Results 81 to 90 of about 98,169 (325)

Cognitive reserve and AβI-42 in mild cognitive impairment (Argentina-Alzheimer’s disease neuroimaging initiative) [PDF]

, 2015
Background: The purpose of this study was to investigate the relationship between cognitive reserve and concentration of Aβ1-42 in the cerebrospinal fluid (CSF) of patients with mild cognitive impairment, those with Alzheimer’s disease, and in control ...
Allegri, Ricardo Francisco, Campos, Jorge, Chrem Mendez, Patricio Alexis, Clarens, María Florencia, Guinjoan, Salvador Martín, Harris, Paula, Martín, María Eugenia, Russo, María Julieta, Sevlever, Gustavo, Suarez, Marcos Fernandez, Surace, Ezequiel Ignacio, Tapajoz Pereira de Sampaio, Fernanda   +11 more
core   +2 more sources

Genotype‐guided cardiac device intervention in LMNA‐related cardiac conduction disorder: The need for timely genetic testing

European Journal of Heart Failure, EarlyView.
Sudden cardiac death is a catastrophic event, making its prevention important. However, patient selection for primary prevention remains controversial. We report two cases of cardiac conduction disorder initially treated with permanent pacemaker implantation.
Shunsuke Inoue, Zhehao Dai, Tsukasa Oshima, Seitaro Nomura, Takashi Hiruma, Ryo Abe, Kanna Fujita, Manami Katoh, Toshiyuki Ko, Yu Shimizu, Masamichi Ito, Kenichiro Yamagata, Junichi Ishida, Eisuke Amiya, Masaru Hatano, Norifumi Takeda, Hiroyuki Morita, Katsuhito Fujiu, Norihiko Takeda, Issei Komuro   +19 more
wiley   +1 more source

Erdheim-Chester Disease: Utility of 18F-FDG Positron Emission Tomography [PDF]

Journal of Clinical and Diagnostic Research, 2018
Erdheim-Chester Disease (ECD) is a rare non Langerhans cell histiocytosis of unknown origin with multiorgan involvement. We report a case of a man who presented to us with haematuria, asthenia, fever, nausea and malleolar oedema.
Angelina Cistaro, Maria Licari, Simone Margotti, Daniele Penna, Vincenzo Arena   +4 more
doaj   +1 more source

A rare case of appendicular skeleton localization in a patient with chronic lymphocytic leukemia successfully treated with salvage radiation therapy [PDF]

, 2017
Bone involvements in chronic lymphocytic leukemia (CLL) are considered rare events, and the English-language medical literature describes them only in sporadic case reports. Consequently, robust indications for a rational clinical management are lacking.
Al Sayyad, Said, Arico, Demetrio, Di Cristofano, Claudio, Marchione, Anna Maria, Petrozza, Vincenzo, Porta, Natale, Ronco, Francesca, Russi, Elvio Grazioso, Sceni, Giuseppe, Stelitano, Caterina, Tuscano, Carmelo, Versace, Paolo, Vincelli, Iolanda Donatella   +12 more
core   +1 more source

Sipple Syndrome: From Diagnosis to Management - A Case Report [PDF]

Middle East Journal of Cancer
Multiple endocrine neoplasia (MEN) is a rare inherited disease caused by multiple complex mutations in the RET gene. It is characterized by the occurrence of tumors involving more than two endocrine glands in the same patient.
Ruwaida Mira, Ranim Mira, Moftah Sherad, Mohamed Rohuma   +3 more
doaj   +1 more source

Shining stars in the sky on the gastric mucosa

Journal of General and Family Medicine, EarlyView.
We report a rare case of an elderly Japanese man diagnosed with sporadic gastric Burkitt lymphoma. Esophagogastroduodenoscopy showed nodular and ulcerated lesions in the lesser curvature of the stomach. Pathological analysis of showed that the gastric lesions are characterized by a diffuse and dense accumulation of dark atypical lymphocytes (night) and
Kosuke Minaga, Hajime Honjo, Tomohiro Watanabe, Masatoshi Kudo   +3 more
wiley   +1 more source

Diagnostic role and prognostic impact of positron emission tomography/computed tomography in patients treated for uterine corpus cancer [PDF]

Srpski Arhiv za Celokupno Lekarstvo
Introduction/Objective. The goal of our research was to evaluate diagnostic and prognostic role of positron emission tomography/computed tomography (PET-CT) in patients previously treated for uterine cancer and compare it to conventional imaging methods (
Stojiljković Milica, Šobić-Šaranović Dragana, Odalović Strahinja, Petrović Jelena, Popović-Krneta Marina, Veljković Miloš, Ranković Nevena, Artiko Vera   +7 more
doaj   +1 more source

Intrapancreatic accessory spleen false positive to 68Ga-Dotatoc: case report and literature review [PDF]

, 2019
Background: Intrapancreatic accessory spleen (IPAS) is an uncommon finding of pancreatic mass. Differential diagnosis with pancreatic tumor, especially with non-functional neuroendocrine tumor (NF-NET), may be very hard and sometimes it entails ...
Bellato, V., Caronna, R., Cerasari, S., Chirletti, P., Ciardi, A., Cicconi, S., Feola, T., Lancellotti, F., Muttillo, E. M., Sacco, L.   +9 more
core   +1 more source

Clinical Images: Penetrating aortic ulceration as an initial presentation of Erdheim‐Chester disease

Arthritis &Rheumatology, EarlyView.
Jerome Razanamahery, Bernard Bonnotte
wiley   +1 more source

Prognostic Impact of Unplanned Total Pancreatectomy in Pancreatic Ductal Adenocarcinoma: A Retrospective Analysis

Journal of Hepato-Biliary-Pancreatic Sciences, EarlyView.
ABSTRACT Background This study evaluated the clinical significance of an unplanned total pancreatectomy (TP) by comparing surgical outcomes of planned and unplanned TP for pancreatic ductal adenocarcinoma (PDAC). Methods Forty‐two patients who underwent TP for PDAC between 2009 and 2020 at the Kindai University Hospital were retrospectively analyzed ...
Dongha Lee, Keiko Kamei, Chihoko Nobori, Yuta Yoshida, Takaaki Murase, Atsushi Takebe, Takuya Nakai, Mamoru Takenaka, Takaaki Chikugo, Ippei Matsumoto   +9 more
wiley   +1 more source