Results 271 to 280 of about 2,023,088 (340)

Employment of the Diagnostic Rhyme Test (Drt) With Normal-Hearing and Sensori-Neural Hearing-Impaired Listeners.

, 1972
Marie H. Olroyd
openalex   +2 more sources

Accelerated Bacterial Identification with MALDI-TOF MS Leads to Fewer Diagnostic Tests and Cost Savings. [PDF]

Antibiotics (Basel)
Uzuriaga M, Guillén-Grima F, Rua M, Leiva J, Yuste JR.   +4 more
europepmc   +1 more source

Comparison of three rapid diagnostic tests for Plasmodium falciparum diagnosis in Ghana. [PDF]

Malar J
Kayode TA, Addo AK, Addison TK, Tweneboah A, Afriyie SO, Abbas DA, Seth A, Badu-Tawiah AK, Badu K, Koepfli C.   +9 more
europepmc   +1 more source

Discontinuation of Immunotherapy in Patients With Relapsing Myelitis Without AQP4/MOG Antibodies

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT This study assesses the outcomes of immunotherapy discontinuation in patients with relapsing seronegative idiopathic myelitis (SIM), a condition that remains uninvestigated due to its rarity. We reviewed records from 77 patients with relapsing SIM at the National Cancer Center of Korea, focusing on 11 who discontinued treatment after a median ...
Ki Hoon Kim, You‐Ri Kang, Jae‐Won Hyun, Su‐Hyun Kim, Ho Jin Kim   +4 more
wiley   +1 more source

Other Diagnostic Tests for Young-Onset Type 2 Diabetes Mellitus. [PDF]

J ASEAN Fed Endocr Soc
Huamán-Chavarry K, Pacco-Valdivia J, Salvador-Carrillo A.   +2 more
europepmc   +1 more source

Validity and Reliability of Clinical and Patient‐Reported Outcomes in Multisystem Proteinopathy 1

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Valosin‐containing protein (VCP)‐associated multisystem proteinopathy 1 (MSP1) is caused by variants in the VCP gene. MSP1 results in various phenotypes including progressive myopathy, Paget's disease of bone, frontotemporal dementia, amyotrophic lateral sclerosis, and parkinsonism, among others.
Lindsay N. Alfano, Megan A. Iammarino, Natalie F. Reash, Linda P. Lowes, Lindsay Pietruszewski, Kathleen Adderley, Lauren Humphrey, Audrey B. Knight, Christopher L. Steiner, Melissa A. Smith, Zarife Sahenk, Anne M. Connolly, Momen Almomen, Eleonora S. D'Ambrosio, Nathan Peck, Allison Peck   +15 more
wiley   +1 more source

The Case of a 67‐Year‐Old Man With Memory Difficulties and Altered Sleep

Annals of Clinical and Translational Neurology, EarlyView.
Wesley Peng, Borna Bonakdarpour
wiley   +1 more source

Compound Heterozygous MRPS14 Variants Associated With Leigh Syndrome

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT MRPS14 (uS14m) is a nuclear‐encoded ribosomal protein important for mitochondria‐specific translation. To date, only a single individual with a recessive MRPS14‐related disorder (also known as COXPD38) has been reported. We report an additional subject possessing novel compound heterozygous MRPS14 variants (p.Asp37Asn, p.Asn60Asp). The subject
Maria Gabriela Otero, Christina Freeman, Ruchi Shah, Renkui Bai, Hong Cui, Marian Castro, Zachary Myers, Eric Choy, Derek Chan, Molly Easter, Sophia Y. Zhao, Madeline Babros, Ruchi Garg, Matthew Deardorff, Franklin Moser, Tyler Mark Pierson   +15 more
wiley   +1 more source

Operational evaluation of the deployment of Malaria/CRP Duo and Dengue Duo rapid diagnostic tests for the management of febrile illness by village malaria workers in rural Cambodia. [PDF]

BMC Infect Dis
Visser MT, Lek D, Adhikari B, Chandna A, Vanna M, Ol S, Bunreth V, Davoeung C, Sovann Y, Umans D, Lubell Y, Chew R, Maude RJ, van der Pluijm RW, Tripura R, Waithira N, Sovannaroth S, van Vugt M, von Seidlein L, Mukaka M, Dondorp A, Peto TJ, Callery JJ.   +22 more
europepmc   +1 more source