Results 101 to 110 of about 368,835 (244)

[Drug therapy for corneo-conjunctival neoplasm].

Farmacia hospitalaria : organo oficial de expresion cientifica de la Sociedad Espanola de Farmacia Hospitalaria, 2005
The goal of therapy for corneo-conjunctival neoplasm is lesion removal, with the most widespread procedure being complete tumor resection with or without associated chemotherapy lines. As this sort of procedure entails a high relapse rate (9-52%) the use of adjuvant therapies to reduce the occurence of relapse becomes a need.
A, Murcia López, J, Borrás Blasco, M C, Alvarado Valero, A, Navarro Ruiz, M, González Delgado, J J, Martínez Toldos   +5 more
openaire   +1 more source

Prognosis and determinants of survival after orbital exenteration for conjunctival melanoma: Experiences from a Dutch Referral Centre

Acta Ophthalmologica, Volume 104, Issue 1, Page e95-e103, February 2026.
Abstract Purpose To assess the prognosis and determinants of survival after orbital exenteration in patients with conjunctival melanoma (CoM). Methods In a retrospective study, 27 consecutive patients who underwent exenteration for CoM from 2001 to 2023 were included.
David Chetroiu, Niels J. Brouwer, Marina Marinkovic, Gregorius P. M. Luyten, Jaco C. Bleeker, Robert M. Verdijk, T. H. Khanh Vu, Stijn W. van der Meeren   +7 more
wiley   +1 more source

Skin manifestations of Bartonella infections. [PDF]

, 2002
peer ...
Arrese Estrada, Jorge, Chian, Cesar A, Pierard, Gérald   +2 more
core   +1 more source

Exploring tear fluid biomarkers and the ocular surface in thyroid eye disease

Acta Ophthalmologica, Volume 104, Issue 1, Page e28-e38, February 2026.
Abstract Purpose To examine ocular surface changes and inflammatory tear fluid biomarkers in patients with thyroid eye disease (TED). Methods We included 106 Graves' disease (GD) patients (36 without TED, 32 with active and 38 with inactive TED) and 106 age‐ and sex‐matched healthy subjects for ophthalmological evaluation, including ocular surface ...
Mikael Thomassen Neset, Roy Miodini Nilsen, Kristian Løvås, Kathrine Halsøy, Håkon Reikvam, Ann‐Elin Meling Stokland, Grethe Åstrøm Ueland, Anette S. B. Wolff, Hans Christian D. Aass, Sjur Reppe, Eystein Sverre Husebye, Eyvind Rødahl, Tor Paaske Utheim, Hans Olav Ueland   +13 more
wiley   +1 more source

Neurological symptoms and natural course of xeroderma pigmentosum [PDF]

, 2008
We have prospectively followed 16 Finnish xeroderma pigmentosum (XP) patients for up to 23 years. Seven patients were assigned by complementation analysis to the group XP-A, two patients to the XP-C group and one patient to the XP-G group.
Anttinen, Anu, Arlett, Colin F, Erkinjuntti,, Matti, Green, Michael H L, Jaspers, Nicolaas G J, Koulu, Leena, Kurki, Timo, Lehmann, Alan R, Marttila, Reijo J, Nikoskelainen, Eeva, Portin,, Raija, Raams, Anja, Wing, Jonathan F   +12 more
core   +3 more sources

WHO classification of skin tumours: key updates in the fifth edition

Histopathology, Volume 88, Issue 3, Page 555-568, February 2026.
This review article summarizes the key updates in the 5th edition of the WHO Classification of Skin Tumours. It provides an overview of the major changes and new entities specific to the skin section, covering areas such as epidermal, melanocytic, mesenchymal and other tumours. The 5th edition of the World Health Organization Classification of Tumours (
Gabrielle Goldman‐Lévy, Raymond Barnhill, Boris C. Bastian, Werner Kempf, David Elder, Pedram Gerami, Wayne Grayson, Dmitry Kazakov, Daniela Massi, Jane Messina, Arnaud de la Fouchardière, Alexander J. Lazar, Thomas Brenn, Brian Rous, Andrew Field, Anthony Gill, Jennelle C. Hodge, Joseph D Khoury, Katia Leite, Shahin Sayed, Puay Hoon Tan, Rosalie Elenitsas, Eduardo Calonje, Lyn M. Duncan, Liang Zhiyong, Holger Moch, Rajendra Singh, Harshima Wijesinghe, Ian Cree, Dilani Lokuhetty   +29 more
wiley   +1 more source

Mediastinal neuroblastoma causing Horner's syndrome in a 7-year-old child: a case report

Journal of Pediatric Surgery Case Reports
Introduction: Peripheral neuroblastic tumors comprise a spectrum of neoplasms (neuroblastoma, ganglioneuroblastoma, ganglioneuroma) that primarily arise from the sympathoadrenal lineage and can cause variety of symptoms.
Alicija Šavareikaitė, Paulius Valatka
doaj   +1 more source

Organoid nevus syndrome: case report [PDF]

, 2001
The authors present a case of a child with organoid nevus syndrome, characterized by epibulbar choristoma in the right eye, Jadassohn's nevus sebaceous in the scalp and arachnoid cist.
Ballalai, Priscilla Luppi, Hirashima, Denise Emiko, Lowen, Marcia Serva, Pólvora, Rafael Piuma, Rigueiro, Moacyr Pezati   +4 more
core   +2 more sources

Comorbidities in People With Intellectual Disability With and Without Schizophrenia and Schizophrenia Without Intellectual Disability: A Swedish Register Study (IDcare)

Journal of Intellectual Disability Research, Volume 70, Issue 2, Page 206-217, February 2026.
ABSTRACT Background Intellectual disability (ID) and schizophrenia are known to separately carry a high risk of comorbidity of mental health and physical conditions. However, the prevalence and risk of comorbidities among people diagnosed with concurrent ID and schizophrenia have to date not been studied.
Trine Lise Bakken, Anna Axmon, Magnus Sandberg   +2 more
wiley   +1 more source

Meibomian Epithelioma of the Lower Eyelid in a Thoroughbred Horse [PDF]

, 2013
A 9-year old, castrated male, thoroughbred horse presented for a left lower eyelid mass with ocular signs of mucopurulent discharge, conjunctival hyperemia and ocular discomfort. On physical examination, there was no other abnormality.
Seong-Kyoon Choi1§, Jin-Kyu Park1§, Won Bae Jeon, Kyung-Hyun Lee2 and Gil-Jae Cho*
core