Results 51 to 60 of about 131,738 (297)

Innovative Minds Shine Bright at the 2023 ConV2X Pitch Competition

open access: yesBlockchain in Healthcare Today, 2023
On Sept 1, 2023, Partners in Digital Health, publisher of Blockchain in Healthcare Today (BHTY,) conducted the 4th Annual ConVerge2Xcelerate (ConV2X) Ignition Pitch Competition.
Tory Cenaj
doaj  

Dispositional Immobility: An Analysis of Non-Decisions as Public Policy in Alberta’s City-Regions

open access: yesSocial Sciences, 2016
For local governments in city-regions, the term “dispositional immobility” can be applied in situations where the question of municipal restructuring becomes an arena for permanent public policy non-decisions.
James Lightbody, Lisa Kline
doaj   +1 more source

The Changing Landscape of Maintenance Therapy in Newly Diagnosed Multiple Myeloma: A Systematic Review With Network Meta‐Analysis of the European Myeloma Network (EMN)

open access: yesAmerican Journal of Hematology, EarlyView.
Our meta‐analysis showed significant improvement of PFS with lenalidomide, proteasome inhibitors, and CD38‐based therapies. A significant OS benefit was noted only with lenalidomide in transplant‐eligible (TE) patients, while CD38‐directed therapy showed a trend toward improved OS.
Heinz Ludwig   +25 more
wiley   +1 more source

Reversible splenic ischemia in inflamma - tory bowel disease

open access: yesJournal of the Belgian Society of Radiology, 2011
A 32-year-old man was admitted to the emergency department complaining of abdominal pain, vomiting and fever. In his medical history we noted Crohn’s disease.
S Van Nieuwenhove   +3 more
doaj   +1 more source

Histidine Supplementation Stabilizes Hearing and Vision and Improves Growth in HARS1‐Related Autosomal Recessive Disorder Associated With Usher‐Like Symptoms

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Autosomal recessive HARS1‐related disorder (originally described as Usher syndrome type 3B) caused by a homozygous Y454S variant in the histidyl‐tRNA synthetase gene (HARS1) is characterized by progressive sensorineural hearing and vision loss and respiratory deterioration with risk for sudden death following febrile illnesses.
Victoria Mok Siu   +23 more
wiley   +1 more source

Enhanced mitochondrial activity reshapes a gut microbiota profile that delays NASH progression

open access: yesHepatology, EarlyView., 2022
Improved mitochondrial activity, due to the lack of methylation‐controlled J protein (MCJ), creates a specific microbiota signature that when transferred through cecal microbiota transplantation delays NASH progression by restoring the gut‐liver axis and enhancing hepatic fatty acid oxidation.
María Juárez‐Fernández   +18 more
wiley   +1 more source

Premier livre illustré de Tory : les Heures de 1525 « à l’antique » : Heures à l'usage de Rome : Annonciation

open access: yes
Livre imprimé sur papier. Reliure de maroquin olive à décor de feuillages dorés, XVII e siècleVoici le premier livre commandé par Tory et vendu dans sa boutique. Comme il ne possède pas encore de presse, il l'a fait imprimer chez son ami Simon de Colines,
Simon de Colines pour Geoffroy Tory
core   +2 more sources

Expanding the Utility of Exome Sequencing in Preventive and Population Genetics

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Carrier screening is a long‐standing genetic testing process offered to at‐risk couples, with or without a family history, who might have pregnancies affected by an autosomal recessive (AR) or X‐linked (XL) disorder. A total of 276 unrelated individuals, initially referred for rare disorder screening by clinicians, were enrolled in this study ...
Charilaos Kostoulas   +6 more
wiley   +1 more source

Tory imprimeur du roi François I er : Ordonnances du Roy nostre sire, sur l’estat des tresoriers et manyment des finances

open access: yes
Geoffroy Tory porte le titre d’imprimeur du roi à partir de l’automne 1531. Cette distinction s’explique en partie par ses relations à la cour de François I er , où il a su faire apprécier ses livres « modernes » à plusieurs grands ...
Geoffroy Tory
core   +2 more sources

The International Consortium for Arthrogryposis: A Collaborative Framework for Early Detection, Care, Research, and Education

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Arthrogryposis multiplex congenita (AMC) is a group of rare congenital conditions, characterized by multiple joint contractures but may involve any body system including central nervous system. AMC is etiologically heterogeneous, with over 400 genetic and many non‐genetic causes implicated in its prenatal development.
Shahrzad Nematollahi   +20 more
wiley   +1 more source

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