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Academic Journal

Multimodal neuroimaging in a case of familial (G114V) juvenile Creutzfeldt-Jakob disease presenting with parkinsonism.

  • Authors : Pascovich C; Nuclear Medicine and Molecular Imaging Centre, Clinics Hospital Doctor Manuel Quintela, Faculty of Medicine, Universidad de la República, Montevideo, Uruguay.; Laboratory of Sleep Neurobiology, Department of Physiology, School of Medicine, Universidad de la República, Montevideo, Uruguay.

Subjects: Creutzfeldt-Jakob Syndrome*/Creutzfeldt-Jakob Syndrome*/Creutzfeldt-Jakob Syndrome*/diagnostic imaging ; Creutzfeldt-Jakob Syndrome*/Creutzfeldt-Jakob Syndrome*/Creutzfeldt-Jakob Syndrome*/genetics ; Creutzfeldt-Jakob Syndrome*/Creutzfeldt-Jakob Syndrome*/Creutzfeldt-Jakob Syndrome*/complications

  • Source: Neurocase [Neurocase] 2025 Dec; Vol. 31 (6), pp. 301-306. Date of Electronic Publication: 2025 Sep 26.Publisher: Routledge Country of Publication: England NLM ID: 9511374 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Expanding the genetic spectrum of corticobasal syndrome: novel CCNF p.M394L variant from a South Asian cohort.

  • Authors : Arshad F; Department of Neurology, National Institute of Mental Health and Neurosciences (nim-Hans), Bengaluru, India.; Udupi GA

Subjects: Cognitive Dysfunction*/Cognitive Dysfunction*/Cognitive Dysfunction*/genetics ; Corticobasal Degeneration*/Corticobasal Degeneration*/Corticobasal Degeneration*/genetics ; Corticobasal Degeneration*/Corticobasal Degeneration*/Corticobasal Degeneration*/diagnostic imaging

  • Source: Neurocase [Neurocase] 2025 Oct; Vol. 31 (5), pp. 221-229. Date of Electronic Publication: 2025 Oct 09.Publisher: Routledge Country of Publication: England NLM ID: 9511374 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

VPS13D-related disorders: a severe case, review, and genotype-phenotype correlation.

  • Authors : Liu WL; Department of Pediatrics, Affiliated Hospital of Guizhou Medical University, Guiyang, P.R. China.; Li F

Subjects: Developmental Disabilities*/Developmental Disabilities*/Developmental Disabilities*/genetics ; Ataxia*/Ataxia*/Ataxia*/genetics; Humans

  • Source: Neurocase [Neurocase] 2025 Aug; Vol. 31 (3), pp. 133-137. Date of Electronic Publication: 2025 Jan 15.Publisher: Routledge Country of Publication: England NLM ID: 9511374 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

The minor allele of the serotonin transporter gene variant rs4251417 is associated with increased resilience in soldiers experiencing acute stress during survival training: preliminary findings.

  • Authors : Petrovick M; Biological & Chemical Technologies, MIT Lincoln Laboratory, Lexington, MA, USA.; Shcherbina A

Subjects: Serotonin Plasma Membrane Transport Proteins*/Serotonin Plasma Membrane Transport Proteins*/Serotonin Plasma Membrane Transport Proteins*/genetics ; Resilience, Psychological* ; Military Personnel*/Military Personnel*/Military Personnel*/psychology

  • Source: Anxiety, stress, and coping [Anxiety Stress Coping] 2025 Mar; Vol. 38 (2), pp. 161-180. Date of Electronic Publication: 2024 Aug 21.Publisher: Routledge Country of Publication: England NLM ID: 9212242 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

The impact of the COVID-19 pandemic on alcohol use disorder symptoms: Testing interactions with polygenic risk.

Subjects: COVID-19*/COVID-19*/COVID-19*/epidemiology ; COVID-19*/COVID-19*/COVID-19*/psychology ; Students*/Students*/Students*/statistics & numerical data

  • Source: Journal of American college health : J of ACH [J Am Coll Health] 2025 Apr; Vol. 73 (4), pp. 1532-1537. Date of Electronic Publication: 2024 Feb 08.Publisher: Routledge Country of Publication: United States NLM ID: 8214119 Publication Model: Print-Electronic Cited Medium:

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  • 1-10 of  1,502 results for ""genetics""