Results 261 to 270 of about 4,987,259 (403)

Image Synthesis in Nuclear Medicine Imaging with Deep Learning: A Review. [PDF]

Sensors (Basel)
Le TD, Shitiri NC, Jung SH, Kwon SY, Lee C.   +4 more
europepmc   +1 more source

RADIATION DOSES OF A FINGER FROM TECHNICS IN NUCLEAR MEDICINE : (A) In Vitro Test : (B) In Vivo Test

, 1980
Tadakazu Fujii, Shuji Nobezawa, Tamotsu Osawa, Toshihiko Kanno, YUKITAMI EGUCHI, Umeo Shirasawa, Nobuaki Yamamura   +6 more
openalex   +2 more sources

Nuclei‐Specific Amygdala Enlargement Is Linked to Psychiatric Comorbidities in Drug‐Resistant Focal Epilepsy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Amygdala enlargement has been the subject of controversial studies regarding its significance in terms of pathogenicity both in epilepsy and in psychiatric comorbidities such as anxiety, depression, and post‐traumatic stress disorder.
Hélène Mourre, Julia Makhalova, Lisa Soncin, Elodie Garnier, Hugo Dary, Arnaud Le Troter, Roy A. M. Haast, Benoit Testud, Marie Arthuis, Samuel Medina Villalon, Stanislas Lagarde, Francesca Pizzo, Christian Bénar, Jean‐Philippe Ranjeva, Maxime Guye, Fabrice Bartolomei   +15 more
wiley   +1 more source

Reconstruction techniques in nuclear medicine time-of-flight PET [PDF]

, 2010
Vandenberghe, Stefaan
core   +1 more source

Editorial: Nuclear medicine advances through artificial intelligence and intelligent informatics. [PDF]

Front Nucl Med
Duff LM, Shi K, Tsoumpas C.
europepmc   +1 more source

Nuclear medicine technology progress report for quarter ending December 31, 1980

, 1981
F. F. Knapp
openalex   +2 more sources

Translating Muscle RNAseq Into the Clinic for the Diagnosis of Muscle Diseases

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Approximately half of patients with hereditary myopathies remain without a definitive genetic diagnosis after DNA next‐generation sequencing (NGS). Here, we implemented transcriptome analysis of muscle biopsies as a complementary diagnostic tool for patients with muscle disease but no definitive genetic diagnosis after exome ...
Alba Segarra‐Casas, Cristina Domínguez‐González, Daniel Natera‐de Benito, Solange Kapetanovic, Aurelio Hernández‐Laín, Berta Estévez‐Arias, Laura Llansó, Carlos Ortez, Cristina Jou, Itxaso Martí‐Carrera, Arístides López‐Márquez, Maria José Rodríguez, Laura González‐Mera, Velina Nedkova, Roberto Fernández‐Torrón, Benjamín Rodríguez‐Santiago, Cecília Jimenez‐Mallebrera, Raul Juntas‐Morales, Adolfo López‐de Munain, Jordi Surrallés, Andrés Nascimento, Eduard Gallardo, Montse Olivé, Pia Gallano, Lidia González‐Quereda   +24 more
wiley   +1 more source

Interpretation and implementation of adult diagnostic reference levels in nuclear medicine and PET in the UK. [PDF]

Nucl Med Commun
Fraser L, Parkar N, Powell A, Richardson M.   +3 more
europepmc   +1 more source

Pathway Analyses of Inherited Neuropathies Identify Putative Common Mechanisms of Axon Degeneration

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Inherited neuropathies (IN) are associated with over 100 different genetic mutations presenting with a variety of phenotypes. This complexity suggests multiple pathways may converge onto a limited number of downstream pathways to effect axonal injury.
Christopher R. Cashman, Craig Blackstone, Reza Sadjadi   +2 more
wiley   +1 more source

Editorial: Theranostics as a driving force in nuclear medicine. [PDF]

Front Oncol
Rowe SP, Werner RA, Ray Banerjee S.
europepmc   +1 more source