Results 231 to 240 of about 25,413,134 (267)

The Role of Calcitonin Gene‐Related Peptide in High‐Altitude Headache: A Prospective Field Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective High‐altitude headache (HAH) is a common neurological condition associated with rapid ascent to high altitude. The pathophysiological mechanisms underlying HAH remain incompletely understood. Calcitonin gene‐related peptide (CGRP), a neuropeptide implicated in migraine pathophysiology, may play a key role in the pathophysiology of ...
Roman Schniepp, Ludwig Karrasch, Helena Breitenstein, Andreas Straube, Katharina Kamm   +4 more
wiley   +1 more source

Prevalence, Patterns, and Factors Associated with Hearing Impairment Among Children and Adolescents with Sickle Cell Disease in Eastern Uganda: A Cross-Sectional Study. [PDF]

Int J Gen Med
Adoch CO, Otto J, Amone D, Abeso J, Malaika N, Achiro K, Chebet M, Katuramu R, Hakizimana T, Pitua I, Otto KA, Abwola MO, Okejomoe AO.   +12 more
europepmc   +1 more source

GAD65 Antibody ELISA With Extended Reportable Range: Validation and Guidance for Neurological Practice

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To (1) validate GAD65‐ELISA detection and quantification for type 1 diabetes mellitus and autoimmune neurological diagnoses, (2) correlate ELISA results (reference range < 5 IU/mL) with established radioimmunoprecipitation assay (RIA; ≤ 0.02 nmol/L), and (3) define ELISA clinical utility and pitfalls.
Andrew McKeon, Dana Olofson, Diana Anissian, Divyanshu Dubey, Eoin P. Flanagan, Max C. Herman, Sarosh R. Irani, Daniel H. Lachance, Maria A. Willrich, Sean Pittock, John R. Mills, Anastasia Zekeridou   +11 more
wiley   +1 more source

Knowledge and awareness of insulin resistance among social media users: A cross-sectional study in Jordan. [PDF]

J Educ Health Promot
Saadeh NA, Alshogran OY, Allan A, Alsheqerat H, Amoorah J, Hasan S.   +5 more
europepmc   +1 more source

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu, Xin Duan, Fatemeh Peymani, Jia Wang, Chengjia Bao, Chaolong Xu, Ying Zou, Zixuan Zhang, Yunxi Zhang, Tongyue Li, Martin Pavlov, Junling Wang, Minhan Song, Tianyu Song, Xiaodi Han, Mingxi Sun, Danmin Shen, Ruoyu Duan, Huafang Jiang, Manting Xu, Holger Prokisch, Fang Fang   +21 more
wiley   +1 more source

Isolated Congenital Ossicular Chain Anomalies. [PDF]

Cureus
Obara N, Okuda H, Nagase N, Ikeda R, Ogawa T.   +4 more
europepmc   +1 more source

Plasma metabolomics in infancy reveals early signatures of a stringently-defined otitis-prone phenotype. [PDF]

Pediatr Allergy Immunol
Prince N, Chen J, Kaur R, Syphurs C, Hoch A, Angelidou A, McEnaney K, Chawes B, Bæk O, Wang T, Brustad N, Levy O, Diray-Arce J, Pichichero M, Lasky-Su JA, IDEaL Consortium.   +15 more
europepmc   +1 more source

Consensus-based clinical and research recommendations for use of glucagon-like peptide-1 receptor agonists in the context of eating disorders: a modified Delphi study. [PDF]

World Psychiatry
Keshen A, Koning E, Allison KC, Amaro A, Bartel S, Belliveau P, Boniferro L, Brar S, Butalia S, Bulik CM, Chao AM, Couturier J, Dennis K, Dixon L, El-Ziftawi D, Gao C, Gamberg S, Goldstone AP, Dalle Grave R, Guerdjikova AI, Halliday TM, Hahn M, Harris A, Himmerich H, Horton WB, Jericho M, Langman B, Lightbody A, Klein DA, Mayer LES, McElroy SL, Mindrum M, Peiper NC, Price C, Raffoul A, Richards J, Schaefer LM, Steinglass J, Taylor VH, Tchang BG, Trappenberg N, Walsh BT, Weintraub MA, White A, Wnuk S.   +44 more
europepmc   +1 more source