Results 221 to 230 of about 8,114 (293)

When Rarity Hits Twice: Hemophagocytic Lymphohistiocytosis in Kabuki Syndrome, A Case Report from Palestine. [PDF]

Lilyan Jarrar, Raya Fuqha, Ahmad Wajdi Mashni, Mohammad O. Hamdan, Sameer Alomari, Mohammad Ataya, Yazan Abed, Laith Abed   +7 more
openalex   +1 more source

Applying an Ethical Lens to the Treatment of People With Multiple Sclerosis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT The practice of neurology requires an understanding of clinical ethics for decision‐making. In multiple sclerosis (MS) care, there are a wide range of ethical considerations that may arise. These involve shared decision‐making around selection of a disease‐modifying therapy (DMT), risks and benefits of well‐studied medications in comparison to
Methma Udawatta, Farrah J. Mateen
wiley   +1 more source

Rare birds in Croatia. Third report of the Croatian Rarities Committee

, 2013
Jelena Kralj, Sanja Barišić
openalex   +1 more source

A Double Rarity: Lost intravascular Catheter Guidewire in Persistent Left Superior Vena Cava and Coronary Sinus - A Case Report

Benjamin Palić, Marija Goluža Sesar, Kristina Galić, Gojko Bogdan, Zrinko Prskalo   +4 more
openalex   +2 more sources

Grossly carious mandibular first molar having supplemental root managed exodontically: A rarity reported

, 2019
Ashvini Kishor Vadane, Amit Sangle, Nashrah Sawant   +2 more
openalex   +2 more sources

Whole‐Body Pattern of Muscle Degeneration and Progression in Sarcoglycanopathies

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterize whole‐body intramuscular fat distribution pattern in patients with sarcoglycanopathies and explore correlations with disease severity, duration and age at onset. Methods Retrospective, cross‐sectional, multicentric study enrolling patients with variants in one of the four sarcoglycan genes who underwent whole‐body ...
Laura Costa‐Comellas, Mauro Monforte, Angel Sanchez‐Montañez, Penélope Romero‐Duque, Elena Pegoraro, Jordi Díaz‐Manera, Dmitry Vlodavets, Lorenzo Maggi, Marco Moscatelli, Adele D‘Amico, Montse Olivé, Jorge Alonso‐Pérez, Giacomo Comi, José Miguel Escudero‐Fernández, Gabriela S. Urcuyo, Anna Pichiecchio, Angela Berardinelli, Kristl G. Claeys, Claudio Bruno, Chiara Panicucci, Sara Bortolani, Eleonora Torchia, Enzo Ricci, Soledad Monges, Jorge A. Bevilacqua, Jorge Diaz‐Jara, Maggie C. Walter, Simone Thiele, Nicoline Løkken, John Vissing, Susana Quijano‐Roy, Robert Y. Carlier, Nicol C. Voermans, Chiara Marini‐Bettolo, Michela Guglieri, Volker Straub, Lea Leonardis, Francina Munell, David Gómez‐Andrés, Giorgio Tasca   +39 more
wiley   +1 more source

Homologation of bird rarities in Mallorca and Formentera. Report 1999 [PDF]

, 1999
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core  

Rare birds in Slovenia in 2019 – Slovenian Rarities Committee’s Report

Acrocephalus, 2020
Mitja Denac, Dejan Bordjan, Luka Božič, Jurij Hanžel, Milan Vogrin   +4 more
openaire   +1 more source

Rarity in Rare: Complicated Disseminated Tuberculosis: A Report of Two Case

Suman Sudha Routray
openalex   +1 more source

Characterization of Clinical Phenotype to Glial Fibrillary Acidic Protein Concentrations in Alexander Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To determine the concentration of glial fibrillary acidic protein (GFAP) in cerebrospinal fluid (CSF) and plasma in Alexander disease (AxD) and whether GFAP levels are predictive of disease phenotypes. Methods CSF and plasma were collected (longitudinally when available) from AxD participants and non‐AxD controls.
Amy T. Waldman, Asako Takanohashi, Joshua Y. Joung, Geraldine W. Liu, Kaley Arnold, Amy Pizzino, Walter Faig, Sarah Woidill, Sona Narula, Adeline L. Vanderver   +9 more
wiley   +1 more source