Results 41 to 50 of about 2,901,254 (317)

Hospital management of community-acquired pneumonia in Malta [PDF]

, 2012
Community-acquired pneumonia (CAP) remains a common diagnosis requiring hospital admission and a leading cause of death worldwide. No local guideline is currently available for the management of CAP.
Mamo, Jonathan, Micallef, Josef, Callus, Roberta, Montefort, Stephen   +3 more
core  

The choice of insider or outsider top executives in acquired companies [PDF]

, 2009
There is considerable debate amongst academics and practitioners over whether top executives of acquired or merged companies should stay or go, post-deal, as studies exploring the link with organisational performance show mixed results.
Angwin, D, Meadows, Maureen, Meadows, M, Angwin, Duncan N., Angwin, Duncan   +4 more
core   +1 more source

Therapeutic Apheresis for Intravenous Methylprednisolone‐Refractory Neuromyelitis Optica Spectrum Disorder: Clinical and Radiological Outcomes in a Single‐Center Case Series

Therapeutic Apheresis and Dialysis, EarlyView.
ABSTRACT Background Neuromyelitis optica spectrum disorder (NMOSD) is a relapsing autoimmune disease of the central nervous system. High‐dose intravenous methylprednisolone (IVMP) is the standard first‐line therapy for acute attacks, although some patients remain refractory.
Wataru Horiguchi, Daisuke Katagiri, Takeyuki Watadani, Shunichi Matsuda, Hiroshi Kaneko, Noritoshi Arai   +5 more
wiley   +1 more source

Tendon transfers for the upper extremity in cerebral palsy

Acta Orthopaedica et Traumatologica Turcica, 2020
Upper extremity deformities in cerebral palsy are caused by the imbalance between spastic and weak muscles acting on unstable joints. The basic goals of surgical treatment of spastic hands and upper extremities of patients with cerebral palsy can be ...
Turker Ozkan, Serdar Tuncer
doaj   +1 more source

Acquired Hypoprothrombinemia [PDF]

Blood, 1957
Abstract Hypoprothrombinemia was encountered in 105 patients including cases of vitamin K deficiency, liver disease, newborns, Dicumarol-type drug therapy and a few miscellaneous disorders. The findings stress the association of acquired hypoprothrombinemia with deficiencies proconvertin and PTC and suggest that these three proteins are ...
J H, FERGUSON, J W, FRESH, J H, LEWIS, E, SPAUGH, M B, ZUCKER   +4 more
openaire   +2 more sources

Therapeutic Apheresis in Nigeria: A Multi‐Center Summary of Abstracts From the Inaugural Nigerian Society for Apheresis Scientific Meeting

Therapeutic Apheresis and Dialysis, EarlyView.
ABSTRACT Background Therapeutic apheresis (TA) is an established treatment modality for hematologic, neurologic, and immunologic disorders, yet access remains severely limited in sub‐Saharan Africa. Donor apheresis, including platelet apheresis collection from healthy donors, represents an important complementary modality supporting blood product ...
Nosa Bazuaye, Chimezie Okwuonu, Evelyn Idam, Folasade Adelekan‐Popoola, Shakirat Gold‐Olufadi, Olufunto Olufela Kalejaiye, Abdullateef Ogala, Zinnah Aloziem, Blossom Amamchukwu, Patience Elimia, Mkpoikanabasi Obot‐Obot, Henry Mbakwe, Praises Maduagwuna, Olatunji Akinrodoye, Chiamaka Anyanwu, Benjamin Anyanwu, Adedamola Akinsiku, Oluwatoyin A. Akinsiku, Muzamil O. Hassan, Fatiu A. Arogundade, Olalekan E. Ojo, Homayemem Weli, Jesupelumi Adenihun, Aderemi Adelaja, Ebun Bamgboye, Olalekan Olatise, Ade E. Faponle, Ayoola Odeyemi, Michael Muoka, Stephen Asaolu, Qudrat Busari, Blessing Dawudu, Michael Naiyeju, Rasheed A. Balogun   +33 more
wiley   +1 more source

Brazilian expert consensus on the diagnosis, classification, screening for complications and treatment of familial partial lipodystrophy

Diabetology & Metabolic Syndrome
Background Partial lipodystrophies are a rare and heterogeneous group of diseases characterized by variable loss of adipose tissue. Around the world, the high heterogeneity in phenotypic expression, limited awareness, and absence of standardized ...
Cynthia Melissa Valerio, Luiz F. Viola, Natália Rossin Guidorizzi, Josivan Gomes Lima, Amélio F. Godoy-Matos, Alexandre Hohl, Fabio R. Trujilho, Joana R. Dantas, Julliane Tamara Araújo de Melo Campos, Lenita Zajdenverg, Raquel Beatriz Gonçalves Muniz, Rodrigo Oliveira Moreira, Virgínia Oliveira Fernandes, Maria Cristina Foss-Freitas, Renan Montenegro   +14 more
doaj   +1 more source

Prevalence of Multidrug-Resistant Tuberculosis in Dalian, China: A Retrospective Study

Infection and Drug Resistance, 2021
Liang Du,1 Yu Zhang,1 Xintong Lv,2 Yuxin Duan,1 Xiaoyan Shi,2 Haoqiang Ji,1 Ruiheng Wu,1 Jia Xu,1 Xu Chen,1 Yang Gao,2 Xiwei Lu,2 Ling Zhou1 1School of Public Health, Dalian Medical University, Dalian, Liaoning, 116044, People’s Republic of China ...
Du L, Zhang Y, Lv X, Duan Y, Shi X, Ji H, Wu R, Xu J, Chen X, Gao Y, Lu X, Zhou L   +11 more
doaj  

Acquired Von Willebrand Factor Deficiency at Patient-Prosthesis Mismatch after AVR Procedure—A Narrative Review

Medicina, 2023
Acquired von Willebrand factor deficiency has been described in patients with aortic valve stenosis due to high shear forces developed during passage through the narrowed valve orifice, which determines structural changes in this molecule.
Andrei Emanuel Grigorescu, Andrei Anghel, Darius Gheorghe Buriman, Horea Feier   +3 more
doaj   +1 more source

Acquired haemophilia A: a case report [PDF]

, 2017
Acquired haemophilia A is rare, autoimmune bleeding disorder caused by the production of autoantibodies against coagulation factor VIII (FVIII). The disorder affects 1.5 people per 1 million population a year, particularly the elderly.
Paulina Stemplewska, Marlena Broncel, Adam Stemplewski, Paulina Gorzelak-Pabiś   +3 more
core   +1 more source