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10 merged results for "Prader Willi Syndrome Association"

Partial results: at least one source did not answer. Available results are shown rather than treating an upstream outage as zero matches.

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  1. Influence of Molecular Genetic Classes on Behavior in Prader-Willi Syndrome.

    Mahmoud R, Butler MG, Park W, Miller JL · 2026 · American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1002/ajmg.b.70034

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  2. Use of Electroconvulsive Therapy for Catatonia in Down Syndrome Regression Disorder: A Systematic Review, Case Series, and Analysis.

    Lim S, Kang K, Oey E, Santoro S · 2026 · Journal of autism and developmental disorders

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1007/s10803-026-07500-3

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  3. An exploratory retrospective analysis of concurrent metabolic and behavioral change in Prader-Willi syndrome during interdisciplinary inpatient stabilization.

    Ravindranathan G, Stockton B, Finnerty J, Collier A · 2026 · Journal of psychiatric research

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1016/j.jpsychires.2026.09.012

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  4. Prevalence of pulmonary hypertension in children with Prader-Willi Syndrome.

    Kohn S, Evans M, Itani R, Wang S · 2026 · Sleep medicine

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1016/j.sleep.2026.109190

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  5. Targeted Epigenetic Reactivation strategies as new treatments for Prader-Willi Syndrome: Achievements and Challenges.

    Alberti S, Cutei I, Broccardi GC, Broccoli V · 2026 · Molecular therapy : the journal of the American Society of Gene Therapy

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1016/j.ymthe.2026.09.023

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  6. Spinal Fusion in Prader-Willi Syndrome: Early Radiographic Outcomes and Complications With a Subset Analysis of Two-year Follow-up in a Multicenter Cohort.

    Lobato AG, Andras L, Vaughan M, Ramo BA · 2026 · Journal of pediatric orthopedics

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1097/bpo.0000000000003467

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  7. Case report: Tirzepatide-responsive refractory diabetes mellitus in an adult female with prader-willi syndrome.

    Li S, Yu J, Wei J, Liang M · 2026 · Medicine

    limited evidence Transparent signal score 45/100 · policy 1.0.0

    Found in pubmed · DOI 10.1097/md.0000000000050605

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    • supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  8. Diagnosing the canvas: challenging the diagnosis of Prader-Willi syndrome in Eugenia Martínez Vallejo (1674-1699).

    Hamiel U, Pinhas-Hamiel O · 2026 · The Journal of clinical endocrinology and metabolism

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in pubmed · DOI 10.1210/clinem/dgag287

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  9. Pulmonary Artery Thromboembolism (PATE) in Paediatrics: Three Clinical Case Presentations.

    Asipauskaitė G, Miškinaitė G, Dagys A, Gurskis V · 2026 · Acta medica Lituanica

    limited evidence Transparent signal score 45/100 · policy 1.0.0

    Found in pubmed · DOI 10.15388/amed.2026.33.1.24

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    • supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  10. A Clinical Genetics-Driven Dual Diagnosis of Prader-Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL.

    Bogliardi FM, D'Ambrosio P, Quattromini G, Di Mario G · 2026 · Genes

    limited evidence Transparent signal score 45/100 · policy 1.0.0

    Found in pubmed · DOI 10.3390/genes17080937

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    • supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer