Results 111 to 120 of about 8,580 (194)

The Lupus Damage Index Revision Program: Results From the Item Generation and Reduction Phases

open access: yesArthritis Care &Research, Volume 78, Issue 10, Page 1449-1466, October 2026.
Objective A data‐driven and expert/patient consensus‐based project to develop a revised Systemic Lupus International Collaborating Clinics (SLICC)/American College of Rheumatology (ACR) Damage Index (SDI) is under way supported by SLICC, ACR, and the Lupus Foundation of America. Our objective is to report the item generation and reduction phase results
Burak Kundakci   +25 more
wiley   +1 more source

Histidine Supplementation Stabilizes Hearing and Vision and Improves Growth in HARS1‐Related Autosomal Recessive Disorder Associated With Usher‐Like Symptoms

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2289-2308, October 2026.
ABSTRACT Autosomal recessive HARS1‐related disorder (originally described as Usher syndrome type 3B) caused by a homozygous Y454S variant in the histidyl‐tRNA synthetase gene (HARS1) is characterized by progressive sensorineural hearing and vision loss and respiratory deterioration with risk for sudden death following febrile illnesses.
Victoria Mok Siu   +23 more
wiley   +1 more source

Oral diazoxide versus placebo for severe or recurrent neonatal hypoglycaemia: Neonatal Glucose Care Optimisation (NeoGluCO) study - a randomised controlled trial. [PDF]

open access: yesBMJ Open, 2022
Laing D   +11 more
europepmc   +1 more source

Cholestatic Liver Failure and Hypoglycemia in a Newborn: A Mitochondrial Pathology due to Citrin Deficiency

open access: yesClinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT In an infant with cholestasis and recurrent hypoglycemia, the combination of hypercitrullinemia, hypermethioninemia, and hyperthreoninemia should prompt testing for citrin deficiency, because early metabolic and genetic diagnosis allows targeted nutritional treatment and rapid clinical improvement.
Julien Neveu   +4 more
wiley   +1 more source

Strategies to improve neurodevelopmental outcomes in babies at risk of neonatal hypoglycaemia. [PDF]

open access: yesLancet Child Adolesc Health, 2021
Alsweiler JM   +3 more
europepmc   +1 more source

Tritrophic Interactions and Parasitoid Community Structure of Gall‐Inducing Herbivores in Arid Desert Ecosystems of Northern Xinjiang, China

open access: yesEcology and Evolution, Volume 16, Issue 10, October 2026.
This study systematically elucidates the complex tritrophic networks among the keystone shrub Lycium ruthenicum, three gall‐inducing pests, and 13 associated parasitoid species in the arid desert ecosystems of northern Xinjiang, China, reporting the globally novel stem gall‐inducing behavior of Scrobipalpa erichiodes.
Gaopeng Yu   +3 more
wiley   +1 more source

Predictors for intrapartum cesarean delivery after labor induction for suspected fetal growth restriction at term

open access: yesInternational Journal of Gynecology &Obstetrics, Volume 175, Issue 1, Page 249-256, October 2026.
Abstract Objective In term pregnancies with suspected fetal growth restriction (FGR) undergoing induction of labor (IOL), predictors for intrapartum cesarean delivery (CD) remain unclear. We aimed to determine predictors for intrapartum CD in this population. Methods This study included a retrospective cohort of singleton pregnancies undergoing IOL at ≥
Matan Anteby   +8 more
wiley   +1 more source

Newborn Screening of Primary Carnitine Deficiency and Prenatal Genetic Diagnosis for a Recurrence‐Risk Family

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 10, October 2026.
We performed large‐scale newborn screening for primary carnitine deficiency (PCD) using tandem mass spectrometry and genetic testing. We determined the local prevalence of PCD and the hotspot variant. Genetic testing was successfully applied for prenatal diagnosis in a recurrence‐risk family.
Huilin Sun   +8 more
wiley   +1 more source

Outcome of neonatal hypoglycaemia [PDF]

open access: yesBMJ, 1999
M. Cornblath   +3 more
openaire   +2 more sources

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