Results 121 to 130 of about 6,612 (269)

Acute and chronic inflammatory polyneuropathies - clinical and therapeutic considerations

, 1981
The Inflammatory Polyneuropathies (IPN) are an important group of acquired neuropathies characterized pathologically by the presence of inflammatory lesions scattered throughout the peripheral nervous system associated with segmental demyelination and ...
Mora, J, Bradley, W, Berkman, E
core  

Australian clinical practice guideline: diagnosis and treatment of idiopathic multicentric Castleman disease

Internal Medicine Journal, EarlyView.
Abstract Idiopathic multicentric Castleman disease (iMCD) is a rare condition. The pathogenesis is incompletely understood; however, interleukin‐6 (IL‐6) is a major mediator. The clinical presentation is heterogeneous, from mild constitutional symptoms to severe multi‐organ failure.
Dipti Talaulikar, Jun Yen Ng, Adam Bryant, Annmarie Bosco, Hugh C. Caterson, Pratyush Giri, Pravin Hissaria, Simon J. Harrison, Stephen Lade, Connull Leslie, Jacinta Perram, H. Miles Prince, Dejan Radeski, Maureen Rischmueller, Craig Wallington‐Gates, Nicholas Weber, Alberta Hoi   +16 more
wiley   +1 more source

Maintenance intravenous immunoglobulin in chronic inflammatory demyelinating polyneuropathy: trends from an Australian tertiary centre

Internal Medicine Journal, EarlyView.
Abstract Background Chronic inflammatory demyelinating polyneuropathy (CIDP) is commonly treated with long‐term intravenous immunoglobulin (IVIg). Individual dosing requirements and duration of IVIg differ among patients, leading to significant heterogeneity in IVIg utilisation.
Kristina T. Pidd, Anthony Khoo
wiley   +1 more source

Successful Multimodal Therapeutic Approach for CD30‐positive Folliculotropic Mycosis Fungoides

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Chiara L. Blomen, Inga Hansen‐Abeck, Andrea Baehr, Stefan W. Schneider, Christoffer Gebhardt, Nina Booken   +5 more
wiley   +1 more source

Sudomotor dysfunction in people with type 1 diabetes with and without clinical peripheral neuropathy: A study from Pune, India

Journal of Diabetes Investigation, EarlyView.
ABSTRACT Background and Aims It is appreciated that current screening tools for diabetic peripheral neuropathy (DPN) often fail to detect early disease. Sudomotor (sweat gland) dysfunction, among the earliest manifestations of DPN, can be measured objectively by the SUDOSCAN® device. We compared SUDOSCAN® with conventional validated screening (Michigan
Rohan Shah, Rishikesh Behere, Aboli Bhalerao, Sanat Phatak, Alma Baptist, Chinmay S. Marathe, Chittaranjan S. Yajnik   +6 more
wiley   +1 more source

Les polyneuropathies dans une double cohorte de pvvih naïfs et sous arv dans trois centres de depistage volontaire et anonyme de Lome, Togo

, 2010
Since the popularized of ARV therapy, the polyneuropathies continue to increase and can lead to stop treatment in PLHIV/AIDS. The study’s goal was to evaluate the frequency and the profile of the polyneuropathies in HIV patients with and without ...
AAK Balogou, Balogou, AAK, Andrianantenaina, AFL, AFL Andrianantenaina, Belo, M, Assogba, K, K Assogba, M Belo   +7 more
core   +1 more source

Concordance of HbA1c, creatinine, LDL cholesterol, HDL cholesterol, and total cholesterol between venous and self‐collected capillary blood samples sent by mail

Journal of Diabetes Investigation, EarlyView.
ABSTRACT Introduction/Aims Self‐collected capillary blood sampling with postal shipment may improve access to routine monitoring of HbA1c, creatinine, and lipid parameters, but evidence on concordance with venous samples under real‐world transport conditions remains limited.
Linda Hoffmeister, Christopher Schuchardt, Angelika Hafke, Eva Hummers, Alexandra Dopfer‐Jablonka, Georg M. N. Behrens, Andrea Stölting, Louis Kuhnke, Julie Schanz, Frank Müller, Christine Happle, Dominik Schröder   +11 more
wiley   +1 more source

Les polyneuropathies axonales chroniques idiopathiques (à propos de 86 cas)

, 2007
L'enquête étiologique d'une polyneuropathie axonale chronique reste très souvent décevante. Les CIAP présentent une faible évolutivité, et le handicap développé au cours du temps reste faible.
DUBOUIS-BONNEFOND, Anne-Gillonne, CLAVELOU, Pierre   +1 more
core  

Epidermal necrolysis sequelae: A cohort study on prevalence and risk factors

Journal of the European Academy of Dermatology and Venereology, EarlyView.
Long‐term sequelae after epidermal necrolysis are frequent, multiple and often severe. Cutaneous, ocular and psychological complications are more frequent, with significant socioeconomic impact. Cluster analysis identifies distinct patient profiles, highlighting the need for personalized multidisciplinary follow‐up.
Thanh Vy Nguyen, Thomas Bettuzzi, Karim Zaghbib, Julie Gueudry, Audrey Colin, Kmar Bel Hareth, Narimane Terkmane, Emilie Sbidian, Nicolas de Prost, Saskia Ingen‐Housz‐Oro   +9 more
wiley   +1 more source

The Dutch neuromuscular database CRAMP (Computer Registry of All Myopathies and Polyneuropathies): development and preliminary data.

, 2007
Contains fulltext : 51646.pdf (Publisher’s version ) (Closed access)Each of the various neuromuscular diseases is rare. Consequently, solid epidemiological data are not available and it is often difficult to find sufficient patients for
Hoeven, J.H. van, Visser, L. H., van Veenendaal, H., Faber, C. G., van der Hoeven, J. H., Janssen, N.G., Schaik, I.N. van, Janssen, N. G., van Schaik, I. N., Verschuuren, J. J. G. M., Notermans, N. C., Engelen, B.G.M. van, Veenendaal, H. van, Doorn, P.A. van, Visser, L.H., van Engelen, B. G. M., Notermans, N.C., Faber, C.G., Verschuuren, J.J., van Doorn, P. A.   +19 more
core   +1 more source