Results 191 to 200 of about 2,033,952 (257)

Just-in-Time Adaptive Intervention for Smoking Cessation in Low-Income Adults: A Randomized Clinical Trial.

JAMA Netw Open
Hébert ET, Kendzor DE, Vidrine DJ, Langford JS, Kezbers KM, Montgomery A, Chen M, Frank-Pearce SG, Vesely SK, Chen S, Barrett ZCW, Businelle MS.   +11 more
europepmc   +1 more source

Just-In-Time Adaptive Interventions to Promote Behavioral Health: Protocol for a Systematic Review. [PDF]

JMIR Res Protoc
Henry LM, Blay-Tofey M, Haeffner CE, Raymond CN, Tandilashvili E, Terry N, Kiderman M, Metcalf O, Brotman MA, Lopez-Guzman S.   +9 more
europepmc   +1 more source

Compound Heterozygote Friedreich Ataxia Patients With Covert Proximal FXN Gene Deletions

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT We present Friedreich ataxia patients with frataxin gene deletions. Data and records were collected at the Children's Hospital of Philadelphia from patients enrolled in the FACOMS natural history study. Patients with proximal deletions initially diagnosed with only one GAA expanded allele had more severe disease than their homozygous expansion
Michael P. Lazaropoulos, Morgan C. Devore, Christina Lam, Courtney Park, Sanjay Bidichandani, David R. Lynch   +5 more
wiley   +1 more source

Suitability of just-in-time adaptive intervention in post-COVID-19-related symptoms: A systematic scoping review. [PDF]

PLOS Digit Health
Schaap G, Butt B, Bode C.
europepmc   +1 more source

Sertraline Treatment Can Mimic Niemann‐Pick Type C Biomarker Profile: A Diagnostic Pitfall

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Oxysterols (cholestane‐3β,5α,6β‐triol and 7‐ketocholesterol) and N‐palmitoyl‐O‐phosphocholineserine (PPCS) are sensitive biomarkers for Niemann‐Pick disease type C (NPC) screening. However, false‐positive results occur, with a biomarker profile suggestive of NPC despite the absence of pathogenic variants in genes involved in NPC or ...
Maria Makrygianni, Cecile Pagan, Antony Citterio‐Quentin, Isabelle Rouvet, Giulia Dingeo, Cyril Hanin, Claudine Laurent‐Levinson, Samia Pichard, Bénédicte Héron, Clément Gourguechon, Daniele Mandia, Jerome Guitton, Carole Lacout, Nicolas Schleinitz, Florient Potier, Olivier Flabeau, Elsa Besse‐Pinot, Foudil Lamari, Magali Pettazzoni, Yann Nadjar   +19 more
wiley   +1 more source

A pilot effectiveness study of a just-in-time micro-randomized controlled trial on the physical activity and sedentary time of young children and their parents: The active family m-health intervention. [PDF]

PLoS One
Phillips SM, Bourke M, Inniss BV, Ahluwalia M, Tucker P.   +4 more
europepmc   +1 more source

MOGAD Is the Most Common Cause of Isolated Optic Neuritis in Children

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives The study aimed to characterize the clinical features, etiologies, and outcomes of isolated, first‐time pediatric ON in the post‐MOG‐IgG era. Methods This was a single‐center retrospective cohort study at Texas Children's Hospital of patients diagnosed with first‐time ON between 2018–2024, with follow‐up data collected through 2025.
Chaitanya Aduru, Akansha Chandrasekar, Kyla Blasingame, Jonathan Rosen, Jesse M. Levine, Karla Salazar, Madhuri Chilakapati, Rod Foroozan, Victoria Hardwick, Jonathan M. Yarimi, Nikita Shukla, Timothy E. Lotze, Kristen S. Fisher, Alexander J. Sandweiss   +13 more
wiley   +1 more source

A just-in-time adaptive mobile application intervention to reduce sodium intake and blood pressure in patients with hypertension: Rationale and design of the LowSalt4Life 2 trial. [PDF]

Am Heart J
Dorsch MP, Dempsey W, Krambrink A, Ganai S, Greer KM, Ali MS, Gesierich C, O'Neill M, Nallamothu BK, Hummel SL.   +9 more
europepmc   +1 more source

Clinical Impact of NOTCH3 Variant Location After First Stroke in CADASIL

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Despite its monogenic origin, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy exhibits marked variability in clinical expression and severity. Variants in the NOTCH3 gene, within epidermal growth factor‐like repeat domains 1–6 or 7–34, are known to influence disease onset, but their impact ...
Léa Aguilhon, Hugues Chabriat, Dominique Hervé, Stéphanie Guey, Sophie Tezenas Du Montcel, Juliette Ortholand   +5 more
wiley   +1 more source

Personalized interventions for behaviour change: A scoping review of just-in-time adaptive interventions. [PDF]

Br J Health Psychol
Hsu TC, Whelan P, Gandrup J, Armitage CJ, Cordingley L, McBeth J.   +5 more
europepmc   +1 more source