Results 251 to 260 of about 16,288,597 (342)

Diagnostic Challenge in Frontal Variant Alzheimer's Disease With Low Amyloid‐β PET Retention

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Diagnosing frontal variant Alzheimer's disease (fvAD) is difficult and could be even more difficult when amyloid‐beta (Aβ) PET retention is low. A 63‐year‐old woman presenting with a 3‐year history of apathy and memory impairment showed executive dysfunction, memory impairment, and severe bilateral frontotemporal atrophy on MRI.
Ryosuke Shimasaki, Masanori Kurihara, Kenji Ishibashi, Aya Midori Tokumaru, Kenji Ishii, Atsushi Iwata   +5 more
wiley   +1 more source

Prevalence of pfhrp2/pfhrp3 gene deletions among patients with Plasmodium falciparum malaria with false-negative in the HRP2-based rapid diagnostic test in Colombia. [PDF]

Mem Inst Oswaldo Cruz
Olivera MJ, Guerra AP, Cortés LJ, Suárez-Jurado AG, Ade MP, Cárdenas IM.   +5 more
europepmc   +1 more source

Methods for LR(k) Testing: (Informative Diagnostics on LALR(k)-Conflicts)

, 1979
Bent Bruun Kristensen, Ole Lehrmann Madsen   +1 more
openalex   +2 more sources

Performance of the Large Language Models in African rheumatology: a diagnostic test accuracy study of ChatGPT-4, Gemini, Copilot, and Claude artificial intelligence. [PDF]

BMC Rheumatol
Bayala YLT, Zabsonré/Tiendrebeogo WJS, Ouedraogo DD, Kaboré F, Sougué C, Yameogo AR, Nacanabo WM, Tinni IA, Ouedraogo A, Zongo YE.   +9 more
europepmc   +1 more source

The Minnesota Percepto‐Diagnostic Test

, 1963

openalex   +1 more source

DIAGNOSTIC PROCEDURE FOR THE EVALUATION OF STRAIN DATA FROM A LINEAR ELASTIC TEST.

, 1972
W. G. Dodge, Jack Smith
openalex   +2 more sources

Spinal Cord Abnormalities in Early Pediatric Multiple Sclerosis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Spinal cord lesions and atrophy in the cervical region are common in adult multiple sclerosis (MS) and correlate with disability. Whether similar abnormalities occur in pediatric MS patients is largely unknown. Clinical and MRI evaluations were performed in 38 pediatric MS patients and 13 healthy controls (HC).
Monica Margoni, Paola Valsasina, Paolo Preziosa, Martina Rubin, Mor Gueye, Lucia Moiola, Maria Assunta Rocca, Massimo Filippi   +7 more
wiley   +1 more source

Diagnostic serum precipitin test in pulmonary aspergillosis; fundamental and clinical studies

, 1972
Takeshi Mori
openalex   +2 more sources

HPDL Variant Type Correlates With Clinical Disease Onset and Severity

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Recently, a mitochondrial encephalopathy due to biallelic HPDL variants was described, associated with a broad range of clinical manifestations ranging from severe, infantile‐onset neurodegeneration to adolescence‐onset hereditary spastic paraplegia. HPDL converts 4‐hydroxyphenylpyruvate acid (4‐HPPA) into 4‐hydroxymandelate (4‐HMA),
Eun Hye Lee, Olivia Kim‐Mcmanus, Jennifer H. Yang, Richard Haas, Maha S. Zaki, Ghada M. H. Abdel‐Salam, Yuji Nakamura, Mohamed S. Abdel‐Hamind, Darius Ebrahimi‐Fakhari, Julian E. Alecu, Nicola Brunetti‐Pierri, Varunvenkat M. Srinivasan, Vykuntaraju K. Gowda, Stephanie Gross, Yasemin Alanay, Paria Najarzadeh Totbati, Manya Yadavilli, Liana Friedman, Naomi Meave Ojeda, Joseph G. Gleeson   +19 more
wiley   +1 more source