Results 251 to 260 of about 2,696,735 (308)

Two distinct growth patterns of preterm infants from birth to 18 months of corrected gestational age: a retrospective cohort study. [PDF]

Transl Pediatr
Wang J, Shang G, He M, Huang Y, Zhang J, Wu F.   +5 more
europepmc   +1 more source

Super‐Refractory Status Epilepticus (SRSE) in a Patient With Compound Heterozygous OPA1 Variants: Case Report and Literature Review

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Super‐Refractory Status Epilepticus (SRSE) is a rare, life‐threatening neurological emergency with unclear etiology in many cases. Mitochondrial dysfunction, often due to disease‐causing genetic variants, is increasingly recognized as a cause, with each gene producing distinct pathophysiological mechanisms.
Pouria Mohammadi, Lara Basovic, Christopher Michael McGraw   +2 more
wiley   +1 more source

Associations between parental history of dementia and plasma markers of inflammation in a multi-ethnic middle-aged community of adults. [PDF]

Alzheimers Dement
Winford ED, Huber BD, Seblova D, Pyne J, Avila-Rieger JF, Turney IC, Mazen JA, Brickman AM, Manly JJ.   +8 more
europepmc   +1 more source

Immune‐Driven Expression in Inclusion Body Myositis With T‐Cell Large Granular Lymphocytic Leukemia

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives T‐cell large granular lymphocytic leukemia (T‐LGLL), reported in up to 58% of inclusion body myositis (IBM) patients, is a rare leukemia of cytotoxic or less commonly helper T cells. The range of myopathies in T‐LGLL and the impact of coexisting T‐LGLL in IBM are not well understood. Our objectives are to investigate the spectrum of
Pannathat Soontrapa, Iago Pinal‐Fernandez, Pritikanta Paul, Michael P. Skolka, Margherita Milone, Min Shi, Mithun V. Shah, Maria Casal‐Dominguez, Katherine Pak, Andrew L. Mammen, Teerin Liewluck   +10 more
wiley   +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

The role of large language models in the diagnosis and management of obstetric patients: a pilot feasibility study using simulated obstetric cases. [PDF]

Arch Gynecol Obstet
Psilopatis I, Redling K, Filippi V, Kappos S, Emons J, Mosimann B, Zwimpfer TA.   +6 more
europepmc   +1 more source

Development of machine learning models for early prediction of small for-gestational-age births using maternal sociodemographic and obstetric data. [PDF]

BMC Pregnancy Childbirth
Bütün Z, Salik EA, Kaya Y, Çelik Ö, Tahta T.   +4 more
europepmc   +1 more source

Adiposity, Fat-Free Mass Index, and Muscular Strength in Children: Independent Effects on Functional Performance in a Tertiary Pediatric Endocrinology Cohort. [PDF]

Medicina (Kaunas)
Pascu BM, Cula AM, Bălănescu A, Bălănescu PC, Gherghina I.   +4 more
europepmc   +1 more source

Receptive-Expressive Language Phenotypes in Infants and Toddlers With Autism Features. [PDF]

Autism Res
Cohenour T, Gulsrud A, Kasari C.
europepmc   +1 more source