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Children and young people's understanding of inherited conditions and their attitudes towards genetic testing: A systematic review

• Authors : McGill, BC ; https://orcid.org/0000-0002-2134-2988; Wakefield, CE

Subjects: 31 Biological Sciences; 3105 Genetics; Prevention

• Source: urn:ISSN:0009-9163; urn:ISSN:1399-0004; Clinical Genetics, 95, 1, 10-22

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Pathology of inherited conditions

• Source: Pathology International. 54

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Children and young people's understanding of inherited conditions and their attitudes towards genetic testing: A systematic review

• Authors : McGill, BC; Wakefield, CE; Vetsch, J

Subjects: 31 Biological Sciences; 3105 Genetics; Clinical Research

• Source: urn:ISSN:0009-9163 ; urn:ISSN:1399-0004 ; Clinical Genetics, 95, 1, 10-22

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A Genetic Counseling Intervention to Facilitate Family Communication About Inherited Conditions

• Authors : Gaff, Clara; Hodgson, Jan

• Source: Journal of Genetic Counseling ; volume 23, issue 5, page 814-823 ; ISSN 1059-7700 1573-3599

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Dual effects of mefenamic acid on the IKs molecular complex.

• Authors : Chan M; Department of Anesthesiology, Pharmacology and Therapeutics, University of British Columbia, Vancouver, British Columbia, Canada.; Pourrier M

Subjects: Mefenamic Acid*/Mefenamic Acid*/Mefenamic Acid*/pharmacology ; Potassium Channels, Voltage-Gated*/Potassium Channels, Voltage-Gated*/Potassium Channels, Voltage-Gated*/genetics ; Potassium Channels, Voltage-Gated*/Potassium Channels, Voltage-Gated*/Potassium Channels, Voltage-Gated*/metabolism

• Source: British journal of pharmacology [Br J Pharmacol] 2025 Feb; Vol. 182 (4), pp. 1075-1089. Date of Electronic Publication: 2024 Nov 08.Publisher: Wiley Country of Publication: England NLM ID: 7502536 Publication Model: Print-Electronic Cited Medium:

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A Review of CEBPA's Role in Hereditary Leukemia

• Authors : Tara Rakiewicz; Neil Palmisiano

Subjects: acute myeloid leukemia; CEBPA; familial

• Source: eJHaem, Vol 7, Iss 2, Pp n/a-n/a (2026)

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A Multisystem Perspective of Pediatric Cell Trafficking Disorders: Within the Cells, Beneath the Signs

• Authors : Merve Yoldaş Çelik; Burcu Köşeci; Ezgi Burgaç

Subjects: cellular trafficking disorders; CTD; endoplasmic reticulum dysfunction

• Source: JIMD Reports, Vol 67, Iss 1, Pp n/a-n/a (2026)

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High‐intensity focused ultrasound: Safety and efficacy of a novel treatment modality for neurofibromatosis type 1 cutaneous neurofibroma

• Authors : Sirkku Peltonen; Jørgen Serup; Mimmi Tang

Subjects: clinical trials; dermatologic therapy; genetic skin disorders

• Source: JEADV Clinical Practice, Vol 3, Iss 4, Pp 1049-1060 (2024)

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Catecholaminergic Polymorphic Ventricular Tachycardia: Advancing From Molecular Insights to Preclinical Models

• Authors : Luca Schneider; Merima Begovic; Xiaobo Zhou

Subjects: 3‐dimensional engineered heart; catecholaminergic polymorphic ventricular tachycardia; CRISPR/Cas9 genome editing

• Source: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 14, Iss 6 (2025)

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A novel TERT variant associated with a telomere biology disorder and challenges in variant classification

• Authors : Vahid Pazhakh; Lucy C. Fox; Nicole Den Elzen

Subjects: genetic anticipation; telomerase activity; telomere biology disorders

• Source: eJHaem, Vol 6, Iss 1, Pp n/a-n/a (2025)

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