Results 81 to 90 of about 2,465 (212)

S2k guideline: Diagnosis and therapy of localized scleroderma

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 4, Page 605-620, April 2024.
Summary The updated S2k guideline deals with the diagnosis and therapy of localized scleroderma (LoS). LoS represents a spectrum of sclerotic skin diseases in which, depending on the subtype and localisation, structures such as adipose tissue, muscles, joints, and bones may also be affected.
Alexander Kreuter, Pia Moinzadeh, Maria Kinberger, Gerd Horneff, Margitta Worm, Ricardo N. Werner, Andreas Hammacher, Thomas Krieg, Jörg Wenzel, Michael Oeschger, Lisa Weibel, Robert Müllegger, Nicolas Hunzelmann   +12 more
wiley   +1 more source

Consensus Paper: Radiological Biomarkers of Cerebellar Diseases [PDF]

, 2015
Hereditary and sporadic cerebellar ataxias represent a vast and still growing group of diseases whose diagnosis and differentiation cannot only rely on clinical evaluation.
A D’Abreu, A Ginestroni, A Ieraci, A Inagaki, A Kelp, A Nocuń, A Poretti, A Poretti, A Rolfs, A Solodkin, A Varrone, AC Stanfield, AG Asokan, AJ Barkovitch, AJ Clapp, Alessandra Vella, Allison Jack, AM Tadesco, AM Wong, Andrea P. Jackowski, Andrea Righini, AR Luft, AR Luft, B Kuemerle, B Soong, BC Jung, C Andrés De, C Cheung, C Garel, C Good, C Jacova, C Limperopoulos, C Lukas, C Moller, C Parazzini, C Scaglione, CC Parker, Cecilia Parazzini, CH Lyoo, Christophe Habas, CJ Stoodley, CW Yoon, D Beitzke, DJG Schutter, DL Vargas, DS Woodruff-Park, E Apartis, E Canu, E Courchesne, E Matsusue, E Matsusue, E Pagani, E Prodi, ED Vidoni, F Brancati, F D’Agata, F Eichler, G Malinger, G Tedeschi, GS Young, H Akhlaghi, H Akhlaghi, H Jacobi, HB Cleavinger, I Ferrer, I Iltis, I Sousa, ID Wilkinson, J Honnorat, J Mazere, J Skefos, J Wegiel, JA Brunberg, JB Schulz, JL Whitwell, JM Kim, Jörg B. Schulz, K Andersen, K Brockmann, K Burk, K Burk, K Ishii, K Lasek, K Nanri, K Nanri, K Pierce, K Reetz, K Reetz, K Reetz, K Reetz, K Specht, K-D Choi, Kathrin Reetz, KB Loh, L Baldaçara, L Ji, L Schols, LA Corben, Leonardo Baldarçara, LI Wallis, LR Ramos, LSK Hokkanen, M Abele, M Anheim, M Bricout, M Catani, M Hadjivassiliou, M Hadjivassiliou, M Hadjivassiliou, M Hadjivassiliou, M Hadjivassiliou, M Mascalchi, M Minnerop, M Rapoport, M Sjobeck, M Verly, M Walterfang, M Walterfang, M. Hadjivassiliou, MA Cheh, Mario Mascalchi, MC Bianchi, ME Steenweg, MR Hatab, N Boddaert, N Gharani, N Kimura, N Kimura, N Kimura, N Ramnani, N Stefano De, Nigel Hoggard, O Bas, OS Cohen, P Braga-Neto, P Brown, P Wang, PA Thomann, PS Wang, R Cabeza, R Della Nave, R Della Nave, R Hashimoto, R Scheid, R Sui, S Alcauter, S Basu, S Currie, S Currie, S Currie, S Currie, S Dohlinger, S Gilman, S Gilman, S Nagamitsu, S Ortega-Cuberoa, S Tanaka, SA Cooper, Sara Jane Webb, SH Fatemi, SH Fatemi, SH Fatemi, SH Fatemi, SJ Webb, SM Boesch, SM Ravizza, Stuart Currie, T Klockgether, T Tarui, T Wu, TD Miller, W Scharmüller, WR Kates, Y Bruecker De, Y Daaboul, Y Hosoi, Y Sunaga   +176 more
core   +1 more source

Dyke-Davidoff-Masson syndrome in an 8-year-old child: Report of a case

Radiology Case Reports
Dyke-Davidoff-Masson syndrome (DDMS) is a rare entity. Few cases have been described in the literature. It can be symptomatic or asymptomatic. The clinical signs are very varied. Imaging is the key to diagnosis.
Nourrelhouda Bahlouli, Fatima Chait, Khadija Laasri, Yahya El Harras, Nazik Allali, Latifa Chat, Siham El Haddad   +6 more
doaj   +1 more source

Localised Unilateral Facial Hemiatrophy

Indian Journal of Dermatology, 2002
A very rare case of localized unilateral facial hemiatrophy is being presented here.
Gangopadhyay Asok, Bandyopadhyay Paritosh   +1 more
doaj  

Adult Presentation of Dyke Davidoff Masson Syndrome With Schizoaffective Disorder — A Case Report

Kerala Journal of Psychiatry, 2018
Dyke Davidoff Masson syndrome (DDMS) is a rare disease with characteristic radiological features, seizures, mental retardation, facial asymmetry, and psychiatric manifestations. Here, we report a case of a 50-year-old female who had a refractory seizure
MK Dinesh Kumar, Denver Steven Pinto
doaj   +1 more source

Presurgical evaluation and surgical treatment of medically refractory epilepsy [PDF]

, 2018
Thanks to today's modern imaging examination techniques and especially to the common use of intracranial electrodes for localizing seizure foci, more and more patients with partial epilepsy can be treated microsurgically.
Siegel, Adrian
core  

Coexistence of Parry-Romberg syndrome with homolateral segmental vitiligo [PDF]

, 2013
Parry-Romberg syndrome or progressive facial hemiatrophy was first described by Caleb Parry in 1825 and Moritz Romberg in 1846. This disorder is characterized by slowly progressing acquired unilateral hemifacial atrophy, which affects subcutaneous ...
Janowska, Marta, Lipko-Godlewska, Sylwia, Podolec, Katarzyna, Wojas-Pelc, Anna   +3 more
core   +2 more sources

Advances in the Medical and Surgical Management of Intractable Partial Complex Seizures [PDF]

, 1974
Seizures can be due to a variety of acute, subacute, or chronic diseases with different etiologies. Clinically, they may manifest as focal or generalized phenomena.
Hooshmand, Hooshang
core   +1 more source

Progressive facial hemiatrophy - A case series

Indian Journal of Dermatology, 2011
Six female patients diagnosed with Progressive Facial Hemiatrophy are presented here. The clinical and serological features are highlighted, and treatment options for the condition are discussed.
Feroze Kaliyadan, Kaberi Biswas, A D Dharmaratnam   +2 more
doaj   +1 more source

Pyogenic Granuloma in a Patient of Sturge-Weber Syndrome with Bilateral Port Wine Stain- A Rare Case Report [PDF]

, 2014
Sturge-Weber syndrome (SWS) also known as encephalotrigeminal angiomatosis. It is a neurocutaneous syndrome, characterized by a facial vascular birthmark and neurological abnormalities.
Mamata G. P, Rajeshwari G. Annigeri, Shakuntala G. K., Shantala Arunkumar   +3 more
core   +1 more source