Results 41 to 50 of about 2,788,561 (295)

C1 Esterase Inhibitor (Human) for the Treatment of Acute Hereditary Angioedema

Clinical Medicine Insights: Blood Disorders, 2011
Hereditary angioedema (HAE) is a relatively rare disease characterized by acute episodes of swelling. These swellings can be disfiguring, painful and life-threatening.
Solange Oliveira Rodrigues Valle, Alfeu Tavares França, Regis A. Campos, Anete Sevciovic Grumach   +3 more
doaj   +1 more source

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

Pediatric 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, Natalie Bradford, David Brain, Sameera Senanayake, Sanjeewa Kularatna, Kate Young, Christine Cashion, Tim Hassall, Susanna Cramb   +8 more
wiley   +1 more source

SUSTAINABLE JURISDICTION AND THE (IM) POSSIBILITY OF REVISION IN ADMINISTRATIVE DECISION ON THE GRATUITY OF EXTRAJUDICIAL EMOLUMENTS GRANTED BY JUDICIAL POWER

Revista Eletrônica de Direito Processual, 2021
Constitutional guarantees of access to the Judiciary were expanded in CPC/2015, which expressly included extrajudicial fees in the concept of free justice. However, § 8 of art.
Antonieta Caetano Gonçalves, Magno Federici Gomes   +1 more
doaj   +1 more source

Is a Revision a Revision? An Analysis of National Arthroplasty Registries’ Definitions of Revision [PDF]

Clinical Orthopaedics & Related Research, 2015
The reported survival of implants depends on the definition used for the endpoint, usually revision. When screening through registry reports from different countries, it appears that revision is defined quite differently.The purposes of this study were to compare the definitions of revision among registry reports and to apply common clinical scenarios ...
Thoralf R, Liebs, Farina, Splietker, Joachim, Hassenpflug   +2 more
openaire   +2 more sources

Inpatient Food Insecurity and Pediatric Hematology Oncology Hospitalization Outcomes

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Children with cancer and blood disorders are at risk for food insecurity (FI). We aimed to describe the association of inpatient food insecurity (IFI) and hospitalization outcomes among patients admitted to the pediatric hematology oncology service. Of 325 caregivers screened for IFI, 60 (18.6%) screened positive.
Joanna M. Robles, Greg Russell, Leila H. DeWitt, Kimberly Montez, Callie L. Brown   +4 more
wiley   +1 more source

Revision of the genus Faucaria (Ruschioideae: Aizoaceae) in South Africa

Bothalia: African Biodiversity & Conservation, 1999
Faucaria Schwantes is a small genus of succulents, concentrated in south-central Eastern Cape. Distinguishing features of Faucaria are the characteristically dotted and toothed leaves and the structure of the seed capsule. A taxonomic review of the genus
L. E. Groen, L. J. G. van der Maesen
doaj   +1 more source

Long-term complications of continent catheterizable channels: a problem for transitional urologists. [PDF]

, 2018
A majority of the transitional urology patient population have neurogenic bladder and many of these patients have undergone creation of continent catheterizable channels (CCCs) to facilitate bladder emptying.
Baradaran, Nima, Elliott, Sean P, Hampson, Lindsay A   +2 more
core  

Space-group changes: a revision to a revision [PDF]

Acta Crystallographica Section B Structural Science, 2001
The space group for the entry under the reference codes FEBMUU and FEBMUU01 in the Cambridge Structural Database (1992) should be further corrected to space group C2/c rather than P1 (FEBMUU) or C2 (FEBMUU01).
Marsh, Richard E., Sparks, Robert A.
openaire   +3 more sources

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

Pediatric 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, Lydie Da Costa, Ludivine David Nguyen, Heloise Chosseler, Audrey Riquet, Benedicte Bruno, Melissa Barbati   +6 more
wiley   +1 more source

Monoflange custom-made partial pelvis replacements offer a viable solution in extensive Paprosky III defects: functional outcome and risk factor analysis in 79 cases

Bone & Joint Open
Aims: Custom-made partial pelvis replacements (PPRs) are increasingly used in the reconstruction of large acetabular defects and have mainly been designed using a triflange approach, requiring extensive soft-tissue dissection.
Yannik Hanusrichter, Carsten Gebert, Maximilian Steinbeck, Marcel Dudda, Jendrik Hardes, Sven Frieler, Lee M. Jeys, Martin Wessling   +7 more
doaj   +1 more source