Results 61 to 70 of about 1,899 (180)

The management of neurogenic arthropathy: a tale of two Charcots [PDF]

Diabetes/Metabolism Research and Reviews, 1999
The pathogenesis and natural history of Charcot neuroarthropathy is often poorly understood. The diagnosis and treatment of Charcot feet can also prove difficult. Two case histories are used to illustrate the key points in the management of this potentially devastating condition.
openaire   +2 more sources

Imaging findings after meniscal repair with degradable polyurethane scaffold: preliminary results. [PDF]

, 2008
Purpose / Introduction: To date, there are no satisfactory solutions to the meniscal originated knee pain post meniscal tear repair. In this study a newly developed polyurethane material that has the intended properties of reducing pain and inducing ...
Huysse, WouterUZGent0019923020938010013388599785210779620000-0001-9847-158801368C42-F0EE-11E1-A9DE-61C894A0A6B4, Sundaram, M.editor, Verdonk, PeterUGent0019921587188010015717609781480314230077B650-F0EE-11E1-A9DE-61C894A0A6B4, Verdonk, RenéUGent801000260947972400350377F37E9FFE-F0ED-11E1-A9DE-61C894A0A6B4, Verstraete, KoenraadGE32UZGent0019791251508010007279610000-0003-3688-1076F46E35F0-F0ED-11E1-A9DE-61C894A0A6B4   +4 more
core   +2 more sources

Neurogenic arthropathy with subclinical inherited neuropathy: A case report.

Orthopedics & Traumatology, 1989
We report here a case demonstrating Charcot Joints at the lumber spine and ankle joints. The patient was a 27-year-old female, presenting the characteristic clinical and radiologic features of neurogenic arthropathy, but with no overt neurologic symptoms. In addition, she had a past history of fractures without pain, and her parents were consanguineous
Tetsuko Okuno, Akio Inoue, Masaaki Kawasaki   +2 more
openaire   +1 more source

Suspected Propofol-Related Infusion Syndrome After Lumbar Spinal Fusion With Total Intravenous Anesthesia: A Case Report [PDF]

, 2018
Propofol-related infusion syndrome (PRIS) is a welldocumented yet rare complication of prolonged infusions of propofol. It is characterized by a myriad of metabolic abnormalities, including cardiac arrhythmias, rhabdomyolysis, acute kidney injury ...
Paterson, Andrew J, Pedri, Tony G, Wharton, Matthew G   +2 more
core   +1 more source

Хирургическая коррекция деформации стопы при остеоартропатии Шарко [PDF]

, 2017
ДИАБЕТИЧЕСКАЯ СТОПА /ХИРОСТЕОАРТРОПАТИЯ ШАРКО /ХИРАРТРОПАТИЯ НЕВРОГЕННАЯСТОПЫ ДЕФОРМАЦИИТРОФИЧЕСКИЕ ЯЗВЫАРТРОДЕЗ СУСТАВОВОРТОПЕДИЧЕСКИЕ ПРОЦЕДУРЫХИРУРГИЧЕСКИЕ ОПЕРАЦИИ ВОССТАНОВИТЕЛЬНЫЕЦель.
Аничкин, В. В., Дмитриенко, А. А., Курек, М. Ф., Маканин, А. Я., Третьяков, А. А.   +4 more
core   +1 more source

The spine in Paget’s disease [PDF]

, 2007
Paget’s disease (PD) is a chronic metabolically active bone disease, characterized by a disturbance in bone modelling and remodelling due to an increase in osteoblastic and osteoclastic activity.
A Hadjipavlou, A Hadjipavlou, A Hadjipavlou, A Relea, A Saifuddin, A Souques, AG Hadjipavlou, AG Hadjipavlou, AG Hadjipavlou, AL Langston, B Maldague, B. J. Tins, BB Heerden Van, BC Berg Vande, BD Nguyen, BJ Tins, BS Epstein, C Cooper, C Marcelli, C. Dell’Atti, CW Hayes, D Rotes-Sala, DA Nicholson, DH Collins, DJ Harris, DL Douglas, DP Davis, E Wallace, ES Siris, ES Siris, F Schajowicz, G Lopez-Abente, G Schmorl, GJ Cook, H Rasmussen, HC Ochsner, HP Brown, HR Cundy, J Lamovec, JD Cody, JM Dennis, JM Mirra, JT Hartman, JW Milgram, L Herzberg, L Hocking, L Klenerman, LS Steinbach, M Castillo, M Sundaram, MA Rosen, MB Zlatkin, MF Basle, MH Schreiber, MJ Nellissery, MR Khairi, P Lander, P. N. M. Tyrrell, PB Guyer, PH Lander, PJ Meunier, PR Clarke, R Mawhinney, R. K. Lalam, RD Altman, RD Altman, RD Altman, RD Boutin, RL Merkow, S Danais, S Hepple, S Sprecher, SA Khan, SI Haslam, SS Siegelman, T Cundy, T Cundy, TP Staa Van, TS Graham, V. N. Cassar-Pullicino, WG Wyllie, WN Estrada   +81 more
core   +2 more sources

Knee Arthrodesis in Navajo Familial Neurogenic Arthropathy

JBJS Case Connector, 2013
Navajo familial neurogenic arthropathy (NFNA) is a rare form of hereditary sensory autonomic neuropathy found in the Navajo population. It usually becomes clinically apparent during the first two decades of life, with unrecognized fractures, Charcot joints as a result of sensory deficits to deep pain, hypohidrosis, and heat intolerance1.
Christina, Brady, Elizabeth A, Szalay
openaire   +3 more sources

Physical Therapy Management of a Patient with Residual Neurologic Deficits Following Lumbar Decompression Surgery [PDF]

, 2018
Background: The symptoms associated with lumbar spinal stenosis (LSS) can severely impact a person’s quality of life. Along with back pain, symptoms might include lower extremity numbness, tingling, pain, cramping, motor control deficits, and weakness ...
Kramer, Austin
core   +1 more source

Caso clínico: Brote agudo de Psoriasis en un infectado por el VIH Clinical case: severe attack of psoriasis in an HIV infected patient

Revista Española de Sanidad Penitenciaria, 2010
La Psoriasis, que parece no tener una mayor prevalencia en infectados por el VIH, sí que presenta en su evolución en estos casos diferencias significativas ligadas no solo a la inmunodepresión, sino también a la propia acción del virus sobre los factores
J.M. Sobrón
doaj  

Roots and fates of congenital insensitivity to pain and anhidrosis: a human phenotype [PDF]

Congenital insensitivity to pain is a rare neurological disorder characterized by the inability to perceive physical pain. Individuals with CIP lack the typical nociceptive responses to harmful stimuli, which poses significant challenges to their safety ...
D. R., Thanushree, George, Robin, K. S., Surabhi, R. K., Rosheni, S. H., Fiza   +4 more
core   +2 more sources