Results 41 to 50 of about 29,978,210 (287)

Pulmonary Dysfunction Is Associated With Sleep Study Abnormalities in Children With Sickle Cell Disease: A Multicenter Study

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Introduction Pulmonary dysfunction and sleep abnormalities are common in children with sickle cell disease (SCD) and are associated with worse clinical outcomes. Whether spirometry abnormalities are associated with polysomnography (PSG) findings remains unclear.
Ammar Saadoon Alishlash   +4 more
wiley   +1 more source

Prevalence and Trajectory of Household Material Hardship Among Children With Advanced Cancer

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background/Objectives Families of children with advanced cancer living in poverty experience inferior outcomes including poor parent mental health and worse child quality of life. Household material hardship (HMH: food, housing, transportation, and/or utility insecurity) is a modifiable poverty exposure—and potential intervention target—that ...
Sarah Wright   +13 more
wiley   +1 more source

Spartan Daily February 22, 2011 [PDF]

open access: yes, 2011
Volume 136, Issue 14https://scholarworks.sjsu.edu/spartandaily/1121/thumbnail ...
San Jose State University, School of Journalism and Mass Communications
core   +1 more source

Financial Burden Associated With Hospitalisation Among Families of Childhood Brain Tumours in Australia

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background Families of children with cancer experience significant financial strain, even with universal healthcare. Indirect costs, such as productivity losses and non‐medical expenses, are rarely included in economic evaluations, and little is known about how effectively financial aid programmes alleviate this burden. Childhood brain tumours
Megumi Lim   +8 more
wiley   +1 more source

Fuldt nummer

open access: yesDansk Universitetspaedagogisk Tidsskrift, 2017
Nummeret indeholder følgende artikler: Hvordan begrunder undervisere forelæsninger? Et interviewstudie med undervisere fra to fagmiljøer Anna Bager-Elsborg Læring i Modvind: Hvordan forbedrer man de studerendes præstation i fag, som de typisk ...
DUT 22
doaj  

Spartan Daily, October 22, 1974 [PDF]

open access: yes, 1974
Volume 63, Issue 24https://scholarworks.sjsu.edu/spartandaily/5908/thumbnail ...
San Jose State University, School of Journalism and Mass Communications
core   +1 more source

The Fate (Outcome) of Clinically Apparent Single Lesion and Oligofocal Nephroblastomatosis Treated According to SIOP/GPOH Protocols for Wilms Tumor

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background The management of clinically apparent single lesions or oligofocal nephroblastomatosis, a facultative precursor of nephroblastoma, remains debated. Methods We retrospectively analyzed 37 patients with clinically apparent single or oligofocal nephroblastomatosis (two to three lesions per kidney) among 2347 patients registered between
Nils Welter   +17 more
wiley   +1 more source

Investigation on Potential Starter of Bacillus spp. for Ivorian Cocoa Beans Fermentation Improvement

open access: yesTurkish Journal of Agriculture: Food Science and Technology, 2018
To investigate some interesting functional properties of Bacillus spp. in cocoa fermentation processing, 702 strains of Bacillus sp. strains were isolated from six main Ivorian cocoa producer regions.
Alalet Luc Zadi   +3 more
doaj   +1 more source

Spartan Daily, September 22, 1980 [PDF]

open access: yes, 1980
Volume 75, Issue 15https://scholarworks.sjsu.edu/spartandaily/6651/thumbnail ...
San Jose State University, School of Journalism and Mass Communications
core   +1 more source

Germline TP53 Mutations Causing Diamond–Blackfan Anemia: A French Report

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Diamond–Blackfan anemia is a rare congenital erythroblastopenia typically caused by mutations in ribosomal protein genes. Recently, gain‐of‐function mutations in TP53 have been identified as a novel cause of Diamond–Blackfan anemia. We report two French patients who both harbored a heterozygous TP53 deletion (NM_000546.5: c.1077delA; p ...
Rafael Moisan   +6 more
wiley   +1 more source

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