Results 81 to 90 of about 119,932 (242)

Impact of Histopathological Response on Outcomes After Surgical Resection Following Carbon‐Ion Radiotherapy for Pancreatic Cancer With Arterial Involvement

open access: yesAnnals of Gastroenterological Surgery, EarlyView.
ABSTRACT Aim Carbon‐ion radiotherapy (CIRT) provides superior dose distribution and higher biological effectiveness than conventional X‐ray radiotherapy and has emerged as a promising component of multidisciplinary treatment for advanced pancreatic ductal adenocarcinoma (PDAC).
Kenichiro Araki   +9 more
wiley   +1 more source

Systemic Bevacizumab for Severe Bleeding From Acquired Gastrointestinal Vascular Malformations

open access: yesAmerican Journal of Hematology, EarlyView.
Targeted antiangiogenic therapy with systemic bevacizumab for bleeding from acquired GI VMs was found to be safe and effective for chronic and severe bleeding from acquired vascular malformations due to idiopathic angiodysplasia, chronic liver disease, and deficiencies of von Willebrand factor, in a patient population comprised mostly of heavily ...
Nardeen E. Ayad   +5 more
wiley   +1 more source

Effets trophiques de la gestation et de la lactation sur le pancréas, le duodénum et l'estomac [PDF]

open access: yes
Au cours des périodes de gestation, de lactation et de post­ lactation, il se produit chez la femelle des augmentations de la consommation de nourriture et des changements morphologiques importants au niveau de certains organes du système digestif ...
Jolicoeur, Lyne
core  

Proximal enteroscopy -Results -Critical appraisal (485 cases) [PDF]

open access: yes, 1982
La duodénojéjunoscopie nous semble devoir remplacer la biopsie à l'aveugle en raison de la validité des biopsies, du raccourcissement du temps de l'examen.
BERGER, F., MARTIN, A., MOULINIER, B.
core  

Actualisation de la prévision des apports en acides aminés digestibles dans l’intestin pour les vaches laitières [PDF]

open access: yes, 2016
Un travail de méta-analyse a été engagé pour revoir le calcul des valeurs d’acides aminés digestibles dans l’intestin (AADI) dans le projet INRA Systali de révision des systèmes d’alimentation des ruminants.
Panzuti, Clémence   +6 more
core   +4 more sources

Superior Mesenteric Artery Syndrome at Pediatric Intensive Care Unit

open access: yesJournal of Pediatric Research, 2017
Superior mesenteric artery syndrome is a rare condition in patients who have oral feeding intolerance. Due to decreased fat tissue around the duodenum, the angle between the superior mesenteric artery and duodenum also decrease.
Emine Burçe Yaşar   +2 more
doaj   +1 more source

The Homozygous p.(Arg215Ter) Variant in XRCC2 Is Associated With Atypical Fanconi Anemia Without Major Hematological Abnormalities in Childhood

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli   +11 more
wiley   +1 more source

Le syndrome de la pince aorto-mésentérique chez l’enfant : à propos d’un cas primitive [PDF]

open access: yes, 2016
Le syndrome de la pince aorto-mésentérique résulte de la compression du troisième duodénum entre l’artère mésentérique supérieure et l’aorte. Elle détermine un tableau d’occlusion intestinale haute aiguë ou chronique.
Bâ, Papa Abdoulaye   +4 more
core   +1 more source

Adenocarcinoma primário de duodeno

open access: yesRevista do Colégio Brasileiro de Cirurgiões
Primary adenocarcinoma of the duodenum is an extremely rare disease, and represents only 0.35 % of all gastrointestinal malignies. Early detection of the disease is dificult because doesn't have pathognomonic simptoms.
Hamilton Petry de Souza   +3 more
doaj   +3 more sources

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young   +6 more
wiley   +1 more source

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