Results 141 to 150 of about 214,123 (285)

Prenatal opioid exposure, and health, social and educational outcomes for school‐aged children: A systematic review

open access: yesAddiction, Volume 121, Issue 10, Page 2633-2645, October 2026.
Abstract Background and aims Recent decades have seen a rise in the number of pregnancies exposed to opioids. Whilst evidence of the impact of such exposure on pregnancy and infant outcomes is fairly robust, the impact of prenatal opioid exposure (POE) on longer‐term outcomes for children and young people remains unclear.
Louise Marryat   +8 more
wiley   +1 more source

Cousin Syndrome Due to TBX15 Gene Variants: Three Novel Cases and Review of the Literature

open access: yesClinical Genetics, Volume 110, Issue 4, Page 480-486, October 2026.
Cousin syndrome (MIM#260660) is a rare recognizable genetic disorder characterized by short stature, pelvi‐scapular dysplasia, and craniofacial dysmorphism due to biallelic pathogenic variants in the TBX15 gene. ABSTRACT Cousin syndrome (MIM#260660) is a rare genetic disorder characterized by short stature, pelvi‐scapular dysplasia and craniofacial ...
Wafaa Alharbi   +6 more
wiley   +1 more source

Clinical and Genetic Profile of One Molecularly Confirmed and One Clinically Suspected Case of LZTR1 ‐Related Noonan Syndrome

open access: yesClinical Genetics, Volume 110, Issue 4, Page 502-507, October 2026.
This study illustrates the phenotypic variability of LZTR1‐related Noonan syndrome type 10 in two pediatric patients, including presentations without congenital heart defects. The findings emphasize the importance of whole‐exome sequencing and longitudinal re‐evaluation of variants of uncertain significance in achieving accurate diagnosis.
Karolina Skrzyńska   +3 more
wiley   +1 more source

Elucidating the Role of SET as a Key Contributor to Neurodevelopmental Disability Within the 9q34.11 Deletion Syndrome Interval

open access: yesClinical Genetics, Volume 110, Issue 4, Page 438-448, October 2026.
This study reports a female proband with a de novo 9q34.11 deletion affecting SET, who underwent a 28‐year diagnostic odyssey after an atypical Rett syndrome clinical diagnosis. Genomic and proteomics analyses confirmed SET haploinsufficiency, refining the critical 9q34.11 region, and supporting speech therapy benefits in improving meaningful ...
Angelo Condell   +14 more
wiley   +1 more source

Clearer Vision, Brighter Futures: Addressing Unmet Pediatric Eye Care Needs Through School‐Based Vision Programs

open access: yesJournal of School Health, Volume 96, Issue 10, October 2026.
ABSTRACT Background Vision impairment affects approximately 1 in 4 school‐aged children in the United States, and yet challenges in connecting to care exist. Poor vision has been linked to diminished academic performance, social development challenges, and poor mental health.
YuQing Xu, Xinxing Guo, Megan Collins
wiley   +1 more source

The Differential Diagnosis of Diplopia. [PDF]

open access: yesDtsch Arztebl Int
Lagrèze WA   +5 more
europepmc   +1 more source

Delivery and Attitude Modulate Shared Neural Processing of Speech Through Distinct Frequency Channels

open access: yesPsychophysiology, Volume 63, Issue 10, October 2026.
ABSTRACT Listeners' brains align when they attend to the same speech, but what determines how strongly they align is not well understood. We asked whether that alignment tracks the communicative relation between a listener and a message, manipulating it from the speaker's side and from the listener's, and bounding the account with a manipulation that ...
Barak Atia   +2 more
wiley   +1 more source

The use of botulinic toxin associated to surgery in non concomitant strabismus

open access: yes, 1997
We evaluated the possibility to associate conventional surgery of non concomitant squint to the use of botulinic toxin and exercises of ocular motility in 12 patients (7 M, 5 I;).
Marullo, M   +6 more
core  

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