 of about 1,401 (195)

Advancing conservation breeding programs for marine invertebrates

open access: yesConservation Biology, EarlyView.
Abstract In the face of ecosystem change and biodiversity loss caused by climate change and other stressors, conservation breeding, or captive breeding, with the aim of reintroduction for wild population recovery, is an emerging tool for preventing species’ extinction and rehabilitating ecosystems.
Elora H. López‐Nandam   +3 more
wiley   +1 more source

Molecular diagnosis of Gilbert's syndrome [PDF]

open access: yes, 2015
Gilbertov sindrom je autosomno-recesivna bolest karakterizirana povećanim vrijednostima nekonjugiranog bilirubina i predstavlja najčešći nasljedni uzrok povišenog bilirubina.
Karaga, Ana
core  

Abernethy Malformation in Combination with Gilbert’s Syndrome

open access: yesРоссийский журнал гастроэнтерологии, гепатологии, колопроктологии, 2020
Aim. To present a clinical case of the Abernethy syndrome.Key points. Abernethy syndrome is a rare vascular anomaly associated with a congenital absence of the portal vein, as a result of which portal blood from the intestines and spleen drains directly ...
N. B. Gubergrits   +7 more
doaj   +1 more source

Quick assessment of quality‐of‐life in itch: An exploratory validation of the 5‐item pruritus life quality

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background and objectives Chronic pruritus (CP) significantly impairs quality of life (QoL), but existing patient‐reported QoL tools are either not specific for CP or are very extensive. Patients and methods The 5‐item pruritus life quality (5PLQ, range: 5–25, 7‐day recall) was developed to assess key itch‐related QoL domains (sensory symptoms,
Claudia Zeidler   +14 more
wiley   +1 more source

Bone Mineral Densities in Individuals with Gilbert’s Syndrome: A Cross-Sectional, Case-Control Pilot Study

open access: yesCanadian Journal of Gastroenterology, 2009
BACKGROUND: Unconjugated bilirubin inhibits osteoblastic proliferative activity in vitro, raising the possibility that Gilbert’s syndrome (GS) patients are at increased risk of osteoporosis.
GY Minuk   +4 more
doaj   +1 more source

Does faster aspart improve time in range in children with type 1 diabetes with glycaemia close to target on insulin pump therapy?

open access: yesDiabetic Medicine, EarlyView.
Abstract Aims To evaluate whether faster insulin aspart (FIA) improves time in range (TIR) compared with standard insulin aspart (SIA) in children and adolescents with type 1 diabetes achieving glycaemia close to target treated with continuous subcutaneous insulin infusion (CSII) and continuous glucose monitoring (CGM).
Kowalczyk‐Korcz Emilia   +3 more
wiley   +1 more source

Gilbert’s Syndrome: Terminology, Epidemiology, Genetics, Pathogenesis (Part I)

open access: yesZdorovʹe Rebenka, 2016
The aim of the review was the analysis of the literature about the prevalence, etiology, genetics and pathogenesis of Gilbert’s syndrome (GS). The scientific literature regarding GS with the keywords «Gilbert's syndrome», «hyperbilirubinemia», «uridine ...
T.V. Sorokman   +2 more
doaj   +1 more source

Management of Gilbert's syndrome with low-dose, diluted hyperbaricity of spinal bupivacaine: A rare-rare combo

open access: yesJournal of the Scientific Society, 2021
Gilbert's syndrome (GS) is an inherited unconjugated hyperbilirubinemia state. Regional anesthesia is recommended over general anesthesia in the management of these patients for surgeries.
Reena Ravindra Kadni   +3 more
doaj   +1 more source

Hepatic Safety of Orforglipron in Adults With Obesity or Overweight and/or Type 2 Diabetes: A Pooled Analysis of the Orforglipron Phase 3 Clinical Trials

open access: yesDiabetes, Obesity and Metabolism, EarlyView.
ABSTRACT Aims Orforglipron is a novel small‐molecule, once daily oral non‐peptide GLP‐1 receptor agonist. The hepatic safety profile in adults with obesity or overweight and/or type 2 diabetes (T2D) across seven orforglipron Phase 3 clinical trials was assessed.
Sean Wharton   +5 more
wiley   +1 more source

Evidence for higher red blood cell mass in persons with unconjugated Hyperbilirubinemia and Gilbert's syndrome

open access: yes, 2008
Background: The genetic polymorphism responsible from Gilbert's syndrome is not sufficient for the clinical phenotype to occur in many persons. Additional factors are believed to contribute in pathogenesis. Red cell mass may be such a factor. Methods: We
Akman, Umit   +7 more
core   +1 more source

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